© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|4083 |
| Gene name | |
| Location | scaffold_32:29691..37876 |
| Strand | + |
| Gene length (bp) | 8185 |
| Transcript length (bp) | 7659 |
| Coding sequence length (bp) | 7656 |
| Protein length (aa) | 2552 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00109 | ketoacyl-synt | Beta-ketoacyl synthase, N-terminal domain | 3.0E-71 | 5 | 256 |
| PF08659 | KR | KR domain | 2.4E-62 | 2164 | 2341 |
| PF00698 | Acyl_transf_1 | Acyl transferase domain | 4.5E-51 | 536 | 816 |
| PF14765 | PS-DH | Polyketide synthase dehydratase | 4.1E-45 | 913 | 1203 |
| PF02801 | Ketoacyl-synt_C | Beta-ketoacyl synthase, C-terminal domain | 6.3E-31 | 265 | 379 |
| PF08242 | Methyltransf_12 | Methyltransferase domain | 3.2E-18 | 1432 | 1538 |
| PF16197 | KAsynt_C_assoc | Ketoacyl-synthetase C-terminal extension | 1.4E-16 | 382 | 505 |
| PF00107 | ADH_zinc_N | Zinc-binding dehydrogenase | 5.1E-14 | 1967 | 2060 |
| PF13602 | ADH_zinc_N_2 | Zinc-binding dehydrogenase | 2.4E-11 | 2005 | 2140 |
| PF00106 | adh_short | short chain dehydrogenase | 1.6E-11 | 2167 | 2313 |
| PF13649 | Methyltransf_25 | Methyltransferase domain | 1.8E-11 | 1430 | 1536 |
| PF08241 | Methyltransf_11 | Methyltransferase domain | 3.1E-11 | 1432 | 1540 |
| PF13489 | Methyltransf_23 | Methyltransferase domain | 1.1E-10 | 1423 | 1588 |
| PF13847 | Methyltransf_31 | Methyltransferase domain | 1.5E-08 | 1425 | 1544 |
| PF13561 | adh_short_C2 | Enoyl-(Acyl carrier protein) reductase | 7.3E-07 | 2173 | 2312 |
| PF08240 | ADH_N | Alcohol dehydrogenase GroES-like domain | 1.6E-06 | 1850 | 1905 |
| PF01209 | Ubie_methyltran | ubiE/COQ5 methyltransferase family | 1.0E-05 | 1419 | 1546 |
| PF00550 | PP-binding | Phosphopantetheine attachment site | 3.7E-05 | 2469 | 2520 |
| 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 | 2 | 2538 | 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 | 6 | 1847 | 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 | 6 | 1185 | 5.0E-170 |
| sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 6 | 1152 | 3.0E-165 |
| sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 6 | 1152 | 1.0E-163 |
| 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 | 2 | 2538 | 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 | 6 | 1847 | 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 | 6 | 1185 | 5.0E-170 |
| sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 6 | 1152 | 3.0E-165 |
| sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 6 | 1152 | 1.0E-163 |
| 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 | 6 | 1182 | 1.0E-137 |
| sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 6 | 1182 | 1.0E-137 |
| sp|P9WQE2|PPSD_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsD PE=3 SV=1 | 6 | 1182 | 1.0E-137 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 6 | 1151 | 2.0E-129 |
| sp|P9WQE9|PHAS_MYCTU | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks2 PE=1 SV=1 | 6 | 1175 | 4.0E-126 |
| sp|P9WQE8|PHAS_MYCTO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=pks2 PE=3 SV=1 | 6 | 1175 | 4.0E-126 |
| sp|A5U9F4|PHAS_MYCTA | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=pks2 PE=3 SV=1 | 6 | 1175 | 4.0E-126 |
| sp|Q7TVK8|PHAS_MYCBO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks2 PE=3 SV=1 | 6 | 1175 | 4.0E-126 |
| sp|A1KQG0|PHAS_MYCBP | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=pks2 PE=3 SV=1 | 6 | 1175 | 7.0E-126 |
| 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 | 6 | 995 | 4.0E-124 |
| sp|P96202|PPSC_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsC PE=1 SV=2 | 6 | 1240 | 4.0E-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 | 6 | 1240 | 4.0E-122 |
| sp|B4XYB8|AZIB_STREG | 5-methyl-1-naphthoate synthase OS=Streptomyces sahachiroi GN=aziB PE=1 SV=1 | 6 | 965 | 2.0E-121 |
| sp|P22367|MSAS_PENPA | 6-methylsalicylic acid synthase OS=Penicillium patulum PE=1 SV=1 | 5 | 964 | 1.0E-120 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 6 | 788 | 3.0E-120 |
| 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 | 6 | 788 | 1.0E-119 |
| sp|P9WQE5|PPSB_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsB PE=1 SV=1 | 6 | 788 | 2.0E-119 |
| sp|P9WQE4|PPSB_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsB PE=3 SV=1 | 6 | 788 | 2.0E-119 |
| 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 | 6 | 995 | 5.0E-119 |
| sp|Q869W9|PKS16_DICDI | Probable polyketide synthase 16 OS=Dictyostelium discoideum GN=pks16 PE=2 SV=1 | 5 | 990 | 3.0E-117 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 6 | 896 | 1.0E-116 |
| sp|Q869X2|PKS17_DICDI | Probable polyketide synthase 17 OS=Dictyostelium discoideum GN=pks17 PE=3 SV=1 | 5 | 990 | 1.0E-116 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 2 | 896 | 3.0E-116 |
| sp|Q02251|MCAS_MYCBO | Mycocerosic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mas PE=1 SV=2 | 6 | 954 | 1.0E-115 |
| sp|Q55E72|PKS1_DICDI | Probable polyketide synthase 1 OS=Dictyostelium discoideum GN=stlA PE=1 SV=1 | 4 | 990 | 7.0E-115 |
| sp|P9WQE6|PPSA_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsA PE=3 SV=1 | 6 | 788 | 2.0E-113 |
| sp|P9WQE7|PPSA_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsA PE=1 SV=1 | 6 | 788 | 3.0E-113 |
| 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 | 6 | 788 | 6.0E-113 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 6 | 813 | 1.0E-112 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 6 | 817 | 9.0E-112 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 6 | 816 | 1.0E-111 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 6 | 816 | 7.0E-105 |
| sp|P12276|FAS_CHICK | Fatty acid synthase OS=Gallus gallus GN=FASN PE=1 SV=5 | 5 | 892 | 5.0E-103 |
| sp|P19096|FAS_MOUSE | Fatty acid synthase OS=Mus musculus GN=Fasn PE=1 SV=2 | 5 | 966 | 6.0E-103 |
| sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 5 | 966 | 8.0E-102 |
| sp|P49327|FAS_HUMAN | Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 | 5 | 966 | 9.0E-102 |
| sp|Q54IX3|PKS26_DICDI | Probable polyketide synthase 26 OS=Dictyostelium discoideum GN=pks26 PE=3 SV=1 | 3 | 1127 | 3.0E-100 |
| sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 6 | 964 | 1.0E-99 |
| sp|Q559A9|PKS13_DICDI | Probable polyketide synthase 13 OS=Dictyostelium discoideum GN=pks13 PE=3 SV=1 | 3 | 967 | 3.0E-99 |
| sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 2 | 985 | 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 | 4 | 907 | 4.0E-98 |
| sp|B0G103|PKS10_DICDI | Probable polyketide synthase 10 OS=Dictyostelium discoideum GN=pks10 PE=3 SV=1 | 3 | 968 | 5.0E-98 |
| sp|Q55CN6|PKS3_DICDI | Probable polyketide synthase 3 OS=Dictyostelium discoideum GN=pks3 PE=3 SV=1 | 14 | 1130 | 6.0E-98 |
| sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 2 | 985 | 2.0E-97 |
| sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 6 | 964 | 4.0E-97 |
| sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 5 | 985 | 1.0E-96 |
| sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 3 | 989 | 2.0E-96 |
| sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 2 | 985 | 8.0E-96 |
| sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 3 | 964 | 9.0E-96 |
| sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 6 | 994 | 2.0E-95 |
| sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 6 | 964 | 5.0E-95 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 6 | 964 | 1.0E-94 |
| sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 6 | 995 | 1.0E-94 |
| sp|B0G100|PKS7_DICDI | Probable polyketide synthase 7 OS=Dictyostelium discoideum GN=pks7 PE=3 SV=1 | 1 | 968 | 2.0E-94 |
| sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 1 | 968 | 8.0E-94 |
| sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 6 | 985 | 1.0E-93 |
| sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 5 | 959 | 2.0E-93 |
| sp|B0G138|PKS21_DICDI | Probable polyketide synthase 21 OS=Dictyostelium discoideum GN=pks21 PE=3 SV=1 | 64 | 957 | 2.0E-93 |
| sp|B0G0Z9|PKS6_DICDI | Probable polyketide synthase 6 OS=Dictyostelium discoideum GN=pks6 PE=3 SV=1 | 1 | 968 | 3.0E-93 |
| sp|Q54KU5|PKS24_DICDI | Probable polyketide synthase 24 OS=Dictyostelium discoideum GN=pks24 PE=3 SV=1 | 6 | 985 | 8.0E-93 |
| sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 7 | 985 | 1.0E-92 |
| sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 5 | 985 | 2.0E-92 |
| 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 | 6 | 890 | 1.0E-91 |
| sp|Q12053|PKSL1_ASPPA | Noranthrone synthase OS=Aspergillus parasiticus GN=pksL1 PE=1 SV=1 | 3 | 915 | 2.0E-91 |
| sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 64 | 957 | 2.0E-91 |
| sp|P9WQE1|PPSE_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsE PE=1 SV=1 | 6 | 901 | 5.0E-91 |
| sp|P9WQE0|PPSE_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsE PE=3 SV=1 | 6 | 901 | 5.0E-91 |
| 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 | 6 | 901 | 5.0E-91 |
| sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 2 | 964 | 1.0E-90 |
| sp|B0G101|PKS8_DICDI | Probable polyketide synthase 8/35 OS=Dictyostelium discoideum GN=pks8 PE=3 SV=1 | 6 | 968 | 2.0E-90 |
| sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 5 | 985 | 6.0E-90 |
| sp|Q86JI5|PKS5_DICDI | Probable polyketide synthase 5 OS=Dictyostelium discoideum GN=pks5 PE=2 SV=1 | 6 | 968 | 3.0E-89 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 6 | 513 | 3.0E-88 |
| sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 5 | 860 | 4.0E-87 |
| sp|Q54B51|PKS44_DICDI | Probable polyketide synthase 44 OS=Dictyostelium discoideum GN=pks44 PE=3 SV=1 | 5 | 966 | 1.0E-86 |
| sp|Q54B49|PKS45_DICDI | Probable polyketide synthase 45 OS=Dictyostelium discoideum GN=pks45 PE=3 SV=2 | 5 | 966 | 2.0E-86 |
| sp|Q55DM7|PKS2_DICDI | Probable polyketide synthase 2 OS=Dictyostelium discoideum GN=pks2 PE=3 SV=1 | 5 | 966 | 4.0E-86 |
| 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 | 6 | 426 | 1.0E-85 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 6 | 540 | 4.0E-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 | 1779 | 2511 | 3.0E-77 |
| 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 | 1779 | 2511 | 3.0E-77 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 6 | 514 | 6.0E-77 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 1 | 519 | 1.0E-76 |
| sp|Q55E72|PKS1_DICDI | Probable polyketide synthase 1 OS=Dictyostelium discoideum GN=stlA PE=1 SV=1 | 1388 | 2533 | 2.0E-73 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 6 | 516 | 2.0E-73 |
| sp|Q9R9J1|MYCA_BACIU | Mycosubtilin synthase subunit A OS=Bacillus subtilis GN=mycA PE=3 SV=1 | 2 | 513 | 7.0E-73 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 5 | 514 | 2.0E-71 |
| 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 | 1823 | 2507 | 4.0E-71 |
| 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 | 1823 | 2507 | 1.0E-70 |
| 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 | 1823 | 2513 | 2.0E-70 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 5 | 518 | 1.0E-69 |
| sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 1422 | 2536 | 7.0E-69 |
| sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 5 | 427 | 2.0E-68 |
| sp|P36189|FAS_ANSAN | Fatty acid synthase (Fragment) OS=Anser anser anser GN=FASN PE=1 SV=1 | 5 | 372 | 9.0E-68 |
| sp|Q02251|MCAS_MYCBO | Mycocerosic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mas PE=1 SV=2 | 1655 | 2338 | 2.0E-67 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 1830 | 2526 | 4.0E-67 |
| sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 1422 | 2536 | 5.0E-67 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 2 | 513 | 5.0E-67 |
| sp|A1KQG0|PHAS_MYCBP | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=pks2 PE=3 SV=1 | 1822 | 2527 | 6.0E-62 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 6 | 513 | 6.0E-62 |
| sp|P9WQE9|PHAS_MYCTU | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks2 PE=1 SV=1 | 1822 | 2527 | 7.0E-62 |
| sp|P9WQE8|PHAS_MYCTO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=pks2 PE=3 SV=1 | 1822 | 2527 | 7.0E-62 |
| sp|A5U9F4|PHAS_MYCTA | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=pks2 PE=3 SV=1 | 1822 | 2527 | 7.0E-62 |
| sp|Q7TVK8|PHAS_MYCBO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks2 PE=3 SV=1 | 1822 | 2527 | 7.0E-62 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 6 | 513 | 1.0E-60 |
| sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 1851 | 2362 | 5.0E-60 |
| sp|P12276|FAS_CHICK | Fatty acid synthase OS=Gallus gallus GN=FASN PE=1 SV=5 | 1856 | 2344 | 1.0E-58 |
| sp|P19096|FAS_MOUSE | Fatty acid synthase OS=Mus musculus GN=Fasn PE=1 SV=2 | 1856 | 2348 | 5.0E-57 |
| sp|P49327|FAS_HUMAN | Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 | 1844 | 2366 | 1.0E-56 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 5 | 426 | 4.0E-56 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 6 | 512 | 5.0E-56 |
| sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 1856 | 2348 | 2.0E-55 |
| sp|Q86JI5|PKS5_DICDI | Probable polyketide synthase 5 OS=Dictyostelium discoideum GN=pks5 PE=2 SV=1 | 1431 | 2511 | 6.0E-54 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 6 | 427 | 6.0E-54 |
| sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 1722 | 2348 | 1.0E-53 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 6 | 519 | 1.0E-52 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 5 | 428 | 2.0E-52 |
| sp|Q54IX3|PKS26_DICDI | Probable polyketide synthase 26 OS=Dictyostelium discoideum GN=pks26 PE=3 SV=1 | 1423 | 2511 | 3.0E-51 |
| sp|Q559A9|PKS13_DICDI | Probable polyketide synthase 13 OS=Dictyostelium discoideum GN=pks13 PE=3 SV=1 | 1399 | 2528 | 4.0E-50 |
| sp|B0G0Z9|PKS6_DICDI | Probable polyketide synthase 6 OS=Dictyostelium discoideum GN=pks6 PE=3 SV=1 | 1431 | 2511 | 1.0E-49 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 5 | 427 | 1.0E-49 |
| sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 1431 | 2533 | 4.0E-49 |
| sp|B0G101|PKS8_DICDI | Probable polyketide synthase 8/35 OS=Dictyostelium discoideum GN=pks8 PE=3 SV=1 | 1431 | 2511 | 3.0E-48 |
| sp|B0G100|PKS7_DICDI | Probable polyketide synthase 7 OS=Dictyostelium discoideum GN=pks7 PE=3 SV=1 | 1431 | 2511 | 4.0E-46 |
| sp|Q55CN6|PKS3_DICDI | Probable polyketide synthase 3 OS=Dictyostelium discoideum GN=pks3 PE=3 SV=1 | 1397 | 2515 | 1.0E-40 |
| sp|Q869X2|PKS17_DICDI | Probable polyketide synthase 17 OS=Dictyostelium discoideum GN=pks17 PE=3 SV=1 | 1842 | 2515 | 3.0E-40 |
| sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 1798 | 2515 | 4.0E-39 |
| sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 1851 | 2510 | 1.0E-38 |
| sp|Q869W9|PKS16_DICDI | Probable polyketide synthase 16 OS=Dictyostelium discoideum GN=pks16 PE=2 SV=1 | 1852 | 2515 | 2.0E-37 |
| sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 1842 | 2529 | 3.0E-37 |
| sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 1847 | 2515 | 6.0E-37 |
| 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 | 494 | 995 | 9.0E-37 |
| sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 1850 | 2515 | 1.0E-36 |
| sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 1850 | 2515 | 4.0E-36 |
| sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 1850 | 2515 | 9.0E-36 |
| sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 1847 | 2511 | 4.0E-35 |
| sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 1847 | 2515 | 1.0E-34 |
| sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 1772 | 2545 | 3.0E-34 |
| sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 1851 | 2511 | 5.0E-34 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 1847 | 2511 | 7.0E-34 |
| sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 1851 | 2511 | 7.0E-34 |
| sp|Q54KU5|PKS24_DICDI | Probable polyketide synthase 24 OS=Dictyostelium discoideum GN=pks24 PE=3 SV=1 | 1851 | 2510 | 1.0E-33 |
| 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 | 2143 | 2535 | 2.0E-33 |
| sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 1850 | 2511 | 6.0E-33 |
| sp|B0G138|PKS21_DICDI | Probable polyketide synthase 21 OS=Dictyostelium discoideum GN=pks21 PE=3 SV=1 | 1843 | 2548 | 8.0E-33 |
| sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 1842 | 2535 | 2.0E-31 |
| sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 1842 | 2537 | 2.0E-30 |
| sp|Q55DM7|PKS2_DICDI | Probable polyketide synthase 2 OS=Dictyostelium discoideum GN=pks2 PE=3 SV=1 | 1852 | 2550 | 2.0E-30 |
| sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 1850 | 2515 | 6.0E-30 |
| sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 1842 | 2535 | 1.0E-29 |
| sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 535 | 1034 | 1.0E-29 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 528 | 985 | 3.0E-28 |
| 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 | 2144 | 2520 | 4.0E-28 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 533 | 863 | 6.0E-26 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 1850 | 2535 | 4.0E-25 |
| sp|Q54B51|PKS44_DICDI | Probable polyketide synthase 44 OS=Dictyostelium discoideum GN=pks44 PE=3 SV=1 | 1842 | 2550 | 1.0E-23 |
| sp|O97764|QOR_BOVIN | Zeta-crystallin OS=Bos taurus GN=CRYZ PE=2 SV=2 | 1813 | 2061 | 1.0E-23 |
| sp|P16538|KAS1_STRGA | Tetracenomycin C polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces glaucescens GN=tcmK PE=3 SV=1 | 2 | 426 | 1.0E-23 |
| sp|Q80TB8|VAT1L_MOUSE | Synaptic vesicle membrane protein VAT-1 homolog-like OS=Mus musculus GN=Vat1l PE=1 SV=2 | 1849 | 2142 | 2.0E-23 |
| sp|Q9HCJ6|VAT1L_HUMAN | Synaptic vesicle membrane protein VAT-1 homolog-like OS=Homo sapiens GN=VAT1L PE=1 SV=2 | 1849 | 2142 | 3.0E-23 |
| sp|P22367|MSAS_PENPA | 6-methylsalicylic acid synthase OS=Penicillium patulum PE=1 SV=1 | 2161 | 2370 | 4.0E-23 |
| sp|Q8JFV8|VAT1_DANRE | Synaptic vesicle membrane protein VAT-1 homolog OS=Danio rerio GN=vat1 PE=2 SV=1 | 1822 | 2140 | 5.0E-23 |
| sp|Q08257|QOR_HUMAN | Quinone oxidoreductase OS=Homo sapiens GN=CRYZ PE=1 SV=1 | 1813 | 2075 | 2.0E-22 |
| sp|Q5R4S7|QOR_PONAB | Quinone oxidoreductase OS=Pongo abelii GN=CRYZ PE=2 SV=1 | 1813 | 2061 | 3.0E-22 |
| sp|P41175|KAS1_STRCM | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cinnamonensis PE=3 SV=1 | 1 | 429 | 4.0E-22 |
| sp|Q99536|VAT1_HUMAN | Synaptic vesicle membrane protein VAT-1 homolog OS=Homo sapiens GN=VAT1 PE=1 SV=2 | 1851 | 2140 | 9.0E-22 |
| sp|P04684|NODE_RHILT | Nodulation protein E OS=Rhizobium leguminosarum bv. trifolii GN=nodE PE=3 SV=2 | 89 | 421 | 1.0E-21 |
| sp|P47199|QOR_MOUSE | Quinone oxidoreductase OS=Mus musculus GN=Cryz PE=1 SV=1 | 1851 | 2058 | 1.0E-21 |
| sp|P11415|QOR_CAVPO | Quinone oxidoreductase OS=Cavia porcellus GN=CRYZ PE=1 SV=1 | 1813 | 2114 | 4.0E-21 |
| sp|Q02578|KAS1_STRCN | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cyaneus GN=curA PE=3 SV=1 | 151 | 431 | 7.0E-21 |
| sp|P72331|NODE_RHIS3 | Nodulation protein E OS=Rhizobium sp. (strain N33) GN=nodE PE=3 SV=1 | 153 | 421 | 1.0E-20 |
| sp|P19333|VAT1_TORCA | Synaptic vesicle membrane protein VAT-1 OS=Torpedo californica PE=1 SV=1 | 1847 | 2159 | 1.0E-20 |
| sp|Q6AYT0|QOR_RAT | Quinone oxidoreductase OS=Rattus norvegicus GN=Cryz PE=2 SV=1 | 1851 | 2101 | 1.0E-20 |
| sp|A7RK30|QORL2_NEMVE | Quinone oxidoreductase-like protein 2 homolog OS=Nematostella vectensis GN=v1g238856 PE=3 SV=1 | 1839 | 2140 | 3.0E-20 |
| 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 | 72 | 426 | 3.0E-20 |
| sp|P39525|CEM1_YEAST | 3-oxoacyl-[acyl-carrier-protein] synthase homolog OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CEM1 PE=1 SV=1 | 95 | 426 | 3.0E-20 |
| sp|Q0MVN8|QOR_PIG | Quinone oxidoreductase OS=Sus scrofa GN=CRYZ PE=2 SV=1 | 1849 | 2058 | 3.0E-20 |
| sp|B4XYB8|AZIB_STREG | 5-methyl-1-naphthoate synthase OS=Streptomyces sahachiroi GN=aziB PE=1 SV=1 | 2152 | 2329 | 6.0E-20 |
| sp|P43678|KAS1_STRRM | Oxytetracycline polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces rimosus PE=3 SV=2 | 6 | 426 | 6.0E-20 |
| sp|Q28452|QOR_LAMGU | Quinone oxidoreductase OS=Lama guanicoe GN=CRYZ PE=2 SV=1 | 1849 | 2058 | 6.0E-20 |
| sp|P9WQE7|PPSA_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsA PE=1 SV=1 | 2158 | 2536 | 7.0E-20 |
| sp|P9WQE6|PPSA_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsA PE=3 SV=1 | 2158 | 2536 | 8.0E-20 |
| 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 | 2158 | 2536 | 8.0E-20 |
| sp|Q05356|KAS1_STRHA | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces halstedii GN=sch1 PE=3 SV=1 | 153 | 428 | 1.0E-19 |
| sp|P06230|NODE_RHIME | Nodulation protein E OS=Rhizobium meliloti (strain 1021) GN=nodE PE=3 SV=1 | 89 | 421 | 2.0E-19 |
| 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 | 1 | 433 | 2.0E-19 |
| sp|Q54B49|PKS45_DICDI | Probable polyketide synthase 45 OS=Dictyostelium discoideum GN=pks45 PE=3 SV=2 | 1842 | 2141 | 3.0E-19 |
| sp|P06231|NOE4_RHIML | Nodulation protein E OS=Rhizobium meliloti GN=nodE PE=3 SV=1 | 89 | 421 | 3.0E-19 |
| sp|P43903|QOR_PSEAE | Quinone oxidoreductase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=qor PE=3 SV=2 | 1851 | 2108 | 5.0E-19 |
| sp|P28304|QOR1_ECOLI | Quinone oxidoreductase 1 OS=Escherichia coli (strain K12) GN=qorA PE=1 SV=1 | 1825 | 2056 | 6.0E-19 |
| sp|P9WQD7|FAB2_MYCTU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kasB PE=1 SV=1 | 174 | 421 | 1.0E-18 |
| sp|P9WQD6|FAB2_MYCTO | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=kasB PE=3 SV=1 | 174 | 421 | 1.0E-18 |
| 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 | 174 | 421 | 1.0E-18 |
| 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 | 6 | 426 | 2.0E-18 |
| sp|P56902|FABF_RHIME | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Rhizobium meliloti (strain 1021) GN=fabF PE=3 SV=2 | 142 | 426 | 3.0E-18 |
| sp|O69473|FAB2_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium leprae (strain TN) GN=kasB PE=3 SV=2 | 174 | 421 | 3.0E-18 |
| sp|Q9D404|OXSM_MOUSE | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Mus musculus GN=Oxsm PE=1 SV=1 | 63 | 428 | 4.0E-18 |
| sp|Q59I44|CAA43_BURSP | 2-haloacrylate reductase OS=Burkholderia sp. GN=caa43 PE=1 SV=1 | 1851 | 2050 | 7.0E-18 |
| sp|P04683|NODE_RHILV | Nodulation protein E OS=Rhizobium leguminosarum bv. viciae GN=nodE PE=3 SV=2 | 153 | 421 | 2.0E-17 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 1420 | 1587 | 3.0E-17 |
| sp|Q0VCA7|OXSM_BOVIN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Bos taurus GN=OXSM PE=2 SV=1 | 110 | 428 | 5.0E-17 |
| sp|P55338|FABF_VIBHA | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Vibrio harveyi GN=fabF PE=3 SV=2 | 66 | 426 | 6.0E-17 |
| sp|Q53FA7|QORX_HUMAN | Quinone oxidoreductase PIG3 OS=Homo sapiens GN=TP53I3 PE=1 SV=2 | 1822 | 2142 | 7.0E-17 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 2165 | 2508 | 9.0E-17 |
| sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 1843 | 2140 | 9.0E-17 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 1361 | 1594 | 1.0E-16 |
| sp|Q3MIE4|VAT1_RAT | Synaptic vesicle membrane protein VAT-1 homolog OS=Rattus norvegicus GN=Vat1 PE=1 SV=1 | 1851 | 2140 | 1.0E-16 |
| sp|Q02K94|FABB_PSEAB | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Pseudomonas aeruginosa (strain UCBPP-PA14) GN=fabB PE=1 SV=1 | 152 | 426 | 1.0E-16 |
| sp|A7Z4X9|BAED_BACMF | Polyketide biosynthesis acyltransferase homolog BaeD OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeD PE=1 SV=1 | 533 | 818 | 2.0E-16 |
| sp|B0BNC9|QORL2_RAT | Quinone oxidoreductase-like protein 2 OS=Rattus norvegicus PE=2 SV=1 | 1843 | 2056 | 3.0E-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 | 80 | 426 | 3.0E-16 |
| sp|P52410|KASC1_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Arabidopsis thaliana GN=KAS1 PE=2 SV=2 | 24 | 421 | 3.0E-16 |
| sp|Q5TKS0|FABF_STAAU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 (Fragment) OS=Staphylococcus aureus GN=fabF PE=3 SV=1 | 154 | 426 | 3.0E-16 |
| sp|Q7A6F8|FABF_STAAN | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain N315) GN=fabF PE=1 SV=1 | 154 | 426 | 3.0E-16 |
| sp|Q99VA6|FABF_STAAM | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabF PE=3 SV=1 | 154 | 426 | 3.0E-16 |
| sp|Q8NXE1|FABF_STAAW | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MW2) GN=fabF PE=1 SV=1 | 154 | 426 | 3.0E-16 |
| sp|Q6GAU2|FABF_STAAS | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MSSA476) GN=fabF PE=3 SV=1 | 154 | 426 | 3.0E-16 |
| sp|Q5HHA1|FABF_STAAC | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain COL) GN=fabF PE=1 SV=1 | 154 | 426 | 3.0E-16 |
| sp|Q6GIA3|FABF_STAAR | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MRSA252) GN=fabF PE=3 SV=1 | 154 | 426 | 3.0E-16 |
| sp|P23902|KASC1_HORVU | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Hordeum vulgare GN=KAS12 PE=1 SV=1 | 127 | 426 | 4.0E-16 |
| sp|Q3UNZ8|QORL2_MOUSE | Quinone oxidoreductase-like protein 2 OS=Mus musculus PE=1 SV=1 | 1840 | 2056 | 4.0E-16 |
| 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 | 153 | 426 | 4.0E-16 |
| sp|Q9NWU1|OXSM_HUMAN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Homo sapiens GN=OXSM PE=1 SV=1 | 110 | 428 | 6.0E-16 |
| sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 1361 | 1594 | 7.0E-16 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 1420 | 1587 | 7.0E-16 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 2180 | 2377 | 1.0E-15 |
| sp|P0AAI8|FABF_SHIFL | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Shigella flexneri GN=fabF PE=3 SV=2 | 142 | 426 | 1.0E-15 |
| sp|P0AAI5|FABF_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli (strain K12) GN=fabF PE=1 SV=2 | 142 | 426 | 1.0E-15 |
| 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 | 142 | 426 | 1.0E-15 |
| sp|P0AAI7|FABF_ECO57 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli O157:H7 GN=fabF PE=3 SV=2 | 142 | 426 | 1.0E-15 |
| sp|P40783|QOR_SALTY | Quinone oxidoreductase OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=qor PE=3 SV=2 | 1825 | 2057 | 1.0E-15 |
| sp|Q62465|VAT1_MOUSE | Synaptic vesicle membrane protein VAT-1 homolog OS=Mus musculus GN=Vat1 PE=1 SV=3 | 1851 | 2140 | 2.0E-15 |
| sp|Q9C9P4|KASC2_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase II, chloroplastic OS=Arabidopsis thaliana GN=KAS2 PE=1 SV=1 | 22 | 426 | 4.0E-15 |
| sp|P0A953|FABB_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Escherichia coli (strain K12) GN=fabB PE=1 SV=1 | 140 | 426 | 7.0E-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 | 140 | 426 | 7.0E-15 |
| sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 1428 | 1617 | 8.0E-15 |
| sp|O34877|PKSD_BACSU | Polyketide biosynthesis acyltransferase homolog PksD OS=Bacillus subtilis (strain 168) GN=pksD PE=1 SV=2 | 533 | 729 | 9.0E-15 |
| sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 1409 | 1594 | 2.0E-14 |
| sp|P16540|KAS1_STRVN | Granaticin polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces violaceoruber GN=gra-orf1 PE=3 SV=1 | 6 | 426 | 2.0E-14 |
| sp|B0G103|PKS10_DICDI | Probable polyketide synthase 10 OS=Dictyostelium discoideum GN=pks10 PE=3 SV=1 | 1423 | 1597 | 5.0E-14 |
| 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 | 2114 | 2346 | 6.0E-14 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 2096 | 2552 | 6.0E-14 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 2180 | 2508 | 8.0E-14 |
| sp|P71019|FABD_BACSU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis (strain 168) GN=fabD PE=3 SV=2 | 533 | 818 | 8.0E-14 |
| sp|A6QQF5|QORL2_BOVIN | Quinone oxidoreductase-like protein 2 OS=Bos taurus PE=2 SV=2 | 1840 | 2056 | 9.0E-14 |
| 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 | 1387 | 1859 | 1.0E-13 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 2180 | 2377 | 1.0E-13 |
| sp|P42865|QOR_LEIAM | Probable quinone oxidoreductase OS=Leishmania amazonensis PE=3 SV=1 | 1852 | 2073 | 1.0E-13 |
| sp|O34340|FABF_BACSU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Bacillus subtilis (strain 168) GN=fabF PE=1 SV=1 | 154 | 426 | 1.0E-13 |
| sp|P73283|FABF_SYNY3 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabF PE=1 SV=1 | 154 | 421 | 1.0E-13 |
| 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 | 103 | 426 | 3.0E-13 |
| sp|P9WQE5|PPSB_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsB PE=1 SV=1 | 2114 | 2346 | 4.0E-13 |
| sp|P9WQE4|PPSB_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsB PE=3 SV=1 | 2114 | 2346 | 4.0E-13 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 2154 | 2516 | 5.0E-13 |
| sp|A7Z4Y0|BAEE_BACMF | Polyketide biosynthesis protein BaeE OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeE PE=1 SV=1 | 533 | 759 | 5.0E-13 |
| sp|P9WQD9|FAB1_MYCTU | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kasA PE=1 SV=1 | 57 | 421 | 7.0E-13 |
| sp|P9WQD8|FAB1_MYCTO | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=kasA PE=3 SV=1 | 57 | 421 | 7.0E-13 |
| 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 | 57 | 421 | 7.0E-13 |
| 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 | 57 | 421 | 7.0E-13 |
| 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 | 136 | 426 | 8.0E-13 |
| 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 | 2146 | 2505 | 9.0E-13 |
| sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 2146 | 2505 | 9.0E-13 |
| sp|P9WQE2|PPSD_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsD PE=3 SV=1 | 2146 | 2505 | 9.0E-13 |
| sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 2224 | 2515 | 9.0E-13 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 2165 | 2377 | 1.0E-12 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 2159 | 2327 | 2.0E-12 |
| 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 | 139 | 426 | 3.0E-12 |
| sp|Q9R9J2|FENF_BACIU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis GN=fenF PE=1 SV=1 | 532 | 838 | 4.0E-12 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 2161 | 2509 | 1.0E-11 |
| 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 | 533 | 759 | 2.0E-11 |
| sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 1428 | 1566 | 3.0E-11 |
| sp|O35017|YOGA_BACSU | Uncharacterized zinc-type alcohol dehydrogenase-like protein YogA OS=Bacillus subtilis (strain 168) GN=yogA PE=3 SV=1 | 1851 | 2056 | 3.0E-11 |
| sp|P73242|FABD_SYNY3 | Malonyl CoA-acyl carrier protein transacylase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabD PE=1 SV=1 | 534 | 759 | 4.0E-11 |
| sp|Q9CBS7|FAB1_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium leprae (strain TN) GN=kasA PE=3 SV=1 | 57 | 421 | 4.0E-11 |
| sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 1428 | 1566 | 5.0E-11 |
| sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 1428 | 1566 | 5.0E-11 |
| sp|P40804|PKSF_BACSU | Polyketide biosynthesis malonyl-ACP decarboxylase PksF OS=Bacillus subtilis (strain 168) GN=pksF PE=1 SV=3 | 163 | 382 | 5.0E-11 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 2165 | 2344 | 6.0E-11 |
| sp|Q8L3X9|KASM_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Arabidopsis thaliana GN=KAS PE=1 SV=1 | 153 | 426 | 8.0E-11 |
| sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 1428 | 1566 | 2.0E-10 |
| sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 1480 | 1594 | 2.0E-10 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 2161 | 2399 | 2.0E-10 |
| sp|O74489|QOR_SCHPO | Probable quinone oxidoreductase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=zta1 PE=1 SV=2 | 1860 | 2057 | 2.0E-10 |
| sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 1428 | 1566 | 3.0E-10 |
| sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 1428 | 1566 | 3.0E-10 |
| sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 1428 | 1566 | 3.0E-10 |
| sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 1428 | 1566 | 5.0E-10 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 1424 | 1587 | 5.0E-10 |
| sp|P34055|INC11_HYPAT | Protein indc11 OS=Hypocrea atroviridis GN=indc11 PE=2 SV=1 | 1835 | 2146 | 8.0E-10 |
| sp|Q8BGC4|ZADH2_MOUSE | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Mus musculus GN=Zadh2 PE=1 SV=1 | 1849 | 2056 | 1.0E-09 |
| sp|O34787|PKSE_BACSU | Polyketide biosynthesis protein PksE OS=Bacillus subtilis (strain 168) GN=pksE PE=1 SV=3 | 533 | 833 | 5.0E-09 |
| 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 | 75 | 425 | 5.0E-09 |
| sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 1428 | 1662 | 6.0E-09 |
| sp|Q6G9Y3|FABD_STAAS | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MSSA476) GN=fabD PE=3 SV=1 | 534 | 818 | 7.0E-09 |
| sp|Q93QD4|FABD_STAAU | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus GN=fabD PE=3 SV=1 | 534 | 818 | 9.0E-09 |
| sp|Q5HGK3|FABD_STAAC | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain COL) GN=fabD PE=3 SV=1 | 534 | 818 | 9.0E-09 |
| sp|Q7A124|FABD_STAAW | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MW2) GN=fabD PE=3 SV=1 | 534 | 818 | 1.0E-08 |
| sp|Q7A5Z3|FABD_STAAN | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain N315) GN=fabD PE=1 SV=1 | 534 | 818 | 1.0E-08 |
| sp|Q99UN8|FABD_STAAM | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabD PE=1 SV=1 | 534 | 818 | 1.0E-08 |
| sp|O95825|QORL1_HUMAN | Quinone oxidoreductase-like protein 1 OS=Homo sapiens GN=CRYZL1 PE=1 SV=2 | 1833 | 2033 | 1.0E-08 |
| sp|Q921W4|QORL1_MOUSE | Quinone oxidoreductase-like protein 1 OS=Mus musculus GN=Cryzl1 PE=1 SV=1 | 1837 | 2033 | 1.0E-08 |
| sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 1428 | 1597 | 2.0E-08 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 2161 | 2544 | 2.0E-08 |
| sp|Q6GHK5|FABD_STAAR | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MRSA252) GN=fabD PE=3 SV=1 | 534 | 818 | 2.0E-08 |
| sp|Q7T3C7|RT4I1_DANRE | Reticulon-4-interacting protein 1 homolog, mitochondrial OS=Danio rerio GN=rtn4ip1 PE=2 SV=2 | 1826 | 2147 | 3.0E-08 |
| sp|Q8N4Q0|ZADH2_HUMAN | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Homo sapiens GN=ZADH2 PE=1 SV=1 | 1849 | 2056 | 4.0E-08 |
| sp|Q9Z311|MECR_RAT | Trans-2-enoyl-CoA reductase, mitochondrial OS=Rattus norvegicus GN=Mecr PE=1 SV=1 | 1851 | 1980 | 6.0E-08 |
| 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 | 621 | 818 | 7.0E-08 |
| sp|P0C842|CJ052_HUMAN | Putative uncharacterized protein encoded by LINC00614 OS=Homo sapiens GN=LINC00614 PE=5 SV=1 | 30 | 143 | 7.0E-08 |
| sp|P0A0I0|FABG_STAAW | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain MW2) GN=fabG PE=3 SV=1 | 2160 | 2313 | 7.0E-08 |
| sp|Q6G9Y2|FABG_STAAS | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain MSSA476) GN=fabG PE=3 SV=1 | 2160 | 2313 | 7.0E-08 |
| sp|Q6GHK4|FABG_STAAR | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain MRSA252) GN=fabG PE=3 SV=1 | 2160 | 2313 | 7.0E-08 |
| sp|P99093|FABG_STAAN | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain N315) GN=fabG PE=1 SV=1 | 2160 | 2313 | 7.0E-08 |
| sp|P0A0H9|FABG_STAAM | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabG PE=1 SV=1 | 2160 | 2313 | 7.0E-08 |
| sp|Q5HGK2|FABG_STAAC | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain COL) GN=fabG PE=3 SV=2 | 2160 | 2313 | 7.0E-08 |
| 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 | 91 | 375 | 8.0E-08 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 2163 | 2335 | 1.0E-07 |
| sp|Q9BV79|MECR_HUMAN | Trans-2-enoyl-CoA reductase, mitochondrial OS=Homo sapiens GN=MECR PE=1 SV=2 | 1851 | 1980 | 1.0E-07 |
| sp|P9WNG5|FABD_MYCTU | Malonyl CoA-acyl carrier protein transacylase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=fabD PE=1 SV=1 | 533 | 818 | 2.0E-07 |
| sp|P9WNG4|FABD_MYCTO | Malonyl CoA-acyl carrier protein transacylase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=fabD PE=3 SV=1 | 533 | 818 | 2.0E-07 |
| 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 | 533 | 818 | 2.0E-07 |
| sp|Q24K16|ZADH2_BOVIN | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Bos taurus GN=ZADH2 PE=2 SV=1 | 1849 | 2056 | 2.0E-07 |
| sp|Q8KA28|FABB_BUCAP | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) GN=fabB PE=3 SV=1 | 141 | 426 | 2.0E-07 |
| sp|Q59A28|QORL1_BOVIN | Quinone oxidoreductase-like protein 1 OS=Bos taurus GN=CRYZL1 PE=2 SV=1 | 1849 | 2033 | 3.0E-07 |
| sp|P38230|QOR_YEAST | Probable quinone oxidoreductase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ZTA1 PE=1 SV=1 | 1849 | 2056 | 3.0E-07 |
| sp|O34825|PKSC_BACSU | Polyketide biosynthesis malonyl CoA-acyl carrier protein transacylase PksC OS=Bacillus subtilis (strain 168) GN=pksC PE=1 SV=1 | 533 | 739 | 3.0E-07 |
| sp|Q9DCS3|MECR_MOUSE | Trans-2-enoyl-CoA reductase, mitochondrial OS=Mus musculus GN=Mecr PE=1 SV=2 | 1851 | 1979 | 4.0E-07 |
| sp|Q8CPI3|FABG_STAES | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus epidermidis (strain ATCC 12228) GN=fabG PE=3 SV=1 | 2163 | 2313 | 6.0E-07 |
| sp|Q5HPW0|FABG_STAEQ | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus epidermidis (strain ATCC 35984 / RP62A) GN=fabG PE=3 SV=1 | 2163 | 2313 | 6.0E-07 |
| sp|Q8H0M1|QORH_SPIOL | Quinone-oxidoreductase homolog, chloroplastic OS=Spinacia oleracea GN=QOR PE=1 SV=1 | 1850 | 1986 | 8.0E-07 |
| sp|P96825|Y0148_MYCTU | Putative short-chain type dehydrogenase/reductase Rv0148 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0148 PE=1 SV=3 | 2163 | 2313 | 8.0E-07 |
| 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 | 1879 | 2142 | 9.0E-07 |
| sp|Q7YS70|MECR_BOVIN | Trans-2-enoyl-CoA reductase, mitochondrial OS=Bos taurus GN=MECR PE=1 SV=1 | 1852 | 2056 | 1.0E-06 |
| sp|P33207|FABG_ARATH | 3-oxoacyl-[acyl-carrier-protein] reductase, chloroplastic OS=Arabidopsis thaliana GN=At1g24360 PE=1 SV=2 | 2167 | 2313 | 1.0E-06 |
| sp|Q93X68|FABG5_BRANA | 3-oxoacyl-[acyl-carrier-protein] reductase 5, chloroplastic (Fragment) OS=Brassica napus GN=bkr1 PE=2 SV=1 | 2167 | 2313 | 2.0E-06 |
| sp|P23238|PHBB_ZOORA | Acetoacetyl-CoA reductase OS=Zoogloea ramigera GN=phbB PE=3 SV=1 | 2167 | 2335 | 3.0E-06 |
| sp|P50204|PHAB_PARDE | Acetoacetyl-CoA reductase OS=Paracoccus denitrificans GN=phaB PE=3 SV=1 | 2167 | 2313 | 9.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0008168 | methyltransferase activity | Yes |
| GO:0003824 | catalytic activity | No |
| GO:0016740 | transferase activity | No |
| GO:0003674 | molecular_function | No |
| GO:0016741 | transferase activity, transferring one-carbon groups | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 20 | 0.45 |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
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 | >Ophio5|4083 MAQADIAIVGIACRFPGEAKSPSAFYQMLVQGRDAWTKVPKSRYDVDAYRHPSRERRGTMVCEGGYFLEDDVSRW DAPFFSCSAVEAQAMDPQQRLLLEVAYESLENAGIPLEAMAESDAACFVGGFTNDYRRIVTSETEAIPQYVMTGN STSMMANRVSWFLNLRGPSVTVDTACSSSMAALHLACETIRSGANETRCALVGGTSLLLDPEDPCCMNALGFLSP DSRCFTFDSRANGYARGEGIAMLVVKHMDDALRDGDAIRAVVRATALNSDGRTAGIVLPNGDAHHRLISHTYRLA GLNPADTQYAELHGTGTRVGDPTEIGAVARTLAAGRPTPLLCGSVKTQIGHTEAAAALAGVLKCVLSMEAGVLPP HKNFIEPNPRLRLEASNIAVPIEPQPWPAADVRRCSVNSFGFGGLNGHIVLDGAAGYLSSRGLAVPSADADSNDA RRPYLFLLSAPEQDAVARQLRAHADYLVSSPDPKLPLLAHTLGARRSVFQWRLAVVARSADELESLWRDEALKPV KAAAAPGVALLFTGQGAQWYAMGRELLALPVFARSVRASASALTAIGCPWDAEAELMAPEAESRVNLAAYSQPLC SVLQIALVDLLRHWGVKPAAVVGHSSGEMAAAYAVGALSREDCLAVAYHRGLVSEMAADRKPGGAMMAVGLSADE VRPRLEDAVTVACVNSPNNVTLAGDRAALERLGESLKRDDIFCRLLQVQNAFHSPQMVAVADEYRRRIANVTPTD MSASFYSTVKGCRIPTSRLTADYWVDNLCSPVELVGALDDMLCADGKGKRSKAPTVIVEVGPHGALAGPFDQFRL ARRGLEHIGYYSLLSRGRDAMQTTMSAAAALWMKGVPVQVGKINGLDETSRPATVLTDLPSYSWNHSVSYWHETW SSRNRRCPPAPKHDLIGWRLHACNPLEPVWKNYLRTSEMPWLKDHQVHGDVVFPAGGVISAVIEAIRQFEAGQDA SREISSFELREFYIPRPLLIPNTELGAETFLHLKRRKSGMGSGAGPWLEFSFYSRQDGDVFVEHAYGLAQAHFAK QPNEVDGGKELREETRAHQRRFRHQSSVCDEPMTSQAHYDFCKSIGLCYGNYFQGLSKVRLHDTTCAFEATIIDT PSCMPGACETEYLIHPTTIDLMFQALLATLPRMQGIQKQGWAPTAVGSIRVSNAVGRGPGTVLYGYGETSPRATH QIVGFVMAGDGAFDSLPGVVMEGIQVSGLGAMQNSSQLSEDSGVKLYAAPYWKPDLLLLEGLRPSRLTSGGPQDH CAAQFCSDSRDIVNEMCRIALERLDGKPDEKLTPPLQKYVEWMRRRNRATLKTFSSITPPISPAFGGFGASLDPN FGIDKLKGFIENFPVDGRLLRHAFASLDAIFSRQTVPIAALMASDDFARFYKESHGAEVIKTIFRNWFDLKAHKK PNLRVIEIGAGTASTTVPVLETLGEAEDETPRFSNYTFTDISPGWFEGARTLLRNWKSRVEYKVLNIEEDPVEQG FEAESYDVVLAVNVLHATKDIHQTLTNCRRLLKPGGNLIVGECTNPDDMLSFIFGILPGWWASEDGRRFGPLLSE AAWDKALKASGFSGTDIAMPDGDDKVGHHRMSVLVSTKPHEQAAALPAKDVVVLMPNDGTDVGAGLASSVCRELE QLGARVSIKELGADIEGKTVVSLLEYETPFLEQVQEADFEQVKNVFLHCRELLWVTRSDAADKSGHPSMRIVSGL LHCIKNEDASRRLHELHLCRNATADVKSTSGAILRRLNSLWQGDGDDGGELVTAERDGAFCIPRYVPDKAMNRSL ARTTESDPALQTEKLIQTCRPLQLKIGRPGMLDTLHFADDDEASQPLLDDEVRIEVQACGLNFRDVLIAMGELRS PSLGYEAAGIVIDTGAKVTRLSPGDRVVCMRPNVMRTRIRAHEWYVHLLPACLSIEDGVTIPVAYATAYRCLVEV ARLQKGESVLIHAAAGGFGQATIHMAKMLGADIFCTVSTEAKKRLVVSLGVKPEHVFSSRDISFETGIRRVTKGR GVDVVVNSLAGELLRRSWACLAPYGRFIEVGKRDIVGNSGLDMQPFDDNAIFACVNLDAMASEPRRLWQLVDKVL RLFEQGSLGLIQPIAVHDFSEVEAVFREMQRGAHMGKLALRVTAESRVPVAPRKQVPLRLRSDATYLLAGGLGGI GRAQALFMAEHGARHLAFVSRSGDAKPEARQLLKTLAEAGVEARAYSGDVADKDRLRAILADAARQMPPIRGVIQ GAMVLDDSLFHKMTYDQWLTATRPKIQGSWNLHELLPSSLDFFVVLSSMAGTIGFLSQSNYAAGNTYQDALVHYR HDKGLPALSIDLGITKGLGYVAEHDDVAAKLKPYGLATVNEQQFFHLMRCALAGTADGESRLNTRQLLAGAGTGG LAQASLATVPETNLYWLTALSTFSYLGEVDVRDTAEAAGEEVTDDVRLIGQLGGAKTMDEAAEAVQDMLLSRIAT IMSVPTTNIDTSKPVHAYGVDSLVAVELRNWLSKRLRSDVSIFDLTGNMAITTLSRKIASRSRLVSAATKGQGDE AA |
| Coding | >Ophio5|4083 ATGGCCCAGGCCGACATCGCCATCGTCGGGATTGCTTGCCGCTTTCCCGGCGAGGCCAAGTCCCCGAGTGCCTTT TACCAGATGCTGGTGCAGGGCCGAGACGCATGGACCAAGGTGCCCAAGTCGCGATACGATGTCGACGCATATAGA CACCCCTCACGCGAGCGTCGCGGAACCATGGTGTGCGAAGGCGGTTACTTTCTGGAAGACGACGTTTCGCGATGG GACGCGCCCTTTTTCTCTTGCTCGGCCGTCGAGGCGCAGGCCATGGATCCCCAACAACGGCTGCTGCTCGAGGTG GCGTACGAGAGTCTGGAGAACGCGGGGATCCCGCTCGAGGCGATGGCGGAGAGCGACGCCGCCTGCTTCGTCGGC GGCTTCACCAACGACTACCGACGCATCGTGACGAGCGAGACGGAGGCGATTCCTCAGTACGTCATGACGGGCAAC TCGACGTCCATGATGGCCAATCGAGTTAGCTGGTTCCTCAACCTGCGCGGGCCGTCCGTCACCGTCGACACGGCC TGCTCGAGCTCAATGGCTGCTCTACATCTGGCGTGCGAGACGATTCGTTCCGGAGCCAACGAGACACGTTGCGCG CTGGTCGGCGGAACGAGCCTGCTTCTGGACCCAGAAGATCCGTGCTGTATGAATGCGCTGGGCTTCCTCAGCCCG GACAGTCGATGCTTCACGTTTGATTCACGGGCCAACGGCTACGCGCGGGGTGAGGGTATCGCGATGCTGGTGGTC AAGCACATGGACGACGCGCTGCGCGACGGCGACGCGATCAGGGCCGTTGTGAGAGCGACGGCATTGAATTCAGAC GGGCGGACTGCCGGCATCGTCCTCCCCAACGGCGACGCCCACCACCGACTCATCAGCCACACCTACCGCCTTGCG GGGCTCAACCCGGCCGACACGCAGTATGCCGAGCTCCACGGCACCGGCACTCGGGTCGGCGACCCCACCGAGATC GGCGCCGTGGCCCGTACCCTCGCTGCCGGCCGCCCGACGCCGCTGCTATGCGGCTCCGTCAAGACGCAGATCGGC CACACCGAGGCCGCCGCCGCCCTAGCCGGTGTCCTGAAATGCGTCCTCTCCATGGAGGCCGGCGTCTTGCCGCCC CACAAGAATTTCATCGAGCCCAATCCGCGGCTCCGGCTCGAGGCCTCGAACATTGCGGTGCCGATAGAGCCGCAG CCGTGGCCCGCCGCCGACGTTCGCCGCTGCTCCGTCAATAGCTTCGGCTTCGGAGGGCTCAACGGTCATATCGTC CTCGACGGAGCGGCCGGTTACCTCAGCAGCCGCGGTCTCGCCGTCCCGAGCGCCGATGCCGACTCCAACGATGCC CGGCGGCCCTACCTCTTCCTCCTCTCCGCCCCGGAGCAGGATGCCGTGGCCCGCCAGCTCCGCGCCCATGCAGAC TATCTCGTCTCGTCGCCGGACCCCAAACTGCCACTTCTCGCCCACACCCTCGGCGCTCGTCGGTCCGTCTTCCAG TGGCGCCTCGCCGTCGTCGCCCGGTCCGCCGACGAGCTCGAGTCTCTGTGGCGCGATGAGGCGCTTAAGCCCGTC AAGGCTGCCGCCGCCCCCGGCGTCGCCCTTCTCTTCACCGGCCAGGGCGCTCAGTGGTACGCCATGGGCCGCGAG CTACTGGCGCTGCCCGTCTTCGCCCGCTCCGTCCGCGCTTCGGCCTCGGCCTTGACCGCCATAGGCTGCCCCTGG GACGCGGAGGCGGAGCTGATGGCTCCCGAGGCCGAGTCGCGCGTCAACCTCGCCGCTTACTCGCAGCCGTTGTGC TCGGTCTTGCAGATTGCCCTCGTCGACCTCCTCCGCCACTGGGGCGTCAAGCCGGCCGCCGTCGTCGGCCACTCT TCGGGCGAGATGGCGGCTGCCTACGCAGTCGGAGCCCTCTCGCGTGAGGACTGCCTGGCCGTCGCCTACCACCGC GGCTTAGTGTCCGAGATGGCTGCCGACCGGAAGCCGGGCGGCGCCATGATGGCCGTTGGTCTGTCCGCCGACGAG GTGCGGCCGCGCCTCGAAGACGCCGTCACCGTCGCCTGCGTCAACAGCCCCAATAATGTGACGCTGGCCGGAGAC CGCGCCGCGCTCGAGAGGCTGGGCGAGTCCCTGAAGCGTGACGACATCTTCTGCCGTCTGCTGCAGGTTCAGAAC GCCTTTCACAGCCCACAGATGGTTGCCGTCGCTGACGAGTACCGTCGACGCATCGCCAACGTGACTCCCACCGAC ATGTCGGCCTCGTTCTATTCGACCGTCAAGGGCTGCCGCATCCCCACGTCGCGCTTGACTGCCGATTACTGGGTC GACAATCTCTGCTCGCCCGTTGAGCTCGTTGGCGCCCTAGACGACATGCTCTGCGCCGACGGCAAGGGCAAGAGG TCCAAAGCGCCCACAGTCATCGTCGAAGTCGGGCCTCATGGCGCCCTCGCTGGCCCCTTTGATCAGTTCCGGCTC GCCCGTCGCGGTCTGGAGCACATCGGCTATTACAGCCTCCTCTCGCGAGGACGGGACGCGATGCAGACAACGATG AGCGCCGCCGCTGCCCTTTGGATGAAGGGCGTTCCCGTTCAAGTCGGCAAGATCAATGGCTTGGACGAGACCTCT CGGCCCGCCACCGTCTTGACCGATCTGCCCTCGTACAGCTGGAACCACTCCGTCTCCTACTGGCATGAGACGTGG AGCTCGCGAAATCGACGCTGCCCGCCAGCTCCCAAGCACGACCTGATCGGATGGCGGCTCCATGCGTGCAACCCG CTAGAGCCCGTGTGGAAAAACTACCTGCGTACCTCGGAGATGCCCTGGCTCAAGGATCACCAGGTCCATGGCGAC GTTGTTTTTCCCGCCGGCGGCGTCATCTCCGCCGTCATCGAGGCCATACGCCAGTTCGAGGCCGGCCAGGACGCG AGCCGTGAAATCTCGAGCTTCGAGCTACGCGAGTTCTATATCCCCCGGCCGCTGCTCATCCCCAACACCGAGCTG GGCGCCGAGACGTTTCTCCACCTCAAACGCAGAAAGTCGGGCATGGGCAGCGGCGCCGGTCCTTGGCTCGAGTTC TCCTTCTACTCGCGCCAGGACGGTGATGTCTTCGTCGAGCACGCCTACGGGCTGGCGCAGGCTCACTTTGCCAAG CAGCCCAACGAGGTGGATGGCGGAAAAGAGCTGCGAGAGGAAACACGGGCGCATCAGCGACGATTCCGGCACCAG AGCAGCGTATGTGACGAGCCGATGACCAGCCAGGCTCACTACGACTTTTGCAAGAGCATTGGCCTCTGCTACGGC AACTATTTTCAGGGTCTCTCCAAGGTGCGGCTTCATGATACGACCTGCGCCTTCGAGGCCACCATCATCGACACA CCGTCGTGCATGCCTGGGGCGTGCGAGACGGAGTACCTCATCCACCCTACGACCATTGATCTCATGTTCCAAGCC CTTCTGGCTACGTTACCCCGGATGCAGGGCATTCAGAAGCAGGGTTGGGCTCCAACGGCTGTCGGCTCGATCCGC GTCTCGAACGCCGTCGGACGCGGACCTGGGACGGTACTGTACGGCTATGGCGAGACGTCTCCCCGCGCGACCCAT CAGATAGTAGGCTTCGTCATGGCAGGCGACGGTGCTTTCGACTCGCTTCCGGGCGTCGTCATGGAAGGCATCCAG GTCTCGGGGCTGGGCGCGATGCAAAACTCATCGCAACTGTCCGAGGACTCGGGCGTCAAGCTGTACGCGGCGCCC TATTGGAAGCCGGATCTGCTACTCCTCGAGGGGCTTCGTCCGTCGAGGCTGACGAGCGGCGGGCCTCAAGACCAT TGTGCGGCTCAGTTCTGCTCCGACAGCCGTGACATTGTCAACGAGATGTGTCGCATTGCCCTGGAGCGGCTGGAC GGCAAGCCAGACGAGAAGCTCACTCCCCCTCTGCAAAAGTACGTCGAGTGGATGCGAAGGCGCAACCGAGCGACC TTGAAGACGTTTAGCAGCATCACGCCGCCCATTAGCCCAGCTTTCGGCGGCTTTGGCGCGAGTCTAGACCCCAAT TTCGGCATCGACAAGCTCAAGGGCTTCATCGAAAACTTCCCGGTCGACGGACGCCTTTTGCGCCACGCCTTTGCC TCGCTCGACGCAATCTTTAGCCGGCAGACGGTCCCCATCGCCGCACTGATGGCGAGCGACGACTTTGCCAGGTTC TACAAGGAGTCTCACGGCGCCGAAGTCATCAAGACCATCTTCCGCAACTGGTTCGACCTCAAGGCGCACAAGAAG CCCAATCTACGCGTCATCGAGATCGGAGCCGGGACGGCGTCGACGACGGTGCCCGTTTTGGAGACGCTGGGGGAG GCCGAAGACGAGACGCCTCGCTTCTCAAACTATACCTTTACCGACATCTCGCCCGGTTGGTTTGAGGGCGCGCGG ACGTTGCTGCGTAACTGGAAGTCTCGGGTTGAGTACAAGGTGCTCAACATTGAGGAGGATCCCGTCGAGCAAGGA TTCGAAGCCGAGTCTTATGACGTGGTGTTGGCTGTCAACGTTCTCCACGCAACCAAAGACATACATCAGACGCTC ACAAACTGCCGCCGCCTGCTCAAGCCCGGCGGCAACCTCATCGTCGGCGAGTGCACCAACCCGGATGACATGCTC TCCTTCATCTTCGGCATCCTGCCCGGCTGGTGGGCCTCGGAAGATGGGAGGCGTTTCGGCCCCCTGCTCAGCGAG GCCGCCTGGGACAAGGCCCTCAAGGCGTCGGGCTTCTCCGGTACTGACATTGCCATGCCTGACGGCGATGACAAG GTTGGCCATCATAGGATGTCGGTTCTGGTCAGCACCAAGCCGCACGAGCAGGCCGCCGCGTTGCCGGCCAAGGAC GTGGTGGTGCTCATGCCCAACGACGGCACCGACGTCGGGGCCGGTCTCGCCTCATCGGTTTGTCGCGAGCTCGAG CAACTCGGAGCTCGTGTCAGCATCAAGGAGCTCGGAGCCGACATCGAGGGCAAGACGGTCGTCTCTCTCCTTGAA TACGAGACGCCTTTTCTCGAGCAGGTTCAGGAAGCCGATTTCGAGCAAGTCAAGAACGTCTTTCTTCACTGCCGC GAGCTCCTCTGGGTCACCCGCTCAGATGCGGCGGACAAGTCAGGCCACCCCAGCATGCGCATTGTCTCCGGGCTG TTGCATTGCATCAAAAATGAGGACGCGTCCCGGCGGCTTCATGAGCTTCACCTCTGCCGCAATGCCACGGCTGAT GTGAAATCGACCAGCGGCGCCATCCTCCGCAGGCTAAACAGCCTGTGGCAGGGCGATGGCGACGACGGCGGGGAG TTGGTGACGGCAGAGCGAGACGGTGCCTTCTGCATCCCTCGTTACGTGCCGGACAAGGCCATGAACCGCAGCCTG GCGCGTACGACCGAGTCGGACCCGGCGCTTCAGACGGAAAAGCTCATCCAGACGTGCCGGCCGCTGCAGCTGAAG ATTGGACGACCGGGGATGCTGGACACGCTGCACTTTGCCGACGATGACGAGGCATCGCAGCCGCTGCTCGACGAC GAGGTCAGGATCGAGGTGCAGGCATGCGGCCTTAACTTCCGAGACGTCTTGATCGCAATGGGCGAGCTCCGGTCC CCCAGTCTGGGCTATGAGGCGGCTGGCATCGTCATCGACACGGGCGCCAAGGTGACTCGACTCTCGCCTGGCGAT AGGGTCGTGTGCATGAGGCCCAACGTGATGCGTACGCGCATCCGCGCTCATGAGTGGTACGTCCATCTGCTGCCG GCCTGCCTATCGATTGAGGACGGCGTGACGATTCCGGTGGCGTATGCAACTGCGTATCGATGCCTTGTCGAGGTG GCGAGGCTGCAAAAGGGCGAGTCGGTGCTTATCCACGCGGCAGCGGGAGGCTTTGGTCAGGCTACAATTCACATG GCCAAGATGCTGGGAGCCGACATCTTCTGCACGGTCAGCACCGAGGCCAAGAAGCGACTGGTCGTCTCTCTGGGC GTCAAGCCCGAACACGTCTTCAGCTCGCGTGACATCTCGTTCGAAACGGGCATCAGGCGGGTGACCAAGGGCCGC GGCGTCGACGTCGTCGTCAACTCGTTGGCAGGTGAGCTTCTACGAAGGAGTTGGGCCTGTCTGGCGCCCTATGGC CGCTTCATTGAGGTCGGCAAGCGAGATATCGTCGGCAACAGTGGGCTCGACATGCAGCCGTTTGACGACAACGCC ATTTTCGCCTGCGTCAATCTTGATGCCATGGCGTCGGAGCCGAGGAGGCTGTGGCAGCTGGTGGACAAGGTGCTG CGGCTTTTCGAGCAGGGCTCTTTGGGACTGATCCAGCCCATCGCCGTCCATGACTTCTCCGAGGTCGAGGCCGTC TTCCGCGAGATGCAGCGAGGCGCCCACATGGGTAAGCTGGCGCTCCGCGTCACGGCCGAATCTCGCGTGCCCGTG GCGCCTCGCAAGCAGGTTCCGCTTCGTCTGCGATCAGACGCCACCTATCTGCTGGCCGGCGGTCTCGGCGGAATC GGCCGGGCTCAGGCGCTGTTCATGGCGGAGCACGGGGCGCGTCACTTGGCCTTTGTCTCGCGTTCTGGCGATGCC AAACCCGAGGCCCGGCAGCTGCTGAAGACGTTGGCCGAGGCCGGCGTCGAGGCCCGGGCTTATTCCGGCGACGTG GCCGACAAGGACCGGCTCCGGGCCATCCTCGCCGATGCGGCGCGCCAAATGCCACCGATCCGCGGCGTCATCCAG GGCGCCATGGTCCTGGACGATTCCCTCTTCCACAAAATGACGTACGACCAGTGGCTGACGGCGACGCGGCCCAAG ATCCAGGGCAGCTGGAATCTGCACGAGTTGCTGCCTTCGAGCCTCGACTTCTTCGTCGTACTCTCCTCCATGGCC GGCACCATCGGCTTCTTGTCTCAGTCCAACTATGCGGCCGGCAACACGTATCAGGACGCGCTGGTGCACTACCGC CACGACAAGGGGCTGCCAGCGCTGAGCATCGACCTGGGCATCACCAAGGGGCTGGGCTACGTGGCCGAGCACGAC GACGTGGCCGCCAAGCTGAAGCCGTACGGGCTGGCTACGGTCAACGAGCAGCAGTTCTTCCATCTCATGCGATGT GCCCTCGCCGGCACCGCCGACGGAGAGAGCCGGCTCAACACGAGACAGCTCCTCGCCGGAGCCGGAACCGGCGGC CTCGCGCAGGCGTCGCTGGCGACGGTGCCGGAGACGAACCTCTACTGGCTCACGGCCCTGTCGACCTTTTCTTAC CTCGGCGAGGTCGACGTTCGGGACACGGCCGAGGCGGCGGGCGAAGAGGTGACGGACGACGTCAGGCTCATCGGC CAGCTCGGAGGGGCCAAGACGATGGACGAGGCGGCCGAGGCGGTCCAGGACATGCTCCTATCTCGCATCGCGACC ATCATGTCGGTGCCGACGACAAACATCGACACGTCCAAGCCGGTGCACGCGTACGGCGTCGACAGCCTGGTGGCC GTCGAGCTACGCAATTGGCTGTCGAAACGGCTGCGGAGCGACGTCAGCATCTTTGACCTGACGGGCAACATGGCC ATTACGACGCTGAGCCGAAAGATTGCCAGCCGGTCGCGTCTGGTGTCTGCCGCGACCAAGGGGCAGGGCGACGAA GCAGCT |
| Transcript | >Ophio5|4083 ATGGCCCAGGCCGACATCGCCATCGTCGGGATTGCTTGCCGCTTTCCCGGCGAGGCCAAGTCCCCGAGTGCCTTT TACCAGATGCTGGTGCAGGGCCGAGACGCATGGACCAAGGTGCCCAAGTCGCGATACGATGTCGACGCATATAGA CACCCCTCACGCGAGCGTCGCGGAACCATGGTGTGCGAAGGCGGTTACTTTCTGGAAGACGACGTTTCGCGATGG GACGCGCCCTTTTTCTCTTGCTCGGCCGTCGAGGCGCAGGCCATGGATCCCCAACAACGGCTGCTGCTCGAGGTG GCGTACGAGAGTCTGGAGAACGCGGGGATCCCGCTCGAGGCGATGGCGGAGAGCGACGCCGCCTGCTTCGTCGGC GGCTTCACCAACGACTACCGACGCATCGTGACGAGCGAGACGGAGGCGATTCCTCAGTACGTCATGACGGGCAAC TCGACGTCCATGATGGCCAATCGAGTTAGCTGGTTCCTCAACCTGCGCGGGCCGTCCGTCACCGTCGACACGGCC TGCTCGAGCTCAATGGCTGCTCTACATCTGGCGTGCGAGACGATTCGTTCCGGAGCCAACGAGACACGTTGCGCG CTGGTCGGCGGAACGAGCCTGCTTCTGGACCCAGAAGATCCGTGCTGTATGAATGCGCTGGGCTTCCTCAGCCCG GACAGTCGATGCTTCACGTTTGATTCACGGGCCAACGGCTACGCGCGGGGTGAGGGTATCGCGATGCTGGTGGTC AAGCACATGGACGACGCGCTGCGCGACGGCGACGCGATCAGGGCCGTTGTGAGAGCGACGGCATTGAATTCAGAC GGGCGGACTGCCGGCATCGTCCTCCCCAACGGCGACGCCCACCACCGACTCATCAGCCACACCTACCGCCTTGCG GGGCTCAACCCGGCCGACACGCAGTATGCCGAGCTCCACGGCACCGGCACTCGGGTCGGCGACCCCACCGAGATC GGCGCCGTGGCCCGTACCCTCGCTGCCGGCCGCCCGACGCCGCTGCTATGCGGCTCCGTCAAGACGCAGATCGGC CACACCGAGGCCGCCGCCGCCCTAGCCGGTGTCCTGAAATGCGTCCTCTCCATGGAGGCCGGCGTCTTGCCGCCC CACAAGAATTTCATCGAGCCCAATCCGCGGCTCCGGCTCGAGGCCTCGAACATTGCGGTGCCGATAGAGCCGCAG CCGTGGCCCGCCGCCGACGTTCGCCGCTGCTCCGTCAATAGCTTCGGCTTCGGAGGGCTCAACGGTCATATCGTC CTCGACGGAGCGGCCGGTTACCTCAGCAGCCGCGGTCTCGCCGTCCCGAGCGCCGATGCCGACTCCAACGATGCC CGGCGGCCCTACCTCTTCCTCCTCTCCGCCCCGGAGCAGGATGCCGTGGCCCGCCAGCTCCGCGCCCATGCAGAC TATCTCGTCTCGTCGCCGGACCCCAAACTGCCACTTCTCGCCCACACCCTCGGCGCTCGTCGGTCCGTCTTCCAG TGGCGCCTCGCCGTCGTCGCCCGGTCCGCCGACGAGCTCGAGTCTCTGTGGCGCGATGAGGCGCTTAAGCCCGTC AAGGCTGCCGCCGCCCCCGGCGTCGCCCTTCTCTTCACCGGCCAGGGCGCTCAGTGGTACGCCATGGGCCGCGAG CTACTGGCGCTGCCCGTCTTCGCCCGCTCCGTCCGCGCTTCGGCCTCGGCCTTGACCGCCATAGGCTGCCCCTGG GACGCGGAGGCGGAGCTGATGGCTCCCGAGGCCGAGTCGCGCGTCAACCTCGCCGCTTACTCGCAGCCGTTGTGC TCGGTCTTGCAGATTGCCCTCGTCGACCTCCTCCGCCACTGGGGCGTCAAGCCGGCCGCCGTCGTCGGCCACTCT TCGGGCGAGATGGCGGCTGCCTACGCAGTCGGAGCCCTCTCGCGTGAGGACTGCCTGGCCGTCGCCTACCACCGC GGCTTAGTGTCCGAGATGGCTGCCGACCGGAAGCCGGGCGGCGCCATGATGGCCGTTGGTCTGTCCGCCGACGAG GTGCGGCCGCGCCTCGAAGACGCCGTCACCGTCGCCTGCGTCAACAGCCCCAATAATGTGACGCTGGCCGGAGAC CGCGCCGCGCTCGAGAGGCTGGGCGAGTCCCTGAAGCGTGACGACATCTTCTGCCGTCTGCTGCAGGTTCAGAAC GCCTTTCACAGCCCACAGATGGTTGCCGTCGCTGACGAGTACCGTCGACGCATCGCCAACGTGACTCCCACCGAC ATGTCGGCCTCGTTCTATTCGACCGTCAAGGGCTGCCGCATCCCCACGTCGCGCTTGACTGCCGATTACTGGGTC GACAATCTCTGCTCGCCCGTTGAGCTCGTTGGCGCCCTAGACGACATGCTCTGCGCCGACGGCAAGGGCAAGAGG TCCAAAGCGCCCACAGTCATCGTCGAAGTCGGGCCTCATGGCGCCCTCGCTGGCCCCTTTGATCAGTTCCGGCTC GCCCGTCGCGGTCTGGAGCACATCGGCTATTACAGCCTCCTCTCGCGAGGACGGGACGCGATGCAGACAACGATG AGCGCCGCCGCTGCCCTTTGGATGAAGGGCGTTCCCGTTCAAGTCGGCAAGATCAATGGCTTGGACGAGACCTCT CGGCCCGCCACCGTCTTGACCGATCTGCCCTCGTACAGCTGGAACCACTCCGTCTCCTACTGGCATGAGACGTGG AGCTCGCGAAATCGACGCTGCCCGCCAGCTCCCAAGCACGACCTGATCGGATGGCGGCTCCATGCGTGCAACCCG CTAGAGCCCGTGTGGAAAAACTACCTGCGTACCTCGGAGATGCCCTGGCTCAAGGATCACCAGGTCCATGGCGAC GTTGTTTTTCCCGCCGGCGGCGTCATCTCCGCCGTCATCGAGGCCATACGCCAGTTCGAGGCCGGCCAGGACGCG AGCCGTGAAATCTCGAGCTTCGAGCTACGCGAGTTCTATATCCCCCGGCCGCTGCTCATCCCCAACACCGAGCTG GGCGCCGAGACGTTTCTCCACCTCAAACGCAGAAAGTCGGGCATGGGCAGCGGCGCCGGTCCTTGGCTCGAGTTC TCCTTCTACTCGCGCCAGGACGGTGATGTCTTCGTCGAGCACGCCTACGGGCTGGCGCAGGCTCACTTTGCCAAG CAGCCCAACGAGGTGGATGGCGGAAAAGAGCTGCGAGAGGAAACACGGGCGCATCAGCGACGATTCCGGCACCAG AGCAGCGTATGTGACGAGCCGATGACCAGCCAGGCTCACTACGACTTTTGCAAGAGCATTGGCCTCTGCTACGGC AACTATTTTCAGGGTCTCTCCAAGGTGCGGCTTCATGATACGACCTGCGCCTTCGAGGCCACCATCATCGACACA CCGTCGTGCATGCCTGGGGCGTGCGAGACGGAGTACCTCATCCACCCTACGACCATTGATCTCATGTTCCAAGCC CTTCTGGCTACGTTACCCCGGATGCAGGGCATTCAGAAGCAGGGTTGGGCTCCAACGGCTGTCGGCTCGATCCGC GTCTCGAACGCCGTCGGACGCGGACCTGGGACGGTACTGTACGGCTATGGCGAGACGTCTCCCCGCGCGACCCAT CAGATAGTAGGCTTCGTCATGGCAGGCGACGGTGCTTTCGACTCGCTTCCGGGCGTCGTCATGGAAGGCATCCAG GTCTCGGGGCTGGGCGCGATGCAAAACTCATCGCAACTGTCCGAGGACTCGGGCGTCAAGCTGTACGCGGCGCCC TATTGGAAGCCGGATCTGCTACTCCTCGAGGGGCTTCGTCCGTCGAGGCTGACGAGCGGCGGGCCTCAAGACCAT TGTGCGGCTCAGTTCTGCTCCGACAGCCGTGACATTGTCAACGAGATGTGTCGCATTGCCCTGGAGCGGCTGGAC GGCAAGCCAGACGAGAAGCTCACTCCCCCTCTGCAAAAGTACGTCGAGTGGATGCGAAGGCGCAACCGAGCGACC TTGAAGACGTTTAGCAGCATCACGCCGCCCATTAGCCCAGCTTTCGGCGGCTTTGGCGCGAGTCTAGACCCCAAT TTCGGCATCGACAAGCTCAAGGGCTTCATCGAAAACTTCCCGGTCGACGGACGCCTTTTGCGCCACGCCTTTGCC TCGCTCGACGCAATCTTTAGCCGGCAGACGGTCCCCATCGCCGCACTGATGGCGAGCGACGACTTTGCCAGGTTC TACAAGGAGTCTCACGGCGCCGAAGTCATCAAGACCATCTTCCGCAACTGGTTCGACCTCAAGGCGCACAAGAAG CCCAATCTACGCGTCATCGAGATCGGAGCCGGGACGGCGTCGACGACGGTGCCCGTTTTGGAGACGCTGGGGGAG GCCGAAGACGAGACGCCTCGCTTCTCAAACTATACCTTTACCGACATCTCGCCCGGTTGGTTTGAGGGCGCGCGG ACGTTGCTGCGTAACTGGAAGTCTCGGGTTGAGTACAAGGTGCTCAACATTGAGGAGGATCCCGTCGAGCAAGGA TTCGAAGCCGAGTCTTATGACGTGGTGTTGGCTGTCAACGTTCTCCACGCAACCAAAGACATACATCAGACGCTC ACAAACTGCCGCCGCCTGCTCAAGCCCGGCGGCAACCTCATCGTCGGCGAGTGCACCAACCCGGATGACATGCTC TCCTTCATCTTCGGCATCCTGCCCGGCTGGTGGGCCTCGGAAGATGGGAGGCGTTTCGGCCCCCTGCTCAGCGAG GCCGCCTGGGACAAGGCCCTCAAGGCGTCGGGCTTCTCCGGTACTGACATTGCCATGCCTGACGGCGATGACAAG GTTGGCCATCATAGGATGTCGGTTCTGGTCAGCACCAAGCCGCACGAGCAGGCCGCCGCGTTGCCGGCCAAGGAC GTGGTGGTGCTCATGCCCAACGACGGCACCGACGTCGGGGCCGGTCTCGCCTCATCGGTTTGTCGCGAGCTCGAG CAACTCGGAGCTCGTGTCAGCATCAAGGAGCTCGGAGCCGACATCGAGGGCAAGACGGTCGTCTCTCTCCTTGAA TACGAGACGCCTTTTCTCGAGCAGGTTCAGGAAGCCGATTTCGAGCAAGTCAAGAACGTCTTTCTTCACTGCCGC GAGCTCCTCTGGGTCACCCGCTCAGATGCGGCGGACAAGTCAGGCCACCCCAGCATGCGCATTGTCTCCGGGCTG TTGCATTGCATCAAAAATGAGGACGCGTCCCGGCGGCTTCATGAGCTTCACCTCTGCCGCAATGCCACGGCTGAT GTGAAATCGACCAGCGGCGCCATCCTCCGCAGGCTAAACAGCCTGTGGCAGGGCGATGGCGACGACGGCGGGGAG TTGGTGACGGCAGAGCGAGACGGTGCCTTCTGCATCCCTCGTTACGTGCCGGACAAGGCCATGAACCGCAGCCTG GCGCGTACGACCGAGTCGGACCCGGCGCTTCAGACGGAAAAGCTCATCCAGACGTGCCGGCCGCTGCAGCTGAAG ATTGGACGACCGGGGATGCTGGACACGCTGCACTTTGCCGACGATGACGAGGCATCGCAGCCGCTGCTCGACGAC GAGGTCAGGATCGAGGTGCAGGCATGCGGCCTTAACTTCCGAGACGTCTTGATCGCAATGGGCGAGCTCCGGTCC CCCAGTCTGGGCTATGAGGCGGCTGGCATCGTCATCGACACGGGCGCCAAGGTGACTCGACTCTCGCCTGGCGAT AGGGTCGTGTGCATGAGGCCCAACGTGATGCGTACGCGCATCCGCGCTCATGAGTGGTACGTCCATCTGCTGCCG GCCTGCCTATCGATTGAGGACGGCGTGACGATTCCGGTGGCGTATGCAACTGCGTATCGATGCCTTGTCGAGGTG GCGAGGCTGCAAAAGGGCGAGTCGGTGCTTATCCACGCGGCAGCGGGAGGCTTTGGTCAGGCTACAATTCACATG GCCAAGATGCTGGGAGCCGACATCTTCTGCACGGTCAGCACCGAGGCCAAGAAGCGACTGGTCGTCTCTCTGGGC GTCAAGCCCGAACACGTCTTCAGCTCGCGTGACATCTCGTTCGAAACGGGCATCAGGCGGGTGACCAAGGGCCGC GGCGTCGACGTCGTCGTCAACTCGTTGGCAGGTGAGCTTCTACGAAGGAGTTGGGCCTGTCTGGCGCCCTATGGC CGCTTCATTGAGGTCGGCAAGCGAGATATCGTCGGCAACAGTGGGCTCGACATGCAGCCGTTTGACGACAACGCC ATTTTCGCCTGCGTCAATCTTGATGCCATGGCGTCGGAGCCGAGGAGGCTGTGGCAGCTGGTGGACAAGGTGCTG CGGCTTTTCGAGCAGGGCTCTTTGGGACTGATCCAGCCCATCGCCGTCCATGACTTCTCCGAGGTCGAGGCCGTC TTCCGCGAGATGCAGCGAGGCGCCCACATGGGTAAGCTGGCGCTCCGCGTCACGGCCGAATCTCGCGTGCCCGTG GCGCCTCGCAAGCAGGTTCCGCTTCGTCTGCGATCAGACGCCACCTATCTGCTGGCCGGCGGTCTCGGCGGAATC GGCCGGGCTCAGGCGCTGTTCATGGCGGAGCACGGGGCGCGTCACTTGGCCTTTGTCTCGCGTTCTGGCGATGCC AAACCCGAGGCCCGGCAGCTGCTGAAGACGTTGGCCGAGGCCGGCGTCGAGGCCCGGGCTTATTCCGGCGACGTG GCCGACAAGGACCGGCTCCGGGCCATCCTCGCCGATGCGGCGCGCCAAATGCCACCGATCCGCGGCGTCATCCAG GGCGCCATGGTCCTGGACGATTCCCTCTTCCACAAAATGACGTACGACCAGTGGCTGACGGCGACGCGGCCCAAG ATCCAGGGCAGCTGGAATCTGCACGAGTTGCTGCCTTCGAGCCTCGACTTCTTCGTCGTACTCTCCTCCATGGCC GGCACCATCGGCTTCTTGTCTCAGTCCAACTATGCGGCCGGCAACACGTATCAGGACGCGCTGGTGCACTACCGC CACGACAAGGGGCTGCCAGCGCTGAGCATCGACCTGGGCATCACCAAGGGGCTGGGCTACGTGGCCGAGCACGAC GACGTGGCCGCCAAGCTGAAGCCGTACGGGCTGGCTACGGTCAACGAGCAGCAGTTCTTCCATCTCATGCGATGT GCCCTCGCCGGCACCGCCGACGGAGAGAGCCGGCTCAACACGAGACAGCTCCTCGCCGGAGCCGGAACCGGCGGC CTCGCGCAGGCGTCGCTGGCGACGGTGCCGGAGACGAACCTCTACTGGCTCACGGCCCTGTCGACCTTTTCTTAC CTCGGCGAGGTCGACGTTCGGGACACGGCCGAGGCGGCGGGCGAAGAGGTGACGGACGACGTCAGGCTCATCGGC CAGCTCGGAGGGGCCAAGACGATGGACGAGGCGGCCGAGGCGGTCCAGGACATGCTCCTATCTCGCATCGCGACC ATCATGTCGGTGCCGACGACAAACATCGACACGTCCAAGCCGGTGCACGCGTACGGCGTCGACAGCCTGGTGGCC GTCGAGCTACGCAATTGGCTGTCGAAACGGCTGCGGAGCGACGTCAGCATCTTTGACCTGACGGGCAACATGGCC ATTACGACGCTGAGCCGAAAGATTGCCAGCCGGTCGCGTCTGGTGTCTGCCGCGACCAAGGGGCAGGGCGACGAA GCAGCTTGA |
| Gene | >Ophio5|4083 ATGGCCCAGGCCGACATCGCCATCGTCGGGATTGCTTGCCGCTTTCCCGGCGAGGCCAAGTCCCCGAGTGCCTTT TACCAGATGCTGGTGCAGGGCCGAGACGCATGGACCAAGGTGCCCAAGTCGCGATACGATGTCGACGCATATAGA CACCCCTCACGCGAGCGTCGCGGAACCATGGTAAGGCAAAAGCACAAAGAGACTTGGACAGGCCCCCGGGGATCG AGGCTGATCTGAATCTCGGTAGGTGTGCGAAGGCGGTTACTTTCTGGAAGACGACGTTTCGCGATGGGACGCGCC CTTTTTCTCTTGCTCGGCCGTCGAGGCGCAGGCCATGGATCCCCAACAACGGCTGCTGCTCGAGGTGGCGTACGA GAGTCTGGAGAACGCGGGGATCCCGCTCGAGGCGATGGCGGAGAGCGACGCCGCCTGCTTCGTCGGCGGCTTCAC CAACGACTACCGACGCATCGTGACGAGCGAGACGGAGGCGATTCCTCAGTACGTCATGACGGGCAACTCGACGTC CATGATGGCCAATCGAGTTAGCTGGTTCCTCAACCTGCGCGGGCCGTCCGTCACCGTCGACACGGCCTGCTCGAG CTCAATGGCTGCTCTACATCTGGCGTGCGAGACGATTCGTTCCGGAGCCAACGAGACACGTTGCGCGCTGGTCGG CGGAACGAGCCTGCTTCTGGACCCAGAAGATCCGTGCTGTATGAATGCGCTGGGCTTCCTCAGCCCGGACAGTCG ATGCTTCACGTTTGATTCACGGGCCAACGGCTACGCGCGGGGTGAGGGTATCGCGATGCTGGTGGTCAAGCACAT GGACGACGCGCTGCGCGACGGCGACGCGATCAGGGCCGTTGTGAGAGCGACGGCATTGAATTCAGACGGGCGGGT GAGTTCATGTTTGTTTCTGTCATGTCGTCGTTAGGGCTAGCAGTCCCAGCACGATGATTGATGATTACCCTTAAC AGGGCTTGCTGACGCATCCGAACACAGACTGCCGGCATCGTCCTCCCCAACGGCGACGCCCACCACCGACTCATC AGCCACACCTACCGCCTTGCGGGGCTCAACCCGGCCGACACGCAGTATGCCGAGCTCCACGGCACCGGCACTCGG GTCGGCGACCCCACCGAGATCGGCGCCGTGGCCCGTACCCTCGCTGCCGGCCGCCCGACGCCGCTGCTATGCGGC TCCGTCAAGACGCAGATCGGCCACACCGAGGCCGCCGCCGCCCTAGCCGGTGTCCTGAAATGCGTCCTCTCCATG GAGGCCGGCGTCTTGCCGCCCCACAAGAATTTCATCGAGCCCAATCCGCGGCTCCGGCTCGAGGCCTCGAACATT GCGGTGCCGATAGAGCCGCAGCCGTGGCCCGCCGCCGACGTTCGCCGCTGCTCCGTCAATAGCTTCGGCTTCGGA GGGCTCAACGGTCATATCGTCCTCGACGGAGCGGCCGGTTACCTCAGCAGCCGCGGTCTCGCCGTCCCGAGCGCC GATGCCGACTCCAACGATGCCCGGCGGCCCTACCTCTTCCTCCTCTCCGCCCCGGAGCAGGATGCCGTGGCCCGC CAGCTCCGCGCCCATGCAGACTATCTCGTCTCGTCGCCGGACCCCAAACTGCCACTTCTCGCCCACACCCTCGGC GCTCGTCGGTCCGTCTTCCAGTGGCGCCTCGCCGTCGTCGCCCGGTCCGCCGACGAGCTCGAGTCTCTGTGGCGC GATGAGGCGCTTAAGCCCGTCAAGGCTGCCGCCGCCCCCGGCGTCGCCCTTCTCTTCACCGGCCAGGGCGCTCAG TGGTACGCCATGGGCCGCGAGCTACTGGCGCTGCCCGTCTTCGCCCGCTCCGTCCGCGCTTCGGCCTCGGCCTTG ACCGCCATAGGCTGCCCCTGGGACGCGGAGGCGGAGCTGATGGCTCCCGAGGCCGAGTCGCGCGTCAACCTCGCC GCTTACTCGCAGCCGTTGTGCTCGGTCTTGCAGATTGCCCTCGTCGACCTCCTCCGCCACTGGGGCGTCAAGCCG GCCGCCGTCGTCGGCCACTCTTCGGGCGAGATGGCGGCTGCCTACGCAGTCGGAGCCCTCTCGCGTGAGGACTGC CTGGCCGTCGCCTACCACCGCGGCTTAGTGTCCGAGATGGCTGCCGACCGGAAGCCGGGCGGCGCCATGATGGCC GTTGGTCTGTCCGCCGACGAGGTGCGGCCGCGCCTCGAAGACGCCGTCACCGTCGCCTGCGTCAACAGCCCCAAT AATGTGACGCTGGCCGGAGACCGCGCCGCGCTCGAGAGGCTGGGCGAGTCCCTGAAGCGTGACGACATCTTCTGC CGTCTGCTGCAGGTTCAGAACGCCTTTCACAGCCCACAGATGGTTGCCGTCGCTGACGAGTACCGTCGACGCATC GCCAACGTGACTCCCACCGACATGTCGGCCTCGTTCTATTCGACCGTCAAGGGCTGCCGCATCCCCACGTCGCGC TTGACTGCCGATTACTGGGTCGACAATCTCTGCTCGCCCGTTGAGCTCGTTGGCGCCCTAGACGACATGCTCTGC GCCGACGGCAAGGGCAAGAGGTCCAAAGCGCCCACAGTCATCGTCGAAGTCGGGCCTCATGGCGCCCTCGCTGGC CCCTTTGATCAGTTCCGGCTCGCCCGTCGCGGTCTGGAGCACATCGGCTATTACAGCCTCCTCTCGCGAGGACGG GACGCGATGCAGACAACGATGAGCGCCGCCGCTGCCCTTTGGATGAAGGGCGTTCCCGTTCAAGTCGGCAAGGTG AGTTGATGTTGCCCTCCAGAACACGCCGTCCGTCTACTCACGCACCGCTCCCAGATCAATGGCTTGGACGAGACC TCTCGGCCCGCCACCGTCTTGACCGATCTGCCCTCGTACAGCTGGAACCACTCCGTCTCCTACTGGCATGAGACG TGGAGCTCGCGAAATCGACGCTGCCCGCCAGCTCCCAAGCACGACCTGATCGGATGGCGGCTCCATGCGTGCAAC CCGCTAGAGCCCGTGTGGAAAAACTACCTGCGTACCTCGGAGATGCCCTGGCTCAAGGATCACCAGGTCCATGGC GACGTTGTTTTTCCCGCCGGCGGCGTCATCTCCGCCGTCATCGAGGCCATACGCCAGTTCGAGGCCGGCCAGGAC GCGAGCCGTGAAATCTCGAGCTTCGAGCTACGCGAGTTCTATATCCCCCGGCCGCTGCTCATCCCCAACACCGAG CTGGGCGCCGAGACGTTTCTCCACCTCAAACGCAGAAAGTCGGGCATGGGCAGCGGCGCCGGTCCTTGGCTCGAG TTCTCCTTCTACTCGCGCCAGGACGGTGATGTCTTCGTCGAGCACGCCTACGGGCTGGCGCAGGCTCACTTTGCC AAGCAGCCCAACGAGGTGGATGGCGGAAAAGAGCTGCGAGAGGAAACACGGGCGCATCAGCGACGATTCCGGCAC CAGAGCAGCGTATGTGACGAGCCGATGACCAGCCAGGCTCACTACGACTTTTGCAAGAGCATTGGCCTCTGCTAC GGCAACTATTTTCAGGGTCTCTCCAAGGTGCGGCTTCATGATACGACCTGCGCCTTCGAGGCCACCATCATCGAC ACACCGTCGTGCATGCCTGGGGCGTGCGAGACGGAGTACCTCATCCACCCTACGACCATTGATCTCATGTTCCAA GCCCTTCTGGCTACGTTACCCCGGATGCAGGGCATTCAGAAGCAGGGTTGGGCTCCAACGGCTGTCGGCTCGATC CGCGTCTCGAACGCCGTCGGACGCGGACCTGGGACGGTACTGTACGGCTATGGCGAGACGTCTCCCCGCGCGACC CATCAGATAGTAGGCTTCGTCATGGCAGGCGACGGTGCTTTCGACTCGCTTCCGGGCGTCGTCATGGAAGGCATC CAGGTCTCGGGGCTGGGCGCGATGCAAAACTCATCGCAACTGTCCGAGGACTCGGGCGTCAAGCTGTACGCGGCG CCCTATTGGAAGCCGGATCTGCTACTCCTCGAGGGGCTTCGTCCGTCGAGGCTGACGAGCGGCGGGCCTCAAGAC CATTGTGCGGCTCAGTTCTGCTCCGACAGCCGTGACATTGTCAACGAGATGTGTCGCATTGCCCTGGAGCGGCTG GACGGCAAGCCAGACGAGAAGCTCACTCCCCCTCTGCAAAAGTACGTCGAGTGGATGCGAAGGCGCAACCGAGCG ACCTTGAAGACGTTTAGCAGCATCACGCCGCCCATTAGCCCAGCTTTCGGCGGCTTTGGCGCGAGTCTAGACCCC AATTTCGGCATCGACAAGCTCAAGGGCTTCATCGAAAACTTCCCGGTCGACGGACGCCTTTTGCGCCACGCCTTT GCCTCGCTCGACGCAATCTTTAGCCGGCAGACGGTCCCCATCGCCGCACTGATGGCGAGCGACGACTTTGCCAGG TTCTACAAGGAGTCTCACGGCGCCGAAGTCATCAAGACCATCTTCCGCAACTGGTTCGACCTCAAGGCGCACAAG AAGCCCAATCTACGCGTCATCGAGATCGGAGCCGGGACGGCGTCGACGACGGTGCCCGTTTTGGAGACGCTGGGG GAGGCCGAAGACGAGACGCCTCGCTTCTCAAACTATACCTTTACCGACATCTCGCCCGGTTGGTTTGAGGGCGCG CGGACGTTGCTGCGTAACTGGAAGTCTCGGGTTGAGTACAAGGTGCTCAACATTGAGGAGGATCCCGTCGAGCAA GGATTCGAAGCCGAGTCTTATGACGTGGTGTTGGCTGTCAACGTACGTCTCTCTCTCTCTCTCTCTCTCTCTCTC TCTCTCTCTCTCTCTGTCTTTCTCTCTTTCTCTCTTTCTCTCTCTGTCTTTCTCTCTTTCTCTCTTTCTCTCTCT CTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTCTCTCTCTTCCTCTCTTTTCTTCTCTCTAACATGTGTTCGCTC TCAGGTTCTCCACGCAACCAAAGACATACATCAGACGCTCACAAACTGCCGCCGCCTGCTCAAGCCCGGCGGCAA CCTCATCGTCGGCGAGTGCACCAACCCGGATGACATGCTCTCCTTCATCTTCGGCATCCTGCCCGGCTGGTGGGC CTCGGAAGATGGGAGGCGTTTCGGCCCCCTGCTCAGCGAGGCCGCCTGGGACAAGGCCCTCAAGGCGTCGGGCTT CTCCGGTACTGACATTGCCATGCCTGACGGCGATGACAAGGTTGGCCATCATAGGATGTCGGTTCTGGTCAGCAC CAAGCCGCACGAGCAGGCCGCCGCGTTGCCGGCCAAGGACGTGGTGGTGCTCATGCCCAACGACGGCACCGACGT CGGGGCCGGTCTCGCCTCATCGGTTTGTCGCGAGCTCGAGCAACTCGGAGCTCGTGTCAGCATCAAGGAGCTCGG AGCCGACATCGAGGGCAAGACGGTCGTCTCTCTCCTTGAATACGAGACGCCTTTTCTCGAGCAGGTTCAGGAAGC CGATTTCGAGCAAGTCAAGAACGTCTTTCTTCACTGCCGCGAGCTCCTCTGGGTCACCCGCTCAGATGCGGCGGA CAAGTCAGGCCACCCCAGCATGCGCATTGTCTCCGGGCTGTTGCATTGCATCAAAAATGAGGACGCGTCCCGGCG GCTTCATGAGCTTCACCTCTGCCGCAATGCCACGGCTGATGTGAAATCGACCAGCGGCGCCATCCTCCGCAGGCT AAACAGCCTGTGGCAGGGCGATGGCGACGACGGCGGGGAGTTGGTGACGGCAGAGCGAGACGGTGCCTTCTGCAT CCCTCGTTACGTGCCGGACAAGGCCATGAACCGCAGCCTGGCGCGTACGACCGAGTCGGACCCGGCGCTTCAGAC GGAAAAGCTCATCCAGACGTGCCGGCCGCTGCAGCTGAAGATTGGACGACCGGGGATGCTGGACACGCTGCACTT TGCCGACGATGACGAGGCATCGCAGCCGCTGCTCGACGACGAGGTCAGGATCGAGGTGCAGGCATGCGGCCTTAA CTTCCGGTAAGAAGTCGTCGTTTCTGATCAAGGGGCTTTGGCGCTAACGAGGCATGGCACAGAGACGTCTTGATC GCAATGGGCGAGCTCCGGTCCCCCAGTCTGGGCTATGAGGCGGCTGGCATCGTCATCGACACGGGCGCCAAGGTG ACTCGACTCTCGCCTGGCGATAGGGTCGTGTGCATGAGGCCCAACGTGATGCGTACGCGCATCCGCGCTCATGAG TGGTACGTCCATCTGCTGCCGGCCTGCCTATCGATTGAGGACGGCGTGACGATTCCGGTGGCGTATGCAACTGCG TATCGATGCCTTGTCGAGGTGGCGAGGCTGCAAAAGGGCGAGTCGGTGCTTATCCACGCGGCAGCGGGAGGTGAG TTTGCAGTCCCACCAAGACTGGCAGTGATTGACTGACCGACGATTTATAGGCTTTGGTCAGGCTACAATTCACAT GGCCAAGATGCTGGGAGCCGACATCTTCTGCACGGTCAGCACCGAGGCCAAGAAGCGACTGGTCGTCTCTCTGGG CGTCAAGCCCGAACACGTCTTCAGCTCGCGTGACATCTCGTTCGAAACGGGCATCAGGCGGGTGACCAAGGGCCG CGGCGTCGACGTCGTCGTCAACTCGTTGGCAGGTGAGCTTCTACGAAGGAGTTGGGCCTGTCTGGCGCCCTATGG CCGCTTCATTGAGGTCGGCAAGCGAGATATCGTCGGCAACAGTGGGCTCGACATGCAGCCGTTTGACGACAACGC CATTTTCGCCTGCGTCAATCTTGATGCCATGGCGTCGGAGCCGAGGAGGCTGTGGCAGCTGGTGGACAAGGTGCT GCGGCTTTTCGAGCAGGGCTCTTTGGGACTGATCCAGCCCATCGCCGTCCATGACTTCTCCGAGGTCGAGGCCGT CTTCCGCGAGATGCAGCGAGGCGCCCACATGGGTAAGCTGGCGCTCCGCGTCACGGCCGAATCTCGCGTGCCCGT GGCGCCTCGCAAGCAGGTTCCGCTTCGTCTGCGATCAGACGCCACCTATCTGCTGGCCGGCGGTCTCGGCGGAAT CGGCCGGGCTCAGGCGCTGTTCATGGCGGAGCACGGGGCGCGTCACTTGGCCTTTGTCTCGCGTTCTGGCGATGC CAAACCCGAGGCCCGGCAGCTGCTGAAGACGTTGGCCGAGGCCGGCGTCGAGGCCCGGGCTTATTCCGGCGACGT GGCCGACAAGGACCGGCTCCGGGCCATCCTCGCCGATGCGGCGCGCCAAATGCCACCGATCCGCGGCGTCATCCA GGGCGCCATGGTCCTGGACGATTCCCTCTTCCACAAAATGACGTACGACCAGTGGCTGACGGCGACGCGGCCCAA GATCCAGGGCAGCTGGAATCTGCACGAGTTGCTGCCTTCGAGCCTCGACTTCTTCGTCGTACTCTCCTCCATGGC CGGCACCATCGGCTTCTTGTCTCAGTCCAACTATGCGGCCGGCAACACGTATCAGGACGCGCTGGTGCACTACCG CCACGACAAGGGGCTGCCAGCGCTGAGCATCGACCTGGGCATCACCAAGGGGCTGGGCTACGTGGCCGAGCACGA CGACGTGGCCGCCAAGCTGAAGCCGTACGGGCTGGCTACGGTCAACGAGCAGCAGTTCTTCCATCTCATGCGATG TGCCCTCGCCGGCACCGCCGACGGAGAGAGCCGGCTCAACACGAGACAGCTCCTCGCCGGAGCCGGAACCGGCGG CCTCGCGCAGGCGTCGCTGGCGACGGTGCCGGAGACGAACCTCTACTGGCTCACGGCCCTGTCGACCTTTTCTTA CCTCGGCGAGGTCGACGTTCGGGACACGGCCGAGGCGGCGGGCGAAGAGGTGACGGACGACGTCAGGCTCATCGG CCAGCTCGGAGGGGCCAAGACGATGGACGAGGCGGCCGAGGCGGTCCAGGACATGCTCCTATCTCGCATCGCGAC CATCATGTCGGTGCCGACGACAAACATCGACACGTCCAAGCCGGTGCACGCGTACGGCGTCGACAGCCTGGTGGC CGTCGAGCTACGCAATTGGCTGTCGAAACGGCTGCGGAGCGACGTCAGCATCTTTGACCTGACGGGCAACATGGC CATTACGACGCTGAGCCGAAAGATTGCCAGCCGGTCGCGTCTGGTGTCTGCCGCGACCAAGGGGCAGGGCGACGA AGCAGCTTGA |