Protein ID | Ophun1|7483 |
Gene name | |
Location | Contig_95:21136..28084 |
Strand | + |
Gene length (bp) | 6948 |
Transcript length (bp) | 6678 |
Coding sequence length (bp) | 6678 |
Protein length (aa) | 2226 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00109 | ketoacyl-synt | Beta-ketoacyl synthase, N-terminal domain | 4.7E-73 | 11 | 261 |
PF08659 | KR | KR domain | 1.8E-67 | 1856 | 2034 |
PF00698 | Acyl_transf_1 | Acyl transferase domain | 5.4E-60 | 538 | 862 |
PF14765 | PS-DH | Polyketide synthase dehydratase | 3.4E-45 | 919 | 1232 |
PF02801 | Ketoacyl-synt_C | Beta-ketoacyl synthase, C-terminal domain | 4.0E-36 | 271 | 387 |
PF16197 | KAsynt_C_assoc | Ketoacyl-synthetase C-terminal extension | 4.3E-19 | 390 | 504 |
PF00106 | adh_short | short chain dehydrogenase | 5.4E-19 | 1858 | 2016 |
PF00107 | ADH_zinc_N | Zinc-binding dehydrogenase | 1.0E-16 | 1658 | 1771 |
PF13602 | ADH_zinc_N_2 | Zinc-binding dehydrogenase | 3.1E-13 | 1698 | 1833 |
PF13561 | adh_short_C2 | Enoyl-(Acyl carrier protein) reductase | 4.7E-13 | 1865 | 2017 |
PF08240 | ADH_N | Alcohol dehydrogenase GroES-like domain | 1.7E-08 | 1541 | 1614 |
PF00550 | PP-binding | Phosphopantetheine attachment site | 1.6E-05 | 2147 | 2210 |
PF02719 | Polysacc_synt_2 | Polysaccharide biosynthesis protein | 1.2E-04 | 1859 | 1991 |
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 | 10 | 1272 | 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 | 11 | 1175 | 4.0E-180 |
sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 11 | 1172 | 9.0E-171 |
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 | 11 | 1186 | 6.0E-169 |
sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 11 | 1031 | 4.0E-168 |
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 | 10 | 1272 | 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 | 11 | 1175 | 4.0E-180 |
sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 11 | 1172 | 9.0E-171 |
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 | 11 | 1186 | 6.0E-169 |
sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 11 | 1031 | 4.0E-168 |
sp|Q9Y7D5|LOVF_ASPTE | Lovastatin diketide synthase LovF OS=Aspergillus terreus GN=lovF PE=1 SV=1 | 1318 | 2217 | 4.0E-146 |
sp|Q55E72|PKS1_DICDI | Probable polyketide synthase 1 OS=Dictyostelium discoideum GN=stlA PE=1 SV=1 | 12 | 1147 | 3.0E-139 |
sp|Q02251|MCAS_MYCBO | Mycocerosic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mas PE=1 SV=2 | 8 | 1024 | 1.0E-136 |
sp|P9WQE9|PHAS_MYCTU | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks2 PE=1 SV=1 | 8 | 1001 | 4.0E-136 |
sp|P9WQE8|PHAS_MYCTO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=pks2 PE=3 SV=1 | 8 | 1001 | 4.0E-136 |
sp|A5U9F4|PHAS_MYCTA | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=pks2 PE=3 SV=1 | 8 | 1001 | 4.0E-136 |
sp|Q7TVK8|PHAS_MYCBO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks2 PE=3 SV=1 | 8 | 1001 | 4.0E-136 |
sp|A1KQG0|PHAS_MYCBP | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=pks2 PE=3 SV=1 | 8 | 1001 | 2.0E-135 |
sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 11 | 1102 | 9.0E-135 |
sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 11 | 902 | 7.0E-132 |
sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 11 | 1141 | 9.0E-130 |
sp|P9WQE2|PPSD_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsD PE=3 SV=1 | 11 | 1141 | 9.0E-130 |
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 | 11 | 1141 | 1.0E-129 |
sp|Q869W9|PKS16_DICDI | Probable polyketide synthase 16 OS=Dictyostelium discoideum GN=pks16 PE=2 SV=1 | 12 | 1191 | 2.0E-129 |
sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 12 | 902 | 5.0E-129 |
sp|Q869X2|PKS17_DICDI | Probable polyketide synthase 17 OS=Dictyostelium discoideum GN=pks17 PE=3 SV=1 | 12 | 1191 | 5.0E-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 | 7 | 1102 | 2.0E-125 |
sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 11 | 906 | 8.0E-125 |
sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 11 | 902 | 1.0E-124 |
sp|P9WQE6|PPSA_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsA PE=3 SV=1 | 11 | 985 | 9.0E-123 |
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 | 7 | 1102 | 1.0E-122 |
sp|P9WQE7|PPSA_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsA PE=1 SV=1 | 11 | 985 | 2.0E-122 |
sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 7 | 830 | 3.0E-122 |
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 | 11 | 985 | 3.0E-122 |
sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 7 | 902 | 2.0E-121 |
sp|B0G100|PKS7_DICDI | Probable polyketide synthase 7 OS=Dictyostelium discoideum GN=pks7 PE=3 SV=1 | 12 | 1002 | 1.0E-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 | 11 | 905 | 6.0E-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 | 11 | 905 | 8.0E-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 | 11 | 905 | 8.0E-119 |
sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 12 | 1147 | 2.0E-118 |
sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 11 | 902 | 3.0E-118 |
sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 12 | 1002 | 1.0E-116 |
sp|B4XYB8|AZIB_STREG | 5-methyl-1-naphthoate synthase OS=Streptomyces sahachiroi GN=aziB PE=1 SV=1 | 11 | 1009 | 3.0E-116 |
sp|Q86JI5|PKS5_DICDI | Probable polyketide synthase 5 OS=Dictyostelium discoideum GN=pks5 PE=2 SV=1 | 7 | 1002 | 1.0E-115 |
sp|B0G0Z9|PKS6_DICDI | Probable polyketide synthase 6 OS=Dictyostelium discoideum GN=pks6 PE=3 SV=1 | 12 | 1002 | 3.0E-115 |
sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 12 | 1147 | 8.0E-115 |
sp|B0G101|PKS8_DICDI | Probable polyketide synthase 8/35 OS=Dictyostelium discoideum GN=pks8 PE=3 SV=1 | 12 | 1002 | 4.0E-111 |
sp|Q55DM7|PKS2_DICDI | Probable polyketide synthase 2 OS=Dictyostelium discoideum GN=pks2 PE=3 SV=1 | 1 | 1179 | 4.0E-110 |
sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 12 | 1147 | 8.0E-110 |
sp|Q54B49|PKS45_DICDI | Probable polyketide synthase 45 OS=Dictyostelium discoideum GN=pks45 PE=3 SV=2 | 12 | 1147 | 2.0E-109 |
sp|Q55CN6|PKS3_DICDI | Probable polyketide synthase 3 OS=Dictyostelium discoideum GN=pks3 PE=3 SV=1 | 20 | 1147 | 2.0E-109 |
sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 12 | 993 | 2.0E-109 |
sp|Q54B51|PKS44_DICDI | Probable polyketide synthase 44 OS=Dictyostelium discoideum GN=pks44 PE=3 SV=1 | 12 | 1147 | 2.0E-108 |
sp|P19096|FAS_MOUSE | Fatty acid synthase OS=Mus musculus GN=Fasn PE=1 SV=2 | 12 | 968 | 2.0E-107 |
sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 12 | 1002 | 2.0E-107 |
sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 12 | 968 | 3.0E-107 |
sp|P49327|FAS_HUMAN | Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 | 12 | 968 | 4.0E-107 |
sp|P96202|PPSC_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsC PE=1 SV=2 | 11 | 1102 | 6.0E-107 |
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 | 11 | 1102 | 6.0E-107 |
sp|Q559A9|PKS13_DICDI | Probable polyketide synthase 13 OS=Dictyostelium discoideum GN=pks13 PE=3 SV=1 | 12 | 1002 | 4.0E-106 |
sp|P22367|MSAS_PENPA | 6-methylsalicylic acid synthase OS=Penicillium patulum PE=1 SV=1 | 12 | 965 | 3.0E-104 |
sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 12 | 1035 | 4.0E-104 |
sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 12 | 1035 | 1.0E-103 |
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 | 1 | 906 | 2.0E-103 |
sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 12 | 1002 | 9.0E-103 |
sp|P12276|FAS_CHICK | Fatty acid synthase OS=Gallus gallus GN=FASN PE=1 SV=5 | 12 | 902 | 2.0E-102 |
sp|B0G103|PKS10_DICDI | Probable polyketide synthase 10 OS=Dictyostelium discoideum GN=pks10 PE=3 SV=1 | 12 | 1147 | 9.0E-102 |
sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 12 | 1050 | 2.0E-101 |
sp|B0G138|PKS21_DICDI | Probable polyketide synthase 21 OS=Dictyostelium discoideum GN=pks21 PE=3 SV=1 | 12 | 1052 | 2.0E-101 |
sp|Q54IX3|PKS26_DICDI | Probable polyketide synthase 26 OS=Dictyostelium discoideum GN=pks26 PE=3 SV=1 | 1 | 1002 | 3.0E-100 |
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 | 3 | 920 | 2.0E-99 |
sp|Q12053|PKSL1_ASPPA | Noranthrone synthase OS=Aspergillus parasiticus GN=pksL1 PE=1 SV=1 | 12 | 902 | 3.0E-96 |
sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 12 | 1147 | 5.0E-94 |
sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 12 | 1003 | 2.0E-90 |
sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 5 | 866 | 7.0E-89 |
sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 12 | 1147 | 7.0E-89 |
sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 4 | 1147 | 1.0E-88 |
sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 81 | 1147 | 1.0E-88 |
sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 12 | 1147 | 6.0E-88 |
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 | 7 | 432 | 7.0E-88 |
sp|P96202|PPSC_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsC PE=1 SV=2 | 1514 | 2209 | 2.0E-87 |
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 | 1514 | 2209 | 2.0E-87 |
sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 12 | 1147 | 1.0E-86 |
sp|Q02251|MCAS_MYCBO | Mycocerosic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mas PE=1 SV=2 | 1417 | 2189 | 6.0E-86 |
sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 12 | 1003 | 8.0E-86 |
sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 13 | 1003 | 3.0E-85 |
sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 12 | 866 | 3.0E-85 |
sp|P9WQE9|PHAS_MYCTU | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks2 PE=1 SV=1 | 1417 | 2189 | 5.0E-85 |
sp|P9WQE8|PHAS_MYCTO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=pks2 PE=3 SV=1 | 1417 | 2189 | 5.0E-85 |
sp|A5U9F4|PHAS_MYCTA | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=pks2 PE=3 SV=1 | 1417 | 2189 | 5.0E-85 |
sp|Q7TVK8|PHAS_MYCBO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks2 PE=3 SV=1 | 1417 | 2189 | 5.0E-85 |
sp|A1KQG0|PHAS_MYCBP | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=pks2 PE=3 SV=1 | 1417 | 2189 | 5.0E-85 |
sp|P9WQE1|PPSE_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsE PE=1 SV=1 | 12 | 824 | 1.0E-84 |
sp|P9WQE0|PPSE_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsE PE=3 SV=1 | 12 | 824 | 1.0E-84 |
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 | 12 | 824 | 1.0E-84 |
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 | 1516 | 2184 | 1.0E-79 |
sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 12 | 520 | 3.0E-79 |
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 | 1516 | 2184 | 5.0E-79 |
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 | 1516 | 2184 | 7.0E-76 |
sp|Q55E72|PKS1_DICDI | Probable polyketide synthase 1 OS=Dictyostelium discoideum GN=stlA PE=1 SV=1 | 1418 | 2196 | 2.0E-75 |
sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 8 | 425 | 4.0E-75 |
sp|Q9R9J1|MYCA_BACIU | Mycosubtilin synthase subunit A OS=Bacillus subtilis GN=mycA PE=3 SV=1 | 12 | 522 | 4.0E-75 |
sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 1523 | 2187 | 6.0E-75 |
sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 12 | 520 | 1.0E-72 |
sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 1 | 520 | 1.0E-72 |
sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 11 | 525 | 4.0E-72 |
sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 12 | 519 | 3.0E-69 |
sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 9 | 525 | 1.0E-68 |
sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 1542 | 2076 | 6.0E-68 |
sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 12 | 522 | 5.0E-67 |
sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 11 | 520 | 5.0E-67 |
sp|P19096|FAS_MOUSE | Fatty acid synthase OS=Mus musculus GN=Fasn PE=1 SV=2 | 1517 | 2050 | 6.0E-67 |
sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 1517 | 2041 | 9.0E-66 |
sp|Q869W9|PKS16_DICDI | Probable polyketide synthase 16 OS=Dictyostelium discoideum GN=pks16 PE=2 SV=1 | 1505 | 2196 | 1.0E-65 |
sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 12 | 546 | 1.0E-65 |
sp|Q869X2|PKS17_DICDI | Probable polyketide synthase 17 OS=Dictyostelium discoideum GN=pks17 PE=3 SV=1 | 1527 | 2196 | 1.0E-64 |
sp|P49327|FAS_HUMAN | Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 | 1552 | 2050 | 5.0E-64 |
sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 12 | 433 | 1.0E-63 |
sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 12 | 434 | 2.0E-63 |
sp|P12276|FAS_CHICK | Fatty acid synthase OS=Gallus gallus GN=FASN PE=1 SV=5 | 1517 | 2050 | 7.0E-63 |
sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 1615 | 2067 | 1.0E-62 |
sp|P36189|FAS_ANSAN | Fatty acid synthase (Fragment) OS=Anser anser anser GN=FASN PE=1 SV=1 | 12 | 379 | 1.0E-60 |
sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 12 | 433 | 5.0E-59 |
sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 12 | 521 | 7.0E-58 |
sp|Q54KU5|PKS24_DICDI | Probable polyketide synthase 24 OS=Dictyostelium discoideum GN=pks24 PE=3 SV=1 | 12 | 434 | 1.0E-56 |
sp|Q55CN6|PKS3_DICDI | Probable polyketide synthase 3 OS=Dictyostelium discoideum GN=pks3 PE=3 SV=1 | 1536 | 2206 | 3.0E-54 |
sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 12 | 519 | 9.0E-54 |
sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 1538 | 2206 | 3.0E-53 |
sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 1538 | 2206 | 2.0E-52 |
sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 12 | 519 | 4.0E-52 |
sp|Q55DM7|PKS2_DICDI | Probable polyketide synthase 2 OS=Dictyostelium discoideum GN=pks2 PE=3 SV=1 | 1543 | 2225 | 3.0E-51 |
sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 1538 | 2206 | 3.0E-51 |
sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 1538 | 2206 | 4.0E-51 |
sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 12 | 526 | 1.0E-50 |
sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 1528 | 2215 | 3.0E-50 |
sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 1527 | 2219 | 3.0E-50 |
sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 1538 | 2205 | 2.0E-49 |
sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 1538 | 2206 | 4.0E-49 |
sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 1528 | 2185 | 1.0E-48 |
sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 1538 | 2206 | 1.0E-48 |
sp|Q54IX3|PKS26_DICDI | Probable polyketide synthase 26 OS=Dictyostelium discoideum GN=pks26 PE=3 SV=1 | 1538 | 2207 | 2.0E-48 |
sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 1538 | 2206 | 7.0E-48 |
sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 1538 | 2193 | 9.0E-48 |
sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 1538 | 2206 | 1.0E-47 |
sp|Q54KU5|PKS24_DICDI | Probable polyketide synthase 24 OS=Dictyostelium discoideum GN=pks24 PE=3 SV=1 | 1542 | 2205 | 1.0E-47 |
sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 1533 | 2190 | 5.0E-47 |
sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 1533 | 2214 | 9.0E-47 |
sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 1533 | 2190 | 6.0E-46 |
sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 1527 | 2206 | 1.0E-45 |
sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 1542 | 2193 | 4.0E-45 |
sp|Q54B49|PKS45_DICDI | Probable polyketide synthase 45 OS=Dictyostelium discoideum GN=pks45 PE=3 SV=2 | 1538 | 2208 | 5.0E-45 |
sp|Q54B51|PKS44_DICDI | Probable polyketide synthase 44 OS=Dictyostelium discoideum GN=pks44 PE=3 SV=1 | 1538 | 2208 | 5.0E-45 |
sp|B0G138|PKS21_DICDI | Probable polyketide synthase 21 OS=Dictyostelium discoideum GN=pks21 PE=3 SV=1 | 1536 | 2205 | 4.0E-43 |
sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 1536 | 2205 | 5.0E-43 |
sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 1538 | 2206 | 6.0E-43 |
sp|B0G0Z9|PKS6_DICDI | Probable polyketide synthase 6 OS=Dictyostelium discoideum GN=pks6 PE=3 SV=1 | 1538 | 2206 | 7.0E-43 |
sp|Q86JI5|PKS5_DICDI | Probable polyketide synthase 5 OS=Dictyostelium discoideum GN=pks5 PE=2 SV=1 | 1538 | 2206 | 1.0E-42 |
sp|B0G100|PKS7_DICDI | Probable polyketide synthase 7 OS=Dictyostelium discoideum GN=pks7 PE=3 SV=1 | 1538 | 2206 | 5.0E-42 |
sp|Q559A9|PKS13_DICDI | Probable polyketide synthase 13 OS=Dictyostelium discoideum GN=pks13 PE=3 SV=1 | 1533 | 2219 | 9.0E-42 |
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 | 1839 | 2221 | 8.0E-41 |
sp|B0G101|PKS8_DICDI | Probable polyketide synthase 8/35 OS=Dictyostelium discoideum GN=pks8 PE=3 SV=1 | 1538 | 2206 | 3.0E-40 |
sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 1538 | 2206 | 9.0E-40 |
sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 516 | 1002 | 1.0E-38 |
sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 1831 | 2209 | 1.0E-36 |
sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 1831 | 2209 | 7.0E-36 |
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 | 531 | 1102 | 1.0E-35 |
sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 536 | 968 | 6.0E-33 |
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 | 12 | 434 | 5.0E-30 |
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 | 1875 | 2208 | 2.0E-29 |
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 | 12 | 434 | 1.0E-28 |
sp|Q8JFV8|VAT1_DANRE | Synaptic vesicle membrane protein VAT-1 homolog OS=Danio rerio GN=vat1 PE=2 SV=1 | 1509 | 1837 | 2.0E-27 |
sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 1857 | 2184 | 3.0E-27 |
sp|P56902|FABF_RHIME | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Rhizobium meliloti (strain 1021) GN=fabF PE=3 SV=2 | 116 | 434 | 1.0E-26 |
sp|Q80TB8|VAT1L_MOUSE | Synaptic vesicle membrane protein VAT-1 homolog-like OS=Mus musculus GN=Vat1l PE=1 SV=2 | 1517 | 1837 | 2.0E-26 |
sp|P72331|NODE_RHIS3 | Nodulation protein E OS=Rhizobium sp. (strain N33) GN=nodE PE=3 SV=1 | 84 | 428 | 3.0E-26 |
sp|Q9HCJ6|VAT1L_HUMAN | Synaptic vesicle membrane protein VAT-1 homolog-like OS=Homo sapiens GN=VAT1L PE=1 SV=2 | 1517 | 1837 | 3.0E-26 |
sp|P55338|FABF_VIBHA | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Vibrio harveyi GN=fabF PE=3 SV=2 | 12 | 434 | 4.0E-26 |
sp|Q8NXE1|FABF_STAAW | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MW2) GN=fabF PE=1 SV=1 | 87 | 434 | 2.0E-25 |
sp|Q6GAU2|FABF_STAAS | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MSSA476) GN=fabF PE=3 SV=1 | 87 | 434 | 2.0E-25 |
sp|Q5HHA1|FABF_STAAC | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain COL) GN=fabF PE=1 SV=1 | 87 | 434 | 2.0E-25 |
sp|Q7A6F8|FABF_STAAN | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain N315) GN=fabF PE=1 SV=1 | 87 | 434 | 2.0E-25 |
sp|Q99VA6|FABF_STAAM | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabF PE=3 SV=1 | 87 | 434 | 2.0E-25 |
sp|Q6GIA3|FABF_STAAR | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MRSA252) GN=fabF PE=3 SV=1 | 87 | 434 | 2.0E-25 |
sp|O97764|QOR_BOVIN | Zeta-crystallin OS=Bos taurus GN=CRYZ PE=2 SV=2 | 1512 | 1833 | 2.0E-25 |
sp|Q5TKS0|FABF_STAAU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 (Fragment) OS=Staphylococcus aureus GN=fabF PE=3 SV=1 | 87 | 433 | 3.0E-25 |
sp|P39525|CEM1_YEAST | 3-oxoacyl-[acyl-carrier-protein] synthase homolog OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CEM1 PE=1 SV=1 | 104 | 434 | 4.0E-25 |
sp|B4XYB8|AZIB_STREG | 5-methyl-1-naphthoate synthase OS=Streptomyces sahachiroi GN=aziB PE=1 SV=1 | 1776 | 2183 | 5.0E-25 |
sp|O34340|FABF_BACSU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Bacillus subtilis (strain 168) GN=fabF PE=1 SV=1 | 90 | 434 | 5.0E-25 |
sp|Q0MVN8|QOR_PIG | Quinone oxidoreductase OS=Sus scrofa GN=CRYZ PE=2 SV=1 | 1512 | 1833 | 6.0E-25 |
sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 497 | 868 | 8.0E-25 |
sp|P06231|NOE4_RHIML | Nodulation protein E OS=Rhizobium meliloti GN=nodE PE=3 SV=1 | 84 | 428 | 1.0E-24 |
sp|P06230|NODE_RHIME | Nodulation protein E OS=Rhizobium meliloti (strain 1021) GN=nodE PE=3 SV=1 | 84 | 428 | 8.0E-24 |
sp|P28304|QOR1_ECOLI | Quinone oxidoreductase 1 OS=Escherichia coli (strain K12) GN=qorA PE=1 SV=1 | 1534 | 1736 | 8.0E-24 |
sp|Q9NWU1|OXSM_HUMAN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Homo sapiens GN=OXSM PE=1 SV=1 | 159 | 431 | 1.0E-23 |
sp|P11415|QOR_CAVPO | Quinone oxidoreductase OS=Cavia porcellus GN=CRYZ PE=1 SV=1 | 1512 | 1795 | 1.0E-23 |
sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 1858 | 2209 | 2.0E-23 |
sp|P40783|QOR_SALTY | Quinone oxidoreductase OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=qor PE=3 SV=2 | 1534 | 1748 | 2.0E-23 |
sp|Q08257|QOR_HUMAN | Quinone oxidoreductase OS=Homo sapiens GN=CRYZ PE=1 SV=1 | 1512 | 1795 | 2.0E-23 |
sp|A7Z4X9|BAED_BACMF | Polyketide biosynthesis acyltransferase homolog BaeD OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeD PE=1 SV=1 | 536 | 830 | 3.0E-23 |
sp|P22367|MSAS_PENPA | 6-methylsalicylic acid synthase OS=Penicillium patulum PE=1 SV=1 | 1857 | 2183 | 4.0E-23 |
sp|P0AAI8|FABF_SHIFL | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Shigella flexneri GN=fabF PE=3 SV=2 | 145 | 434 | 4.0E-23 |
sp|P0AAI5|FABF_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli (strain K12) GN=fabF PE=1 SV=2 | 145 | 434 | 4.0E-23 |
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 | 145 | 434 | 4.0E-23 |
sp|P0AAI7|FABF_ECO57 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli O157:H7 GN=fabF PE=3 SV=2 | 145 | 434 | 4.0E-23 |
sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 1872 | 2215 | 5.0E-23 |
sp|P9WQE2|PPSD_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsD PE=3 SV=1 | 1872 | 2215 | 5.0E-23 |
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 | 1872 | 2215 | 5.0E-23 |
sp|Q5R4S7|QOR_PONAB | Quinone oxidoreductase OS=Pongo abelii GN=CRYZ PE=2 SV=1 | 1512 | 1762 | 7.0E-23 |
sp|Q9D404|OXSM_MOUSE | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Mus musculus GN=Oxsm PE=1 SV=1 | 12 | 431 | 1.0E-22 |
sp|P04684|NODE_RHILT | Nodulation protein E OS=Rhizobium leguminosarum bv. trifolii GN=nodE PE=3 SV=2 | 84 | 428 | 2.0E-22 |
sp|P16540|KAS1_STRVN | Granaticin polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces violaceoruber GN=gra-orf1 PE=3 SV=1 | 12 | 436 | 4.0E-22 |
sp|A7RK30|QORL2_NEMVE | Quinone oxidoreductase-like protein 2 homolog OS=Nematostella vectensis GN=v1g238856 PE=3 SV=1 | 1538 | 1836 | 6.0E-22 |
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 | 12 | 433 | 6.0E-22 |
sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 1872 | 2184 | 1.0E-21 |
sp|P47199|QOR_MOUSE | Quinone oxidoreductase OS=Mus musculus GN=Cryz PE=1 SV=1 | 1512 | 1762 | 1.0E-21 |
sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 1872 | 2184 | 2.0E-21 |
sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 1776 | 2189 | 2.0E-21 |
sp|P04683|NODE_RHILV | Nodulation protein E OS=Rhizobium leguminosarum bv. viciae GN=nodE PE=3 SV=2 | 84 | 428 | 2.0E-21 |
sp|P41175|KAS1_STRCM | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cinnamonensis PE=3 SV=1 | 12 | 432 | 2.0E-21 |
sp|Q6AYT0|QOR_RAT | Quinone oxidoreductase OS=Rattus norvegicus GN=Cryz PE=2 SV=1 | 1539 | 1762 | 3.0E-21 |
sp|Q28452|QOR_LAMGU | Quinone oxidoreductase OS=Lama guanicoe GN=CRYZ PE=2 SV=1 | 1512 | 1795 | 5.0E-21 |
sp|P19333|VAT1_TORCA | Synaptic vesicle membrane protein VAT-1 OS=Torpedo californica PE=1 SV=1 | 1538 | 1748 | 6.0E-21 |
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 | 162 | 434 | 9.0E-21 |
sp|Q0VCA7|OXSM_BOVIN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Bos taurus GN=OXSM PE=2 SV=1 | 12 | 431 | 1.0E-20 |
sp|O34877|PKSD_BACSU | Polyketide biosynthesis acyltransferase homolog PksD OS=Bacillus subtilis (strain 168) GN=pksD PE=1 SV=2 | 536 | 830 | 1.0E-20 |
sp|P73283|FABF_SYNY3 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabF PE=1 SV=1 | 12 | 434 | 2.0E-20 |
sp|P71019|FABD_BACSU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis (strain 168) GN=fabD PE=3 SV=2 | 535 | 833 | 3.0E-20 |
sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 1826 | 2028 | 5.0E-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 | 1856 | 2051 | 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 | 1856 | 2051 | 6.0E-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 | 1856 | 2051 | 6.0E-20 |
sp|Q99536|VAT1_HUMAN | Synaptic vesicle membrane protein VAT-1 homolog OS=Homo sapiens GN=VAT1 PE=1 SV=2 | 1542 | 1837 | 1.0E-19 |
sp|A6QQF5|QORL2_BOVIN | Quinone oxidoreductase-like protein 2 OS=Bos taurus PE=2 SV=2 | 1536 | 1834 | 1.0E-19 |
sp|Q05356|KAS1_STRHA | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces halstedii GN=sch1 PE=3 SV=1 | 12 | 436 | 1.0E-19 |
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 | 109 | 434 | 2.0E-19 |
sp|Q53FA7|QORX_HUMAN | Quinone oxidoreductase PIG3 OS=Homo sapiens GN=TP53I3 PE=1 SV=2 | 1523 | 1833 | 3.0E-19 |
sp|Q02K94|FABB_PSEAB | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Pseudomonas aeruginosa (strain UCBPP-PA14) GN=fabB PE=1 SV=1 | 109 | 434 | 6.0E-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 | 1513 | 1748 | 7.0E-19 |
sp|P16538|KAS1_STRGA | Tetracenomycin C polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces glaucescens GN=tcmK PE=3 SV=1 | 12 | 435 | 8.0E-19 |
sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 1855 | 2194 | 1.0E-18 |
sp|B0BNC9|QORL2_RAT | Quinone oxidoreductase-like protein 2 OS=Rattus norvegicus PE=2 SV=1 | 1536 | 1748 | 4.0E-18 |
sp|P9WQD7|FAB2_MYCTU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kasB PE=1 SV=1 | 180 | 434 | 7.0E-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 | 180 | 434 | 7.0E-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 | 180 | 434 | 7.0E-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 | 12 | 432 | 9.0E-18 |
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 | 1852 | 2029 | 1.0E-17 |
sp|P9WQE5|PPSB_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsB PE=1 SV=1 | 1852 | 2029 | 1.0E-17 |
sp|P9WQE4|PPSB_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsB PE=3 SV=1 | 1852 | 2029 | 1.0E-17 |
sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 1871 | 2028 | 2.0E-17 |
sp|Q59I44|CAA43_BURSP | 2-haloacrylate reductase OS=Burkholderia sp. GN=caa43 PE=1 SV=1 | 1542 | 1738 | 2.0E-17 |
sp|Q02578|KAS1_STRCN | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cyaneus GN=curA PE=3 SV=1 | 12 | 435 | 2.0E-17 |
sp|A7Z4Y0|BAEE_BACMF | Polyketide biosynthesis protein BaeE OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeE PE=1 SV=1 | 536 | 756 | 3.0E-17 |
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 | 147 | 434 | 3.0E-17 |
sp|Q3UNZ8|QORL2_MOUSE | Quinone oxidoreductase-like protein 2 OS=Mus musculus PE=1 SV=1 | 1536 | 1834 | 4.0E-17 |
sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 1850 | 2077 | 8.0E-17 |
sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 1839 | 2019 | 2.0E-16 |
sp|O69473|FAB2_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium leprae (strain TN) GN=kasB PE=3 SV=2 | 180 | 427 | 2.0E-16 |
sp|Q8L3X9|KASM_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Arabidopsis thaliana GN=KAS PE=1 SV=1 | 159 | 432 | 2.0E-16 |
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 | 88 | 434 | 4.0E-16 |
sp|P0A953|FABB_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Escherichia coli (strain K12) GN=fabB PE=1 SV=1 | 109 | 434 | 7.0E-16 |
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 | 109 | 434 | 7.0E-16 |
sp|Q7A124|FABD_STAAW | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MW2) GN=fabD PE=3 SV=1 | 535 | 833 | 1.0E-15 |
sp|Q7A5Z3|FABD_STAAN | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain N315) GN=fabD PE=1 SV=1 | 535 | 833 | 1.0E-15 |
sp|Q99UN8|FABD_STAAM | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabD PE=1 SV=1 | 535 | 833 | 1.0E-15 |
sp|Q93QD4|FABD_STAAU | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus GN=fabD PE=3 SV=1 | 535 | 833 | 1.0E-15 |
sp|Q6G9Y3|FABD_STAAS | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MSSA476) GN=fabD PE=3 SV=1 | 535 | 833 | 1.0E-15 |
sp|Q5HGK3|FABD_STAAC | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain COL) GN=fabD PE=3 SV=1 | 535 | 833 | 1.0E-15 |
sp|Q6GHK5|FABD_STAAR | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MRSA252) GN=fabD PE=3 SV=1 | 535 | 833 | 1.0E-15 |
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 | 536 | 756 | 2.0E-15 |
sp|P43712|FABD_HAEIN | Malonyl CoA-acyl carrier protein transacylase OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=fabD PE=3 SV=1 | 535 | 841 | 2.0E-15 |
sp|P23902|KASC1_HORVU | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Hordeum vulgare GN=KAS12 PE=1 SV=1 | 26 | 432 | 2.0E-15 |
sp|O34825|PKSC_BACSU | Polyketide biosynthesis malonyl CoA-acyl carrier protein transacylase PksC OS=Bacillus subtilis (strain 168) GN=pksC PE=1 SV=1 | 536 | 749 | 2.0E-15 |
sp|P52410|KASC1_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Arabidopsis thaliana GN=KAS1 PE=2 SV=2 | 171 | 428 | 3.0E-15 |
sp|Q3MIE4|VAT1_RAT | Synaptic vesicle membrane protein VAT-1 homolog OS=Rattus norvegicus GN=Vat1 PE=1 SV=1 | 1542 | 1840 | 4.0E-15 |
sp|O34787|PKSE_BACSU | Polyketide biosynthesis protein PksE OS=Bacillus subtilis (strain 168) GN=pksE PE=1 SV=3 | 536 | 845 | 4.0E-15 |
sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 1842 | 2020 | 6.0E-15 |
sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 1859 | 2037 | 1.0E-14 |
sp|Q9CBS7|FAB1_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium leprae (strain TN) GN=kasA PE=3 SV=1 | 173 | 434 | 1.0E-14 |
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 | 97 | 385 | 3.0E-14 |
sp|Q62465|VAT1_MOUSE | Synaptic vesicle membrane protein VAT-1 homolog OS=Mus musculus GN=Vat1 PE=1 SV=3 | 1542 | 1840 | 4.0E-14 |
sp|P38230|QOR_YEAST | Probable quinone oxidoreductase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ZTA1 PE=1 SV=1 | 1517 | 1748 | 6.0E-14 |
sp|Q9C9P4|KASC2_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase II, chloroplastic OS=Arabidopsis thaliana GN=KAS2 PE=1 SV=1 | 96 | 432 | 1.0E-13 |
sp|A4YGN2|ACAR_METS5 | Acryloyl-coenzyme A reductase OS=Metallosphaera sedula (strain ATCC 51363 / DSM 5348) GN=Msed_1426 PE=1 SV=1 | 1542 | 1761 | 2.0E-13 |
sp|P42865|QOR_LEIAM | Probable quinone oxidoreductase OS=Leishmania amazonensis PE=3 SV=1 | 1543 | 1833 | 2.0E-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 | 180 | 434 | 5.0E-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 | 180 | 434 | 5.0E-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 | 180 | 434 | 5.0E-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 | 180 | 434 | 5.0E-13 |
sp|Q975C8|ACAR_SULTO | Acryloyl-coenzyme A reductase OS=Sulfolobus tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) GN=STK_04800 PE=1 SV=1 | 1541 | 1835 | 6.0E-13 |
sp|Q9R9J2|FENF_BACIU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis GN=fenF PE=1 SV=1 | 536 | 829 | 6.0E-13 |
sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 1857 | 2028 | 1.0E-12 |
sp|Q8H0M1|QORH_SPIOL | Quinone-oxidoreductase homolog, chloroplastic OS=Spinacia oleracea GN=QOR PE=1 SV=1 | 1520 | 1835 | 1.0E-12 |
sp|O74489|QOR_SCHPO | Probable quinone oxidoreductase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=zta1 PE=1 SV=2 | 1545 | 1748 | 2.0E-12 |
sp|O85140|FABD_SALTY | Malonyl CoA-acyl carrier protein transacylase OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=fabD PE=1 SV=3 | 535 | 830 | 6.0E-12 |
sp|P40804|PKSF_BACSU | Polyketide biosynthesis malonyl-ACP decarboxylase PksF OS=Bacillus subtilis (strain 168) GN=pksF PE=1 SV=3 | 159 | 433 | 1.0E-11 |
sp|P0AAI9|FABD_ECOLI | Malonyl CoA-acyl carrier protein transacylase OS=Escherichia coli (strain K12) GN=fabD PE=1 SV=2 | 535 | 830 | 2.0E-11 |
sp|P0AAJ0|FABD_ECOL6 | Malonyl CoA-acyl carrier protein transacylase OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=fabD PE=3 SV=2 | 535 | 830 | 2.0E-11 |
sp|Q8X8I7|FABD_ECO57 | Malonyl CoA-acyl carrier protein transacylase OS=Escherichia coli O157:H7 GN=fabD PE=3 SV=3 | 535 | 830 | 2.0E-11 |
sp|P43678|KAS1_STRRM | Oxytetracycline polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces rimosus PE=3 SV=2 | 12 | 435 | 2.0E-11 |
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 | 138 | 434 | 3.0E-11 |
sp|P0C842|CJ052_HUMAN | Putative uncharacterized protein encoded by LINC00614 OS=Homo sapiens GN=LINC00614 PE=5 SV=1 | 44 | 145 | 5.0E-11 |
sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 1859 | 2052 | 6.0E-11 |
sp|Q7T3C7|RT4I1_DANRE | Reticulon-4-interacting protein 1 homolog, mitochondrial OS=Danio rerio GN=rtn4ip1 PE=2 SV=2 | 1519 | 1834 | 1.0E-10 |
sp|P73242|FABD_SYNY3 | Malonyl CoA-acyl carrier protein transacylase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabD PE=1 SV=1 | 535 | 836 | 1.0E-10 |
sp|P51831|FABG_BACSU | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Bacillus subtilis (strain 168) GN=fabG PE=3 SV=3 | 1857 | 2007 | 3.0E-10 |
sp|Q84V25|ENOXE_FRAAN | 2-methylene-furan-3-one reductase OS=Fragaria ananassa GN=EO PE=1 SV=1 | 1526 | 1837 | 4.0E-10 |
sp|Q24K16|ZADH2_BOVIN | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Bos taurus GN=ZADH2 PE=2 SV=1 | 1540 | 1748 | 1.0E-09 |
sp|Q8BGC4|ZADH2_MOUSE | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Mus musculus GN=Zadh2 PE=1 SV=1 | 1532 | 1837 | 2.0E-09 |
sp|P16539|KAS2_STRGA | Tetracenomycin C polyketide putative beta-ketoacyl synthase 2 OS=Streptomyces glaucescens GN=tcmL PE=3 SV=2 | 10 | 434 | 2.0E-09 |
sp|P0A2C9|FABG_SALTY | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=fabG PE=1 SV=1 | 1859 | 2014 | 3.0E-09 |
sp|P0A2D0|FABG_SALTI | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Salmonella typhi GN=fabG PE=3 SV=1 | 1859 | 2014 | 3.0E-09 |
sp|Q39172|P1_ARATH | NADP-dependent alkenal double bond reductase P1 OS=Arabidopsis thaliana GN=P1 PE=1 SV=1 | 1633 | 1833 | 3.0E-09 |
sp|Q9BV79|MECR_HUMAN | Trans-2-enoyl-CoA reductase, mitochondrial OS=Homo sapiens GN=MECR PE=1 SV=2 | 1538 | 1690 | 3.0E-09 |
sp|P34055|INC11_HYPAT | Protein indc11 OS=Hypocrea atroviridis GN=indc11 PE=2 SV=1 | 1516 | 1755 | 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 | 86 | 435 | 7.0E-09 |
sp|Q39173|P2_ARATH | NADP-dependent alkenal double bond reductase P2 OS=Arabidopsis thaliana GN=P2 PE=2 SV=2 | 1633 | 1833 | 7.0E-09 |
sp|Q6P0H7|CBR4_DANRE | Carbonyl reductase family member 4 OS=Danio rerio GN=cbr4 PE=2 SV=1 | 1859 | 2075 | 8.0E-09 |
sp|Q7TS56|CBR4_RAT | Carbonyl reductase family member 4 OS=Rattus norvegicus GN=Cbr4 PE=2 SV=1 | 1860 | 2014 | 8.0E-09 |
sp|Q8N4Q0|ZADH2_HUMAN | Zinc-binding alcohol dehydrogenase domain-containing protein 2 OS=Homo sapiens GN=ZADH2 PE=1 SV=1 | 1532 | 1833 | 9.0E-09 |
sp|K4BW79|ENOX_SOLLC | 2-methylene-furan-3-one reductase OS=Solanum lycopersicum GN=EO PE=1 SV=1 | 1522 | 1687 | 9.0E-09 |
sp|Q02207|FOX2_YEAST | Peroxisomal hydratase-dehydrogenase-epimerase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FOX2 PE=2 SV=1 | 1859 | 2022 | 1.0E-08 |
sp|Q9Z311|MECR_RAT | Trans-2-enoyl-CoA reductase, mitochondrial OS=Rattus norvegicus GN=Mecr PE=1 SV=1 | 1542 | 1671 | 1.0E-08 |
sp|P73574|FABG1_SYNY3 | 3-oxoacyl-[acyl-carrier-protein] reductase 1 OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabG1 PE=1 SV=1 | 1859 | 2065 | 1.0E-08 |
sp|P96825|Y0148_MYCTU | Putative short-chain type dehydrogenase/reductase Rv0148 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0148 PE=1 SV=3 | 1859 | 2016 | 2.0E-08 |
sp|O94038|ADH2_CANAL | Alcohol dehydrogenase 2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=ADH2 PE=3 SV=1 | 1599 | 1833 | 2.0E-08 |
sp|P07246|ADH3_YEAST | Alcohol dehydrogenase 3, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ADH3 PE=1 SV=2 | 1528 | 1833 | 2.0E-08 |
sp|Q9X248|FABG_THEMA | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Thermotoga maritima (strain ATCC 43589 / MSB8 / DSM 3109 / JCM 10099) GN=fabG PE=3 SV=1 | 1859 | 2007 | 2.0E-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 | 625 | 831 | 4.0E-08 |
sp|Q9KQH7|FABG_VIBCH | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) GN=fabG PE=1 SV=2 | 1859 | 2016 | 4.0E-08 |
sp|Q941I0|ENOXC_FRAAN | 2-methylene-furan-3-one reductase OS=Fragaria ananassa GN=EO PE=1 SV=2 | 1526 | 1837 | 4.0E-08 |
sp|O67610|FABG_AQUAE | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Aquifex aeolicus (strain VF5) GN=fabG PE=1 SV=1 | 1859 | 2016 | 5.0E-08 |
sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 1872 | 2020 | 6.0E-08 |
sp|Q6WAU0|PULR_MENPI | (+)-pulegone reductase OS=Mentha piperita PE=1 SV=1 | 1633 | 1743 | 6.0E-08 |
sp|Q9DCS3|MECR_MOUSE | Trans-2-enoyl-CoA reductase, mitochondrial OS=Mus musculus GN=Mecr PE=1 SV=2 | 1542 | 1667 | 6.0E-08 |
sp|A4IFA7|CBR4_BOVIN | Carbonyl reductase family member 4 OS=Bos taurus GN=CBR4 PE=2 SV=1 | 1860 | 2014 | 8.0E-08 |
sp|O23939|ENOX_FRAVE | 2-methylene-furan-3-one reductase OS=Fragaria vesca GN=EO PE=2 SV=2 | 1526 | 1837 | 8.0E-08 |
sp|O94564|YGD6_SCHPO | Zinc-type alcohol dehydrogenase-like protein C1773.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1773.06c PE=3 SV=1 | 1536 | 1748 | 9.0E-08 |
sp|O35017|YOGA_BACSU | Uncharacterized zinc-type alcohol dehydrogenase-like protein YogA OS=Bacillus subtilis (strain 168) GN=yogA PE=3 SV=1 | 1524 | 1748 | 9.0E-08 |
sp|Q9SV68|QORH_ARATH | Putative quinone-oxidoreductase homolog, chloroplastic OS=Arabidopsis thaliana GN=At4g13010 PE=2 SV=1 | 1523 | 1835 | 1.0E-07 |
sp|Q9C0Y6|YKM8_SCHPO | Zinc-type alcohol dehydrogenase-like protein PB24D3.08c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAPB24D3.08c PE=3 SV=1 | 1633 | 1833 | 1.0E-07 |
sp|Q9SLN8|DBR_TOBAC | 2-alkenal reductase (NADP(+)-dependent) OS=Nicotiana tabacum GN=DBR PE=1 SV=1 | 1633 | 1833 | 1.0E-07 |
sp|Q7YS70|MECR_BOVIN | Trans-2-enoyl-CoA reductase, mitochondrial OS=Bos taurus GN=MECR PE=1 SV=1 | 1543 | 1667 | 2.0E-07 |
sp|P0AEK3|FABG_SHIFL | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Shigella flexneri GN=fabG PE=3 SV=1 | 1859 | 2014 | 2.0E-07 |
sp|P0AEK2|FABG_ECOLI | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Escherichia coli (strain K12) GN=fabG PE=1 SV=1 | 1859 | 2014 | 2.0E-07 |
sp|Q6GQN8|MECR_DANRE | Trans-2-enoyl-CoA reductase, mitochondrial OS=Danio rerio GN=mecr PE=2 SV=2 | 1543 | 1667 | 2.0E-07 |
sp|P49384|ADH3_KLULA | Alcohol dehydrogenase 3, mitochondrial OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=ADH3 PE=3 SV=2 | 1528 | 1833 | 2.0E-07 |
sp|P49385|ADH4_KLULA | Alcohol dehydrogenase 4, mitochondrial OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=ADH4 PE=3 SV=2 | 1528 | 1833 | 3.0E-07 |
sp|Q28GQ2|MECR_XENTR | Trans-2-enoyl-CoA reductase, mitochondrial OS=Xenopus tropicalis GN=mecr PE=2 SV=1 | 1540 | 1671 | 4.0E-07 |
sp|B0G103|PKS10_DICDI | Probable polyketide synthase 10 OS=Dictyostelium discoideum GN=pks10 PE=3 SV=1 | 1859 | 2190 | 7.0E-07 |
sp|P99173|ZDH1_STAAN | Zinc-type alcohol dehydrogenase-like protein SA1988 OS=Staphylococcus aureus (strain N315) GN=SA1988 PE=1 SV=1 | 1523 | 1677 | 7.0E-07 |
sp|P63475|ZDH1_STAAM | Zinc-type alcohol dehydrogenase-like protein SAV2186 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=SAV2186 PE=3 SV=1 | 1523 | 1677 | 7.0E-07 |
sp|Q91VT4|CBR4_MOUSE | Carbonyl reductase family member 4 OS=Mus musculus GN=Cbr4 PE=1 SV=2 | 1860 | 2014 | 8.0E-07 |
sp|Q93X67|FABG2_BRANA | 3-oxoacyl-[acyl-carrier-protein] reductase 2, chloroplastic OS=Brassica napus GN=bkr2 PE=2 SV=1 | 1859 | 2067 | 8.0E-07 |
sp|Q6GEP3|ZDH1_STAAR | Zinc-type alcohol dehydrogenase-like protein SAR2277 OS=Staphylococcus aureus (strain MRSA252) GN=SAR2277 PE=3 SV=1 | 1523 | 1677 | 8.0E-07 |
sp|Q9Y7D0|LOVC_ASPTE | Enoyl reductase LovC OS=Aspergillus terreus GN=lovC PE=1 SV=1 | 1534 | 1638 | 8.0E-07 |
sp|Q8NVD1|ZDH1_STAAW | Zinc-type alcohol dehydrogenase-like protein MW2112 OS=Staphylococcus aureus (strain MW2) GN=MW2112 PE=3 SV=1 | 1523 | 1677 | 1.0E-06 |
sp|Q6G7C8|ZDH1_STAAS | Zinc-type alcohol dehydrogenase-like protein SAS2087 OS=Staphylococcus aureus (strain MSSA476) GN=SAS2087 PE=3 SV=1 | 1523 | 1677 | 1.0E-06 |
sp|Q5HE19|ZDH1_STAAC | Zinc-type alcohol dehydrogenase-like protein SACOL2177 OS=Staphylococcus aureus (strain COL) GN=SACOL2177 PE=3 SV=1 | 1523 | 1677 | 1.0E-06 |
sp|Q3SZJ4|PTGR1_BOVIN | Prostaglandin reductase 1 OS=Bos taurus GN=PTGR1 PE=2 SV=1 | 1633 | 1756 | 1.0E-06 |
sp|Q14914|PTGR1_HUMAN | Prostaglandin reductase 1 OS=Homo sapiens GN=PTGR1 PE=1 SV=2 | 1633 | 1744 | 1.0E-06 |
sp|Q07288|ADH1_KLUMA | Alcohol dehydrogenase 1 OS=Kluyveromyces marxianus GN=ADH1 PE=3 SV=1 | 1528 | 1833 | 2.0E-06 |
sp|Q93X68|FABG5_BRANA | 3-oxoacyl-[acyl-carrier-protein] reductase 5, chloroplastic (Fragment) OS=Brassica napus GN=bkr1 PE=2 SV=1 | 1859 | 2067 | 2.0E-06 |
sp|P33207|FABG_ARATH | 3-oxoacyl-[acyl-carrier-protein] reductase, chloroplastic OS=Arabidopsis thaliana GN=At1g24360 PE=1 SV=2 | 1837 | 2067 | 2.0E-06 |
sp|P55336|FABG_VIBHA | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Vibrio harveyi GN=fabG PE=3 SV=1 | 1859 | 2065 | 2.0E-06 |
sp|P43713|FABG_HAEIN | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=fabG PE=3 SV=1 | 1859 | 2014 | 2.0E-06 |
sp|P66782|Y1385_MYCBO | Uncharacterized oxidoreductase Mb1385 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=fabG2 PE=3 SV=1 | 1849 | 2008 | 3.0E-06 |
sp|P9WGR9|Y1350_MYCTU | Uncharacterized oxidoreductase Rv1350 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=fabG2 PE=1 SV=1 | 1849 | 2008 | 3.0E-06 |
sp|P9WGR8|Y1350_MYCTO | Uncharacterized oxidoreductase MT1393 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=fabG2 PE=3 SV=1 | 1849 | 2008 | 3.0E-06 |
sp|P0A0I0|FABG_STAAW | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain MW2) GN=fabG PE=3 SV=1 | 1859 | 2006 | 3.0E-06 |
sp|Q6G9Y2|FABG_STAAS | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain MSSA476) GN=fabG PE=3 SV=1 | 1859 | 2006 | 3.0E-06 |
sp|Q6GHK4|FABG_STAAR | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain MRSA252) GN=fabG PE=3 SV=1 | 1859 | 2006 | 3.0E-06 |
sp|P99093|FABG_STAAN | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain N315) GN=fabG PE=1 SV=1 | 1859 | 2006 | 3.0E-06 |
sp|P0A0H9|FABG_STAAM | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabG PE=1 SV=1 | 1859 | 2006 | 3.0E-06 |
sp|Q5HGK2|FABG_STAAC | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Staphylococcus aureus (strain COL) GN=fabG PE=3 SV=2 | 1859 | 2006 | 3.0E-06 |
sp|P51660|DHB4_MOUSE | Peroxisomal multifunctional enzyme type 2 OS=Mus musculus GN=Hsd17b4 PE=1 SV=3 | 1859 | 2007 | 4.0E-06 |
sp|P97852|DHB4_RAT | Peroxisomal multifunctional enzyme type 2 OS=Rattus norvegicus GN=Hsd17b4 PE=1 SV=3 | 1859 | 2011 | 4.0E-06 |
sp|Q949M3|FABG3_BRANA | 3-oxoacyl-[acyl-carrier-protein] reductase 3, chloroplastic OS=Brassica napus GN=bkr3 PE=2 SV=1 | 1859 | 2067 | 4.0E-06 |
sp|Q29073|PTGR1_PIG | Prostaglandin reductase 1 OS=Sus scrofa GN=PTGR1 PE=1 SV=1 | 1633 | 1743 | 5.0E-06 |
sp|Q93X62|FABG1_BRANA | 3-oxoacyl-[acyl-carrier-protein] reductase 1, chloroplastic OS=Brassica napus GN=gbkr1 PE=1 SV=1 | 1859 | 2067 | 5.0E-06 |
sp|P97584|PTGR1_RAT | Prostaglandin reductase 1 OS=Rattus norvegicus GN=Ptgr1 PE=2 SV=3 | 1633 | 1744 | 6.0E-06 |
sp|Q9Z8P2|FABG_CHLPN | 3-oxoacyl-[acyl-carrier-protein] reductase FabG OS=Chlamydia pneumoniae GN=fabG PE=3 SV=1 | 1859 | 2016 | 6.0E-06 |
sp|P28643|FABG_CUPLA | 3-oxoacyl-[acyl-carrier-protein] reductase, chloroplastic OS=Cuphea lanceolata GN=CLKR27 PE=2 SV=1 | 1859 | 2067 | 6.0E-06 |
sp|Q9EQZ5|PTGR1_CAVPO | Prostaglandin reductase 1 OS=Cavia porcellus GN=Ptgr1 PE=1 SV=1 | 1633 | 1759 | 7.0E-06 |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 28 | 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 | >Ophun1|7483 MASDNGRKLAPVAVVGMSCRLPGGVSTLDDFWTMLSRARSGWREIPEDRFSSKAFFHPNPQKKGCFNARGGYFMD HDLSLFDAPFFNITKQEALAMDPKQRQLLECTYEALENAGISKESVAGSNMGVFVGGSVSDYAMSTFRDPDSIPM FDVTGNHQSILSGRISHAFDLRGPCFSVDTACSSGLYALHAAVQSIRSGDCDSAVVAGCHLHLQPDHWVSMSMSG LFAEHGKTYAFDHRAKSGFARGEGVGCLILKSLDRARADKDQIRSIIVNTGANQDGRTVGLSTPSVEAQEQLIRD VYTKAGVNVQEVGFVEAHGTGTKIGDPIEARAIYNALGEGRTKRQPLYMGSVKTNIGHLENASGIISVIKASLML EKGFILPNVNFEKANPSIPLDEWNIKVPTNLRSWPAQKRFISVNNFGFGGSNAHCILQRPDLVPSSLTQEKSDNH HKLFVLSGYTEDAAKQRSKHLGIYAEQHPEVFQKRLVNNLAYTLCQRRSHLPWRVAVTATCCSEIVEALNSIDAK PARASGKAPKIAFVFTGQGAQWHAMGRELMTSHPVFADTMREADACLSRLGADFSLLEELAKDKETSEVNKARLS QPACTAVQLALVRLLASWGIEPQAVVGHSSGEIGAAFATGAISLEDAMAAAFQRGQATLRMKAEHPDLKGGMLAV GASPAEVRKTIKALGLEGAAVACENSPGSTTVSGDVQDVEKLAAELESRKVFNRKLLVDVAYHSSHMELVAEEYT RSIKNIKATEGSSKTSFFSSLQGKALDSLTSLTAEYWRDNLVKPVLFSSALEALCREAEPTVLVEIGPHAALEGP IKQVLREMGDKVASSIKYCPTLVRNKDASAAALQTAGRLYVMGQPIRFEEVNQMNEADPPSVIEDMLPYPWTHEK YWHETRMSREHRIKEFARHDLLGRLSTSSSDFEHRWRNILTTDDVPWLRDHKMQSLVTFPFAGFIAMVAEAASQR AAMKRVSFDRFCLREVQITSPLIMNDGDEYEVTLSLSRYAEGTRSYSNAWDSFCVSSWTQQRGWVEHCRGLVSVR KNEAANPVGLTVRRDARRRFDRASGVCNEVVDKDKFYADLTGNGAEYGPLFRIDDDTLVGEGHSLTTIKVPDTSA CMPHNYEAPSILSAAVLDMFFHLTFAILGAGRGLMPNLYMPNAVKHMEFSKEFPATPGKTMRAICEGYPDTVNLI PADFFIDVWESPDSAQPLFSTQGFTMTPVNDRVNEQLEPPSICFKVEWEELGGKESPAAVENGQANGSNGHDSNG VNGHSNGHSNGHSNGTNGVNGSNGVHDLNGHADVEADSPPEFSAPVVIISDNKGESDPLAKALVDLIALKTGATP TICPLDTLDATDKICIAVCELNSPVISNISGKAFDKLQKVILTAHALLWVSAGTFKNAKHPDSALAQGLLRTVRS ETSKMAATLDLDPDSPLDNGSRSELIIQALRRVLASETELGPSDFEFAESEGKLVVPRVVEDEEMNQLVQHQTQP TGPYLQPFDQYGRRLQIAIGTYGALDSLYFCDQPARPLRDDEVEVKIAATGMNFKDVVIAMGQVPSPYLGVECSG TISNVGAKVTSLSVGDRVCAMSLGAYGTFARCRATSAAVIPHDMSFETAASIPVVYSTAYYGMVELARIQAGESI LIHAASGGVGQAAIQLAHMIGAEIYATVGGADKKQLLMDKYGIPEDRIFYSRTADFGPAIREATGGHGVDVVLNS LAGELLRESWESLAHFGRFIEIGKRDITSNTRLDMNKFEHNVTFSSVDLTLVASERPKIMSSVLNSVMELMGKKS IAPIGPITVLGISELETALRTLQSGKSTGKLIISPRPGEQVKVTHRPAATILNGHATYIIIGGTGGLGRSMAKRM VQRGAKHIVLLSRAGRMTAELAQLSDECRGLGATITVKACNVANEGSVRQVVEECTRSLPPIRGVIHAAMVLRDM LFEKMSFDDFHQVMESKVAGTWNFHRALSSHQLDFFIMLSSVAGIVGNRGQAAYAAANTFLDAFVQYRTQRGLPA TSIDLTAVEDVGYLAENAARSKEVLKTLEGNSFGEAEVLALLEAGIRGQISQLSNSQCITGLSFAGSSLPFYADD ARFVRLREAYQSTMQMNDAAAPGQSLPSQELIQAPSYDEAVNVVSQRISEKLCAILMLQPGDVDTKTSVKSYGLD SLNAIELRNWIGKEYLAHLQVLELLTSGAISDLAALTMKKSKIQHAHKEP* |
Coding | >Ophun1|7483 ATGGCGTCAGACAATGGCCGGAAGCTGGCCCCTGTCGCCGTGGTCGGCATGTCATGCCGTCTCCCCGGCGGCGTC TCGACTCTCGATGACTTTTGGACAATGCTCTCGCGTGCCCGCTCCGGCTGGCGGGAGATTCCAGAGGACCGTTTC AGCAGCAAGGCGTTTTTCCACCCGAATCCGCAGAAGAAGGGCTGCTTCAACGCCCGGGGCGGCTATTTCATGGAC CACGACCTGAGCTTGTTTGACGCTCCATTCTTCAACATTACCAAGCAAGAGGCCCTGGCCATGGATCCCAAGCAG CGGCAGCTCCTCGAGTGCACTTACGAGGCCCTCGAAAACGCCGGCATCTCCAAGGAGAGCGTAGCCGGCAGCAAC ATGGGCGTCTTCGTCGGCGGCTCCGTCTCTGATTACGCCATGAGCACCTTTCGCGACCCGGACTCGATTCCCATG TTTGACGTGACGGGCAACCATCAGTCGATTCTGTCCGGTCGTATCTCTCACGCCTTTGACCTCCGTGGGCCGTGC TTCTCCGTCGACACGGCCTGTTCATCCGGCCTGTACGCTCTGCACGCGGCGGTGCAGAGCATCCGTAGCGGGGAC TGTGACTCTGCCGTCGTTGCAGGCTGTCACCTGCATCTGCAGCCGGATCATTGGGTCTCCATGTCCATGTCTGGC CTCTTTGCCGAACATGGCAAGACGTATGCCTTTGATCACCGCGCCAAGTCCGGCTTCGCCCGTGGAGAGGGAGTC GGCTGCCTTATCCTCAAGTCACTGGATCGGGCTCGAGCGGACAAGGACCAGATCAGGTCCATCATCGTCAACACT GGCGCCAACCAGGATGGCAGGACCGTCGGACTGTCGACCCCAAGCGTCGAGGCGCAAGAGCAGCTGATCCGTGAC GTTTATACCAAAGCTGGCGTCAACGTCCAGGAAGTCGGTTTCGTCGAGGCTCACGGAACAGGCACCAAGATCGGC GATCCGATAGAGGCCAGGGCCATCTACAACGCCCTCGGCGAGGGCCGCACCAAGAGGCAGCCGCTGTACATGGGC TCGGTCAAAACCAACATTGGCCATCTGGAGAACGCCAGCGGTATCATCTCGGTCATCAAGGCGTCCCTCATGCTG GAAAAGGGCTTCATTCTGCCCAATGTCAATTTCGAAAAGGCCAACCCCAGCATTCCGCTCGATGAGTGGAACATC AAGGTTCCCACCAACCTGCGGTCATGGCCTGCTCAGAAGCGATTCATCAGCGTCAACAACTTTGGCTTCGGAGGA TCCAACGCTCACTGCATCCTCCAGCGTCCCGACCTCGTACCCTCCTCGCTCACCCAGGAAAAGTCGGACAACCAT CATAAACTCTTCGTCCTGTCCGGCTACACCGAGGATGCCGCCAAGCAGCGGTCCAAGCACCTCGGCATCTACGCC GAGCAGCATCCGGAGGTCTTCCAGAAGCGTCTCGTCAACAACCTGGCTTACACCTTGTGCCAGCGACGATCTCAC CTCCCCTGGCGCGTTGCCGTAACGGCCACCTGCTGCAGCGAAATCGTCGAGGCACTCAACAGCATCGATGCCAAG CCGGCTCGCGCCTCGGGCAAGGCGCCCAAGATTGCCTTCGTCTTCACCGGCCAGGGCGCTCAGTGGCACGCCATG GGTCGCGAGCTGATGACGTCACACCCGGTCTTCGCCGACACTATGCGCGAGGCCGACGCCTGTCTGTCGCGTCTG GGAGCCGACTTTTCTCTTCTCGAGGAGCTGGCCAAGGACAAGGAGACGTCCGAGGTCAACAAGGCCAGGCTGAGT CAGCCGGCCTGCACCGCCGTTCAACTTGCCCTCGTCCGCCTGCTGGCATCGTGGGGGATCGAGCCCCAGGCCGTC GTTGGCCATTCGAGCGGTGAGATCGGCGCAGCCTTCGCTACAGGCGCCATCAGCCTGGAAGATGCCATGGCAGCT GCCTTCCAGCGAGGCCAGGCCACGCTGCGGATGAAGGCCGAGCACCCGGATCTCAAGGGCGGCATGTTGGCTGTG GGCGCGAGTCCGGCCGAGGTGCGCAAGACGATCAAGGCTCTGGGCCTCGAGGGCGCTGCTGTCGCCTGCGAGAAC TCGCCTGGATCGACTACCGTCTCGGGAGACGTCCAGGATGTCGAGAAGCTGGCCGCCGAGCTGGAGAGCCGCAAG GTCTTCAACCGCAAGCTGCTCGTTGACGTCGCCTACCACTCGTCGCACATGGAGCTCGTGGCCGAAGAGTACACG CGTTCTATCAAGAATATCAAGGCGACCGAGGGCAGCTCCAAGACGTCCTTCTTCTCTTCCCTTCAGGGCAAGGCC TTGGACAGCCTCACGTCGTTGACGGCCGAGTACTGGCGCGACAATCTCGTCAAGCCCGTGCTGTTCTCGTCGGCG CTCGAGGCCCTCTGCCGCGAGGCCGAGCCGACGGTCCTGGTCGAGATCGGGCCTCATGCCGCTCTCGAGGGTCCC ATCAAGCAAGTGCTCCGCGAGATGGGTGACAAGGTGGCCAGCAGCATCAAGTATTGTCCTACTCTTGTTCGCAAC AAGGATGCCAGCGCAGCGGCTCTCCAGACCGCTGGGCGACTCTACGTCATGGGCCAGCCCATCCGCTTTGAAGAG GTCAATCAGATGAATGAGGCTGACCCGCCGAGCGTCATTGAAGACATGCTCCCATACCCCTGGACGCACGAAAAG TACTGGCACGAGACGCGCATGAGCCGCGAGCATCGGATCAAGGAGTTTGCTCGCCATGACCTTCTCGGACGCCTG AGCACCTCGTCCAGCGACTTTGAGCATCGCTGGCGCAACATCCTCACCACCGACGACGTGCCGTGGCTGAGGGAT CACAAGATGCAGTCGCTCGTTACCTTTCCCTTTGCCGGCTTCATCGCCATGGTCGCCGAGGCCGCCTCGCAGCGG GCGGCCATGAAGCGCGTCTCCTTCGATCGCTTCTGCTTGCGCGAGGTCCAGATTACTTCGCCGCTCATCATGAAC GACGGCGACGAGTATGAGGTGACGTTGAGCCTGAGCCGGTACGCCGAGGGCACGCGCTCCTACTCCAACGCTTGG GACTCGTTCTGCGTCTCATCGTGGACGCAGCAGAGGGGATGGGTCGAGCACTGCCGCGGTCTCGTTTCTGTTCGC AAGAACGAGGCTGCCAATCCGGTCGGCTTGACGGTCAGGAGAGACGCTCGCCGCCGGTTCGACAGGGCCTCTGGC GTGTGTAACGAAGTTGTCGACAAGGACAAGTTTTACGCTGACTTGACCGGCAACGGAGCCGAGTACGGGCCCCTG TTCCGGATCGACGACGATACCCTCGTTGGCGAGGGACACTCCCTCACCACCATCAAGGTTCCCGACACGTCCGCC TGCATGCCTCACAACTACGAGGCGCCCTCGATCCTATCGGCAGCCGTGCTTGACATGTTCTTCCACCTGACGTTT GCCATCCTCGGAGCTGGACGCGGCCTGATGCCGAATCTGTACATGCCAAATGCCGTCAAGCACATGGAGTTTAGC AAGGAGTTCCCTGCCACTCCAGGTAAGACGATGCGGGCCATCTGCGAGGGCTATCCCGACACGGTCAATCTGATT CCCGCCGACTTCTTCATCGACGTGTGGGAATCGCCGGACTCGGCTCAGCCGCTGTTCAGCACCCAGGGATTCACC ATGACGCCCGTCAACGATCGCGTCAATGAGCAGCTTGAGCCGCCTTCCATCTGCTTCAAGGTTGAGTGGGAGGAG CTTGGAGGCAAGGAGAGTCCCGCTGCAGTTGAAAATGGGCAAGCCAATGGCAGCAATGGACATGACAGCAACGGC GTCAATGGCCACTCAAACGGTCACAGCAACGGCCACAGCAACGGGACCAACGGAGTCAACGGCTCCAATGGAGTC CACGATTTGAACGGTCACGCCGACGTTGAAGCCGACAGCCCCCCCGAGTTCTCGGCCCCCGTCGTCATCATCTCC GACAACAAGGGCGAAAGTGACCCCTTGGCCAAAGCCCTCGTCGACCTCATCGCCCTCAAGACGGGAGCGACGCCA ACCATCTGCCCGCTCGACACTCTCGACGCCACCGACAAGATCTGCATCGCCGTCTGCGAGCTCAACAGCCCCGTC ATCTCCAACATCAGCGGCAAGGCTTTTGACAAGCTGCAAAAGGTCATTCTCACCGCCCACGCCCTGCTCTGGGTC AGCGCCGGCACTTTCAAGAATGCCAAGCACCCGGATAGCGCGTTGGCTCAGGGTCTGCTGCGGACGGTGCGCTCT GAGACGAGCAAGATGGCCGCCACGCTTGACCTTGACCCGGACTCTCCTCTCGACAACGGGTCCCGGTCCGAGCTC ATCATCCAGGCCTTGCGGCGCGTTCTGGCGTCCGAGACGGAGCTTGGGCCGAGTGACTTCGAGTTTGCCGAGAGT GAGGGCAAGCTCGTCGTCCCCCGTGTCGTCGAAGATGAAGAGATGAACCAGCTCGTCCAGCACCAGACGCAACCG ACTGGACCCTACCTTCAGCCCTTTGACCAGTACGGTCGCCGGCTACAGATCGCCATCGGCACCTACGGCGCGCTC GACTCGCTGTACTTTTGCGATCAGCCGGCCCGGCCGTTGCGAGATGACGAGGTCGAGGTCAAGATTGCTGCCACC GGCATGAACTTCAAGGACGTTGTCATCGCCATGGGTCAGGTTCCCAGCCCCTATCTCGGCGTCGAGTGCAGTGGT ACCATCTCCAACGTGGGCGCCAAGGTCACCTCGCTCTCGGTTGGCGATCGCGTCTGTGCAATGTCCCTGGGGGCG TACGGCACCTTTGCCCGCTGTCGGGCGACGAGCGCGGCTGTCATTCCTCACGACATGAGTTTCGAGACGGCGGCC TCGATCCCTGTCGTCTACTCGACCGCCTACTACGGCATGGTCGAGCTGGCCCGCATCCAGGCCGGGGAGAGTATC CTGATCCACGCTGCCTCGGGCGGTGTCGGTCAGGCTGCCATCCAGCTGGCCCACATGATCGGAGCCGAGATATAC GCCACGGTTGGCGGCGCCGACAAGAAGCAGCTGCTGATGGACAAGTACGGCATCCCTGAGGACCGCATCTTCTAC AGTCGTACCGCCGACTTCGGCCCGGCCATCCGCGAAGCCACTGGCGGCCACGGTGTCGACGTCGTCCTCAACTCG CTGGCCGGCGAGCTGCTGCGCGAGTCGTGGGAGAGTCTGGCGCACTTTGGACGCTTCATCGAGATTGGCAAGCGT GATATCACGTCCAACACGCGTCTCGACATGAACAAGTTTGAGCACAACGTCACCTTTAGCTCCGTCGATCTGACG CTCGTCGCCTCGGAGAGACCAAAGATCATGAGCAGCGTCCTCAACTCTGTCATGGAGCTGATGGGTAAGAAGAGC ATCGCGCCCATCGGTCCCATTACCGTCCTCGGCATCTCTGAGCTCGAGACGGCTCTGCGCACGCTCCAGAGCGGC AAGTCGACGGGGAAGCTCATCATCTCTCCGCGTCCGGGGGAGCAAGTCAAGGTCACCCATCGCCCAGCAGCCACC ATCCTCAACGGTCATGCCACCTACATCATCATCGGCGGTACGGGCGGCCTGGGGAGATCCATGGCTAAGCGTATG GTCCAGCGAGGCGCCAAGCACATTGTGCTCCTGTCCCGAGCCGGTCGCATGACGGCTGAGCTGGCGCAGCTGAGC GACGAGTGCCGCGGCCTCGGCGCTACCATCACCGTCAAGGCTTGCAACGTTGCCAACGAGGGGAGTGTCAGGCAG GTTGTCGAAGAGTGTACCCGGTCTCTGCCGCCCATCCGAGGTGTCATCCACGCGGCCATGGTCCTCCGGGACATG CTGTTCGAGAAGATGTCGTTCGATGACTTCCATCAGGTCATGGAATCCAAGGTGGCTGGCACCTGGAACTTCCAC CGCGCTCTGAGCAGCCACCAGCTCGACTTCTTTATCATGCTCTCGTCAGTCGCTGGTATCGTCGGAAACAGGGGT CAAGCCGCCTACGCAGCGGCCAACACTTTCCTCGACGCCTTCGTTCAGTACAGGACACAGAGGGGCCTGCCAGCC ACGTCGATCGACCTGACGGCCGTTGAGGACGTGGGTTATCTGGCCGAGAACGCTGCTCGATCCAAGGAGGTGCTC AAGACTCTCGAGGGCAACTCTTTCGGCGAGGCAGAGGTGCTGGCCCTGCTCGAGGCCGGCATTCGTGGTCAAATC TCGCAGTTGTCCAACAGCCAGTGCATCACGGGTCTCAGCTTCGCCGGTTCGTCACTGCCCTTCTACGCCGACGAC GCCCGCTTTGTCCGTCTCCGCGAGGCCTACCAGTCGACGATGCAGATGAACGACGCCGCGGCTCCCGGCCAGTCA CTGCCGTCGCAGGAGCTCATCCAGGCTCCCTCATACGACGAGGCCGTCAATGTGGTCAGCCAGAGGATAAGCGAG AAGCTCTGCGCCATCTTGATGCTGCAGCCGGGCGACGTGGATACCAAGACGTCGGTCAAGTCGTACGGCCTCGAC TCGCTCAACGCCATCGAGCTGCGCAACTGGATCGGCAAGGAGTATCTCGCTCATCTGCAGGTCCTCGAGCTGTTG ACCTCGGGCGCCATCTCGGATCTCGCGGCGCTGACGATGAAGAAGTCCAAGATTCAGCATGCGCACAAGGAGCCT TGA |
Transcript | >Ophun1|7483 ATGGCGTCAGACAATGGCCGGAAGCTGGCCCCTGTCGCCGTGGTCGGCATGTCATGCCGTCTCCCCGGCGGCGTC TCGACTCTCGATGACTTTTGGACAATGCTCTCGCGTGCCCGCTCCGGCTGGCGGGAGATTCCAGAGGACCGTTTC AGCAGCAAGGCGTTTTTCCACCCGAATCCGCAGAAGAAGGGCTGCTTCAACGCCCGGGGCGGCTATTTCATGGAC CACGACCTGAGCTTGTTTGACGCTCCATTCTTCAACATTACCAAGCAAGAGGCCCTGGCCATGGATCCCAAGCAG CGGCAGCTCCTCGAGTGCACTTACGAGGCCCTCGAAAACGCCGGCATCTCCAAGGAGAGCGTAGCCGGCAGCAAC ATGGGCGTCTTCGTCGGCGGCTCCGTCTCTGATTACGCCATGAGCACCTTTCGCGACCCGGACTCGATTCCCATG TTTGACGTGACGGGCAACCATCAGTCGATTCTGTCCGGTCGTATCTCTCACGCCTTTGACCTCCGTGGGCCGTGC TTCTCCGTCGACACGGCCTGTTCATCCGGCCTGTACGCTCTGCACGCGGCGGTGCAGAGCATCCGTAGCGGGGAC TGTGACTCTGCCGTCGTTGCAGGCTGTCACCTGCATCTGCAGCCGGATCATTGGGTCTCCATGTCCATGTCTGGC CTCTTTGCCGAACATGGCAAGACGTATGCCTTTGATCACCGCGCCAAGTCCGGCTTCGCCCGTGGAGAGGGAGTC GGCTGCCTTATCCTCAAGTCACTGGATCGGGCTCGAGCGGACAAGGACCAGATCAGGTCCATCATCGTCAACACT GGCGCCAACCAGGATGGCAGGACCGTCGGACTGTCGACCCCAAGCGTCGAGGCGCAAGAGCAGCTGATCCGTGAC GTTTATACCAAAGCTGGCGTCAACGTCCAGGAAGTCGGTTTCGTCGAGGCTCACGGAACAGGCACCAAGATCGGC GATCCGATAGAGGCCAGGGCCATCTACAACGCCCTCGGCGAGGGCCGCACCAAGAGGCAGCCGCTGTACATGGGC TCGGTCAAAACCAACATTGGCCATCTGGAGAACGCCAGCGGTATCATCTCGGTCATCAAGGCGTCCCTCATGCTG GAAAAGGGCTTCATTCTGCCCAATGTCAATTTCGAAAAGGCCAACCCCAGCATTCCGCTCGATGAGTGGAACATC AAGGTTCCCACCAACCTGCGGTCATGGCCTGCTCAGAAGCGATTCATCAGCGTCAACAACTTTGGCTTCGGAGGA TCCAACGCTCACTGCATCCTCCAGCGTCCCGACCTCGTACCCTCCTCGCTCACCCAGGAAAAGTCGGACAACCAT CATAAACTCTTCGTCCTGTCCGGCTACACCGAGGATGCCGCCAAGCAGCGGTCCAAGCACCTCGGCATCTACGCC GAGCAGCATCCGGAGGTCTTCCAGAAGCGTCTCGTCAACAACCTGGCTTACACCTTGTGCCAGCGACGATCTCAC CTCCCCTGGCGCGTTGCCGTAACGGCCACCTGCTGCAGCGAAATCGTCGAGGCACTCAACAGCATCGATGCCAAG CCGGCTCGCGCCTCGGGCAAGGCGCCCAAGATTGCCTTCGTCTTCACCGGCCAGGGCGCTCAGTGGCACGCCATG GGTCGCGAGCTGATGACGTCACACCCGGTCTTCGCCGACACTATGCGCGAGGCCGACGCCTGTCTGTCGCGTCTG GGAGCCGACTTTTCTCTTCTCGAGGAGCTGGCCAAGGACAAGGAGACGTCCGAGGTCAACAAGGCCAGGCTGAGT CAGCCGGCCTGCACCGCCGTTCAACTTGCCCTCGTCCGCCTGCTGGCATCGTGGGGGATCGAGCCCCAGGCCGTC GTTGGCCATTCGAGCGGTGAGATCGGCGCAGCCTTCGCTACAGGCGCCATCAGCCTGGAAGATGCCATGGCAGCT GCCTTCCAGCGAGGCCAGGCCACGCTGCGGATGAAGGCCGAGCACCCGGATCTCAAGGGCGGCATGTTGGCTGTG GGCGCGAGTCCGGCCGAGGTGCGCAAGACGATCAAGGCTCTGGGCCTCGAGGGCGCTGCTGTCGCCTGCGAGAAC TCGCCTGGATCGACTACCGTCTCGGGAGACGTCCAGGATGTCGAGAAGCTGGCCGCCGAGCTGGAGAGCCGCAAG GTCTTCAACCGCAAGCTGCTCGTTGACGTCGCCTACCACTCGTCGCACATGGAGCTCGTGGCCGAAGAGTACACG CGTTCTATCAAGAATATCAAGGCGACCGAGGGCAGCTCCAAGACGTCCTTCTTCTCTTCCCTTCAGGGCAAGGCC TTGGACAGCCTCACGTCGTTGACGGCCGAGTACTGGCGCGACAATCTCGTCAAGCCCGTGCTGTTCTCGTCGGCG CTCGAGGCCCTCTGCCGCGAGGCCGAGCCGACGGTCCTGGTCGAGATCGGGCCTCATGCCGCTCTCGAGGGTCCC ATCAAGCAAGTGCTCCGCGAGATGGGTGACAAGGTGGCCAGCAGCATCAAGTATTGTCCTACTCTTGTTCGCAAC AAGGATGCCAGCGCAGCGGCTCTCCAGACCGCTGGGCGACTCTACGTCATGGGCCAGCCCATCCGCTTTGAAGAG GTCAATCAGATGAATGAGGCTGACCCGCCGAGCGTCATTGAAGACATGCTCCCATACCCCTGGACGCACGAAAAG TACTGGCACGAGACGCGCATGAGCCGCGAGCATCGGATCAAGGAGTTTGCTCGCCATGACCTTCTCGGACGCCTG AGCACCTCGTCCAGCGACTTTGAGCATCGCTGGCGCAACATCCTCACCACCGACGACGTGCCGTGGCTGAGGGAT CACAAGATGCAGTCGCTCGTTACCTTTCCCTTTGCCGGCTTCATCGCCATGGTCGCCGAGGCCGCCTCGCAGCGG GCGGCCATGAAGCGCGTCTCCTTCGATCGCTTCTGCTTGCGCGAGGTCCAGATTACTTCGCCGCTCATCATGAAC GACGGCGACGAGTATGAGGTGACGTTGAGCCTGAGCCGGTACGCCGAGGGCACGCGCTCCTACTCCAACGCTTGG GACTCGTTCTGCGTCTCATCGTGGACGCAGCAGAGGGGATGGGTCGAGCACTGCCGCGGTCTCGTTTCTGTTCGC AAGAACGAGGCTGCCAATCCGGTCGGCTTGACGGTCAGGAGAGACGCTCGCCGCCGGTTCGACAGGGCCTCTGGC GTGTGTAACGAAGTTGTCGACAAGGACAAGTTTTACGCTGACTTGACCGGCAACGGAGCCGAGTACGGGCCCCTG TTCCGGATCGACGACGATACCCTCGTTGGCGAGGGACACTCCCTCACCACCATCAAGGTTCCCGACACGTCCGCC TGCATGCCTCACAACTACGAGGCGCCCTCGATCCTATCGGCAGCCGTGCTTGACATGTTCTTCCACCTGACGTTT GCCATCCTCGGAGCTGGACGCGGCCTGATGCCGAATCTGTACATGCCAAATGCCGTCAAGCACATGGAGTTTAGC AAGGAGTTCCCTGCCACTCCAGGTAAGACGATGCGGGCCATCTGCGAGGGCTATCCCGACACGGTCAATCTGATT CCCGCCGACTTCTTCATCGACGTGTGGGAATCGCCGGACTCGGCTCAGCCGCTGTTCAGCACCCAGGGATTCACC ATGACGCCCGTCAACGATCGCGTCAATGAGCAGCTTGAGCCGCCTTCCATCTGCTTCAAGGTTGAGTGGGAGGAG CTTGGAGGCAAGGAGAGTCCCGCTGCAGTTGAAAATGGGCAAGCCAATGGCAGCAATGGACATGACAGCAACGGC GTCAATGGCCACTCAAACGGTCACAGCAACGGCCACAGCAACGGGACCAACGGAGTCAACGGCTCCAATGGAGTC CACGATTTGAACGGTCACGCCGACGTTGAAGCCGACAGCCCCCCCGAGTTCTCGGCCCCCGTCGTCATCATCTCC GACAACAAGGGCGAAAGTGACCCCTTGGCCAAAGCCCTCGTCGACCTCATCGCCCTCAAGACGGGAGCGACGCCA ACCATCTGCCCGCTCGACACTCTCGACGCCACCGACAAGATCTGCATCGCCGTCTGCGAGCTCAACAGCCCCGTC ATCTCCAACATCAGCGGCAAGGCTTTTGACAAGCTGCAAAAGGTCATTCTCACCGCCCACGCCCTGCTCTGGGTC AGCGCCGGCACTTTCAAGAATGCCAAGCACCCGGATAGCGCGTTGGCTCAGGGTCTGCTGCGGACGGTGCGCTCT GAGACGAGCAAGATGGCCGCCACGCTTGACCTTGACCCGGACTCTCCTCTCGACAACGGGTCCCGGTCCGAGCTC ATCATCCAGGCCTTGCGGCGCGTTCTGGCGTCCGAGACGGAGCTTGGGCCGAGTGACTTCGAGTTTGCCGAGAGT GAGGGCAAGCTCGTCGTCCCCCGTGTCGTCGAAGATGAAGAGATGAACCAGCTCGTCCAGCACCAGACGCAACCG ACTGGACCCTACCTTCAGCCCTTTGACCAGTACGGTCGCCGGCTACAGATCGCCATCGGCACCTACGGCGCGCTC GACTCGCTGTACTTTTGCGATCAGCCGGCCCGGCCGTTGCGAGATGACGAGGTCGAGGTCAAGATTGCTGCCACC GGCATGAACTTCAAGGACGTTGTCATCGCCATGGGTCAGGTTCCCAGCCCCTATCTCGGCGTCGAGTGCAGTGGT ACCATCTCCAACGTGGGCGCCAAGGTCACCTCGCTCTCGGTTGGCGATCGCGTCTGTGCAATGTCCCTGGGGGCG TACGGCACCTTTGCCCGCTGTCGGGCGACGAGCGCGGCTGTCATTCCTCACGACATGAGTTTCGAGACGGCGGCC TCGATCCCTGTCGTCTACTCGACCGCCTACTACGGCATGGTCGAGCTGGCCCGCATCCAGGCCGGGGAGAGTATC CTGATCCACGCTGCCTCGGGCGGTGTCGGTCAGGCTGCCATCCAGCTGGCCCACATGATCGGAGCCGAGATATAC GCCACGGTTGGCGGCGCCGACAAGAAGCAGCTGCTGATGGACAAGTACGGCATCCCTGAGGACCGCATCTTCTAC AGTCGTACCGCCGACTTCGGCCCGGCCATCCGCGAAGCCACTGGCGGCCACGGTGTCGACGTCGTCCTCAACTCG CTGGCCGGCGAGCTGCTGCGCGAGTCGTGGGAGAGTCTGGCGCACTTTGGACGCTTCATCGAGATTGGCAAGCGT GATATCACGTCCAACACGCGTCTCGACATGAACAAGTTTGAGCACAACGTCACCTTTAGCTCCGTCGATCTGACG CTCGTCGCCTCGGAGAGACCAAAGATCATGAGCAGCGTCCTCAACTCTGTCATGGAGCTGATGGGTAAGAAGAGC ATCGCGCCCATCGGTCCCATTACCGTCCTCGGCATCTCTGAGCTCGAGACGGCTCTGCGCACGCTCCAGAGCGGC AAGTCGACGGGGAAGCTCATCATCTCTCCGCGTCCGGGGGAGCAAGTCAAGGTCACCCATCGCCCAGCAGCCACC ATCCTCAACGGTCATGCCACCTACATCATCATCGGCGGTACGGGCGGCCTGGGGAGATCCATGGCTAAGCGTATG GTCCAGCGAGGCGCCAAGCACATTGTGCTCCTGTCCCGAGCCGGTCGCATGACGGCTGAGCTGGCGCAGCTGAGC GACGAGTGCCGCGGCCTCGGCGCTACCATCACCGTCAAGGCTTGCAACGTTGCCAACGAGGGGAGTGTCAGGCAG GTTGTCGAAGAGTGTACCCGGTCTCTGCCGCCCATCCGAGGTGTCATCCACGCGGCCATGGTCCTCCGGGACATG CTGTTCGAGAAGATGTCGTTCGATGACTTCCATCAGGTCATGGAATCCAAGGTGGCTGGCACCTGGAACTTCCAC CGCGCTCTGAGCAGCCACCAGCTCGACTTCTTTATCATGCTCTCGTCAGTCGCTGGTATCGTCGGAAACAGGGGT CAAGCCGCCTACGCAGCGGCCAACACTTTCCTCGACGCCTTCGTTCAGTACAGGACACAGAGGGGCCTGCCAGCC ACGTCGATCGACCTGACGGCCGTTGAGGACGTGGGTTATCTGGCCGAGAACGCTGCTCGATCCAAGGAGGTGCTC AAGACTCTCGAGGGCAACTCTTTCGGCGAGGCAGAGGTGCTGGCCCTGCTCGAGGCCGGCATTCGTGGTCAAATC TCGCAGTTGTCCAACAGCCAGTGCATCACGGGTCTCAGCTTCGCCGGTTCGTCACTGCCCTTCTACGCCGACGAC GCCCGCTTTGTCCGTCTCCGCGAGGCCTACCAGTCGACGATGCAGATGAACGACGCCGCGGCTCCCGGCCAGTCA CTGCCGTCGCAGGAGCTCATCCAGGCTCCCTCATACGACGAGGCCGTCAATGTGGTCAGCCAGAGGATAAGCGAG AAGCTCTGCGCCATCTTGATGCTGCAGCCGGGCGACGTGGATACCAAGACGTCGGTCAAGTCGTACGGCCTCGAC TCGCTCAACGCCATCGAGCTGCGCAACTGGATCGGCAAGGAGTATCTCGCTCATCTGCAGGTCCTCGAGCTGTTG ACCTCGGGCGCCATCTCGGATCTCGCGGCGCTGACGATGAAGAAGTCCAAGATTCAGCATGCGCACAAGGAGCCT TGA |
Gene | >Ophun1|7483 ATGGCGTCAGACAATGGCCGGAAGCTGGCCCCTGTCGCCGTGGTCGGCATGTCATGCCGTCTCCCCGGCGGCGTC TCGACTCTCGATGACTTTTGGACAATGCTCTCGCGTGCCCGCTCCGGCTGGCGGGAGATTCCAGAGGACCGTTTC AGCAGCAAGGCGTTTTTCCACCCGAATCCGCAGAAGAAGGGCTGCTTCAACGCCCGGGGCGGCTATTTCATGGAC CACGACCTGAGCTTGTTTGACGCTCCATTCTTCAACATTACCAAGCAAGAGGCCCTGGCCATGGGTATGTCCCCT GCAAGAGGGTAGAAGAGGAAGAAGACTAACAAGGACGTACAGATCCCAAGCAGCGGCAGCTCCTCGAGTGCACTT ACGAGGCCCTCGAAAACGCCGGCATCTCCAAGGAGAGCGTAGCCGGCAGCAACATGGGCGTCTTCGTCGGCGGCT CCGTCTCTGATTACGCCATGAGCACCTTTCGCGACCCGGACTCGATTCCCATGTTTGACGTGACGGGCAACCATC AGTCGATTCTGTCCGGTCGTATCTCTCACGCCTTTGACCTCCGTGGGCCGTGCTTCTCCGTCGACACGGCCTGTT CATCCGGCCTGTACGCTCTGCACGCGGCGGTGCAGAGCATCCGTAGCGGGGACTGTGACTCTGCCGTCGTTGCAG GCTGTCACCTGCATCTGCAGCCGGATCATTGGGTCTCCATGTCCATGTCTGGGTAGGTGAATCTCTTTCCTCGGC TTCGTGGGCTTGACTGAACATCTGGACGCAGCCTCTTTGCCGAACATGGCAAGACGTATGCCTTTGATCACCGCG CCAAGTCCGGCTTCGCCCGTGGAGAGGGAGTCGGCTGCCTTATCCTCAAGTCACTGGATCGGGCTCGAGCGGACA AGGACCAGATCAGGTCCATCATCGTCAACACTGGCGCCAACCAGGATGGCAGGACCGTCGGTAAGGCCATCTTTC TCTTCTCTGTATGTTTCTGATACTGACCACATATTCAGGACTGTCGACCCCAAGCGTCGAGGCGCAAGAGCAGCT GATCCGTGACGTTTATACCAAAGCTGGCGTCAACGTCCAGGAAGTCGGTTTCGTCGAGGCTCACGGAACAGGCAC CAAGATCGGCGATCCGATAGAGGCCAGGGCCATCTACAACGCCCTCGGCGAGGGCCGCACCAAGAGGCAGCCGCT GTACATGGGCTCGGTCAAAACCAACATTGGCCATCTGGAGAACGCCAGCGGTATCATCTCGGTCATCAAGGCGTC CCTCATGCTGGAAAAGGGCTTCATTCTGCCCAATGTCAATTTCGAAAAGGCCAACCCCAGCATTCCGCTCGATGA GTGGAACATCAAGGTTCCCACCAACCTGCGGTCATGGCCTGCTCAGAAGCGATTCATCAGCGTCAACAACTTTGG CTTCGGAGGATCCAACGCTCACTGCATCCTCCAGCGTCCCGACCTCGTACCCTCCTCGCTCACCCAGGAAAAGTC GGACAACCATCATAAACTCTTCGTCCTGTCCGGCTACACCGAGGATGCCGCCAAGCAGCGGTCCAAGCACCTCGG CATCTACGCCGAGCAGCATCCGGAGGTCTTCCAGAAGCGTCTCGTCAACAACCTGGCTTACACCTTGTGCCAGCG ACGATCTCACCTCCCCTGGCGCGTTGCCGTAACGGCCACCTGCTGCAGCGAAATCGTCGAGGCACTCAACAGCAT CGATGCCAAGCCGGCTCGCGCCTCGGGCAAGGCGCCCAAGATTGCCTTCGTCTTCACCGGCCAGGGCGCTCAGTG GCACGCCATGGGTCGCGAGCTGATGACGTCACACCCGGTCTTCGCCGACACTATGCGCGAGGCCGACGCCTGTCT GTCGCGTCTGGGAGCCGACTTTTCTCTTCTCGAGGAGCTGGCCAAGGACAAGGAGACGTCCGAGGTCAACAAGGC CAGGCTGAGTCAGCCGGCCTGCACCGCCGTTCAACTTGCCCTCGTCCGCCTGCTGGCATCGTGGGGGATCGAGCC CCAGGCCGTCGTTGGCCATTCGAGCGGTGAGATCGGCGCAGCCTTCGCTACAGGCGCCATCAGCCTGGAAGATGC CATGGCAGCTGCCTTCCAGCGAGGCCAGGCCACGCTGCGGATGAAGGCCGAGCACCCGGATCTCAAGGGCGGCAT GTTGGCTGTGGGCGCGAGTCCGGCCGAGGTGCGCAAGACGATCAAGGCTCTGGGCCTCGAGGGCGCTGCTGTCGC CTGCGAGAACTCGCCTGGATCGACTACCGTCTCGGGAGACGTCCAGGATGTCGAGAAGCTGGCCGCCGAGCTGGA GAGCCGCAAGGTCTTCAACCGCAAGCTGCTCGTTGACGTCGCCTACCACTCGTCGCACATGGAGCTCGTGGCCGA AGAGTACACGCGTTCTATCAAGAATATCAAGGCGACCGAGGGCAGCTCCAAGACGTCCTTCTTCTCTTCCCTTCA GGGCAAGGCCTTGGACAGCCTCACGTCGTTGACGGCCGAGTACTGGCGCGACAATCTCGTCAAGCCCGTGCTGTT CTCGTCGGCGCTCGAGGCCCTCTGCCGCGAGGCCGAGCCGACGGTCCTGGTCGAGATCGGGCCTCATGCCGCTCT CGAGGGTCCCATCAAGCAAGTGCTCCGCGAGATGGGTGACAAGGTGGCCAGCAGCATCAAGTATTGTCCTACTCT TGTTCGCAACAAGGATGCCAGCGCAGCGGCTCTCCAGACCGCTGGGCGACTCTACGTCATGGGCCAGCCCATCCG CTTTGAAGAGGTCAATCAGATGAATGAGGCTGACCCGCCGAGCGTCATTGAAGACATGCTCCCATACCCCTGGAC GCACGAAAAGTACTGGCACGAGACGCGCATGAGCCGCGAGCATCGGATCAAGGAGTTTGCTCGCCATGACCTTCT CGGACGCCTGAGCACCTCGTCCAGCGACTTTGAGCATCGCTGGCGCAACATCCTCACCACCGACGACGTGCCGTG GCTGAGGGATCACAAGATGCAGTCGCTCGTTACCTTTCCCTTTGCCGGCTTCATCGCCATGGTCGCCGAGGCCGC CTCGCAGCGGGCGGCCATGAAGCGCGTCTCCTTCGATCGCTTCTGCTTGCGCGAGGTCCAGATTACTTCGCCGCT CATCATGAACGACGGCGACGAGTATGAGGTGACGTTGAGCCTGAGCCGGTACGCCGAGGGCACGCGCTCCTACTC CAACGCTTGGGACTCGTTCTGCGTCTCATCGTGGACGCAGCAGAGGGGATGGGTCGAGCACTGCCGCGGTCTCGT TTCTGTTCGCAAGAACGAGGCTGCCAATCCGGTCGGCTTGACGGTCAGGAGAGACGCTCGCCGCCGGTTCGACAG GGCCTCTGGCGTGTGTAACGAAGTTGTCGACAAGGACAAGTTTTACGCTGACTTGACCGGCAACGGAGCCGAGTA CGGGCCCCTGTTCCGGATCGACGACGATACCCTCGTTGGCGAGGGACACTCCCTCACCACCATCAAGGTTCCCGA CACGTCCGCCTGCATGCCTCACAACTACGAGGCGCCCTCGATCCTATCGGCAGCCGTGCTTGACATGTTCTTCCA CCTGACGTTTGCCATCCTCGGAGCTGGACGCGGCCTGATGCCGAATCTGTACATGCCAAATGCCGTCAAGCACAT GGAGTTTAGCAAGGAGTTCCCTGCCACTCCAGGTAAGACGATGCGGGCCATCTGCGAGGGCTATCCCGACACGGT CAATCTGATTCCCGCCGACTTCTTCATCGACGTGTGGGAATCGCCGGACTCGGCTCAGCCGCTGTTCAGCACCCA GGGATTCACCATGACGCCCGTCAACGATCGCGTCAATGAGCAGCTTGAGCCGCCTTCCATCTGCTTCAAGGTTGA GTGGGAGGAGCTTGGAGGCAAGGAGAGTCCCGCTGCAGTTGAAAATGGGCAAGCCAATGGCAGCAATGGACATGA CAGCAACGGCGTCAATGGCCACTCAAACGGTCACAGCAACGGCCACAGCAACGGGACCAACGGAGTCAACGGCTC CAATGGAGTCCACGATTTGAACGGTCACGCCGACGTTGAAGCCGACAGCCCCCCCGAGTTCTCGGCCCCCGTCGT CATCATCTCCGACAACAAGGGCGAAAGTGACCCCTTGGCCAAAGCCCTCGTCGACCTCATCGCCCTCAAGACGGG AGCGACGCCAACCATCTGCCCGCTCGACACTCTCGACGCCACCGACAAGATCTGCATCGCCGTCTGCGAGCTCAA CAGCCCCGTCATCTCCAACATCAGCGGCAAGGCTTTTGACAAGCTGCAAAAGGTCATTCTCACCGCCCACGCCCT GCTCTGGGTCAGCGCCGGCACTTTCAAGAATGCCAAGCACCCGGATAGCGCGTTGGCTCAGGGTCTGCTGCGGAC GGTGCGCTCTGAGACGAGCAAGATGGCCGCCACGCTTGACCTTGACCCGGACTCTCCTCTCGACAACGGGTCCCG GTCCGAGCTCATCATCCAGGCCTTGCGGCGCGTTCTGGCGTCCGAGACGGAGCTTGGGCCGAGTGACTTCGAGTT TGCCGAGAGTGAGGGCAAGCTCGTCGTCCCCCGTGTCGTCGAAGATGAAGAGATGAACCAGCTCGTCCAGCACCA GACGCAACCGACTGGACCCTACCTTCAGCCCTTTGACCAGTACGGTCGCCGGCTACAGATCGCCATCGGCACCTA CGGCGCGCTCGACTCGCTGTACTTTTGCGATCAGCCGGCCCGGCCGTTGCGAGATGACGAGGTCGAGGTCAAGAT TGCTGCCACCGGCATGAACTTCAAGGACGTTGTCATCGCCATGGGTCAGGTTCCCAGCCCCTATCTCGGCGTCGA GTGCAGTGGTACCATCTCCAACGTGGGCGCCAAGGTCACCTCGCTCTCGGTTGGCGATCGCGTCTGTGCAATGTC CCTGGGGGCGTACGGCACCTTTGCCCGCTGTCGGGCGACGAGCGCGGCTGTCATTCCTCACGACATGAGTTTCGA GACGGCGGCCTCGATCCCTGTCGTCTACTCGACCGCCTACTACGGCATGGTCGAGCTGGCCCGCATCCAGGCCGG GGAGAGTATCCTGATCCACGCTGCCTCGGGCGGTGTCGGTCAGGCTGCCATCCAGCTGGCCCACATGATCGGAGC CGAGATATACGCCACGGTTGGCGGCGCCGACAAGAAGCAGCTGCTGATGGACAAGTACGGCATCCCTGAGGACCG CATCTTCTACAGTCGTACCGCCGACTTCGGCCCGGCCATCCGCGAAGCCACTGGCGGCCACGGTGTCGACGTCGT CCTCAACTCGCTGGCCGGCGAGCTGCTGCGCGAGTCGTGGGAGAGTCTGGCGCACTTTGGACGCTTCATCGAGAT TGGCAAGCGTGATATCACGTCCAACACGCGTCTCGACATGAACAAGTTTGAGCACAACGTCACCTTTAGCTCCGT CGATCTGACGCTCGTCGCCTCGGAGAGACCAAAGATCATGAGCAGCGTCCTCAACTCTGTCATGGAGCTGATGGG TAAGAAGAGCATCGCGCCCATCGGTCCCATTACCGTCCTCGGCATCTCTGAGCTCGAGACGGCTCTGCGCACGCT CCAGAGCGGCAAGTCGACGGGGAAGCTCATCATCTCTCCGCGTCCGGGGGAGCAAGTCAAGGTACTTTACTGTTC TTCTCTCTGATGTGTCTCGTGGATGCTAACGCGAGGTTATCATAGGTCACCCATCGCCCAGCAGCCACCATCCTC AACGGTCATGCCACCTACATCATCATCGGCGGTACGGGCGGCCTGGGGAGATCCATGGCTAAGCGTATGGTCCAG CGAGGCGCCAAGCACATTGTGCTCCTGTCCCGAGCCGGTCGCATGACGGCTGAGCTGGCGCAGCTGAGCGACGAG TGCCGCGGCCTCGGCGCTACCATCACCGTCAAGGCTTGCAACGTTGCCAACGAGGGGAGTGTCAGGCAGGTTGTC GAAGAGTGTACCCGGTCTCTGCCGCCCATCCGAGGTGTCATCCACGCGGCCATGGTCCTCCGGGTATGATTGTCT ACAGACGTATCTTGATCTCGCGAAACTAACGCTTCGCAGGACATGCTGTTCGAGAAGATGTCGTTCGATGACTTC CATCAGGTCATGGAATCCAAGGTGGCTGGCACCTGGAACTTCCACCGCGCTCTGAGCAGCCACCAGCTCGACTTC TTTATCATGCTCTCGTCAGTCGCTGGTATCGTCGGAAACAGGGGTCAAGCCGCCTACGCAGCGGCCAACACTTTC CTCGACGCCTTCGTTCAGTACAGGACACAGAGGGGCCTGCCAGCCACGTCGATCGACCTGACGGCCGTTGAGGAC GTGGGTTATCTGGCCGAGAACGCTGCTCGATCCAAGGAGGTGCTCAAGACTCTCGAGGGCAACTCTTTCGGCGAG GCAGAGGTGCTGGCCCTGCTCGAGGCCGGCATTCGTGGTCAAATCTCGCAGTTGTCCAACAGCCAGTGCATCACG GGTCTCAGCTTCGCCGGTTCGTCACTGCCCTTCTACGCCGACGACGCCCGCTTTGTCCGTCTCCGCGAGGCCTAC CAGTCGACGATGCAGATGAACGACGCCGCGGCTCCCGGCCAGTCACTGCCGTCGCAGGAGCTCATCCAGGCTCCC TCATACGACGAGGCCGTCAATGTGGTCAGCCAGAGGATAAGCGAGAAGCTCTGCGCCATCTTGATGCTGCAGCCG GGCGACGTGGATACCAAGACGTCGGTCAAGTCGTACGGCCTCGACTCGCTCAACGCCATCGAGCTGCGCAACTGG ATCGGCAAGGAGTATCTCGCTCATCTGCAGGTCCTCGAGCTGTTGACCTCGGGCGCCATCTCGGATCTCGCGGCG CTGACGATGAAGAAGTCCAAGATTCAGCATGCGCACAAGGAGCCTTGA |