© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophun1|2808 |
| Gene name | |
| Location | Contig_25:43161..52818 |
| Strand | - |
| Gene length (bp) | 9657 |
| Transcript length (bp) | 8544 |
| Coding sequence length (bp) | 8544 |
| Protein length (aa) | 2848 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00109 | ketoacyl-synt | Beta-ketoacyl synthase, N-terminal domain | 1.2E-70 | 299 | 550 |
| PF08659 | KR | KR domain | 3.3E-62 | 2455 | 2632 |
| PF00698 | Acyl_transf_1 | Acyl transferase domain | 1.2E-49 | 831 | 1114 |
| PF14765 | PS-DH | Polyketide synthase dehydratase | 2.0E-47 | 1210 | 1496 |
| PF02801 | Ketoacyl-synt_C | Beta-ketoacyl synthase, C-terminal domain | 7.8E-32 | 559 | 673 |
| PF08242 | Methyltransf_12 | Methyltransferase domain | 1.5E-17 | 1724 | 1831 |
| PF16197 | KAsynt_C_assoc | Ketoacyl-synthetase C-terminal extension | 8.3E-17 | 676 | 799 |
| PF00107 | ADH_zinc_N | Zinc-binding dehydrogenase | 3.6E-15 | 2258 | 2360 |
| PF03959 | FSH1 | Serine hydrolase (FSH1) | 7.6E-14 | 2 | 273 |
| PF13602 | ADH_zinc_N_2 | Zinc-binding dehydrogenase | 1.8E-11 | 2296 | 2431 |
| PF13649 | Methyltransf_25 | Methyltransferase domain | 1.1E-10 | 1723 | 1829 |
| PF00106 | adh_short | short chain dehydrogenase | 5.5E-10 | 2458 | 2604 |
| PF08241 | Methyltransf_11 | Methyltransferase domain | 1.7E-09 | 1724 | 1833 |
| PF13489 | Methyltransf_23 | Methyltransferase domain | 1.1E-09 | 1717 | 1881 |
| PF13847 | Methyltransf_31 | Methyltransferase domain | 9.9E-08 | 1719 | 1837 |
| PF01209 | Ubie_methyltran | ubiE/COQ5 methyltransferase family | 1.6E-05 | 1713 | 1839 |
| PF00550 | PP-binding | Phosphopantetheine attachment site | 3.7E-05 | 2760 | 2811 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q9Y7D5|LOVF_ASPTE | Lovastatin diketide synthase LovF OS=Aspergillus terreus GN=lovF PE=1 SV=1 | 296 | 2829 | 0.0E+00 |
| sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 300 | 2843 | 0.0E+00 |
| sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 300 | 2843 | 0.0E+00 |
| sp|A1CLY8|CCSA_ASPCL | Polyketide synthase-nonribosomal peptide synthetase OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=ccsA PE=3 SV=1 | 300 | 2094 | 0.0E+00 |
| sp|Q4WAZ9|NRP14_ASPFU | Nonribosomal peptide synthetase 14 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=NRPS14 PE=2 SV=2 | 300 | 2112 | 0.0E+00 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q9Y7D5|LOVF_ASPTE | Lovastatin diketide synthase LovF OS=Aspergillus terreus GN=lovF PE=1 SV=1 | 296 | 2829 | 0.0E+00 |
| sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 300 | 2843 | 0.0E+00 |
| sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 300 | 2843 | 0.0E+00 |
| sp|A1CLY8|CCSA_ASPCL | Polyketide synthase-nonribosomal peptide synthetase OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=ccsA PE=3 SV=1 | 300 | 2094 | 0.0E+00 |
| sp|Q4WAZ9|NRP14_ASPFU | Nonribosomal peptide synthetase 14 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=NRPS14 PE=2 SV=2 | 300 | 2112 | 0.0E+00 |
| sp|Q7TXL7|PPSD_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsD PE=3 SV=1 | 300 | 1475 | 9.0E-134 |
| sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 300 | 1475 | 1.0E-133 |
| sp|P9WQE2|PPSD_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsD PE=3 SV=1 | 300 | 1475 | 1.0E-133 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 289 | 1444 | 2.0E-127 |
| sp|P22367|MSAS_PENPA | 6-methylsalicylic acid synthase OS=Penicillium patulum PE=1 SV=1 | 288 | 1261 | 2.0E-125 |
| sp|Q7TXL9|PPSB_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsB PE=1 SV=1 | 282 | 1093 | 3.0E-123 |
| sp|P9WQE5|PPSB_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsB PE=1 SV=1 | 282 | 1093 | 4.0E-123 |
| sp|P9WQE4|PPSB_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsB PE=3 SV=1 | 282 | 1093 | 4.0E-123 |
| sp|P96202|PPSC_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsC PE=1 SV=2 | 300 | 1529 | 2.0E-122 |
| sp|Q7TXL8|PPSC_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsC PE=1 SV=1 | 300 | 1529 | 2.0E-122 |
| sp|P9WQE9|PHAS_MYCTU | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks2 PE=1 SV=1 | 300 | 1264 | 4.0E-120 |
| sp|P9WQE8|PHAS_MYCTO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=pks2 PE=3 SV=1 | 300 | 1264 | 4.0E-120 |
| sp|A5U9F4|PHAS_MYCTA | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=pks2 PE=3 SV=1 | 300 | 1264 | 4.0E-120 |
| sp|Q7TVK8|PHAS_MYCBO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks2 PE=3 SV=1 | 300 | 1264 | 4.0E-120 |
| sp|A1KQG0|PHAS_MYCBP | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=pks2 PE=3 SV=1 | 300 | 1264 | 8.0E-120 |
| sp|B4XYB8|AZIB_STREG | 5-methyl-1-naphthoate synthase OS=Streptomyces sahachiroi GN=aziB PE=1 SV=1 | 292 | 1262 | 1.0E-119 |
| sp|Q869W9|PKS16_DICDI | Probable polyketide synthase 16 OS=Dictyostelium discoideum GN=pks16 PE=2 SV=1 | 299 | 1446 | 2.0E-119 |
| sp|Q869X2|PKS17_DICDI | Probable polyketide synthase 17 OS=Dictyostelium discoideum GN=pks17 PE=3 SV=1 | 299 | 1446 | 1.0E-118 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 300 | 1193 | 4.0E-118 |
| sp|Q7TXK8|MSL7_MYCBO | Phenolphthiocerol synthesis polyketide synthase type I Pks15/1 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks15/1 PE=1 SV=1 | 300 | 1288 | 2.0E-117 |
| sp|B2HIL7|MSL7_MYCMM | Phenolphthiocerol synthesis polyketide synthase type I Pks15/1 OS=Mycobacterium marinum (strain ATCC BAA-535 / M) GN=pks15/1 PE=1 SV=1 | 300 | 1456 | 5.0E-117 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 300 | 1120 | 1.0E-116 |
| sp|P9WQE6|PPSA_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsA PE=3 SV=1 | 300 | 1113 | 1.0E-115 |
| sp|P9WQE7|PPSA_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsA PE=1 SV=1 | 300 | 1113 | 2.0E-115 |
| sp|Q7TXM0|PPSA_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsA PE=1 SV=1 | 300 | 1113 | 2.0E-115 |
| sp|Q02251|MCAS_MYCBO | Mycocerosic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mas PE=1 SV=2 | 300 | 1276 | 5.0E-115 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 300 | 1193 | 7.0E-115 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 289 | 1215 | 7.0E-115 |
| sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 299 | 1887 | 1.0E-113 |
| sp|Q55E72|PKS1_DICDI | Probable polyketide synthase 1 OS=Dictyostelium discoideum GN=stlA PE=1 SV=1 | 299 | 1261 | 2.0E-113 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 271 | 1113 | 3.0E-113 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 273 | 1084 | 1.0E-112 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 300 | 1120 | 1.0E-110 |
| sp|P12276|FAS_CHICK | Fatty acid synthase OS=Gallus gallus GN=FASN PE=1 SV=5 | 299 | 1113 | 2.0E-102 |
| sp|P19096|FAS_MOUSE | Fatty acid synthase OS=Mus musculus GN=Fasn PE=1 SV=2 | 299 | 1263 | 3.0E-102 |
| sp|P49327|FAS_HUMAN | Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 | 299 | 1292 | 8.0E-102 |
| sp|Q54IX3|PKS26_DICDI | Probable polyketide synthase 26 OS=Dictyostelium discoideum GN=pks26 PE=3 SV=1 | 299 | 1419 | 3.0E-101 |
| sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 299 | 1197 | 6.0E-101 |
| sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 299 | 1260 | 2.0E-99 |
| sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 299 | 1260 | 3.0E-99 |
| sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 300 | 1261 | 4.0E-99 |
| sp|Q03149|WA_EMENI | Conidial yellow pigment biosynthesis polyketide synthase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=wA PE=1 SV=2 | 300 | 1115 | 1.0E-98 |
| sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 299 | 1303 | 3.0E-98 |
| sp|B0G103|PKS10_DICDI | Probable polyketide synthase 10 OS=Dictyostelium discoideum GN=pks10 PE=3 SV=1 | 299 | 1286 | 6.0E-98 |
| sp|Q559A9|PKS13_DICDI | Probable polyketide synthase 13 OS=Dictyostelium discoideum GN=pks13 PE=3 SV=1 | 299 | 1264 | 2.0E-97 |
| sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 299 | 1260 | 8.0E-97 |
| sp|B0G138|PKS21_DICDI | Probable polyketide synthase 21 OS=Dictyostelium discoideum GN=pks21 PE=3 SV=1 | 358 | 1254 | 8.0E-97 |
| sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 300 | 1261 | 3.0E-96 |
| sp|Q12053|PKSL1_ASPPA | Noranthrone synthase OS=Aspergillus parasiticus GN=pksL1 PE=1 SV=1 | 267 | 1115 | 7.0E-96 |
| sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 273 | 1260 | 8.0E-96 |
| sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 358 | 1254 | 4.0E-95 |
| sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 285 | 1261 | 4.0E-95 |
| sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 300 | 1278 | 1.0E-94 |
| sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 301 | 1260 | 1.0E-94 |
| sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 299 | 1256 | 5.0E-94 |
| sp|B0G0Z9|PKS6_DICDI | Probable polyketide synthase 6 OS=Dictyostelium discoideum GN=pks6 PE=3 SV=1 | 292 | 1307 | 6.0E-94 |
| sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 300 | 1260 | 6.0E-94 |
| sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 294 | 1307 | 6.0E-94 |
| sp|B0G101|PKS8_DICDI | Probable polyketide synthase 8/35 OS=Dictyostelium discoideum GN=pks8 PE=3 SV=1 | 292 | 1307 | 3.0E-93 |
| sp|Q54KU5|PKS24_DICDI | Probable polyketide synthase 24 OS=Dictyostelium discoideum GN=pks24 PE=3 SV=1 | 300 | 1261 | 4.0E-93 |
| sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 299 | 1254 | 6.0E-93 |
| sp|Q55CN6|PKS3_DICDI | Probable polyketide synthase 3 OS=Dictyostelium discoideum GN=pks3 PE=3 SV=1 | 358 | 1423 | 1.0E-92 |
| sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 300 | 1263 | 3.0E-92 |
| sp|B0G100|PKS7_DICDI | Probable polyketide synthase 7 OS=Dictyostelium discoideum GN=pks7 PE=3 SV=1 | 294 | 1265 | 1.0E-91 |
| sp|Q54B49|PKS45_DICDI | Probable polyketide synthase 45 OS=Dictyostelium discoideum GN=pks45 PE=3 SV=2 | 299 | 1403 | 1.0E-91 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 300 | 1263 | 4.0E-91 |
| sp|Q54B51|PKS44_DICDI | Probable polyketide synthase 44 OS=Dictyostelium discoideum GN=pks44 PE=3 SV=1 | 299 | 1263 | 4.0E-91 |
| sp|Q55DM7|PKS2_DICDI | Probable polyketide synthase 2 OS=Dictyostelium discoideum GN=pks2 PE=3 SV=1 | 299 | 1286 | 1.0E-90 |
| sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 299 | 1260 | 3.0E-90 |
| sp|Q86JI5|PKS5_DICDI | Probable polyketide synthase 5 OS=Dictyostelium discoideum GN=pks5 PE=2 SV=1 | 292 | 1265 | 2.0E-89 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 300 | 808 | 7.0E-89 |
| sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 293 | 1261 | 1.0E-88 |
| sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 299 | 1260 | 3.0E-87 |
| sp|Q12397|STCA_EMENI | Putative sterigmatocystin biosynthesis polyketide synthase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=stcA PE=3 SV=2 | 300 | 1115 | 9.0E-87 |
| sp|P96284|PKS15_MYCTU | Putative inactive phenolphthiocerol synthesis polyketide synthase type I Pks15 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks15 PE=1 SV=2 | 300 | 720 | 9.0E-85 |
| sp|Q7TXL6|PPSE_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsE PE=1 SV=1 | 300 | 1201 | 1.0E-83 |
| sp|P9WQE1|PPSE_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsE PE=1 SV=1 | 300 | 1201 | 1.0E-83 |
| sp|P9WQE0|PPSE_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsE PE=3 SV=1 | 300 | 1201 | 1.0E-83 |
| sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 300 | 713 | 5.0E-79 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 292 | 809 | 6.0E-79 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 226 | 835 | 1.0E-78 |
| sp|P96202|PPSC_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsC PE=1 SV=2 | 2067 | 2802 | 1.0E-76 |
| sp|Q7TXL8|PPSC_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsC PE=1 SV=1 | 2067 | 2802 | 1.0E-76 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 300 | 811 | 1.0E-74 |
| sp|Q55E72|PKS1_DICDI | Probable polyketide synthase 1 OS=Dictyostelium discoideum GN=stlA PE=1 SV=1 | 1646 | 2824 | 4.0E-74 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 293 | 809 | 6.0E-74 |
| sp|Q9R9J1|MYCA_BACIU | Mycosubtilin synthase subunit A OS=Bacillus subtilis GN=mycA PE=3 SV=1 | 296 | 808 | 4.0E-73 |
| sp|Q7TXK8|MSL7_MYCBO | Phenolphthiocerol synthesis polyketide synthase type I Pks15/1 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks15/1 PE=1 SV=1 | 2156 | 2798 | 2.0E-72 |
| sp|P96285|PKS1_MYCTU | Putative inactive phenolphthiocerol synthesis polyketide synthase type I Pks1 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks1 PE=1 SV=4 | 2156 | 2798 | 4.0E-72 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 287 | 809 | 5.0E-72 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 299 | 821 | 3.0E-70 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 296 | 808 | 7.0E-69 |
| sp|B2HIL7|MSL7_MYCMM | Phenolphthiocerol synthesis polyketide synthase type I Pks15/1 OS=Mycobacterium marinum (strain ATCC BAA-535 / M) GN=pks15/1 PE=1 SV=1 | 2120 | 2804 | 1.0E-68 |
| sp|P36189|FAS_ANSAN | Fatty acid synthase (Fragment) OS=Anser anser anser GN=FASN PE=1 SV=1 | 299 | 666 | 2.0E-66 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 2127 | 2817 | 6.0E-66 |
| sp|Q02251|MCAS_MYCBO | Mycocerosic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mas PE=1 SV=2 | 1987 | 2643 | 1.0E-64 |
| sp|P12276|FAS_CHICK | Fatty acid synthase OS=Gallus gallus GN=FASN PE=1 SV=5 | 1976 | 2635 | 5.0E-64 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 296 | 808 | 2.0E-61 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 300 | 808 | 4.0E-61 |
| sp|P9WQE9|PHAS_MYCTU | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks2 PE=1 SV=1 | 2075 | 2635 | 1.0E-57 |
| sp|P9WQE8|PHAS_MYCTO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=pks2 PE=3 SV=1 | 2075 | 2635 | 1.0E-57 |
| sp|A5U9F4|PHAS_MYCTA | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=pks2 PE=3 SV=1 | 2075 | 2635 | 1.0E-57 |
| sp|Q7TVK8|PHAS_MYCBO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks2 PE=3 SV=1 | 2075 | 2635 | 1.0E-57 |
| sp|A1KQG0|PHAS_MYCBP | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=pks2 PE=3 SV=1 | 2075 | 2635 | 1.0E-57 |
| sp|P19096|FAS_MOUSE | Fatty acid synthase OS=Mus musculus GN=Fasn PE=1 SV=2 | 2156 | 2639 | 7.0E-56 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 300 | 721 | 3.0E-55 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 299 | 720 | 3.0E-55 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 300 | 807 | 5.0E-55 |
| sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 2156 | 2639 | 6.0E-55 |
| sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 2186 | 2639 | 1.0E-54 |
| sp|P49327|FAS_HUMAN | Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 | 1944 | 2639 | 2.0E-54 |
| sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 2142 | 2660 | 2.0E-54 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 268 | 722 | 6.0E-53 |
| sp|Q86JI5|PKS5_DICDI | Probable polyketide synthase 5 OS=Dictyostelium discoideum GN=pks5 PE=2 SV=1 | 1724 | 2802 | 2.0E-52 |
| sp|Q54IX3|PKS26_DICDI | Probable polyketide synthase 26 OS=Dictyostelium discoideum GN=pks26 PE=3 SV=1 | 1716 | 2802 | 2.0E-50 |
| sp|Q559A9|PKS13_DICDI | Probable polyketide synthase 13 OS=Dictyostelium discoideum GN=pks13 PE=3 SV=1 | 1692 | 2819 | 2.0E-50 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 300 | 809 | 1.0E-49 |
| sp|B0G0Z9|PKS6_DICDI | Probable polyketide synthase 6 OS=Dictyostelium discoideum GN=pks6 PE=3 SV=1 | 1587 | 2802 | 6.0E-49 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 293 | 721 | 9.0E-49 |
| sp|B0G101|PKS8_DICDI | Probable polyketide synthase 8/35 OS=Dictyostelium discoideum GN=pks8 PE=3 SV=1 | 1724 | 2802 | 5.0E-45 |
| sp|B0G100|PKS7_DICDI | Probable polyketide synthase 7 OS=Dictyostelium discoideum GN=pks7 PE=3 SV=1 | 1724 | 2802 | 9.0E-44 |
| sp|Q55CN6|PKS3_DICDI | Probable polyketide synthase 3 OS=Dictyostelium discoideum GN=pks3 PE=3 SV=1 | 2069 | 2845 | 1.0E-41 |
| sp|Q869X2|PKS17_DICDI | Probable polyketide synthase 17 OS=Dictyostelium discoideum GN=pks17 PE=3 SV=1 | 2153 | 2806 | 7.0E-41 |
| sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 2045 | 2820 | 7.0E-41 |
| sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 1775 | 2828 | 1.0E-40 |
| sp|Q4WAZ9|NRP14_ASPFU | Nonribosomal peptide synthetase 14 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=NRPS14 PE=2 SV=2 | 2451 | 2826 | 4.0E-40 |
| sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 2138 | 2801 | 4.0E-40 |
| sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 2095 | 2806 | 4.0E-39 |
| sp|Q869W9|PKS16_DICDI | Probable polyketide synthase 16 OS=Dictyostelium discoideum GN=pks16 PE=2 SV=1 | 2153 | 2806 | 1.0E-37 |
| sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 2164 | 2806 | 2.0E-37 |
| sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 2164 | 2806 | 2.0E-37 |
| sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 2166 | 2806 | 2.0E-36 |
| sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 2164 | 2806 | 8.0E-36 |
| sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 2164 | 2806 | 1.0E-35 |
| sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 2164 | 2802 | 4.0E-35 |
| sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 2167 | 2824 | 2.0E-33 |
| sp|Q54KU5|PKS24_DICDI | Probable polyketide synthase 24 OS=Dictyostelium discoideum GN=pks24 PE=3 SV=1 | 2161 | 2801 | 3.0E-33 |
| sp|P96285|PKS1_MYCTU | Putative inactive phenolphthiocerol synthesis polyketide synthase type I Pks1 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks1 PE=1 SV=4 | 789 | 1288 | 9.0E-33 |
| sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 2144 | 2802 | 1.0E-32 |
| sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 2164 | 2802 | 1.0E-32 |
| sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 2162 | 2841 | 6.0E-32 |
| sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 2164 | 2802 | 8.0E-32 |
| sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 2139 | 2836 | 1.0E-30 |
| sp|Q55DM7|PKS2_DICDI | Probable polyketide synthase 2 OS=Dictyostelium discoideum GN=pks2 PE=3 SV=1 | 1715 | 2820 | 6.0E-30 |
| sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 2164 | 2806 | 1.0E-29 |
| sp|A1CLY8|CCSA_ASPCL | Polyketide synthase-nonribosomal peptide synthetase OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=ccsA PE=3 SV=1 | 2437 | 2832 | 9.0E-28 |
| sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 2139 | 2826 | 1.0E-27 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 825 | 1415 | 2.0E-27 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 820 | 1160 | 1.0E-24 |
| sp|Q54B51|PKS44_DICDI | Probable polyketide synthase 44 OS=Dictyostelium discoideum GN=pks44 PE=3 SV=1 | 2162 | 2825 | 1.0E-24 |
| sp|P22367|MSAS_PENPA | 6-methylsalicylic acid synthase OS=Penicillium patulum PE=1 SV=1 | 2453 | 2668 | 1.0E-23 |
| sp|Q54B49|PKS45_DICDI | Probable polyketide synthase 45 OS=Dictyostelium discoideum GN=pks45 PE=3 SV=2 | 2162 | 2825 | 7.0E-23 |
| sp|B4XYB8|AZIB_STREG | 5-methyl-1-naphthoate synthase OS=Streptomyces sahachiroi GN=aziB PE=1 SV=1 | 2443 | 2826 | 2.0E-22 |
| sp|P16538|KAS1_STRGA | Tetracenomycin C polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces glaucescens GN=tcmK PE=3 SV=1 | 300 | 720 | 2.0E-22 |
| sp|Q83E37|FABF_COXBU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Coxiella burnetii (strain RSA 493 / Nine Mile phase I) GN=fabF PE=1 SV=1 | 389 | 720 | 7.0E-22 |
| sp|P04684|NODE_RHILT | Nodulation protein E OS=Rhizobium leguminosarum bv. trifolii GN=nodE PE=3 SV=2 | 383 | 715 | 4.0E-21 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 1716 | 1887 | 4.0E-20 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 2453 | 2799 | 5.0E-20 |
| sp|Q02578|KAS1_STRCN | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cyaneus GN=curA PE=3 SV=1 | 445 | 724 | 6.0E-20 |
| sp|P06230|NODE_RHIME | Nodulation protein E OS=Rhizobium meliloti (strain 1021) GN=nodE PE=3 SV=1 | 383 | 715 | 7.0E-20 |
| sp|P06231|NOE4_RHIML | Nodulation protein E OS=Rhizobium meliloti GN=nodE PE=3 SV=1 | 383 | 715 | 8.0E-20 |
| sp|Q8JFV8|VAT1_DANRE | Synaptic vesicle membrane protein VAT-1 homolog OS=Danio rerio GN=vat1 PE=2 SV=1 | 2144 | 2435 | 9.0E-20 |
| sp|Q9D404|OXSM_MOUSE | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Mus musculus GN=Oxsm PE=1 SV=1 | 448 | 722 | 1.0E-19 |
| sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 1716 | 1887 | 2.0E-19 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 2144 | 2431 | 2.0E-19 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 2471 | 2668 | 5.0E-19 |
| sp|P41175|KAS1_STRCM | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cinnamonensis PE=3 SV=1 | 300 | 723 | 7.0E-19 |
| sp|P72331|NODE_RHIS3 | Nodulation protein E OS=Rhizobium sp. (strain N33) GN=nodE PE=3 SV=1 | 450 | 715 | 7.0E-19 |
| sp|Q05356|KAS1_STRHA | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces halstedii GN=sch1 PE=3 SV=1 | 447 | 722 | 1.0E-18 |
| sp|P23155|KAS1_STRCO | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO5318 PE=3 SV=1 | 300 | 723 | 3.0E-18 |
| sp|Q99536|VAT1_HUMAN | Synaptic vesicle membrane protein VAT-1 homolog OS=Homo sapiens GN=VAT1 PE=1 SV=2 | 2170 | 2438 | 4.0E-18 |
| sp|O97764|QOR_BOVIN | Zeta-crystallin OS=Bos taurus GN=CRYZ PE=2 SV=2 | 2170 | 2352 | 4.0E-18 |
| sp|P9WQE6|PPSA_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsA PE=3 SV=1 | 2449 | 2827 | 5.0E-18 |
| sp|P9WQE7|PPSA_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsA PE=1 SV=1 | 2449 | 2827 | 5.0E-18 |
| sp|Q7TXM0|PPSA_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsA PE=1 SV=1 | 2449 | 2827 | 5.0E-18 |
| sp|Q5R4S7|QOR_PONAB | Quinone oxidoreductase OS=Pongo abelii GN=CRYZ PE=2 SV=1 | 2170 | 2366 | 7.0E-18 |
| sp|Q0VCA7|OXSM_BOVIN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Bos taurus GN=OXSM PE=2 SV=1 | 448 | 722 | 9.0E-18 |
| sp|Q08257|QOR_HUMAN | Quinone oxidoreductase OS=Homo sapiens GN=CRYZ PE=1 SV=1 | 2143 | 2366 | 9.0E-18 |
| sp|Q9NWU1|OXSM_HUMAN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Homo sapiens GN=OXSM PE=1 SV=1 | 448 | 722 | 1.0E-17 |
| sp|P04683|NODE_RHILV | Nodulation protein E OS=Rhizobium leguminosarum bv. viciae GN=nodE PE=3 SV=2 | 425 | 715 | 1.0E-17 |
| sp|P9WQD7|FAB2_MYCTU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kasB PE=1 SV=1 | 504 | 715 | 1.0E-17 |
| sp|P9WQD6|FAB2_MYCTO | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=kasB PE=3 SV=1 | 504 | 715 | 1.0E-17 |
| sp|P63457|FAB2_MYCBO | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=kasB PE=3 SV=1 | 504 | 715 | 1.0E-17 |
| sp|Q02059|KASA_STRCO | Actinorhodin polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO5087 PE=1 SV=2 | 300 | 720 | 4.0E-17 |
| sp|P52410|KASC1_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Arabidopsis thaliana GN=KAS1 PE=2 SV=2 | 318 | 715 | 5.0E-17 |
| sp|Q5TKS0|FABF_STAAU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 (Fragment) OS=Staphylococcus aureus GN=fabF PE=3 SV=1 | 448 | 720 | 5.0E-17 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 2387 | 2807 | 6.0E-17 |
| sp|P39525|CEM1_YEAST | 3-oxoacyl-[acyl-carrier-protein] synthase homolog OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CEM1 PE=1 SV=1 | 389 | 720 | 6.0E-17 |
| sp|O34340|FABF_BACSU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Bacillus subtilis (strain 168) GN=fabF PE=1 SV=1 | 448 | 720 | 8.0E-17 |
| sp|Q6GIA3|FABF_STAAR | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MRSA252) GN=fabF PE=3 SV=1 | 448 | 720 | 9.0E-17 |
| sp|Q8NXE1|FABF_STAAW | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MW2) GN=fabF PE=1 SV=1 | 448 | 720 | 9.0E-17 |
| sp|Q6GAU2|FABF_STAAS | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MSSA476) GN=fabF PE=3 SV=1 | 448 | 720 | 9.0E-17 |
| sp|Q5HHA1|FABF_STAAC | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain COL) GN=fabF PE=1 SV=1 | 448 | 720 | 9.0E-17 |
| sp|Q7A6F8|FABF_STAAN | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain N315) GN=fabF PE=1 SV=1 | 448 | 720 | 9.0E-17 |
| sp|Q99VA6|FABF_STAAM | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabF PE=3 SV=1 | 448 | 720 | 9.0E-17 |
| sp|P43678|KAS1_STRRM | Oxytetracycline polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces rimosus PE=3 SV=2 | 300 | 720 | 1.0E-16 |
| sp|P0AAI8|FABF_SHIFL | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Shigella flexneri GN=fabF PE=3 SV=2 | 448 | 720 | 1.0E-16 |
| sp|P0AAI5|FABF_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli (strain K12) GN=fabF PE=1 SV=2 | 448 | 720 | 1.0E-16 |
| sp|P0AAI6|FABF_ECOL6 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=fabF PE=3 SV=2 | 448 | 720 | 1.0E-16 |
| sp|P0AAI7|FABF_ECO57 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli O157:H7 GN=fabF PE=3 SV=2 | 448 | 720 | 1.0E-16 |
| sp|P55338|FABF_VIBHA | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Vibrio harveyi GN=fabF PE=3 SV=2 | 448 | 720 | 1.0E-16 |
| sp|Q9C9P4|KASC2_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase II, chloroplastic OS=Arabidopsis thaliana GN=KAS2 PE=1 SV=1 | 316 | 720 | 1.0E-16 |
| sp|P47199|QOR_MOUSE | Quinone oxidoreductase OS=Mus musculus GN=Cryz PE=1 SV=1 | 2165 | 2349 | 1.0E-16 |
| sp|P73283|FABF_SYNY3 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabF PE=1 SV=1 | 294 | 715 | 2.0E-16 |
| sp|Q6AYT0|QOR_RAT | Quinone oxidoreductase OS=Rattus norvegicus GN=Cryz PE=2 SV=1 | 2165 | 2366 | 2.0E-16 |
| sp|P56902|FABF_RHIME | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Rhizobium meliloti (strain 1021) GN=fabF PE=3 SV=2 | 439 | 720 | 2.0E-16 |
| sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 1716 | 1913 | 3.0E-16 |
| sp|P23902|KASC1_HORVU | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Hordeum vulgare GN=KAS12 PE=1 SV=1 | 439 | 720 | 3.0E-16 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 2162 | 2427 | 5.0E-16 |
| sp|Q9KQH9|FABF_VIBCH | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) GN=fabF PE=1 SV=3 | 448 | 720 | 6.0E-16 |
| sp|Q80TB8|VAT1L_MOUSE | Synaptic vesicle membrane protein VAT-1 homolog-like OS=Mus musculus GN=Vat1l PE=1 SV=2 | 2156 | 2433 | 7.0E-16 |
| sp|Q9HCJ6|VAT1L_HUMAN | Synaptic vesicle membrane protein VAT-1 homolog-like OS=Homo sapiens GN=VAT1L PE=1 SV=2 | 2156 | 2433 | 8.0E-16 |
| sp|O69473|FAB2_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium leprae (strain TN) GN=kasB PE=3 SV=2 | 518 | 715 | 9.0E-16 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 2471 | 2799 | 2.0E-15 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 2471 | 2635 | 2.0E-15 |
| sp|B0G103|PKS10_DICDI | Probable polyketide synthase 10 OS=Dictyostelium discoideum GN=pks10 PE=3 SV=1 | 1716 | 1890 | 2.0E-15 |
| sp|Q59I44|CAA43_BURSP | 2-haloacrylate reductase OS=Burkholderia sp. GN=caa43 PE=1 SV=1 | 2169 | 2341 | 2.0E-15 |
| sp|P11415|QOR_CAVPO | Quinone oxidoreductase OS=Cavia porcellus GN=CRYZ PE=1 SV=1 | 2143 | 2405 | 2.0E-15 |
| sp|P43903|QOR_PSEAE | Quinone oxidoreductase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=qor PE=3 SV=2 | 2168 | 2399 | 2.0E-15 |
| sp|P0A953|FABB_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Escherichia coli (strain K12) GN=fabB PE=1 SV=1 | 446 | 720 | 2.0E-15 |
| sp|P0A954|FABB_ECOL6 | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=fabB PE=3 SV=1 | 446 | 720 | 2.0E-15 |
| sp|Q0MVN8|QOR_PIG | Quinone oxidoreductase OS=Sus scrofa GN=CRYZ PE=2 SV=1 | 2170 | 2349 | 3.0E-15 |
| sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 828 | 1288 | 5.0E-15 |
| sp|A7RK30|QORL2_NEMVE | Quinone oxidoreductase-like protein 2 homolog OS=Nematostella vectensis GN=v1g238856 PE=3 SV=1 | 2136 | 2399 | 8.0E-15 |
| sp|Q02K94|FABB_PSEAB | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Pseudomonas aeruginosa (strain UCBPP-PA14) GN=fabB PE=1 SV=1 | 446 | 720 | 1.0E-14 |
| sp|O94297|OXSM_SCHPO | Putative 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.13c PE=3 SV=1 | 448 | 715 | 1.0E-14 |
| sp|Q3MIE4|VAT1_RAT | Synaptic vesicle membrane protein VAT-1 homolog OS=Rattus norvegicus GN=Vat1 PE=1 SV=1 | 2190 | 2437 | 2.0E-14 |
| sp|P16540|KAS1_STRVN | Granaticin polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces violaceoruber GN=gra-orf1 PE=3 SV=1 | 300 | 720 | 3.0E-14 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 2438 | 2635 | 4.0E-14 |
| sp|Q28452|QOR_LAMGU | Quinone oxidoreductase OS=Lama guanicoe GN=CRYZ PE=2 SV=1 | 2148 | 2349 | 4.0E-14 |
| sp|P19333|VAT1_TORCA | Synaptic vesicle membrane protein VAT-1 OS=Torpedo californica PE=1 SV=1 | 2144 | 2447 | 5.0E-14 |
| sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 2142 | 2431 | 7.0E-14 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 2457 | 2807 | 8.0E-14 |
| sp|Q62465|VAT1_MOUSE | Synaptic vesicle membrane protein VAT-1 homolog OS=Mus musculus GN=Vat1 PE=1 SV=3 | 2190 | 2437 | 8.0E-14 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 1713 | 1880 | 9.0E-14 |
| sp|O34877|PKSD_BACSU | Polyketide biosynthesis acyltransferase homolog PksD OS=Bacillus subtilis (strain 168) GN=pksD PE=1 SV=2 | 828 | 1044 | 1.0E-13 |
| sp|P71019|FABD_BACSU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis (strain 168) GN=fabD PE=3 SV=2 | 828 | 1115 | 1.0E-13 |
| sp|Q6G9Y3|FABD_STAAS | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MSSA476) GN=fabD PE=3 SV=1 | 829 | 1121 | 2.0E-13 |
| sp|P28304|QOR1_ECOLI | Quinone oxidoreductase 1 OS=Escherichia coli (strain K12) GN=qorA PE=1 SV=1 | 2122 | 2347 | 2.0E-13 |
| sp|Q7A124|FABD_STAAW | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MW2) GN=fabD PE=3 SV=1 | 829 | 1121 | 2.0E-13 |
| sp|Q7A5Z3|FABD_STAAN | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain N315) GN=fabD PE=1 SV=1 | 829 | 1121 | 2.0E-13 |
| sp|Q99UN8|FABD_STAAM | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabD PE=1 SV=1 | 829 | 1121 | 2.0E-13 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 2437 | 2633 | 3.0E-13 |
| sp|Q93QD4|FABD_STAAU | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus GN=fabD PE=3 SV=1 | 829 | 1121 | 3.0E-13 |
| sp|Q5HGK3|FABD_STAAC | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain COL) GN=fabD PE=3 SV=1 | 829 | 1121 | 3.0E-13 |
| sp|Q53FA7|QORX_HUMAN | Quinone oxidoreductase PIG3 OS=Homo sapiens GN=TP53I3 PE=1 SV=2 | 2155 | 2347 | 3.0E-13 |
| sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 1724 | 1887 | 4.0E-13 |
| sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 1721 | 1952 | 4.0E-13 |
| sp|Q6GHK5|FABD_STAAR | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MRSA252) GN=fabD PE=3 SV=1 | 829 | 1121 | 4.0E-13 |
| sp|Q7TXL9|PPSB_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsB PE=1 SV=1 | 2439 | 2637 | 6.0E-13 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 2450 | 2617 | 6.0E-13 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 1713 | 1880 | 6.0E-13 |
| sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 1721 | 1890 | 8.0E-13 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 2457 | 2800 | 1.0E-12 |
| sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 1721 | 1859 | 2.0E-12 |
| sp|B0G138|PKS21_DICDI | Probable polyketide synthase 21 OS=Dictyostelium discoideum GN=pks21 PE=3 SV=1 | 2142 | 2431 | 2.0E-12 |
| sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 1721 | 1859 | 2.0E-12 |
| sp|P42865|QOR_LEIAM | Probable quinone oxidoreductase OS=Leishmania amazonensis PE=3 SV=1 | 2170 | 2347 | 2.0E-12 |
| sp|Q89AY4|FABB_BUCBP | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) GN=fabB PE=3 SV=1 | 430 | 720 | 2.0E-12 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 2457 | 2670 | 3.0E-12 |
| sp|P9WQE5|PPSB_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsB PE=1 SV=1 | 2439 | 2637 | 4.0E-12 |
| sp|P9WQE4|PPSB_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsB PE=3 SV=1 | 2439 | 2637 | 4.0E-12 |
| sp|P9WQD9|FAB1_MYCTU | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kasA PE=1 SV=1 | 351 | 715 | 4.0E-12 |
| sp|P9WQD8|FAB1_MYCTO | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=kasA PE=3 SV=1 | 351 | 715 | 4.0E-12 |
| sp|H8ESN0|FAB1_MYCTE | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium tuberculosis (strain ATCC 35801 / TMC 107 / Erdman) GN=kasA PE=2 SV=2 | 351 | 715 | 4.0E-12 |
| sp|P63455|FAB1_MYCBO | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=kasA PE=3 SV=1 | 351 | 715 | 4.0E-12 |
| sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 1721 | 1859 | 7.0E-12 |
| sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 1721 | 1890 | 8.0E-12 |
| sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 1721 | 1859 | 8.0E-12 |
| sp|Q7TXL7|PPSD_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsD PE=3 SV=1 | 2471 | 2796 | 1.0E-11 |
| sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 2471 | 2796 | 1.0E-11 |
| sp|P9WQE2|PPSD_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsD PE=3 SV=1 | 2471 | 2796 | 1.0E-11 |
| sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 1721 | 1859 | 1.0E-11 |
| sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 1721 | 1890 | 1.0E-11 |
| sp|P73242|FABD_SYNY3 | Malonyl CoA-acyl carrier protein transacylase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabD PE=1 SV=1 | 829 | 1055 | 1.0E-11 |
| sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 1721 | 1952 | 2.0E-11 |
| sp|P40783|QOR_SALTY | Quinone oxidoreductase OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=qor PE=3 SV=2 | 2122 | 2347 | 2.0E-11 |
| sp|P43710|FABB_HAEIN | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=fabB PE=3 SV=1 | 397 | 720 | 3.0E-11 |
| sp|A7Z4X9|BAED_BACMF | Polyketide biosynthesis acyltransferase homolog BaeD OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeD PE=1 SV=1 | 828 | 1115 | 5.0E-11 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 2454 | 2807 | 8.0E-11 |
| sp|P57193|FABB_BUCAI | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) GN=fabB PE=3 SV=1 | 519 | 720 | 9.0E-11 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 2449 | 2806 | 2.0E-10 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 2598 | 2802 | 4.0E-10 |
| sp|B0BNC9|QORL2_RAT | Quinone oxidoreductase-like protein 2 OS=Rattus norvegicus PE=2 SV=1 | 2140 | 2347 | 4.0E-10 |
| sp|Q3UNZ8|QORL2_MOUSE | Quinone oxidoreductase-like protein 2 OS=Mus musculus PE=1 SV=1 | 2140 | 2347 | 4.0E-10 |
| sp|P40804|PKSF_BACSU | Polyketide biosynthesis malonyl-ACP decarboxylase PksF OS=Bacillus subtilis (strain 168) GN=pksF PE=1 SV=3 | 425 | 720 | 4.0E-10 |
| sp|Q8L3X9|KASM_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Arabidopsis thaliana GN=KAS PE=1 SV=1 | 448 | 720 | 4.0E-10 |
| sp|O35017|YOGA_BACSU | Uncharacterized zinc-type alcohol dehydrogenase-like protein YogA OS=Bacillus subtilis (strain 168) GN=yogA PE=3 SV=1 | 2216 | 2347 | 2.0E-09 |
| sp|Q9CBS7|FAB1_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium leprae (strain TN) GN=kasA PE=3 SV=1 | 519 | 715 | 2.0E-09 |
| sp|O74489|QOR_SCHPO | Probable quinone oxidoreductase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=zta1 PE=1 SV=2 | 2170 | 2348 | 3.0E-09 |
| sp|A0R0B2|FABD_MYCS2 | Malonyl CoA-acyl carrier protein transacylase OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=fabD PE=1 SV=1 | 916 | 1115 | 4.0E-09 |
| sp|Q9R9J2|FENF_BACIU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis GN=fenF PE=1 SV=1 | 827 | 1135 | 6.0E-09 |
| sp|P38230|QOR_YEAST | Probable quinone oxidoreductase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ZTA1 PE=1 SV=1 | 2169 | 2347 | 6.0E-09 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 1717 | 1880 | 1.0E-08 |
| sp|P34055|INC11_HYPAT | Protein indc11 OS=Hypocrea atroviridis GN=indc11 PE=2 SV=1 | 2139 | 2433 | 1.0E-08 |
| sp|Q8BGC4|ZADH2_MOUSE | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Mus musculus GN=Zadh2 PE=1 SV=1 | 2164 | 2347 | 1.0E-08 |
| sp|A7Z4X8|BAEC_BACMF | Polyketide biosynthesis malonyl CoA-acyl carrier protein transacylase BaeC OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeC PE=1 SV=1 | 828 | 1056 | 2.0E-08 |
| sp|A6QQF5|QORL2_BOVIN | Quinone oxidoreductase-like protein 2 OS=Bos taurus PE=2 SV=2 | 2142 | 2347 | 3.0E-08 |
| sp|O94038|ADH2_CANAL | Alcohol dehydrogenase 2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=ADH2 PE=3 SV=1 | 2170 | 2431 | 4.0E-08 |
| sp|Q00681|STCJ_EMENI | Sterigmatocystin biosynthesis fatty acid synthase subunit alpha OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=stcJ PE=3 SV=2 | 369 | 777 | 9.0E-08 |
| sp|P0C842|CJ052_HUMAN | Putative uncharacterized protein encoded by LINC00614 OS=Homo sapiens GN=LINC00614 PE=5 SV=1 | 366 | 442 | 1.0E-07 |
| sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 1715 | 1833 | 2.0E-07 |
| sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 1715 | 1833 | 2.0E-07 |
| sp|Q503Y4|OVCA2_DANRE | Ovarian cancer-associated gene 2 protein homolog OS=Danio rerio GN=ovca2 PE=2 SV=1 | 1 | 131 | 2.0E-07 |
| sp|Q8N4Q0|ZADH2_HUMAN | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Homo sapiens GN=ZADH2 PE=1 SV=1 | 2168 | 2347 | 5.0E-07 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 2409 | 2626 | 1.0E-06 |
| sp|P9WNG5|FABD_MYCTU | Malonyl CoA-acyl carrier protein transacylase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=fabD PE=1 SV=1 | 828 | 1115 | 1.0E-06 |
| sp|P9WNG4|FABD_MYCTO | Malonyl CoA-acyl carrier protein transacylase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=fabD PE=3 SV=1 | 828 | 1115 | 1.0E-06 |
| sp|P63459|FABD_MYCBO | Malonyl CoA-acyl carrier protein transacylase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=fabD PE=3 SV=1 | 828 | 1115 | 1.0E-06 |
| sp|Q24K16|ZADH2_BOVIN | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Bos taurus GN=ZADH2 PE=2 SV=1 | 2225 | 2347 | 1.0E-06 |
| sp|O42909|YBI2_SCHPO | Zinc-type alcohol dehydrogenase-like protein C16A3.02c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC16A3.02c PE=3 SV=1 | 2158 | 2347 | 1.0E-06 |
| sp|Q89AH0|FABD_BUCBP | Malonyl CoA-acyl carrier protein transacylase OS=Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) GN=fabD PE=3 SV=1 | 830 | 1039 | 3.0E-06 |
| sp|Q02062|KASB_STRCO | Actinorhodin polyketide putative beta-ketoacyl synthase 2 OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO5088 PE=1 SV=1 | 385 | 672 | 5.0E-06 |
| sp|P0DN30|RTAI1_ARTBC | Probable zinc-binding oxidoreductase, mitochondrial OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_02327-2 PE=3 SV=1 | 2216 | 2433 | 5.0E-06 |
| sp|Q9EQZ5|PTGR1_CAVPO | Prostaglandin reductase 1 OS=Cavia porcellus GN=Ptgr1 PE=1 SV=1 | 2215 | 2428 | 6.0E-06 |
| sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 1721 | 1833 | 7.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0008168 | methyltransferase activity | Yes |
| GO:0003674 | molecular_function | No |
| GO:0016740 | transferase activity | No |
| GO:0003824 | catalytic activity | No |
| GO:0016741 | transferase activity, transferring one-carbon groups | No |
| Gene cluster ID | Type of secondary metabolism gene |
|---|---|
| Cluster 14 | PKS |
| Orthofinder run ID | 4 |
| Orthogroup | 11 |
| Change Orthofinder run |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
| Protein | >Ophun1|2808 MRILCVHGAAINGDIFASKTEKLRALLPADYSYEWPEGEHEVTPIQSLSDTYPGPYLSHLEEITTRGIRNSIERL EACIEEDGPFDGVMAICEVLSFRHPGAMLVAGLLFKRQMEDPTGPLPFRFAIFIAGAPPLTWSDSVGQNMFNQVM SEDPLDVDKDNFDEPEAGIQGRPNIEYIKEFGRKLYRDLTPELEKWVQTVEDMGTDPDKARLMPHAILPQLHPDR LDLPTAHMWGRNDVLSSHSGLLFRLCNPDFALSHVHDGVHDVPQSSKDNEIFSNLVRKTILRSQFAVNNMAAVDI AIVGLACRFPGEAKSPKAFYQMLVQGRDAWSKVPKSRYDVDAYRHPSRERRGTMVCEGGYFLEDDVSRWDAPFFA CSTVEAHAMDPQQRLLLEVAYESLENAGIPMEALAESDAACFVGGFTNDYQRIVTSESEATPQYTMTGNSTAMMA NRVSWFLNLRGPSVTVDTACSSSMAAFHLACETIRSESNETRCAMVGGTSLLFNPDDPCGMNALGFLSPDSRCYS FDSRANGYARGEGVAMLVLKHMDDALRDGDAIRGVVRASALNSDGRTAGIVLPNGEAHQRLINHTYRLAGFHPAD TQYAELHGTGTRVGDPTEISAVARTLAADRSTPLLCGSVKTQIGHSEAAAAMAGILKCVLSMEAGILPPNKNFVE PNPRLRLEASNIVVPTESQPWPVAAVRRCSINSFGFGGLNGHVILDGAASYLGSRGLAVPDVDADAEAKARPRLF LLSAPEQSAVARQLRTHADYLTDSSPPVSLPLLAHTLGARRSVFQWRLAVVARSADELESLWRQNGPAPIKAVAS PGVALIFTGQGAQWHAMGRELLALPVFARSVRASAAALVAQGCPWDAWTELMRPEAESRVGQAVYSQPLTSLLQI ALVDLLRYWGVTPSAVVGHSSGEMAAAYAVGALSREDCLTIAYHRGVVSEMAAQREPGGAMMAVGLSADEIRPRL VSSAITVACINSPNNVTLAGDAAALEELAESLKRDDVFCRVLKVQNAFHSPQMQTVADEYRRRIAGVKPVDVTAA FHSTVHGCRIPTSKLTADYWVANLCSPVELVRALDDMLCTNDGKGKRSKAPTIMVEVGPHGVLAGPFEQFRLARR GLEHLGYYSLLSRGRDAMITAMTAASALWMRGAAVRVDKINDLDEASRPATVLTDLPSYSWNHSVSYWHETWGSR NRRWPSAPKHDLIGWRLPACNPLEPVWKNYLRVGEIPWLKDHQVHGDVVFPAAGVISAVIEAMRQFESGHDITSF ELREFYIPRPLLIPSTELGAETFLHLKRRKTGMGSGAGPWLEFSFYSRQDDDTFVEHAHGLVQAHFAKQCNEVDG GRELREETLAHQRRFRHQVKTCDEPLTSQAHYEFCRSIGLVYGDNFQGLCNVRLRDTNVAFEVSVVDTPACMPGA CESDYLVHPTTIDLLFQALLATLPNMRDAEKQGWAPTAVGSIRVSTAIRRGPGTVLQGHGELSSGAAHQMVGFVM AGDGVFDSFPAVVMDGIQVSALGTMQSASVNASEDSIVKLYATPAWKPDLLLLEGRRPARLAVGATQDHDAARFS IDSREIVDDMCRAALQRLDDEAIAELAPHLQQYVSWMQKRTSETRTFASITPPISPGFSAYDVKVDEYFSINKLK SFIDRFPVDGRLLQHAFACIDPIFSGETTPIAALMASDDFARFYKESNGAEVMIPIFRNWFDLKAHKKPSLRILE VGGGTGAMTVPILETMGDAEGETPRFSGFTFTDISPGWFEGARTLLRRWKSRVDYKVLNIEVDPVEQGFEPESYD VILAFNVLHATKSIKTSLENCRRLLKPGGNLIVGECTNPDDMLSFIFGLLPGWWAAEDGRQFGPLLSESAWDKTL KDAGFSGTDIAMPDGDDEAGHHRMSVMVSTKPHEQETSSSTKDVVVLVANNSINDIGKSLAASVRRDLEQLGARV SIKVLGSSEIKFEGKTVISLLEYGMPILQQVQEADFENIKHVLLHCRELLWVTRSDAADKEGHPSMRIISGLLHC LKNEDASRRLHELHLCRNVTASVAKTSDVILRRLNSLWQGEGEEAAELVTVERDGEFCIPRYVPEKTMNRSLART TDSDLELQTEKLVQAGRPLRLKIGRPGMLDTLHFGDDDEALQPLAKDEVMIEVLADVLIAMGELRSPNLGYEAAG IIVGTGAKVTRLSVGDRVLCLRPAVMRTRIRTNQWHVHLLPACLSIENGVTIPVAYATAYRCLVEVARLEKGETV LIHAAAGGFGQASIHMAKMLGADIFCTVSSEAKKRLVVSLGVKPEHVFSSRDVSFEAGIKRITNGRGVDVVVNSL AGELLRRSWACMAPYGRFVEVGKRDIVGNSGLDMQPFDNNAVFACVNLDAMTSEPRRLWELVDKVLRLFEQGSLG LIQPIAVHDFSDLEAVFREMQRGAHMGKLALRVTPESRVPVAPRKTVPLKLSPDATYLLAGGLGGLGRAQALFMV EHGARHLAFVSRSGDSRPEARKLLDTLAKAGVKTRAYAGDVADRDGLGAILDDVARRMPPIRGVIQGAMVLDDAL FQNMSYDQWQNATRPKIQGSWNLHELLPADLDFFVVLSSMAGAIGFVSQANYAAGNTYQDALAHYRHARGLPALS IDLGITKGFGYVAEHEEVAAKLKPYGLATVNEQQLFHLLRCAMAGTADGDNKLPTRQLLAGAGTGGLAQASLATV PETNLFWLSALASFSYLGEVDMRASAETAGDEMTDDARLVGQLSASKTMDEAAEVVQDMLLARISTIMSVPTADI DTAKPVHAYGVDSLVAVELRNWLSKRLRSDVSIFDLTGNMAITTLSRKIASRSRLVPTAAKGQGGNETGVAE* |
| Coding | >Ophun1|2808 ATGCGTATTCTCTGCGTCCACGGAGCCGCTATCAACGGCGACATCTTCGCTTCCAAGACGGAGAAGCTTCGAGCT CTGCTGCCGGCCGACTACTCATATGAATGGCCCGAAGGCGAGCACGAGGTGACACCCATCCAAAGCCTCTCCGAC ACTTATCCCGGACCCTATCTTTCGCACCTAGAAGAAATCACCACCCGCGGCATCCGGAATTCCATCGAGAGACTC GAGGCTTGCATCGAGGAGGACGGTCCGTTTGACGGTGTCATGGCCATCTGCGAGGTGCTCTCCTTCCGACACCCC GGTGCTATGCTCGTCGCAGGCCTGCTCTTCAAACGGCAGATGGAAGACCCAACGGGGCCGCTGCCGTTCAGGTTC GCCATCTTCATCGCAGGCGCTCCTCCGCTCACCTGGTCCGACTCAGTCGGGCAGAACATGTTCAATCAGGTCATG AGTGAAGACCCCCTCGACGTCGACAAGGACAACTTTGACGAGCCGGAGGCCGGGATCCAAGGCAGGCCCAATATC GAGTACATCAAGGAATTTGGCCGCAAGCTGTACCGAGACCTGACTCCCGAGCTGGAGAAATGGGTGCAAACCGTC GAGGACATGGGCACCGATCCCGACAAGGCACGCCTCATGCCGCACGCGATACTGCCTCAGCTGCATCCGGATAGA CTCGATCTGCCCACGGCTCACATGTGGGGACGTAACGACGTCTTGAGCAGCCACTCGGGCCTCTTGTTCCGGCTC TGCAACCCGGACTTTGCACTGAGCCACGTGCATGATGGGGTACACGACGTCCCGCAGTCGTCCAAGGACAACGAG ATCTTTAGCAACTTGGTCCGTAAGACAATTCTGCGCAGCCAATTCGCAGTAAACAACATGGCCGCTGTCGACATC GCCATCGTCGGGCTCGCGTGCCGCTTTCCCGGTGAGGCCAAGTCCCCAAAGGCCTTTTACCAGATGCTGGTGCAA GGCCGTGATGCTTGGTCCAAAGTGCCCAAATCACGGTACGATGTCGACGCGTACCGACACCCGTCGCGTGAGCGC CGCGGGACAATGGTGTGTGAAGGCGGCTACTTTTTAGAAGACGACGTCTCTCGGTGGGACGCGCCCTTTTTCGCC TGCTCGACCGTCGAGGCGCATGCCATGGATCCGCAGCAGAGGCTGCTACTCGAAGTCGCCTACGAGAGCCTGGAG AACGCGGGCATCCCGATGGAGGCGTTGGCCGAAAGCGACGCGGCCTGCTTCGTCGGCGGCTTCACCAACGACTAC CAGCGCATCGTGACGAGCGAGTCGGAGGCGACGCCACAGTATACCATGACGGGAAACTCGACGGCCATGATGGCC AACCGCGTCAGCTGGTTCCTCAACCTACGCGGGCCGTCGGTGACGGTCGACACGGCCTGCTCCAGCTCCATGGCG GCGTTTCATCTGGCTTGCGAGACGATCCGGTCCGAGTCCAACGAAACGCGATGCGCCATGGTCGGTGGCACCAGC CTGCTGTTCAACCCGGACGATCCATGCGGTATGAATGCGCTGGGCTTCCTGAGCCCGGATAGCCGATGCTATAGC TTCGATTCGCGAGCCAACGGCTACGCGCGTGGTGAAGGCGTCGCGATGCTGGTGCTCAAGCACATGGATGACGCG CTGCGAGACGGAGATGCCATTCGGGGCGTGGTGCGTGCATCGGCGCTGAATTCAGACGGACGGACGGCCGGCATC GTCCTCCCCAATGGAGAGGCTCATCAGCGCCTCATCAATCACACCTATCGCCTAGCGGGCTTCCATCCCGCCGAT ACGCAGTATGCCGAGCTCCACGGCACCGGCACTCGCGTCGGCGATCCCACCGAAATCAGTGCCGTGGCCCGGACC CTCGCCGCCGATCGATCCACGCCGCTGCTATGTGGCTCCGTCAAGACGCAGATTGGTCACTCCGAGGCGGCCGCC GCCATGGCCGGCATTCTCAAATGCGTCCTCTCCATGGAGGCTGGCATCCTGCCGCCAAACAAGAACTTTGTTGAG CCAAATCCGCGGCTCCGGCTCGAGGCCTCCAACATCGTGGTGCCGACCGAGTCGCAGCCGTGGCCCGTAGCCGCC GTCCGCCGCTGCTCTATTAATAGCTTCGGCTTCGGTGGGCTCAACGGTCACGTTATCCTCGACGGTGCTGCTAGC TACCTCGGCAGCCGCGGACTCGCCGTTCCGGACGTCGATGCCGATGCCGAAGCAAAGGCCCGGCCCCGTCTCTTC CTCCTGTCCGCCCCGGAACAGAGCGCCGTGGCCCGCCAGCTCCGCACCCACGCCGACTACCTGACCGACTCCTCG CCGCCCGTCTCTCTGCCGCTCCTCGCTCATACGCTGGGCGCCCGCCGCTCCGTCTTTCAGTGGCGCCTCGCCGTC GTCGCCCGCTCTGCCGACGAGCTCGAGTCCCTCTGGCGTCAGAATGGGCCGGCGCCTATCAAGGCCGTTGCCTCG CCTGGCGTGGCTCTCATCTTCACTGGCCAGGGCGCCCAGTGGCACGCCATGGGTCGCGAGCTACTGGCCCTGCCC GTCTTTGCCCGCTCCGTCCGCGCCTCGGCCGCTGCGCTGGTCGCCCAGGGCTGCCCCTGGGATGCTTGGACCGAG CTCATGCGTCCAGAAGCCGAGTCGCGCGTTGGTCAGGCCGTCTACTCCCAGCCGTTGACGTCGCTACTTCAGATT GCCCTCGTCGACCTCCTCCGCTACTGGGGTGTCACGCCGTCCGCCGTCGTTGGCCATTCGTCGGGTGAGATGGCG GCCGCTTATGCCGTCGGCGCCCTATCCCGCGAGGACTGCCTCACTATTGCCTATCATCGCGGTGTGGTATCTGAA ATGGCAGCCCAACGCGAGCCTGGCGGTGCCATGATGGCCGTCGGTCTCTCTGCCGACGAGATCCGGCCGCGACTG GTCAGCTCCGCCATCACCGTGGCTTGCATCAACAGCCCCAACAACGTGACGCTGGCGGGAGACGCCGCGGCTCTC GAGGAACTGGCCGAGTCTCTGAAGCGCGACGACGTCTTCTGCCGCGTTCTGAAGGTTCAAAACGCCTTCCACAGC CCGCAGATGCAGACTGTGGCCGATGAGTACCGTCGACGTATCGCCGGCGTCAAGCCCGTCGACGTTACGGCCGCC TTCCACTCCACCGTCCACGGCTGCCGGATTCCCACATCGAAGCTGACGGCTGACTACTGGGTGGCCAATCTCTGC TCTCCCGTCGAGCTCGTCCGAGCCTTGGACGACATGCTGTGCACCAACGACGGCAAGGGTAAGAGATCCAAGGCA CCCACCATCATGGTTGAAGTCGGGCCTCACGGCGTCCTCGCCGGCCCCTTTGAGCAGTTCCGGCTCGCCCGCCGC GGCCTGGAGCACCTCGGCTACTACAGTCTTCTCTCACGGGGACGGGACGCCATGATTACGGCAATGACAGCCGCT TCCGCTCTCTGGATGAGGGGTGCTGCTGTTCGGGTCGACAAGATTAATGACTTGGACGAGGCCTCTCGGCCCGCC ACCGTCCTCACTGATCTGCCGTCCTACAGCTGGAATCACTCCGTCTCGTACTGGCACGAGACATGGGGCTCGCGA AACCGCCGCTGGCCATCGGCTCCCAAGCACGATCTGATCGGGTGGCGGCTCCCTGCATGCAACCCGCTGGAGCCC GTGTGGAAGAATTACCTGCGCGTCGGCGAGATTCCCTGGCTCAAGGATCACCAGGTGCACGGCGACGTTGTGTTT CCCGCTGCCGGCGTCATCAGCGCCGTCATCGAGGCCATGCGCCAGTTTGAAAGCGGTCATGACATCACGAGCTTC GAGCTCCGCGAGTTCTACATCCCCCGGCCCCTTCTCATCCCCAGTACCGAGCTCGGTGCCGAGACCTTCCTCCAC CTGAAGCGCAGGAAAACGGGCATGGGCAGCGGGGCCGGCCCCTGGCTCGAATTCTCCTTTTACTCGCGTCAGGAC GACGACACCTTTGTCGAGCACGCCCATGGGCTCGTCCAGGCTCACTTTGCCAAGCAGTGCAACGAGGTGGACGGA GGCAGGGAGCTGCGGGAGGAGACGCTGGCGCACCAGAGACGCTTCCGACATCAGGTCAAAACGTGCGACGAGCCG CTCACTAGCCAAGCTCACTACGAGTTTTGCAGGAGCATAGGCCTCGTTTACGGTGACAACTTTCAGGGCCTATGC AATGTGCGGCTCAGAGACACCAACGTCGCCTTTGAGGTTTCCGTCGTCGACACGCCGGCCTGCATGCCGGGAGCG TGTGAGTCGGATTACCTGGTTCACCCGACGACCATCGACCTCTTGTTCCAGGCCCTCCTGGCGACGCTACCCAAC ATGCGGGACGCCGAGAAGCAGGGATGGGCCCCGACGGCCGTCGGCTCGATCCGTGTCTCGACGGCCATTCGACGC GGTCCCGGCACGGTACTTCAGGGCCACGGTGAGCTGTCCTCCGGGGCTGCCCATCAGATGGTGGGCTTCGTCATG GCGGGCGACGGCGTCTTCGACTCGTTTCCGGCAGTTGTCATGGACGGAATCCAGGTTTCGGCTCTGGGCACCATG CAGAGCGCTTCGGTTAATGCGTCCGAGGACTCGATTGTCAAGCTGTACGCGACGCCTGCCTGGAAGCCAGACCTG CTTCTCCTCGAGGGACGACGTCCGGCGCGGCTGGCCGTGGGGGCGACTCAGGACCATGACGCGGCTCGGTTCAGC ATCGACAGCCGCGAGATCGTCGACGACATGTGCCGCGCCGCCTTGCAGCGTCTGGACGACGAGGCCATCGCGGAG CTGGCCCCCCATTTGCAGCAGTACGTCTCCTGGATGCAGAAGCGCACCAGCGAGACCAGGACGTTCGCCAGCATC ACGCCGCCCATTAGCCCGGGCTTCAGCGCCTACGACGTCAAGGTGGACGAGTACTTTAGCATCAACAAGCTCAAG AGCTTCATCGACAGGTTTCCTGTCGACGGGCGCCTCTTGCAGCACGCCTTTGCCTGCATCGACCCCATCTTCAGC GGGGAGACGACACCGATCGCGGCCCTGATGGCGAGCGACGATTTCGCCCGCTTCTACAAGGAGTCCAACGGTGCC GAGGTCATGATACCCATCTTCCGCAACTGGTTCGACCTCAAGGCACACAAGAAGCCAAGCCTGCGCATTCTCGAA GTCGGGGGCGGCACGGGCGCGATGACGGTGCCCATTCTGGAGACGATGGGAGACGCCGAGGGCGAGACGCCACGT TTCTCAGGCTTTACCTTTACCGACATCTCACCCGGCTGGTTCGAGGGCGCCCGGACGCTGCTGCGTCGCTGGAAG TCTCGTGTCGATTACAAGGTGCTCAACATTGAGGTTGATCCCGTTGAGCAGGGGTTCGAGCCCGAGTCTTATGAT GTCATCTTGGCTTTCAATGTCCTCCATGCCACGAAAAGCATAAAAACGTCGCTCGAAAACTGCCGCCGGCTGCTC AAGCCCGGAGGCAACCTCATCGTCGGCGAATGCACTAATCCCGACGATATGCTCAGCTTCATCTTTGGCCTCTTG CCCGGCTGGTGGGCCGCCGAGGACGGCAGGCAGTTTGGCCCCTTGCTGAGCGAGTCCGCCTGGGATAAGACGCTC AAGGATGCTGGCTTCTCCGGCACCGATATCGCCATGCCGGACGGCGACGATGAGGCTGGCCATCATCGGATGTCG GTCATGGTCAGTACCAAGCCGCACGAGCAGGAGACATCCTCTTCGACCAAAGACGTCGTCGTTCTCGTTGCCAAC AATAGCATCAACGACATCGGGAAAAGCCTCGCCGCCTCCGTCCGCCGCGATCTTGAGCAGCTCGGAGCCCGCGTC AGTATCAAAGTTTTGGGATCGTCCGAGATCAAATTCGAGGGCAAGACGGTCATCTCTCTCTTGGAGTACGGCATG CCGATCCTCCAACAGGTCCAGGAAGCCGACTTCGAGAACATCAAGCACGTCTTGCTTCATTGCCGCGAGCTCCTC TGGGTTACGCGCTCGGATGCGGCGGACAAGGAGGGACATCCCAGTATGCGCATCATCTCGGGCCTGCTTCACTGC CTCAAGAACGAGGACGCGTCTCGAAGGCTTCACGAGCTGCATCTTTGCCGAAACGTCACGGCTAGCGTGGCCAAG ACCAGCGACGTCATTCTCCGCAGGCTCAACAGTCTGTGGCAAGGTGAAGGGGAAGAGGCAGCGGAGCTGGTCACG GTGGAGCGAGACGGCGAATTCTGCATTCCCCGTTACGTGCCGGAAAAGACGATGAACCGCAGCCTGGCGCGCACG ACCGATTCTGATCTGGAGCTGCAGACAGAGAAGCTCGTGCAGGCCGGCCGGCCATTGCGGCTCAAAATTGGGCGG CCAGGGATGTTGGACACGCTTCATTTCGGCGACGATGATGAGGCCTTGCAGCCGCTGGCCAAAGACGAAGTCATG ATTGAGGTGTTGGCGGACGTCTTGATTGCAATGGGCGAGCTCCGGTCGCCGAATCTGGGCTACGAGGCAGCCGGC ATCATCGTCGGCACCGGGGCCAAGGTGACGCGGCTGTCGGTCGGCGATCGGGTTCTGTGCCTGAGGCCGGCCGTG ATGCGCACGCGGATCCGCACCAACCAGTGGCACGTCCACCTGCTGCCGGCCTGCTTGTCGATTGAGAACGGCGTG ACGATTCCGGTGGCATACGCCACTGCGTATCGTTGTCTTGTCGAAGTGGCGAGGCTGGAAAAGGGGGAGACGGTG CTGATTCACGCCGCAGCGGGGGGCTTCGGACAGGCTTCGATCCACATGGCCAAGATGCTGGGTGCCGACATCTTC TGTACGGTCAGCTCCGAGGCCAAGAAGCGGCTGGTCGTCTCGCTCGGGGTCAAGCCCGAGCATGTCTTTAGCTCG CGCGATGTCTCGTTCGAGGCAGGCATCAAGAGGATCACTAACGGCCGTGGCGTCGACGTCGTCGTCAATTCGCTT GCCGGCGAGCTGCTACGCCGAAGCTGGGCCTGTATGGCTCCCTACGGCCGCTTCGTCGAGGTCGGCAAGCGAGAC ATTGTGGGCAATAGCGGGCTAGACATGCAGCCGTTCGATAACAACGCCGTGTTCGCGTGCGTTAACCTCGATGCT ATGACGTCTGAGCCGCGGCGGCTGTGGGAGCTGGTGGACAAGGTGCTTCGCTTGTTTGAGCAGGGCTCGCTGGGA CTGATCCAGCCCATTGCCGTCCATGACTTCTCCGACCTCGAAGCCGTCTTCCGCGAAATGCAACGAGGAGCGCAT ATGGGCAAGCTGGCGCTGCGCGTGACGCCCGAGTCGCGGGTTCCGGTTGCGCCGCGAAAGACGGTGCCCCTGAAG CTGTCGCCGGATGCGACATACCTGCTGGCCGGCGGCCTCGGCGGACTTGGCCGGGCCCAGGCTCTGTTTATGGTC GAACACGGGGCTCGGCACTTGGCCTTTGTGTCGCGGTCCGGCGACTCGCGGCCCGAGGCCCGGAAGCTGCTGGAC ACGCTGGCAAAGGCCGGGGTCAAGACCCGGGCCTACGCCGGCGACGTGGCCGACCGCGACGGGCTAGGTGCCATT CTCGACGACGTGGCGCGCCGCATGCCGCCTATACGCGGTGTCATTCAGGGCGCCATGGTGCTCGACGACGCCCTC TTCCAGAATATGTCATACGACCAGTGGCAGAATGCGACACGGCCCAAGATCCAGGGCAGCTGGAACCTTCACGAA CTGCTGCCGGCCGACCTCGACTTCTTCGTCGTCCTCTCCTCCATGGCTGGAGCCATCGGCTTCGTCTCCCAGGCC AACTACGCGGCCGGCAACACATACCAGGACGCGCTGGCCCATTACCGACACGCCCGGGGTCTGCCAGCGTTGAGC ATCGACCTCGGCATCACAAAGGGCTTTGGCTACGTGGCCGAGCACGAGGAGGTTGCAGCTAAGCTGAAGCCGTAC GGGCTGGCGACGGTCAACGAGCAGCAGCTATTTCACCTACTACGCTGCGCCATGGCCGGCACCGCCGACGGCGAC AATAAGCTGCCCACGCGGCAGCTGCTCGCCGGCGCCGGTACGGGGGGTCTGGCTCAGGCGTCACTTGCGACGGTG CCCGAGACGAACCTGTTCTGGCTCTCGGCCCTGGCGTCCTTCTCTTACCTGGGCGAGGTGGACATGAGAGCCTCG GCCGAGACGGCGGGCGATGAGATGACGGACGACGCGCGGCTCGTCGGCCAGCTATCAGCGTCCAAGACGATGGAC GAGGCGGCCGAGGTGGTGCAAGACATGCTGCTGGCGCGCATCTCGACCATCATGTCGGTGCCGACGGCTGACATC GACACAGCCAAGCCGGTTCACGCGTACGGCGTCGACAGTTTGGTGGCCGTTGAGCTGCGAAACTGGCTGTCGAAG CGGCTGCGTAGCGACGTCAGCATCTTTGACCTGACGGGCAACATGGCCATTACGACGCTGAGCCGGAAGATTGCC AGCCGGTCACGCCTGGTCCCCACTGCGGCCAAAGGGCAGGGCGGCAACGAGACTGGTGTTGCTGAGTGA |
| Transcript | >Ophun1|2808 ATGCGTATTCTCTGCGTCCACGGAGCCGCTATCAACGGCGACATCTTCGCTTCCAAGACGGAGAAGCTTCGAGCT CTGCTGCCGGCCGACTACTCATATGAATGGCCCGAAGGCGAGCACGAGGTGACACCCATCCAAAGCCTCTCCGAC ACTTATCCCGGACCCTATCTTTCGCACCTAGAAGAAATCACCACCCGCGGCATCCGGAATTCCATCGAGAGACTC GAGGCTTGCATCGAGGAGGACGGTCCGTTTGACGGTGTCATGGCCATCTGCGAGGTGCTCTCCTTCCGACACCCC GGTGCTATGCTCGTCGCAGGCCTGCTCTTCAAACGGCAGATGGAAGACCCAACGGGGCCGCTGCCGTTCAGGTTC GCCATCTTCATCGCAGGCGCTCCTCCGCTCACCTGGTCCGACTCAGTCGGGCAGAACATGTTCAATCAGGTCATG AGTGAAGACCCCCTCGACGTCGACAAGGACAACTTTGACGAGCCGGAGGCCGGGATCCAAGGCAGGCCCAATATC GAGTACATCAAGGAATTTGGCCGCAAGCTGTACCGAGACCTGACTCCCGAGCTGGAGAAATGGGTGCAAACCGTC GAGGACATGGGCACCGATCCCGACAAGGCACGCCTCATGCCGCACGCGATACTGCCTCAGCTGCATCCGGATAGA CTCGATCTGCCCACGGCTCACATGTGGGGACGTAACGACGTCTTGAGCAGCCACTCGGGCCTCTTGTTCCGGCTC TGCAACCCGGACTTTGCACTGAGCCACGTGCATGATGGGGTACACGACGTCCCGCAGTCGTCCAAGGACAACGAG ATCTTTAGCAACTTGGTCCGTAAGACAATTCTGCGCAGCCAATTCGCAGTAAACAACATGGCCGCTGTCGACATC GCCATCGTCGGGCTCGCGTGCCGCTTTCCCGGTGAGGCCAAGTCCCCAAAGGCCTTTTACCAGATGCTGGTGCAA GGCCGTGATGCTTGGTCCAAAGTGCCCAAATCACGGTACGATGTCGACGCGTACCGACACCCGTCGCGTGAGCGC CGCGGGACAATGGTGTGTGAAGGCGGCTACTTTTTAGAAGACGACGTCTCTCGGTGGGACGCGCCCTTTTTCGCC TGCTCGACCGTCGAGGCGCATGCCATGGATCCGCAGCAGAGGCTGCTACTCGAAGTCGCCTACGAGAGCCTGGAG AACGCGGGCATCCCGATGGAGGCGTTGGCCGAAAGCGACGCGGCCTGCTTCGTCGGCGGCTTCACCAACGACTAC CAGCGCATCGTGACGAGCGAGTCGGAGGCGACGCCACAGTATACCATGACGGGAAACTCGACGGCCATGATGGCC AACCGCGTCAGCTGGTTCCTCAACCTACGCGGGCCGTCGGTGACGGTCGACACGGCCTGCTCCAGCTCCATGGCG GCGTTTCATCTGGCTTGCGAGACGATCCGGTCCGAGTCCAACGAAACGCGATGCGCCATGGTCGGTGGCACCAGC CTGCTGTTCAACCCGGACGATCCATGCGGTATGAATGCGCTGGGCTTCCTGAGCCCGGATAGCCGATGCTATAGC TTCGATTCGCGAGCCAACGGCTACGCGCGTGGTGAAGGCGTCGCGATGCTGGTGCTCAAGCACATGGATGACGCG CTGCGAGACGGAGATGCCATTCGGGGCGTGGTGCGTGCATCGGCGCTGAATTCAGACGGACGGACGGCCGGCATC GTCCTCCCCAATGGAGAGGCTCATCAGCGCCTCATCAATCACACCTATCGCCTAGCGGGCTTCCATCCCGCCGAT ACGCAGTATGCCGAGCTCCACGGCACCGGCACTCGCGTCGGCGATCCCACCGAAATCAGTGCCGTGGCCCGGACC CTCGCCGCCGATCGATCCACGCCGCTGCTATGTGGCTCCGTCAAGACGCAGATTGGTCACTCCGAGGCGGCCGCC GCCATGGCCGGCATTCTCAAATGCGTCCTCTCCATGGAGGCTGGCATCCTGCCGCCAAACAAGAACTTTGTTGAG CCAAATCCGCGGCTCCGGCTCGAGGCCTCCAACATCGTGGTGCCGACCGAGTCGCAGCCGTGGCCCGTAGCCGCC GTCCGCCGCTGCTCTATTAATAGCTTCGGCTTCGGTGGGCTCAACGGTCACGTTATCCTCGACGGTGCTGCTAGC TACCTCGGCAGCCGCGGACTCGCCGTTCCGGACGTCGATGCCGATGCCGAAGCAAAGGCCCGGCCCCGTCTCTTC CTCCTGTCCGCCCCGGAACAGAGCGCCGTGGCCCGCCAGCTCCGCACCCACGCCGACTACCTGACCGACTCCTCG CCGCCCGTCTCTCTGCCGCTCCTCGCTCATACGCTGGGCGCCCGCCGCTCCGTCTTTCAGTGGCGCCTCGCCGTC GTCGCCCGCTCTGCCGACGAGCTCGAGTCCCTCTGGCGTCAGAATGGGCCGGCGCCTATCAAGGCCGTTGCCTCG CCTGGCGTGGCTCTCATCTTCACTGGCCAGGGCGCCCAGTGGCACGCCATGGGTCGCGAGCTACTGGCCCTGCCC GTCTTTGCCCGCTCCGTCCGCGCCTCGGCCGCTGCGCTGGTCGCCCAGGGCTGCCCCTGGGATGCTTGGACCGAG CTCATGCGTCCAGAAGCCGAGTCGCGCGTTGGTCAGGCCGTCTACTCCCAGCCGTTGACGTCGCTACTTCAGATT GCCCTCGTCGACCTCCTCCGCTACTGGGGTGTCACGCCGTCCGCCGTCGTTGGCCATTCGTCGGGTGAGATGGCG GCCGCTTATGCCGTCGGCGCCCTATCCCGCGAGGACTGCCTCACTATTGCCTATCATCGCGGTGTGGTATCTGAA ATGGCAGCCCAACGCGAGCCTGGCGGTGCCATGATGGCCGTCGGTCTCTCTGCCGACGAGATCCGGCCGCGACTG GTCAGCTCCGCCATCACCGTGGCTTGCATCAACAGCCCCAACAACGTGACGCTGGCGGGAGACGCCGCGGCTCTC GAGGAACTGGCCGAGTCTCTGAAGCGCGACGACGTCTTCTGCCGCGTTCTGAAGGTTCAAAACGCCTTCCACAGC CCGCAGATGCAGACTGTGGCCGATGAGTACCGTCGACGTATCGCCGGCGTCAAGCCCGTCGACGTTACGGCCGCC TTCCACTCCACCGTCCACGGCTGCCGGATTCCCACATCGAAGCTGACGGCTGACTACTGGGTGGCCAATCTCTGC TCTCCCGTCGAGCTCGTCCGAGCCTTGGACGACATGCTGTGCACCAACGACGGCAAGGGTAAGAGATCCAAGGCA CCCACCATCATGGTTGAAGTCGGGCCTCACGGCGTCCTCGCCGGCCCCTTTGAGCAGTTCCGGCTCGCCCGCCGC GGCCTGGAGCACCTCGGCTACTACAGTCTTCTCTCACGGGGACGGGACGCCATGATTACGGCAATGACAGCCGCT TCCGCTCTCTGGATGAGGGGTGCTGCTGTTCGGGTCGACAAGATTAATGACTTGGACGAGGCCTCTCGGCCCGCC ACCGTCCTCACTGATCTGCCGTCCTACAGCTGGAATCACTCCGTCTCGTACTGGCACGAGACATGGGGCTCGCGA AACCGCCGCTGGCCATCGGCTCCCAAGCACGATCTGATCGGGTGGCGGCTCCCTGCATGCAACCCGCTGGAGCCC GTGTGGAAGAATTACCTGCGCGTCGGCGAGATTCCCTGGCTCAAGGATCACCAGGTGCACGGCGACGTTGTGTTT CCCGCTGCCGGCGTCATCAGCGCCGTCATCGAGGCCATGCGCCAGTTTGAAAGCGGTCATGACATCACGAGCTTC GAGCTCCGCGAGTTCTACATCCCCCGGCCCCTTCTCATCCCCAGTACCGAGCTCGGTGCCGAGACCTTCCTCCAC CTGAAGCGCAGGAAAACGGGCATGGGCAGCGGGGCCGGCCCCTGGCTCGAATTCTCCTTTTACTCGCGTCAGGAC GACGACACCTTTGTCGAGCACGCCCATGGGCTCGTCCAGGCTCACTTTGCCAAGCAGTGCAACGAGGTGGACGGA GGCAGGGAGCTGCGGGAGGAGACGCTGGCGCACCAGAGACGCTTCCGACATCAGGTCAAAACGTGCGACGAGCCG CTCACTAGCCAAGCTCACTACGAGTTTTGCAGGAGCATAGGCCTCGTTTACGGTGACAACTTTCAGGGCCTATGC AATGTGCGGCTCAGAGACACCAACGTCGCCTTTGAGGTTTCCGTCGTCGACACGCCGGCCTGCATGCCGGGAGCG TGTGAGTCGGATTACCTGGTTCACCCGACGACCATCGACCTCTTGTTCCAGGCCCTCCTGGCGACGCTACCCAAC ATGCGGGACGCCGAGAAGCAGGGATGGGCCCCGACGGCCGTCGGCTCGATCCGTGTCTCGACGGCCATTCGACGC GGTCCCGGCACGGTACTTCAGGGCCACGGTGAGCTGTCCTCCGGGGCTGCCCATCAGATGGTGGGCTTCGTCATG GCGGGCGACGGCGTCTTCGACTCGTTTCCGGCAGTTGTCATGGACGGAATCCAGGTTTCGGCTCTGGGCACCATG CAGAGCGCTTCGGTTAATGCGTCCGAGGACTCGATTGTCAAGCTGTACGCGACGCCTGCCTGGAAGCCAGACCTG CTTCTCCTCGAGGGACGACGTCCGGCGCGGCTGGCCGTGGGGGCGACTCAGGACCATGACGCGGCTCGGTTCAGC ATCGACAGCCGCGAGATCGTCGACGACATGTGCCGCGCCGCCTTGCAGCGTCTGGACGACGAGGCCATCGCGGAG CTGGCCCCCCATTTGCAGCAGTACGTCTCCTGGATGCAGAAGCGCACCAGCGAGACCAGGACGTTCGCCAGCATC ACGCCGCCCATTAGCCCGGGCTTCAGCGCCTACGACGTCAAGGTGGACGAGTACTTTAGCATCAACAAGCTCAAG AGCTTCATCGACAGGTTTCCTGTCGACGGGCGCCTCTTGCAGCACGCCTTTGCCTGCATCGACCCCATCTTCAGC GGGGAGACGACACCGATCGCGGCCCTGATGGCGAGCGACGATTTCGCCCGCTTCTACAAGGAGTCCAACGGTGCC GAGGTCATGATACCCATCTTCCGCAACTGGTTCGACCTCAAGGCACACAAGAAGCCAAGCCTGCGCATTCTCGAA GTCGGGGGCGGCACGGGCGCGATGACGGTGCCCATTCTGGAGACGATGGGAGACGCCGAGGGCGAGACGCCACGT TTCTCAGGCTTTACCTTTACCGACATCTCACCCGGCTGGTTCGAGGGCGCCCGGACGCTGCTGCGTCGCTGGAAG TCTCGTGTCGATTACAAGGTGCTCAACATTGAGGTTGATCCCGTTGAGCAGGGGTTCGAGCCCGAGTCTTATGAT GTCATCTTGGCTTTCAATGTCCTCCATGCCACGAAAAGCATAAAAACGTCGCTCGAAAACTGCCGCCGGCTGCTC AAGCCCGGAGGCAACCTCATCGTCGGCGAATGCACTAATCCCGACGATATGCTCAGCTTCATCTTTGGCCTCTTG CCCGGCTGGTGGGCCGCCGAGGACGGCAGGCAGTTTGGCCCCTTGCTGAGCGAGTCCGCCTGGGATAAGACGCTC AAGGATGCTGGCTTCTCCGGCACCGATATCGCCATGCCGGACGGCGACGATGAGGCTGGCCATCATCGGATGTCG GTCATGGTCAGTACCAAGCCGCACGAGCAGGAGACATCCTCTTCGACCAAAGACGTCGTCGTTCTCGTTGCCAAC AATAGCATCAACGACATCGGGAAAAGCCTCGCCGCCTCCGTCCGCCGCGATCTTGAGCAGCTCGGAGCCCGCGTC AGTATCAAAGTTTTGGGATCGTCCGAGATCAAATTCGAGGGCAAGACGGTCATCTCTCTCTTGGAGTACGGCATG CCGATCCTCCAACAGGTCCAGGAAGCCGACTTCGAGAACATCAAGCACGTCTTGCTTCATTGCCGCGAGCTCCTC TGGGTTACGCGCTCGGATGCGGCGGACAAGGAGGGACATCCCAGTATGCGCATCATCTCGGGCCTGCTTCACTGC CTCAAGAACGAGGACGCGTCTCGAAGGCTTCACGAGCTGCATCTTTGCCGAAACGTCACGGCTAGCGTGGCCAAG ACCAGCGACGTCATTCTCCGCAGGCTCAACAGTCTGTGGCAAGGTGAAGGGGAAGAGGCAGCGGAGCTGGTCACG GTGGAGCGAGACGGCGAATTCTGCATTCCCCGTTACGTGCCGGAAAAGACGATGAACCGCAGCCTGGCGCGCACG ACCGATTCTGATCTGGAGCTGCAGACAGAGAAGCTCGTGCAGGCCGGCCGGCCATTGCGGCTCAAAATTGGGCGG CCAGGGATGTTGGACACGCTTCATTTCGGCGACGATGATGAGGCCTTGCAGCCGCTGGCCAAAGACGAAGTCATG ATTGAGGTGTTGGCGGACGTCTTGATTGCAATGGGCGAGCTCCGGTCGCCGAATCTGGGCTACGAGGCAGCCGGC ATCATCGTCGGCACCGGGGCCAAGGTGACGCGGCTGTCGGTCGGCGATCGGGTTCTGTGCCTGAGGCCGGCCGTG ATGCGCACGCGGATCCGCACCAACCAGTGGCACGTCCACCTGCTGCCGGCCTGCTTGTCGATTGAGAACGGCGTG ACGATTCCGGTGGCATACGCCACTGCGTATCGTTGTCTTGTCGAAGTGGCGAGGCTGGAAAAGGGGGAGACGGTG CTGATTCACGCCGCAGCGGGGGGCTTCGGACAGGCTTCGATCCACATGGCCAAGATGCTGGGTGCCGACATCTTC TGTACGGTCAGCTCCGAGGCCAAGAAGCGGCTGGTCGTCTCGCTCGGGGTCAAGCCCGAGCATGTCTTTAGCTCG CGCGATGTCTCGTTCGAGGCAGGCATCAAGAGGATCACTAACGGCCGTGGCGTCGACGTCGTCGTCAATTCGCTT GCCGGCGAGCTGCTACGCCGAAGCTGGGCCTGTATGGCTCCCTACGGCCGCTTCGTCGAGGTCGGCAAGCGAGAC ATTGTGGGCAATAGCGGGCTAGACATGCAGCCGTTCGATAACAACGCCGTGTTCGCGTGCGTTAACCTCGATGCT ATGACGTCTGAGCCGCGGCGGCTGTGGGAGCTGGTGGACAAGGTGCTTCGCTTGTTTGAGCAGGGCTCGCTGGGA CTGATCCAGCCCATTGCCGTCCATGACTTCTCCGACCTCGAAGCCGTCTTCCGCGAAATGCAACGAGGAGCGCAT ATGGGCAAGCTGGCGCTGCGCGTGACGCCCGAGTCGCGGGTTCCGGTTGCGCCGCGAAAGACGGTGCCCCTGAAG CTGTCGCCGGATGCGACATACCTGCTGGCCGGCGGCCTCGGCGGACTTGGCCGGGCCCAGGCTCTGTTTATGGTC GAACACGGGGCTCGGCACTTGGCCTTTGTGTCGCGGTCCGGCGACTCGCGGCCCGAGGCCCGGAAGCTGCTGGAC ACGCTGGCAAAGGCCGGGGTCAAGACCCGGGCCTACGCCGGCGACGTGGCCGACCGCGACGGGCTAGGTGCCATT CTCGACGACGTGGCGCGCCGCATGCCGCCTATACGCGGTGTCATTCAGGGCGCCATGGTGCTCGACGACGCCCTC TTCCAGAATATGTCATACGACCAGTGGCAGAATGCGACACGGCCCAAGATCCAGGGCAGCTGGAACCTTCACGAA CTGCTGCCGGCCGACCTCGACTTCTTCGTCGTCCTCTCCTCCATGGCTGGAGCCATCGGCTTCGTCTCCCAGGCC AACTACGCGGCCGGCAACACATACCAGGACGCGCTGGCCCATTACCGACACGCCCGGGGTCTGCCAGCGTTGAGC ATCGACCTCGGCATCACAAAGGGCTTTGGCTACGTGGCCGAGCACGAGGAGGTTGCAGCTAAGCTGAAGCCGTAC GGGCTGGCGACGGTCAACGAGCAGCAGCTATTTCACCTACTACGCTGCGCCATGGCCGGCACCGCCGACGGCGAC AATAAGCTGCCCACGCGGCAGCTGCTCGCCGGCGCCGGTACGGGGGGTCTGGCTCAGGCGTCACTTGCGACGGTG CCCGAGACGAACCTGTTCTGGCTCTCGGCCCTGGCGTCCTTCTCTTACCTGGGCGAGGTGGACATGAGAGCCTCG GCCGAGACGGCGGGCGATGAGATGACGGACGACGCGCGGCTCGTCGGCCAGCTATCAGCGTCCAAGACGATGGAC GAGGCGGCCGAGGTGGTGCAAGACATGCTGCTGGCGCGCATCTCGACCATCATGTCGGTGCCGACGGCTGACATC GACACAGCCAAGCCGGTTCACGCGTACGGCGTCGACAGTTTGGTGGCCGTTGAGCTGCGAAACTGGCTGTCGAAG CGGCTGCGTAGCGACGTCAGCATCTTTGACCTGACGGGCAACATGGCCATTACGACGCTGAGCCGGAAGATTGCC AGCCGGTCACGCCTGGTCCCCACTGCGGCCAAAGGGCAGGGCGGCAACGAGACTGGTGTTGCTGAGTGA |
| Gene | >Ophun1|2808 ATGCGTATTCTCTGCGTCCACGGAGCCGCTATCAACGGCGACATCTTCGCTTCCAAGACGGAGAAGCTTCGAGCT CTGCTGCCGGCCGACTACTCATATGAATGGCCCGAAGGCGAGCACGAGGTGACACCCATCCAAAGCCTCTCCGAC ACTTATCCCGGACCCTATCTTTCGCACCTAGAAGAAATCACCACCCGCGGCATCCGGAATTCCATCGAGAGACTC GAGGCTTGCATCGAGGAGGACGGTCCGTTTGACGGTGTCATGGCCATCTGCGAGGTGCTCTCCTTCCGACACCCC GTCGTTCCCTCGCGATTGAACAAAGACTGACTGGCAAACGCACCAAGCAGGGTGCTATGCTCGTCGCAGGCCTGC TCTTCAAACGGCAGATGGAAGACCCAACGGGGCCGCTGCCGTTCAGGTTCGCCATCTTCATCGCAGGCGCTCCTC CGCTCACCTGGTCCGACTCAGTCGGGCAGAACATGTTCAATCAGGTCATGAGTGAAGACCCCCTCGACGTCGACA AGGACAACTTTGACGAGCCGGAGGCCGGGATCCAAGGCAGGCCCAATATCGAGTACATCAAGGAATTTGGCCGCA AGCTGTACCGAGACCTGACTCCCGAGCTGGAGAAATGGGTGCAAACCGTCGAGGACATGGGCACCGATCCCGACA AGGCACGCCTCATGCCGCACGCGATACTGCCTCAGCTGCATCCGGATAGACTCGATCTGCCCACGGCTCACATGT GGGGACGTAACGACGTCTTGAGCAGCCACTCGGGCCTCTTGTTCCGGCTCTGCAACCCGGACTTTGCACTGAGCC ACGTGCATGATGGGGTACACGACGTCCCGCAGTCGTCCAAGGACAACGAGATCTTTAGCAACTTGGTCCGTAAGA CAATTCTGCGCAGCCAATTCGCAGTGTAGTAGATGATGGGGGGGTGAAACAATCGGCGGAGGGATGGACATGGGA GGGGAATATCGGCGGAACGAGAATGACAAAGCCTTGTATCCAGGCAGTCGGTTTCGAGACATGACATAGATATCT ATAGGTGGCCTAGTTGAGCAGGGATGAGATAATGTTGTTGCTGAAGTTTCGAGCTTCCTCAATCCTCGCCGTTTC TAGTGAAACGGATCCAACCGGCTTCAGCTGACGCAACACGTTGTTAGGTCTCCAAACGAGTGAATGGGTTTCTCT TCCGTCGTCATCCCAACCGCATCGACAAAAGAGGAAGCTTGACGCACCTTTCGTCTCGATGGCTCGGAGTAATGG CTGGATCGGGGCGATCCGATCTGGCGCTCGCCTGTGCACAAGAACAAGTCCCGGGCAACCATCGAGAAAGAATAC ACGGCTGGAGGAGGCACCGTTCCTCCGTCGACGGGAAGAGTCAGCTCCAATGCAATATAAGAAAGACGCTCTCTC TTGAGCAAGCAAAATATATGCCCAATCTGTTGAAGTCGTAATCTTTGCTACCGACTATCGCAGAAACAACATGGC CGCTGTCGACATCGCCATCGTCGGGCTCGCGTGCCGCTTTCCCGGTGAGGCCAAGTCCCCAAAGGCCTTTTACCA GATGCTGGTGCAAGGCCGTGATGCTTGGTCCAAAGTGCCCAAATCACGGTACGATGTCGACGCGTACCGACACCC GTCGCGTGAGCGCCGCGGGACAATGGTAGGAACAGACAGACGCGAGGCGAGTCCATGGGGTTGGTAGAAGCTGAC GGGTCTTTAACAGGTGTGTGAAGGCGGCTACTTTTTAGAAGACGACGTCTCTCGGTGGGACGCGCCCTTTTTCGC CTGCTCGACCGTCGAGGCGCATGCCATGGATCCGCAGCAGAGGCTGCTACTCGAAGTCGCCTACGAGAGCCTGGA GAACGCGGGCATCCCGATGGAGGCGTTGGCCGAAAGCGACGCGGCCTGCTTCGTCGGCGGCTTCACCAACGACTA CCAGCGCATCGTGACGAGCGAGTCGGAGGCGACGCCACAGTATACCATGACGGGAAACTCGACGGCCATGATGGC CAACCGCGTCAGCTGGTTCCTCAACCTACGCGGGCCGTCGGTGACGGTCGACACGGCCTGCTCCAGCTCCATGGC GGCGTTTCATCTGGCTTGCGAGACGATCCGGTCCGAGTCCAACGAAACGCGATGCGCCATGGTCGGTGGCACCAG CCTGCTGTTCAACCCGGACGATCCATGCGGTATGAATGCGCTGGGCTTCCTGAGCCCGGATAGCCGATGCTATAG CTTCGATTCGCGAGCCAACGGCTACGCGCGTGGTGAAGGCGTCGCGATGCTGGTGCTCAAGCACATGGATGACGC GCTGCGAGACGGAGATGCCATTCGGGGCGTGGTGCGTGCATCGGCGCTGAATTCAGACGGACGGGTGAGTCTCTC AAGATTGGTGATGATGTGGGCGACGTTCGATGGTGCCTGAGTGGTAGTAAGCAGATGGACGATAAGGGCTTGCTG ACATGATATCAAAACACCAAGACGGCCGGCATCGTCCTCCCCAATGGAGAGGCTCATCAGCGCCTCATCAATCAC ACCTATCGCCTAGCGGGCTTCCATCCCGCCGATACGCAGTATGCCGAGCTCCACGGCACCGGCACTCGCGTCGGC GATCCCACCGAAATCAGTGCCGTGGCCCGGACCCTCGCCGCCGATCGATCCACGCCGCTGCTATGTGGCTCCGTC AAGACGCAGATTGGTCACTCCGAGGCGGCCGCCGCCATGGCCGGCATTCTCAAATGCGTCCTCTCCATGGAGGCT GGCATCCTGCCGCCAAACAAGAACTTTGTTGAGCCAAATCCGCGGCTCCGGCTCGAGGCCTCCAACATCGTGGTG CCGACCGAGTCGCAGCCGTGGCCCGTAGCCGCCGTCCGCCGCTGCTCTATTAATAGCTTCGGCTTCGGTGGGCTC AACGGTCACGTTATCCTCGACGGTGCTGCTAGCTACCTCGGCAGCCGCGGACTCGCCGTTCCGGACGTCGATGCC GATGCCGAAGCAAAGGCCCGGCCCCGTCTCTTCCTCCTGTCCGCCCCGGAACAGAGCGCCGTGGCCCGCCAGCTC CGCACCCACGCCGACTACCTGACCGACTCCTCGCCGCCCGTCTCTCTGCCGCTCCTCGCTCATACGCTGGGCGCC CGCCGCTCCGTCTTTCAGTGGCGCCTCGCCGTCGTCGCCCGCTCTGCCGACGAGCTCGAGTCCCTCTGGCGTCAG AATGGGCCGGCGCCTATCAAGGCCGTTGCCTCGCCTGGCGTGGCTCTCATCTTCACTGGCCAGGGCGCCCAGTGG CACGCCATGGGTCGCGAGCTACTGGCCCTGCCCGTCTTTGCCCGCTCCGTCCGCGCCTCGGCCGCTGCGCTGGTC GCCCAGGGCTGCCCCTGGGATGCTTGGACCGAGCTCATGCGTCCAGAAGCCGAGTCGCGCGTTGGTCAGGCCGTC TACTCCCAGCCGTTGACGTCGCTACTTCAGATTGCCCTCGTCGACCTCCTCCGCTACTGGGGTGTCACGCCGTCC GCCGTCGTTGGCCATTCGTCGGGTGAGATGGCGGCCGCTTATGCCGTCGGCGCCCTATCCCGCGAGGACTGCCTC ACTATTGCCTATCATCGCGGTGTGGTATCTGAAATGGCAGCCCAACGCGAGCCTGGCGGTGCCATGATGGCCGTC GGTCTCTCTGCCGACGAGATCCGGCCGCGACTGGTCAGCTCCGCCATCACCGTGGCTTGCATCAACAGCCCCAAC AACGTGACGCTGGCGGGAGACGCCGCGGCTCTCGAGGAACTGGCCGAGTCTCTGAAGCGCGACGACGTCTTCTGC CGCGTTCTGAAGGTTCAAAACGCCTTCCACAGCCCGCAGATGCAGACTGTGGCCGATGAGTACCGTCGACGTATC GCCGGCGTCAAGCCCGTCGACGTTACGGCCGCCTTCCACTCCACCGTCCACGGCTGCCGGATTCCCACATCGAAG CTGACGGCTGACTACTGGGTGGCCAATCTCTGCTCTCCCGTCGAGCTCGTCCGAGCCTTGGACGACATGCTGTGC ACCAACGACGGCAAGGGTAAGAGATCCAAGGCACCCACCATCATGGTTGAAGTCGGGCCTCACGGCGTCCTCGCC GGCCCCTTTGAGCAGTTCCGGCTCGCCCGCCGCGGCCTGGAGCACCTCGGCTACTACAGTCTTCTCTCACGGGGA CGGGACGCCATGATTACGGCAATGACAGCCGCTTCCGCTCTCTGGATGAGGGGTGCTGCTGTTCGGGTCGACAAG GTGAGTCTCGACATCTTTTACCCTTCGACAGAGAGCCATCTTGCTGACGCGTCCGCTTCCAGATTAATGACTTGG ACGAGGCCTCTCGGCCCGCCACCGTCCTCACTGATCTGCCGTCCTACAGCTGGAATCACTCCGTCTCGTACTGGC ACGAGACATGGGGCTCGCGAAACCGCCGCTGGCCATCGGCTCCCAAGCACGATCTGATCGGGTGGCGGCTCCCTG CATGCAACCCGCTGGAGCCCGTGTGGAAGAATTACCTGCGCGTCGGCGAGATTCCCTGGCTCAAGGATCACCAGG TGCACGGCGACGTTGTGTTTCCCGCTGCCGGCGTCATCAGCGCCGTCATCGAGGCCATGCGCCAGTTTGAAAGCG GTCATGACATCACGAGCTTCGAGCTCCGCGAGTTCTACATCCCCCGGCCCCTTCTCATCCCCAGTACCGAGCTCG GTGCCGAGACCTTCCTCCACCTGAAGCGCAGGAAAACGGGCATGGGCAGCGGGGCCGGCCCCTGGCTCGAATTCT CCTTTTACTCGCGTCAGGACGACGACACCTTTGTCGAGCACGCCCATGGGCTCGTCCAGGCTCACTTTGCCAAGC AGTGCAACGAGGTGGACGGAGGCAGGGAGCTGCGGGAGGAGACGCTGGCGCACCAGAGACGCTTCCGACATCAGG TCAAAACGTGCGACGAGCCGCTCACTAGCCAAGCTCACTACGAGTTTTGCAGGAGCATAGGCCTCGTTTACGGTA TGTGCAGTTGTCTGGCTGCTGTTCTGTGCGCTTTGGTTGCTGAATGATGGACAGGTGACAACTTTCAGGGCCTAT GCAATGTGCGGCTCAGAGACACCAACGTCGCCTTTGAGGTTTCCGTCGTCGACACGCCGGCCTGCATGCCGGGAG CGTGTGAGTCGGATTACCTGGTTCACCCGACGACCATCGACCTCTTGTTCCAGGCCCTCCTGGCGACGCTACCCA ACATGCGGGACGCCGAGAAGCAGGGATGGGCCCCGACGGCCGTCGGCTCGATCCGTGTCTCGACGGCCATTCGAC GCGGTCCCGGCACGGTACTTCAGGGCCACGGTGAGCTGTCCTCCGGGGCTGCCCATCAGATGGTGGGCTTCGTCA TGGCGGGCGACGGCGTCTTCGACTCGTTTCCGGCAGTTGTCATGGACGGAATCCAGGTTTCGGCTCTGGGCACCA TGCAGAGCGCTTCGGTTAATGCGTCCGAGGACTCGATTGTCAAGCTGTACGCGACGCCTGCCTGGAAGCCAGACC TGCTTCTCCTCGAGGGACGACGTCCGGCGCGGCTGGCCGTGGGGGCGACTCAGGACCATGACGCGGCTCGGTTCA GCATCGACAGCCGCGAGATCGTCGACGACATGTGCCGCGCCGCCTTGCAGCGTCTGGACGACGAGGCCATCGCGG AGCTGGCCCCCCATTTGCAGCAGTACGTCTCCTGGATGCAGAAGCGCACCAGCGAGACCAGGACGTTCGCCAGCA TCACGCCGCCCATTAGCCCGGGCTTCAGCGCCTACGACGTCAAGGTGGACGAGTACTTTAGCATCAACAAGCTCA AGAGCTTCATCGACAGGTTTCCTGTCGACGGGCGCCTCTTGCAGCACGCCTTTGCCTGCATCGACCCCATCTTCA GCGGGGAGACGACACCGATCGCGGCCCTGATGGCGAGCGACGATTTCGCCCGCTTCTACAAGGAGTCCAACGGTG CCGAGGTCATGATACCCATCTTCCGCAACTGGTTCGACCTCAAGGCACACAAGAAGCCAAGCCTGCGCATTCTCG AAGTCGGGGGCGGCACGGGCGCGATGACGGTGCCCATTCTGGAGACGATGGGAGACGCCGAGGGCGAGACGCCAC GTTTCTCAGGCTTTACCTTTACCGACATCTCACCCGGCTGGTTCGAGGGCGCCCGGACGCTGCTGCGTCGCTGGA AGTCTCGTGTCGATTACAAGGTGCTCAACATTGAGGTTGATCCCGTTGAGCAGGGGTTCGAGCCCGAGTCTTATG ATGTCATCTTGGCTTTCAATGTACGAAGCACATTCTCCTTCTTTCATTCTTCCTCTTCTTCTCCTTTGCCCTCCT TCCTCTCGTTCTGACATCATCTACAGGTCCTCCATGCCACGAAAAGCATAAAAACGTCGCTCGAAAACTGCCGCC GGCTGCTCAAGCCCGGAGGCAACCTCATCGTCGGCGAATGCACTAATCCCGACGATATGCTCAGCTTCATCTTTG GCCTCTTGCCCGGCTGGTGGGCCGCCGAGGACGGCAGGCAGTTTGGCCCCTTGCTGAGCGAGTCCGCCTGGGATA AGACGCTCAAGGATGCTGGCTTCTCCGGCACCGATATCGCCATGCCGGACGGCGACGATGAGGCTGGCCATCATC GGATGTCGGTCATGGTCAGTACCAAGCCGCACGAGCAGGAGACATCCTCTTCGACCAAAGACGTCGTCGTTCTCG TTGCCAACAATAGCATCAACGACATCGGGAAAAGCCTCGCCGCCTCCGTCCGCCGCGATCTTGAGCAGCTCGGAG CCCGCGTCAGTATCAAAGTTTTGGGATCGTCCGAGATCAAATTCGAGGGCAAGACGGTCATCTCTCTCTTGGAGT ACGGCATGCCGATCCTCCAACAGGTCCAGGAAGCCGACTTCGAGAACATCAAGCACGTCTTGCTTCATTGCCGCG AGCTCCTCTGGGTTACGCGCTCGGATGCGGCGGACAAGGAGGGACATCCCAGTATGCGCATCATCTCGGGCCTGC TTCACTGCCTCAAGAACGAGGACGCGTCTCGAAGGCTTCACGAGCTGCATCTTTGCCGAAACGTCACGGCTAGCG TGGCCAAGACCAGCGACGTCATTCTCCGCAGGCTCAACAGTCTGTGGCAAGGTGAAGGGGAAGAGGCAGCGGAGC TGGTCACGGTGGAGCGAGACGGCGAATTCTGCATTCCCCGTTACGTGCCGGAAAAGACGATGAACCGCAGCCTGG CGCGCACGACCGATTCTGATCTGGAGCTGCAGACAGAGAAGCTCGTGCAGGCCGGCCGGCCATTGCGGCTCAAAA TTGGGCGGCCAGGGATGTTGGACACGCTTCATTTCGGCGACGATGATGAGGCCTTGCAGCCGCTGGCCAAAGACG AAGTCATGATTGAGGTGTTGGCGTGTGGCCTCAACTTCCGGCAGGTTTATACGCGCCCACGAGGCAGAGATGTTG CTAACGAACCATATACAGGGACGTCTTGATTGCAATGGGCGAGCTCCGGTCGCCGAATCTGGGCTACGAGGCAGC CGGCATCATCGTCGGCACCGGGGCCAAGGTGACGCGGCTGTCGGTCGGCGATCGGGTTCTGTGCCTGAGGCCGGC CGTGATGCGCACGCGGATCCGCACCAACCAGTGGCACGTCCACCTGCTGCCGGCCTGCTTGTCGATTGAGAACGG CGTGACGATTCCGGTGGCATACGCCACTGCGTATCGTTGTCTTGTCGAAGTGGCGAGGCTGGAAAAGGGGGAGAC GGTGCTGATTCACGCCGCAGCGGGGGGTGAGTAGGCTCCGCGACTACGGTGGGAACGTTGTGATTAACGGATATT CTTTCTCTAGGCTTCGGACAGGCTTCGATCCACATGGCCAAGATGCTGGGTGCCGACATCTTCTGTACGGTCAGC TCCGAGGCCAAGAAGCGGCTGGTCGTCTCGCTCGGGGTCAAGCCCGAGCATGTCTTTAGCTCGCGCGATGTCTCG TTCGAGGCAGGCATCAAGAGGATCACTAACGGCCGTGGCGTCGACGTCGTCGTCAATTCGCTTGCCGGCGAGCTG CTACGCCGAAGCTGGGCCTGTATGGCTCCCTACGGCCGCTTCGTCGAGGTCGGCAAGCGAGACATTGTGGGCAAT AGCGGGCTAGACATGCAGCCGTTCGATAACAACGCCGTGTTCGCGTGCGTTAACCTCGATGCTATGACGTCTGAG CCGCGGCGGCTGTGGGAGCTGGTGGACAAGGTGCTTCGCTTGTTTGAGCAGGGCTCGCTGGGACTGATCCAGCCC ATTGCCGTCCATGACTTCTCCGACCTCGAAGCCGTCTTCCGCGAAATGCAACGAGGAGCGCATATGGGCAAGCTG GCGCTGCGCGTGACGCCCGAGTCGCGGGTTCCGGTTGCGCCGCGAAAGACGGTGCCCCTGAAGCTGTCGCCGGAT GCGACATACCTGCTGGCCGGCGGCCTCGGCGGACTTGGCCGGGCCCAGGCTCTGTTTATGGTCGAACACGGGGCT CGGCACTTGGCCTTTGTGTCGCGGTCCGGCGACTCGCGGCCCGAGGCCCGGAAGCTGCTGGACACGCTGGCAAAG GCCGGGGTCAAGACCCGGGCCTACGCCGGCGACGTGGCCGACCGCGACGGGCTAGGTGCCATTCTCGACGACGTG GCGCGCCGCATGCCGCCTATACGCGGTGTCATTCAGGGCGCCATGGTGCTCGACGACGCCCTCTTCCAGAATATG TCATACGACCAGTGGCAGAATGCGACACGGCCCAAGATCCAGGGCAGCTGGAACCTTCACGAACTGCTGCCGGCC GACCTCGACTTCTTCGTCGTCCTCTCCTCCATGGCTGGAGCCATCGGCTTCGTCTCCCAGGCCAACTACGCGGCC GGCAACACATACCAGGACGCGCTGGCCCATTACCGACACGCCCGGGGTCTGCCAGCGTTGAGCATCGACCTCGGC ATCACAAAGGGCTTTGGCTACGTGGCCGAGCACGAGGAGGTTGCAGCTAAGCTGAAGCCGTACGGGCTGGCGACG GTCAACGAGCAGCAGCTATTTCACCTACTACGCTGCGCCATGGCCGGCACCGCCGACGGCGACAATAAGCTGCCC ACGCGGCAGCTGCTCGCCGGCGCCGGTACGGGGGGTCTGGCTCAGGCGTCACTTGCGACGGTGCCCGAGACGAAC CTGTTCTGGCTCTCGGCCCTGGCGTCCTTCTCTTACCTGGGCGAGGTGGACATGAGAGCCTCGGCCGAGACGGCG GGCGATGAGATGACGGACGACGCGCGGCTCGTCGGCCAGCTATCAGCGTCCAAGACGATGGACGAGGCGGCCGAG GTGGTGCAAGACATGCTGCTGGCGCGCATCTCGACCATCATGTCGGTGCCGACGGCTGACATCGACACAGCCAAG CCGGTTCACGCGTACGGCGTCGACAGTTTGGTGGCCGTTGAGCTGCGAAACTGGCTGTCGAAGCGGCTGCGTAGC GACGTCAGCATCTTTGACCTGACGGGCAACATGGCCATTACGACGCTGAGCCGGAAGATTGCCAGCCGGTCACGC CTGGTCCCCACTGCGGCCAAAGGGCAGGGCGGCAACGAGACTGGTGTTGCTGAGTGA |