© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|7364 |
| Gene name | |
| Location | Contig_424:4270..9060 |
| Strand | + |
| Gene length (bp) | 4790 |
| Transcript length (bp) | 4521 |
| Coding sequence length (bp) | 4521 |
| Protein length (aa) | 1507 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00109 | ketoacyl-synt | Beta-ketoacyl synthase, N-terminal domain | 7.1E-64 | 18 | 265 |
| PF00698 | Acyl_transf_1 | Acyl transferase domain | 3.0E-43 | 581 | 895 |
| PF14765 | PS-DH | Polyketide synthase dehydratase | 3.7E-37 | 968 | 1265 |
| PF02801 | Ketoacyl-synt_C | Beta-ketoacyl synthase, C-terminal domain | 4.7E-16 | 275 | 375 |
| PF02801 | Ketoacyl-synt_C | Beta-ketoacyl synthase, C-terminal domain | 2.8E-05 | 384 | 414 |
| PF16197 | KAsynt_C_assoc | Ketoacyl-synthetase C-terminal extension | 2.5E-12 | 429 | 530 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| 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 | 18 | 1494 | 0.0E+00 |
| sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 17 | 1494 | 0.0E+00 |
| sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 17 | 1494 | 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 | 17 | 1495 | 0.0E+00 |
| sp|Q9Y7D5|LOVF_ASPTE | Lovastatin diketide synthase LovF OS=Aspergillus terreus GN=lovF PE=1 SV=1 | 20 | 1494 | 2.0E-176 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| 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 | 18 | 1494 | 0.0E+00 |
| sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 17 | 1494 | 0.0E+00 |
| sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 17 | 1494 | 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 | 17 | 1495 | 0.0E+00 |
| sp|Q9Y7D5|LOVF_ASPTE | Lovastatin diketide synthase LovF OS=Aspergillus terreus GN=lovF PE=1 SV=1 | 20 | 1494 | 2.0E-176 |
| sp|Q869W9|PKS16_DICDI | Probable polyketide synthase 16 OS=Dictyostelium discoideum GN=pks16 PE=2 SV=1 | 13 | 1018 | 1.0E-111 |
| sp|Q869X2|PKS17_DICDI | Probable polyketide synthase 17 OS=Dictyostelium discoideum GN=pks17 PE=3 SV=1 | 13 | 1018 | 4.0E-109 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 18 | 1193 | 5.0E-109 |
| sp|Q55E72|PKS1_DICDI | Probable polyketide synthase 1 OS=Dictyostelium discoideum GN=stlA PE=1 SV=1 | 10 | 1019 | 1.0E-105 |
| 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 | 1024 | 4.0E-103 |
| 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 | 1024 | 7.0E-103 |
| 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 | 1024 | 1.0E-102 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 5 | 923 | 4.0E-100 |
| sp|P9WQE9|PHAS_MYCTU | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks2 PE=1 SV=1 | 20 | 1060 | 1.0E-99 |
| sp|P9WQE8|PHAS_MYCTO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=pks2 PE=3 SV=1 | 20 | 1060 | 1.0E-99 |
| sp|A5U9F4|PHAS_MYCTA | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=pks2 PE=3 SV=1 | 20 | 1060 | 1.0E-99 |
| sp|Q7TVK8|PHAS_MYCBO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks2 PE=3 SV=1 | 20 | 1060 | 1.0E-99 |
| sp|A1KQG0|PHAS_MYCBP | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=pks2 PE=3 SV=1 | 20 | 1060 | 2.0E-99 |
| 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 | 18 | 885 | 7.0E-99 |
| sp|P9WQE5|PPSB_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsB PE=1 SV=1 | 18 | 885 | 7.0E-99 |
| sp|P9WQE4|PPSB_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsB PE=3 SV=1 | 18 | 885 | 7.0E-99 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 20 | 868 | 1.0E-98 |
| sp|Q559A9|PKS13_DICDI | Probable polyketide synthase 13 OS=Dictyostelium discoideum GN=pks13 PE=3 SV=1 | 14 | 1046 | 5.0E-97 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 18 | 882 | 6.0E-97 |
| sp|Q54IX3|PKS26_DICDI | Probable polyketide synthase 26 OS=Dictyostelium discoideum GN=pks26 PE=3 SV=1 | 17 | 1183 | 4.0E-96 |
| sp|B0G103|PKS10_DICDI | Probable polyketide synthase 10 OS=Dictyostelium discoideum GN=pks10 PE=3 SV=1 | 17 | 1205 | 9.0E-95 |
| sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 1 | 1178 | 1.0E-93 |
| sp|Q55CN6|PKS3_DICDI | Probable polyketide synthase 3 OS=Dictyostelium discoideum GN=pks3 PE=3 SV=1 | 27 | 1142 | 4.0E-93 |
| sp|P96202|PPSC_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsC PE=1 SV=2 | 12 | 1009 | 6.0E-93 |
| 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 | 12 | 1009 | 6.0E-93 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 18 | 923 | 2.0E-92 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 15 | 917 | 3.0E-92 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 18 | 894 | 3.0E-92 |
| sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 18 | 1021 | 1.0E-91 |
| sp|P9WQE2|PPSD_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsD PE=3 SV=1 | 18 | 1021 | 1.0E-91 |
| 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 | 18 | 1021 | 1.0E-91 |
| sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 20 | 1046 | 4.0E-91 |
| sp|B0G100|PKS7_DICDI | Probable polyketide synthase 7 OS=Dictyostelium discoideum GN=pks7 PE=3 SV=1 | 17 | 1176 | 9.0E-91 |
| sp|P22367|MSAS_PENPA | 6-methylsalicylic acid synthase OS=Penicillium patulum PE=1 SV=1 | 18 | 1019 | 2.0E-90 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 20 | 1046 | 3.0E-90 |
| sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 17 | 1019 | 3.0E-89 |
| 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 | 18 | 1020 | 3.0E-89 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 17 | 880 | 5.0E-89 |
| sp|B4XYB8|AZIB_STREG | 5-methyl-1-naphthoate synthase OS=Streptomyces sahachiroi GN=aziB PE=1 SV=1 | 13 | 1023 | 5.0E-89 |
| sp|Q02251|MCAS_MYCBO | Mycocerosic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mas PE=1 SV=2 | 20 | 1059 | 1.0E-88 |
| sp|B0G101|PKS8_DICDI | Probable polyketide synthase 8/35 OS=Dictyostelium discoideum GN=pks8 PE=3 SV=1 | 85 | 1191 | 5.0E-88 |
| sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 16 | 1084 | 9.0E-88 |
| sp|B0G0Z9|PKS6_DICDI | Probable polyketide synthase 6 OS=Dictyostelium discoideum GN=pks6 PE=3 SV=1 | 17 | 1191 | 2.0E-87 |
| 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 | 18 | 1193 | 1.0E-86 |
| sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 16 | 1019 | 2.0E-86 |
| sp|B0G138|PKS21_DICDI | Probable polyketide synthase 21 OS=Dictyostelium discoideum GN=pks21 PE=3 SV=1 | 17 | 1019 | 6.0E-86 |
| sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 20 | 1050 | 2.0E-85 |
| sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 13 | 1019 | 2.0E-85 |
| sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 17 | 1046 | 2.0E-85 |
| sp|P19096|FAS_MOUSE | Fatty acid synthase OS=Mus musculus GN=Fasn PE=1 SV=2 | 86 | 1142 | 3.0E-84 |
| sp|P12276|FAS_CHICK | Fatty acid synthase OS=Gallus gallus GN=FASN PE=1 SV=5 | 85 | 1015 | 1.0E-83 |
| sp|P49327|FAS_HUMAN | Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 | 86 | 1014 | 1.0E-82 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 17 | 1084 | 2.0E-82 |
| sp|Q86JI5|PKS5_DICDI | Probable polyketide synthase 5 OS=Dictyostelium discoideum GN=pks5 PE=2 SV=1 | 20 | 1019 | 3.0E-82 |
| sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 19 | 1144 | 1.0E-81 |
| sp|Q54KU5|PKS24_DICDI | Probable polyketide synthase 24 OS=Dictyostelium discoideum GN=pks24 PE=3 SV=1 | 17 | 1019 | 3.0E-81 |
| sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 13 | 1019 | 4.0E-81 |
| sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 16 | 1045 | 7.0E-81 |
| sp|Q54B49|PKS45_DICDI | Probable polyketide synthase 45 OS=Dictyostelium discoideum GN=pks45 PE=3 SV=2 | 14 | 1176 | 1.0E-79 |
| sp|Q54B51|PKS44_DICDI | Probable polyketide synthase 44 OS=Dictyostelium discoideum GN=pks44 PE=3 SV=1 | 14 | 1176 | 3.0E-79 |
| sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 16 | 1186 | 1.0E-78 |
| sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 20 | 1186 | 2.0E-78 |
| sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 16 | 1185 | 3.0E-78 |
| sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 19 | 871 | 1.0E-76 |
| sp|Q12053|PKSL1_ASPPA | Noranthrone synthase OS=Aspergillus parasiticus GN=pksL1 PE=1 SV=1 | 8 | 945 | 1.0E-76 |
| sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 21 | 1185 | 3.0E-76 |
| sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 19 | 1075 | 4.0E-76 |
| sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 19 | 871 | 6.0E-75 |
| sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 19 | 1186 | 7.0E-75 |
| 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 | 17 | 957 | 2.0E-74 |
| sp|P9WQE1|PPSE_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsE PE=1 SV=1 | 17 | 957 | 2.0E-74 |
| sp|P9WQE0|PPSE_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsE PE=3 SV=1 | 17 | 957 | 2.0E-74 |
| 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 | 18 | 465 | 1.0E-73 |
| sp|Q55DM7|PKS2_DICDI | Probable polyketide synthase 2 OS=Dictyostelium discoideum GN=pks2 PE=3 SV=1 | 19 | 1020 | 5.0E-73 |
| 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 | 20 | 867 | 3.0E-69 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 16 | 548 | 1.0E-66 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 14 | 553 | 2.0E-66 |
| 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 | 12 | 945 | 2.0E-65 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 18 | 552 | 3.0E-65 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 13 | 547 | 9.0E-65 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 19 | 557 | 1.0E-64 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 18 | 547 | 2.0E-64 |
| sp|Q9R9J1|MYCA_BACIU | Mycosubtilin synthase subunit A OS=Bacillus subtilis GN=mycA PE=3 SV=1 | 9 | 578 | 3.0E-64 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 7 | 552 | 1.0E-63 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 18 | 548 | 7.0E-62 |
| sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 86 | 469 | 3.0E-61 |
| sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 86 | 469 | 6.0E-61 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 19 | 556 | 1.0E-60 |
| sp|P36189|FAS_ANSAN | Fatty acid synthase (Fragment) OS=Anser anser anser GN=FASN PE=1 SV=1 | 86 | 408 | 4.0E-56 |
| sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 17 | 458 | 1.0E-54 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 20 | 553 | 6.0E-53 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 17 | 548 | 4.0E-46 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 18 | 594 | 1.0E-44 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 18 | 493 | 9.0E-43 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 17 | 547 | 1.0E-42 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 18 | 477 | 7.0E-42 |
| sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 581 | 1212 | 3.0E-27 |
| 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 | 77 | 465 | 3.0E-22 |
| sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 567 | 1046 | 2.0E-19 |
| sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 563 | 1046 | 2.0E-18 |
| sp|P0AAI8|FABF_SHIFL | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Shigella flexneri GN=fabF PE=3 SV=2 | 154 | 466 | 8.0E-18 |
| sp|P0AAI5|FABF_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli (strain K12) GN=fabF PE=1 SV=2 | 154 | 466 | 8.0E-18 |
| 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 | 154 | 466 | 8.0E-18 |
| sp|P0AAI7|FABF_ECO57 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli O157:H7 GN=fabF PE=3 SV=2 | 154 | 466 | 8.0E-18 |
| 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 | 94 | 466 | 1.0E-17 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 524 | 911 | 3.0E-14 |
| sp|P55338|FABF_VIBHA | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Vibrio harveyi GN=fabF PE=3 SV=2 | 85 | 466 | 4.0E-14 |
| 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 | 112 | 469 | 1.0E-13 |
| sp|O34877|PKSD_BACSU | Polyketide biosynthesis acyltransferase homolog PksD OS=Bacillus subtilis (strain 168) GN=pksD PE=1 SV=2 | 578 | 872 | 2.0E-13 |
| 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 | 166 | 461 | 2.0E-13 |
| sp|P06230|NODE_RHIME | Nodulation protein E OS=Rhizobium meliloti (strain 1021) GN=nodE PE=3 SV=1 | 101 | 461 | 2.0E-13 |
| sp|P9WQD7|FAB2_MYCTU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kasB PE=1 SV=1 | 136 | 460 | 9.0E-13 |
| sp|P9WQD6|FAB2_MYCTO | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=kasB PE=3 SV=1 | 136 | 460 | 9.0E-13 |
| 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 | 136 | 460 | 9.0E-13 |
| sp|P06231|NOE4_RHIML | Nodulation protein E OS=Rhizobium meliloti GN=nodE PE=3 SV=1 | 170 | 461 | 1.0E-12 |
| sp|P52410|KASC1_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Arabidopsis thaliana GN=KAS1 PE=2 SV=2 | 102 | 470 | 2.0E-12 |
| sp|P72331|NODE_RHIS3 | Nodulation protein E OS=Rhizobium sp. (strain N33) GN=nodE PE=3 SV=1 | 151 | 346 | 4.0E-12 |
| sp|O69473|FAB2_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium leprae (strain TN) GN=kasB PE=3 SV=2 | 186 | 460 | 7.0E-12 |
| 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 | 485 | 1020 | 8.0E-12 |
| sp|P39525|CEM1_YEAST | 3-oxoacyl-[acyl-carrier-protein] synthase homolog OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CEM1 PE=1 SV=1 | 106 | 466 | 1.0E-11 |
| sp|P04684|NODE_RHILT | Nodulation protein E OS=Rhizobium leguminosarum bv. trifolii GN=nodE PE=3 SV=2 | 151 | 461 | 3.0E-11 |
| sp|Q9C9P4|KASC2_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase II, chloroplastic OS=Arabidopsis thaliana GN=KAS2 PE=1 SV=1 | 166 | 465 | 3.0E-10 |
| sp|P71019|FABD_BACSU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis (strain 168) GN=fabD PE=3 SV=2 | 581 | 870 | 4.0E-10 |
| sp|Q8L3X9|KASM_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Arabidopsis thaliana GN=KAS PE=1 SV=1 | 166 | 467 | 4.0E-10 |
| sp|P56902|FABF_RHIME | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Rhizobium meliloti (strain 1021) GN=fabF PE=3 SV=2 | 154 | 469 | 4.0E-10 |
| 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 | 153 | 468 | 8.0E-10 |
| sp|Q5TKS0|FABF_STAAU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 (Fragment) OS=Staphylococcus aureus GN=fabF PE=3 SV=1 | 94 | 461 | 9.0E-10 |
| sp|Q6GIA3|FABF_STAAR | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MRSA252) GN=fabF PE=3 SV=1 | 94 | 461 | 2.0E-09 |
| sp|Q8NXE1|FABF_STAAW | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MW2) GN=fabF PE=1 SV=1 | 94 | 461 | 2.0E-09 |
| sp|Q6GAU2|FABF_STAAS | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MSSA476) GN=fabF PE=3 SV=1 | 94 | 461 | 2.0E-09 |
| sp|Q5HHA1|FABF_STAAC | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain COL) GN=fabF PE=1 SV=1 | 94 | 461 | 2.0E-09 |
| sp|Q9D404|OXSM_MOUSE | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Mus musculus GN=Oxsm PE=1 SV=1 | 166 | 461 | 2.0E-09 |
| sp|Q7A6F8|FABF_STAAN | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain N315) GN=fabF PE=1 SV=1 | 94 | 461 | 2.0E-09 |
| sp|Q99VA6|FABF_STAAM | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabF PE=3 SV=1 | 94 | 461 | 2.0E-09 |
| sp|Q9CBS7|FAB1_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium leprae (strain TN) GN=kasA PE=3 SV=1 | 186 | 460 | 3.0E-09 |
| sp|P04683|NODE_RHILV | Nodulation protein E OS=Rhizobium leguminosarum bv. viciae GN=nodE PE=3 SV=2 | 151 | 461 | 8.0E-09 |
| sp|P23902|KASC1_HORVU | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Hordeum vulgare GN=KAS12 PE=1 SV=1 | 77 | 470 | 1.0E-08 |
| sp|P0C842|CJ052_HUMAN | Putative uncharacterized protein encoded by LINC00614 OS=Homo sapiens GN=LINC00614 PE=5 SV=1 | 56 | 149 | 1.0E-08 |
| sp|A7Z4X9|BAED_BACMF | Polyketide biosynthesis acyltransferase homolog BaeD OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeD PE=1 SV=1 | 578 | 878 | 2.0E-08 |
| sp|P0A953|FABB_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Escherichia coli (strain K12) GN=fabB PE=1 SV=1 | 93 | 465 | 2.0E-08 |
| 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 | 93 | 465 | 2.0E-08 |
| 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 | 149 | 468 | 4.0E-08 |
| sp|P16538|KAS1_STRGA | Tetracenomycin C polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces glaucescens GN=tcmK PE=3 SV=1 | 14 | 413 | 8.0E-08 |
| sp|Q02K94|FABB_PSEAB | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Pseudomonas aeruginosa (strain UCBPP-PA14) GN=fabB PE=1 SV=1 | 115 | 466 | 2.0E-07 |
| sp|Q9NWU1|OXSM_HUMAN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Homo sapiens GN=OXSM PE=1 SV=1 | 166 | 461 | 7.0E-07 |
| sp|Q02578|KAS1_STRCN | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cyaneus GN=curA PE=3 SV=1 | 63 | 413 | 1.0E-06 |
| sp|P73242|FABD_SYNY3 | Malonyl CoA-acyl carrier protein transacylase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabD PE=1 SV=1 | 581 | 801 | 2.0E-06 |
| sp|P41175|KAS1_STRCM | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cinnamonensis PE=3 SV=1 | 171 | 467 | 2.0E-06 |
| sp|Q0VCA7|OXSM_BOVIN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Bos taurus GN=OXSM PE=2 SV=1 | 166 | 461 | 3.0E-06 |
| sp|P73283|FABF_SYNY3 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabF PE=1 SV=1 | 85 | 460 | 3.0E-06 |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 51 | 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 | >Hirsu2|7364 MTAAAAAAAAAARRPGEEDIAIVGSAYRFPGDATSPSRLWALLRAPSVVASRVPALEGYHHADGLYHGHTNVREA YLLAGEAPQRRFDAGFFGVSPAEAAAMDPQLRLLLETVYEAVEAGGLPLDRLRGSDTAVYAGQMLGEYEQLMGRD LDGLSRYHASGTARAMTSNRLSYAFDWRGPSVTIDTACSSSLVALHCAVQQLRAGHSRVAVAAGANLLLDVGTFV AQSKMQMLSPAGRSRMWDAGADGYARGDGVAAVVLKTRRAAEADGDAIEAVIRETAVNQDGRTPGPTSPSASAQA QLIRDCYARAGLDLSDPAHRPQYFEAHGTGTPAGDPVEAEAISSAFFPAGSAPDPPLYVGGIKVILPRPCAAYTA ARLTPAHETVIGHSEGAAGLAGIVKASLALQNAAIPPNLLGRLHGRVEPFCRHLRVPVSLTAWPALPGGGPRRAS VNSFGFGGTNAHAILESHSPLSRRQQPRAVFIPFVFSAASETSLKAYLAGFCAYLGAEQAVQVDLRDLAYTLDAR RTRLPVAAAVAASTAEQLRAKLETKLDEARADPDRRVGFKLVRQPGAERKPRLLGVFTGQGAQWPQMGLDLVTAS PAARRVLERLDARLAGLPAAHRPSWSLLEELQKEGSSSRIMEAAVAQPLCTAIQILQVHIVRAAGIDLTAVVGHS SGEIAAAYAAGFVTAEDAVCIAYYRGLFAGLSRGASGREAAMMAVETSAEDARQLLRFPEFEGRACVAAVNSSTS VTLSGDRDAIHELKTVFDDEQKLARLLRVDMAYHSHHMRACSAAYLDALAALGIQLGSGDRTTWFSSVYGSQMDQ HQLLKGPYWDANMVSPVLFMQAVDSAAASARRFDMVVELGPHPALRAPTLQTLQDRLRKSVPYTGLFRRGVSAST SVADGLAYAWTHLDKGAVDLQGYDGFVAGESAPRLVKGLPGYAWDHTKEHWHEPRYSRAIRLRPGPVHELLGHLT PNSTEHDMRWRHVLRISELPWLAGHRLQNSVVFPASGYVVGVLEAALSLCSARPATLIELCDVDFRSALVFDHDD SSIETVVALTDISRREPHTIEAGFKYHAASSKDNGALELKACGRVRIQLGQPCDSSLPPRPPRRPNLVPTCERSF YDLISPDFQYSGQFKALERLARKLGAATGFIAKVEPTNLVMHPAVVDAAFHSTFLAYAAPDDGAQIPMHIPRRIR HVTVNPSLCFSDGTSQEALAFDSAVPVDFPHANMVCDIDVYPHNHRHAMMQVEGLECVPLAQQVAKEDKEVFCNV VWGPANPDAQAVIAGDGPATPHQLELARGLEKVASFYLHRLQLQLPSNDPCRAREPCSGLLRLTALQPRWGHETQ EELIAACEPFANTVDMRLLLCICQGLLATAEVVDVEPGLVREWYASGLGIATGTRHLARISKQLVHRNPHMHILE VVADIGAATAAIRDEIGRESASYTITGQARAAQDSAPLPSEAGDHVIASDLSKDLRDQGLSEGAYDLVICLPHRH CLGVNF* |
| Coding | >Hirsu2|7364 ATGACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGCAGGCCGGGGGAGGAGGACATCGCCATCGTGGGATCG GCGTACCGCTTCCCCGGGGACGCCACGTCGCCGTCCCGGCTGTGGGCCCTGCTGCGGGCGCCGTCCGTCGTGGCC AGCCGGGTGCCGGCGCTCGAGGGCTACCACCACGCCGACGGGCTGTACCACGGGCACACCAACGTGCGCGAGGCG TACCTGCTGGCGGGCGAGGCGCCGCAGCGGCGCTTCGACGCCGGCTTCTTCGGCGTCAGCCCGGCCGAGGCGGCC GCCATGGACCCGCAGCTGCGGCTCCTGCTCGAGACCGTCTACGAGGCGGTCGAGGCCGGCGGCCTGCCGCTGGAC CGGCTCCGGGGCTCCGACACGGCCGTCTACGCCGGCCAGATGCTGGGCGAGTACGAGCAGCTGATGGGGCGCGAC CTCGACGGCCTCAGCCGCTACCACGCGTCCGGCACCGCCCGCGCCATGACGTCCAACCGGCTGTCGTACGCCTTC GACTGGCGCGGCCCGTCCGTCACCATCGACACCGCCTGCAGCTCCAGCCTGGTGGCTCTGCACTGCGCCGTCCAG CAACTGCGCGCCGGCCACTCGCGCGTCGCCGTCGCCGCCGGCGCCAACTTGCTGCTCGACGTTGGCACCTTCGTC GCCCAGAGCAAGATGCAGATGCTGTCGCCGGCCGGCCGCTCCCGCATGTGGGACGCCGGCGCCGACGGCTACGCC CGCGGCGACGGCGTCGCCGCCGTCGTGCTCAAGACGCGCCGCGCCGCCGAGGCCGACGGAGACGCCATCGAGGCC GTCATCCGCGAGACGGCCGTCAACCAGGACGGCAGGACGCCCGGCCCGACCTCGCCCAGCGCTTCCGCCCAGGCC CAGCTTATCCGCGACTGCTACGCGCGGGCCGGCCTCGACTTGTCCGATCCTGCGCACCGGCCGCAGTACTTCGAG GCCCACGGCACCGGTACCCCGGCCGGCGACCCCGTCGAGGCCGAGGCCATCAGCTCCGCCTTCTTCCCCGCCGGA TCCGCGCCGGACCCGCCTCTCTACGTCGGCGGCATCAAGGTAATCCTCCCTCGACCCTGCGCGGCCTACACGGCG GCCAGGCTAACACCGGCCCACGAGACCGTCATCGGCCACAGCGAAGGGGCGGCCGGCCTGGCCGGTATCGTCAAG GCCTCGCTGGCCTTGCAGAATGCTGCCATTCCGCCCAACCTCCTGGGCCGGCTCCATGGCCGAGTCGAGCCCTTC TGCCGACACTTACGTGTCCCTGTGTCCCTGACGGCCTGGCCGGCCCTCCCCGGCGGCGGCCCTCGCCGTGCGAGC GTCAACAGCTTCGGCTTCGGCGGCACCAATGCCCACGCCATTCTCGAGAGCCACTCGCCGCTCTCCAGGCGCCAG CAGCCGCGGGCCGTCTTCATCCCCTTCGTCTTCTCCGCGGCCTCCGAGACCTCGCTCAAGGCGTACCTGGCAGGC TTCTGCGCCTACCTCGGAGCGGAGCAGGCCGTGCAAGTCGACCTTCGCGACCTGGCTTACACCCTGGACGCTCGC CGGACGCGGCTGCCCGTGGCGGCGGCCGTGGCGGCCTCCACCGCCGAGCAGCTGCGCGCCAAGCTCGAGACGAAG CTCGACGAGGCCCGCGCAGACCCTGACCGGCGTGTCGGCTTCAAGCTCGTGCGCCAGCCCGGCGCCGAGCGGAAG CCCCGGCTGCTGGGAGTCTTCACGGGGCAGGGGGCGCAGTGGCCCCAGATGGGGCTAGACCTCGTCACCGCGTCT CCGGCCGCGCGACGCGTCCTGGAGAGACTCGACGCTCGGCTGGCAGGACTGCCCGCCGCCCATCGCCCCTCGTGG TCCCTTCTGGAGGAGCTGCAGAAAGAGGGCTCGTCGTCGCGCATCATGGAGGCCGCCGTCGCCCAGCCGCTGTGT ACGGCGATCCAGATCCTCCAGGTCCATATCGTGCGCGCCGCCGGCATTGACCTGACCGCCGTTGTCGGCCATTCG TCGGGAGAGATCGCGGCGGCCTACGCGGCGGGTTTCGTCACGGCCGAGGACGCCGTATGCATCGCCTACTACCGC GGTCTGTTCGCGGGCCTCTCGCGCGGAGCCTCGGGCCGCGAGGCCGCCATGATGGCGGTCGAGACGTCGGCCGAA GATGCCCGCCAACTCCTCCGCTTTCCCGAATTCGAGGGTCGTGCCTGTGTGGCCGCGGTGAATTCGTCCACGAGC GTCACCCTCTCCGGGGACCGGGATGCCATTCACGAGCTCAAGACCGTCTTCGACGACGAGCAAAAGCTTGCCAGG CTTCTCAGAGTCGACATGGCGTACCACTCGCACCATATGCGAGCGTGCTCTGCCGCATACCTCGATGCTCTGGCG GCGCTGGGTATCCAGCTGGGTTCCGGCGACCGCACCACCTGGTTCTCGAGCGTCTATGGCTCGCAAATGGACCAG CACCAGCTCCTCAAGGGACCGTACTGGGACGCCAACATGGTCAGCCCCGTGCTCTTCATGCAGGCCGTCGACAGC GCCGCCGCCTCCGCCCGCCGGTTCGACATGGTCGTAGAGCTGGGCCCTCATCCGGCGCTCAGGGCCCCTACTCTG CAGACGCTCCAGGATCGTCTGCGGAAGTCTGTCCCGTACACCGGCCTCTTTCGCCGCGGCGTCTCGGCCAGCACA TCCGTGGCCGACGGCCTCGCGTATGCCTGGACCCATCTGGACAAGGGAGCGGTCGACTTACAGGGCTATGACGGC TTCGTGGCCGGCGAGTCGGCCCCTCGGCTGGTCAAGGGGCTTCCCGGCTATGCCTGGGACCACACGAAAGAGCAC TGGCACGAGCCGAGATACTCCAGGGCGATTCGTCTGCGGCCGGGCCCGGTGCACGAGCTGCTGGGCCATCTGACC CCCAACAGCACCGAGCATGACATGCGATGGCGGCACGTCCTGCGCATCTCCGAGCTGCCCTGGCTCGCGGGCCAC CGGCTTCAGAATTCTGTCGTCTTTCCGGCCTCTGGATACGTGGTAGGCGTGCTGGAGGCGGCCCTTTCCCTGTGC AGTGCCCGTCCGGCGACGCTCATCGAGCTCTGTGACGTGGACTTTCGCTCCGCCCTGGTCTTCGACCACGACGAC TCGAGCATAGAGACCGTCGTCGCCCTCACGGACATCTCGAGGAGAGAGCCACACACCATCGAGGCCGGCTTCAAG TACCACGCGGCTTCGAGCAAAGACAACGGCGCGCTCGAGCTCAAGGCATGCGGTCGCGTGCGGATCCAACTGGGC CAGCCCTGCGACAGCAGCCTGCCCCCCCGGCCCCCGAGGCGGCCGAACCTTGTCCCGACCTGCGAAAGAAGTTTC TACGACTTGATCTCTCCGGACTTCCAGTATTCCGGCCAGTTCAAGGCCCTCGAGAGGCTGGCGAGGAAGCTCGGG GCCGCTACAGGATTCATTGCCAAGGTTGAGCCGACGAATCTTGTCATGCACCCGGCAGTGGTTGACGCTGCTTTT CATTCCACGTTCCTGGCGTATGCCGCCCCTGACGACGGAGCCCAGATTCCTATGCACATCCCGCGCAGGATCCGG CACGTCACGGTAAACCCGAGCCTCTGCTTCAGTGACGGGACCAGCCAAGAGGCCCTGGCCTTCGACTCGGCCGTG CCTGTGGATTTCCCACATGCGAACATGGTGTGCGACATTGACGTCTACCCACATAACCATCGACATGCCATGATG CAAGTCGAAGGTCTGGAGTGCGTGCCCCTCGCCCAGCAGGTGGCCAAGGAAGACAAGGAGGTCTTTTGCAACGTC GTGTGGGGACCGGCAAACCCAGATGCCCAGGCAGTAATAGCTGGTGACGGTCCGGCAACGCCACATCAGCTCGAG CTCGCACGCGGCCTCGAGAAGGTCGCAAGCTTCTACTTGCACCGCCTGCAGCTCCAGCTCCCTTCCAACGACCCT TGTCGAGCCCGAGAGCCCTGTAGCGGGCTGTTGCGGCTTACCGCTCTGCAGCCGCGATGGGGACATGAGACGCAG GAAGAGCTCATCGCAGCATGTGAGCCCTTTGCGAATACAGTCGATATGAGACTGCTGCTTTGCATCTGCCAGGGA CTGCTTGCCACCGCTGAGGTTGTCGACGTGGAACCGGGCCTTGTCAGGGAGTGGTACGCAAGTGGCCTCGGAATT GCGACCGGCACGAGGCATCTGGCTCGCATATCGAAGCAACTTGTCCATAGGAACCCTCACATGCATATTCTCGAG GTTGTCGCCGACATTGGAGCCGCAACTGCGGCCATCCGGGATGAGATTGGCCGTGAATCGGCCTCGTACACCATC ACCGGCCAGGCTCGTGCCGCGCAGGATTCAGCACCACTGCCGTCCGAGGCAGGCGACCACGTGATAGCCTCGGAT CTCTCCAAGGACCTCCGGGATCAGGGCCTCTCCGAGGGGGCATACGATCTGGTCATCTGCTTGCCGCACCGCCAC TGCCTCGGAGTCAATTTCTAA |
| Transcript | >Hirsu2|7364 ATGACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGCAGGCCGGGGGAGGAGGACATCGCCATCGTGGGATCG GCGTACCGCTTCCCCGGGGACGCCACGTCGCCGTCCCGGCTGTGGGCCCTGCTGCGGGCGCCGTCCGTCGTGGCC AGCCGGGTGCCGGCGCTCGAGGGCTACCACCACGCCGACGGGCTGTACCACGGGCACACCAACGTGCGCGAGGCG TACCTGCTGGCGGGCGAGGCGCCGCAGCGGCGCTTCGACGCCGGCTTCTTCGGCGTCAGCCCGGCCGAGGCGGCC GCCATGGACCCGCAGCTGCGGCTCCTGCTCGAGACCGTCTACGAGGCGGTCGAGGCCGGCGGCCTGCCGCTGGAC CGGCTCCGGGGCTCCGACACGGCCGTCTACGCCGGCCAGATGCTGGGCGAGTACGAGCAGCTGATGGGGCGCGAC CTCGACGGCCTCAGCCGCTACCACGCGTCCGGCACCGCCCGCGCCATGACGTCCAACCGGCTGTCGTACGCCTTC GACTGGCGCGGCCCGTCCGTCACCATCGACACCGCCTGCAGCTCCAGCCTGGTGGCTCTGCACTGCGCCGTCCAG CAACTGCGCGCCGGCCACTCGCGCGTCGCCGTCGCCGCCGGCGCCAACTTGCTGCTCGACGTTGGCACCTTCGTC GCCCAGAGCAAGATGCAGATGCTGTCGCCGGCCGGCCGCTCCCGCATGTGGGACGCCGGCGCCGACGGCTACGCC CGCGGCGACGGCGTCGCCGCCGTCGTGCTCAAGACGCGCCGCGCCGCCGAGGCCGACGGAGACGCCATCGAGGCC GTCATCCGCGAGACGGCCGTCAACCAGGACGGCAGGACGCCCGGCCCGACCTCGCCCAGCGCTTCCGCCCAGGCC CAGCTTATCCGCGACTGCTACGCGCGGGCCGGCCTCGACTTGTCCGATCCTGCGCACCGGCCGCAGTACTTCGAG GCCCACGGCACCGGTACCCCGGCCGGCGACCCCGTCGAGGCCGAGGCCATCAGCTCCGCCTTCTTCCCCGCCGGA TCCGCGCCGGACCCGCCTCTCTACGTCGGCGGCATCAAGGTAATCCTCCCTCGACCCTGCGCGGCCTACACGGCG GCCAGGCTAACACCGGCCCACGAGACCGTCATCGGCCACAGCGAAGGGGCGGCCGGCCTGGCCGGTATCGTCAAG GCCTCGCTGGCCTTGCAGAATGCTGCCATTCCGCCCAACCTCCTGGGCCGGCTCCATGGCCGAGTCGAGCCCTTC TGCCGACACTTACGTGTCCCTGTGTCCCTGACGGCCTGGCCGGCCCTCCCCGGCGGCGGCCCTCGCCGTGCGAGC GTCAACAGCTTCGGCTTCGGCGGCACCAATGCCCACGCCATTCTCGAGAGCCACTCGCCGCTCTCCAGGCGCCAG CAGCCGCGGGCCGTCTTCATCCCCTTCGTCTTCTCCGCGGCCTCCGAGACCTCGCTCAAGGCGTACCTGGCAGGC TTCTGCGCCTACCTCGGAGCGGAGCAGGCCGTGCAAGTCGACCTTCGCGACCTGGCTTACACCCTGGACGCTCGC CGGACGCGGCTGCCCGTGGCGGCGGCCGTGGCGGCCTCCACCGCCGAGCAGCTGCGCGCCAAGCTCGAGACGAAG CTCGACGAGGCCCGCGCAGACCCTGACCGGCGTGTCGGCTTCAAGCTCGTGCGCCAGCCCGGCGCCGAGCGGAAG CCCCGGCTGCTGGGAGTCTTCACGGGGCAGGGGGCGCAGTGGCCCCAGATGGGGCTAGACCTCGTCACCGCGTCT CCGGCCGCGCGACGCGTCCTGGAGAGACTCGACGCTCGGCTGGCAGGACTGCCCGCCGCCCATCGCCCCTCGTGG TCCCTTCTGGAGGAGCTGCAGAAAGAGGGCTCGTCGTCGCGCATCATGGAGGCCGCCGTCGCCCAGCCGCTGTGT ACGGCGATCCAGATCCTCCAGGTCCATATCGTGCGCGCCGCCGGCATTGACCTGACCGCCGTTGTCGGCCATTCG TCGGGAGAGATCGCGGCGGCCTACGCGGCGGGTTTCGTCACGGCCGAGGACGCCGTATGCATCGCCTACTACCGC GGTCTGTTCGCGGGCCTCTCGCGCGGAGCCTCGGGCCGCGAGGCCGCCATGATGGCGGTCGAGACGTCGGCCGAA GATGCCCGCCAACTCCTCCGCTTTCCCGAATTCGAGGGTCGTGCCTGTGTGGCCGCGGTGAATTCGTCCACGAGC GTCACCCTCTCCGGGGACCGGGATGCCATTCACGAGCTCAAGACCGTCTTCGACGACGAGCAAAAGCTTGCCAGG CTTCTCAGAGTCGACATGGCGTACCACTCGCACCATATGCGAGCGTGCTCTGCCGCATACCTCGATGCTCTGGCG GCGCTGGGTATCCAGCTGGGTTCCGGCGACCGCACCACCTGGTTCTCGAGCGTCTATGGCTCGCAAATGGACCAG CACCAGCTCCTCAAGGGACCGTACTGGGACGCCAACATGGTCAGCCCCGTGCTCTTCATGCAGGCCGTCGACAGC GCCGCCGCCTCCGCCCGCCGGTTCGACATGGTCGTAGAGCTGGGCCCTCATCCGGCGCTCAGGGCCCCTACTCTG CAGACGCTCCAGGATCGTCTGCGGAAGTCTGTCCCGTACACCGGCCTCTTTCGCCGCGGCGTCTCGGCCAGCACA TCCGTGGCCGACGGCCTCGCGTATGCCTGGACCCATCTGGACAAGGGAGCGGTCGACTTACAGGGCTATGACGGC TTCGTGGCCGGCGAGTCGGCCCCTCGGCTGGTCAAGGGGCTTCCCGGCTATGCCTGGGACCACACGAAAGAGCAC TGGCACGAGCCGAGATACTCCAGGGCGATTCGTCTGCGGCCGGGCCCGGTGCACGAGCTGCTGGGCCATCTGACC CCCAACAGCACCGAGCATGACATGCGATGGCGGCACGTCCTGCGCATCTCCGAGCTGCCCTGGCTCGCGGGCCAC CGGCTTCAGAATTCTGTCGTCTTTCCGGCCTCTGGATACGTGGTAGGCGTGCTGGAGGCGGCCCTTTCCCTGTGC AGTGCCCGTCCGGCGACGCTCATCGAGCTCTGTGACGTGGACTTTCGCTCCGCCCTGGTCTTCGACCACGACGAC TCGAGCATAGAGACCGTCGTCGCCCTCACGGACATCTCGAGGAGAGAGCCACACACCATCGAGGCCGGCTTCAAG TACCACGCGGCTTCGAGCAAAGACAACGGCGCGCTCGAGCTCAAGGCATGCGGTCGCGTGCGGATCCAACTGGGC CAGCCCTGCGACAGCAGCCTGCCCCCCCGGCCCCCGAGGCGGCCGAACCTTGTCCCGACCTGCGAAAGAAGTTTC TACGACTTGATCTCTCCGGACTTCCAGTATTCCGGCCAGTTCAAGGCCCTCGAGAGGCTGGCGAGGAAGCTCGGG GCCGCTACAGGATTCATTGCCAAGGTTGAGCCGACGAATCTTGTCATGCACCCGGCAGTGGTTGACGCTGCTTTT CATTCCACGTTCCTGGCGTATGCCGCCCCTGACGACGGAGCCCAGATTCCTATGCACATCCCGCGCAGGATCCGG CACGTCACGGTAAACCCGAGCCTCTGCTTCAGTGACGGGACCAGCCAAGAGGCCCTGGCCTTCGACTCGGCCGTG CCTGTGGATTTCCCACATGCGAACATGGTGTGCGACATTGACGTCTACCCACATAACCATCGACATGCCATGATG CAAGTCGAAGGTCTGGAGTGCGTGCCCCTCGCCCAGCAGGTGGCCAAGGAAGACAAGGAGGTCTTTTGCAACGTC GTGTGGGGACCGGCAAACCCAGATGCCCAGGCAGTAATAGCTGGTGACGGTCCGGCAACGCCACATCAGCTCGAG CTCGCACGCGGCCTCGAGAAGGTCGCAAGCTTCTACTTGCACCGCCTGCAGCTCCAGCTCCCTTCCAACGACCCT TGTCGAGCCCGAGAGCCCTGTAGCGGGCTGTTGCGGCTTACCGCTCTGCAGCCGCGATGGGGACATGAGACGCAG GAAGAGCTCATCGCAGCATGTGAGCCCTTTGCGAATACAGTCGATATGAGACTGCTGCTTTGCATCTGCCAGGGA CTGCTTGCCACCGCTGAGGTTGTCGACGTGGAACCGGGCCTTGTCAGGGAGTGGTACGCAAGTGGCCTCGGAATT GCGACCGGCACGAGGCATCTGGCTCGCATATCGAAGCAACTTGTCCATAGGAACCCTCACATGCATATTCTCGAG GTTGTCGCCGACATTGGAGCCGCAACTGCGGCCATCCGGGATGAGATTGGCCGTGAATCGGCCTCGTACACCATC ACCGGCCAGGCTCGTGCCGCGCAGGATTCAGCACCACTGCCGTCCGAGGCAGGCGACCACGTGATAGCCTCGGAT CTCTCCAAGGACCTCCGGGATCAGGGCCTCTCCGAGGGGGCATACGATCTGGTCATCTGCTTGCCGCACCGCCAC TGCCTCGGAGTCAATTTCTAA |
| Gene | >Hirsu2|7364 ATGACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGCAGGCCGGGGGAGGAGGACATCGCCATCGTGGGATCG GCGTACCGCTTCCCCGGGGACGCCACGTCGCCGTCCCGGCTGTGGGCCCTGCTGCGGGCGCCGTCCGTCGTGGCC AGCCGGGTGCCGGCGCTCGAGGGCTACCACCACGCCGACGGGCTGTACCACGGGCACACCAACGTGCGCGAGGCG TACCTGCTGGCGGGCGAGGCGCCGCAGCGGCGCTTCGACGCCGGCTTCTTCGGCGTCAGCCCGGCCGAGGCGGCC GCCATGGACCCGCAGCTGCGGCTCCTGCTCGAGACCGTCTACGAGGCGGTCGAGGCCGGCGGCCTGCCGCTGGAC CGGCTCCGGGGCTCCGACACGGCCGTCTACGCCGGCCAGATGCTGGGCGAGTACGAGCAGCTGATGGGGCGCGAC CTCGACGGCCTCAGCCGCTACCACGCGTCCGGCACCGCCCGCGCCATGACGTCCAACCGGCTGTCGTACGCCTTC GACTGGCGCGGCCCGTCCGTCACCATCGACACCGCCTGCAGCTCCAGCCTGGTGGCTCTGCACTGCGCCGTCCAG CAACTGCGCGCCGGCCACTCGCGCGTCGCCGTCGCCGCCGGCGCCAACTTGCTGCTCGACGTTGGCACCTTCGTC GCCCAGAGCAAGATGCAGATGCTGTCGCCGGCCGGCCGCTCCCGCATGTGGGACGCCGGCGCCGACGGCTACGCC CGCGGCGACGGCGTCGCCGCCGTCGTGCTCAAGACGCGCCGCGCCGCCGAGGCCGACGGAGACGCCATCGAGGCC GTCATCCGCGAGACGGCCGTCAACCAGGACGGCAGGACGCCCGGCCCGACCTCGTCAGTCCCCCCTTTTCTCCTC GTCTAGGCCGACGACGTGCCTGACCCGTATCTTGCCTGGCTGCCAGGCCCAGCGCTTCCGCCCAGGCCCAGCTTA TCCGCGACTGCTACGCGCGGGCCGGCCTCGACTTGTCCGATCCTGCGCACCGGCCGCAGTACTTCGAGGCCCACG GCACCGGTACCCCGGCCGGCGACCCCGTCGAGGCCGAGGCCATCAGCTCCGCCTTCTTCCCCGCCGGATCCGCGC CGGACCCGCCTCTCTACGTCGGCGGCATCAAGGTAATCCTCCCTCGACCCTGCGCGGCCTACACGGCGGCCAGGC TAACACCGGCCCACGAGACCGTCATCGGCCACAGCGAAGGGGCGGCCGGCCTGGCCGGTATCGTCAAGGCCTCGC TGGCCTTGCAGAATGCTGCCATTCCGCCCAACCTCCTGGGCCGGCTCCATGGCCGAGTCGAGCCCTTCTGCCGAC ACTTACGTGTCCCTGTGTCCCTGACGGCCTGGCCGGCCCTCCCCGGCGGCGGCCCTCGCCGTGCGAGCGTCAACA GGTAACGTTTGCGCCACTGTCCCTTCCACGGCCCGGCCCTGACTCCGAGCCGTGCCCCAGCTTCGGCTTCGGCGG CACCAATGCCCACGCCATTCTCGAGAGCCACTCGCCGCTCTCCAGGCGCCAGCAGCCGCGGGCCGTCTTCATCCC CTTCGTCTTCTCCGCGGCCTCCGAGACCTCGCTCAAGGCGTACCTGGCAGGCTTCTGCGCCTACCTCGGAGCGGA GCAGGCCGTGCAAGTCGACCTTCGCGACCTGGCTTACACCCTGGACGCTCGCCGGACGCGGCTGCCCGTGGCGGC GGCCGTGGCGGCCTCCACCGCCGAGCAGCTGCGCGCCAAGCTCGAGACGAAGCTCGACGAGGCCCGCGCAGACCC TGACCGGCGTGTCGGCTTCAAGCTCGTGCGCCAGCCCGGCGCCGAGCGGAAGCCCCGGCTGCTGGGAGTCTTCAC GGGGCAGGGGGCGCAGTGGCCCCAGATGGGGCTAGACCTCGTCACCGCGTCTCCGGCCGCGCGACGCGTCCTGGA GAGACTCGACGCTCGGCTGGCAGGACTGCCCGCCGCCCATCGCCCCTCGTGGTCCCTTCTGGAGGAGCTGCAGAA AGAGGGCTCGTCGTCGCGCATCATGGAGGCCGCCGTCGCCCAGCCGCTGTGTACGGCGATCCAGATCCTCCAGGT CCATATCGTGCGCGCCGCCGGCATTGACCTGACCGCCGTTGTCGGCCATTCGTCGGGAGAGATCGCGGCGGCCTA CGCGGCGGGTTTCGTCACGGCCGAGGACGCCGTATGCATCGCCTACTACCGCGGTCTGTTCGCGGGCCTCTCGCG CGGAGCCTCGGGCCGCGAGGCCGCCATGATGGCGGTCGAGACGTCGGCCGAAGATGCCCGCCAACTCCTCCGCTT TCCCGAATTCGAGGGTCGTGCCTGTGTGGCCGCGGTGAATTCGTCCACGAGCGTCACCCTCTCCGGGGACCGGGA TGCCATTCACGAGCTCAAGACCGTCTTCGACGACGAGCAAAAGCTTGCCAGGCTTCTCAGAGTCGACATGGCGTA CCACTCGCACCATATGCGAGCGTGCTCTGCCGCATACCTCGATGCTCTGGCGGCGCTGGGTATCCAGCTGGGTTC CGGCGACCGCACCACCTGGTTCTCGAGCGTCTATGGCTCGCAAATGGACCAGCACCAGCTCCTCAAGGGACCGTA CTGGGACGCCAACATGGTCAGCCCCGTGCTCTTCATGCAGGCCGTCGACAGCGCCGCCGCCTCCGCCCGCCGGTT CGACATGGTCGTAGAGCTGGGCCCTCATCCGGCGCTCAGGGCCCCTACTCTGCAGACGCTCCAGGATCGTCTGCG GAAGTCTGTCCCGTACACCGGCCTCTTTCGCCGCGGCGTCTCGGCCAGCACATCCGTGGCCGACGGCCTCGCGTA TGCCTGGACCCATCTGGACAAGGGAGCGGTCGACTTACAGGGCTATGACGGCTTCGTGGCCGGCGAGTCGGCCCC TCGGCTGGTCAAGGGGCTTCCCGGCTATGCCTGGGACCACACGAAAGAGCACTGGCACGAGCCGAGATACTCCAG GGCGATTCGTCTGCGGCCGGGCCCGGTGCACGAGCTGCTGGGCCATCTGACCCCCAACAGCACCGAGCATGACAT GCGATGGCGGCACGTCCTGCGCATCTCCGAGCTGCCCTGGCTCGCGGGCCACCGGCTTCAGAATTCTGTCGTCTT TCCGGCCTCTGGATACGTGGTAGGCGTGCTGGAGGCGGCCCTTTCCCTGTGCAGTGCCCGTCCGGCGACGCTCAT CGAGCTCTGTGACGTGGACTTTCGCTCCGCCCTGGTCTTCGACCACGACGACTCGAGCATAGAGACCGTCGTCGC CCTCACGGACATCTCGAGGAGAGAGCCACACACCATCGAGGCCGGCTTCAAGTACCACGCGGCTTCGAGCAAAGA CAACGGCGCGCTCGAGCTCAAGGCATGCGGTCGCGTGCGGATCCAACTGGGCCAGCCCTGCGACAGCAGCCTGCC CCCCCGGCCCCCGAGGCGGCCGAACCTTGTCCCGACCTGCGAAAGAAGTTTCTACGACTTGATCTCTCCGGACTT CCAGTATTCCGGCCAGTTCAAGGCCCTCGAGAGGCTGGCGAGGAAGCTCGGGGCCGCTACAGGATTCATTGCCAA GGTTGAGCCGACGAATCTTGTCATGCACCCGGCAGTGGTTGACGCTGCTTTTGTACGTCCATCCGCGTCGAATCC GCCTCGTCGTCTCCAGCTAACGTCGTTGCAGCATTCCACGTTCCTGGCGTATGCCGCCCCTGACGACGGAGCCCA GATTCCTATGCACATCCCGCGCAGGATCCGGCACGTCACGGTAAACCCGAGCCTCTGCTTCAGTGACGGGACCAG CCAAGAGGCCCTGGCCTTCGACTCGGCCGTGCCTGTGGATTTCCCACATGCGAACATGGTGTGCGACATTGACGT CTACCCACATAACCATCGACATGCCATGATGCAAGTCGAAGGTCTGGAGTGCGTGCCCCTCGCCCAGCAGGTGGC CAAGGAAGACAAGGAGGTCTTTTGCAACGTCGTGTGGGGACCGGCAAACCCAGATGCCCAGGCAGTAATAGCTGG TGACGGTCCGGCAACGCCACATCAGCTCGAGCTCGCACGCGGCCTCGAGAAGGTCGCAAGCTTCTACTTGCACCG CCTGCAGCTCCAGCTCCCTTCCAACGACCCTTGTCGAGCCCGAGAGCCCTGTAGCGGGCTGTTGCGGCTTACCGC TCTGCAGCCGCGATGGGGACATGAGACGCAGGAAGAGCTCATCGCAGCATGTGAGCCCTTTGCGAATACAGTCGA TATGAGACTGCTGCTTTGCATCTGCCAGGGACTGCTTGCCACCGCTGAGGTTGTCGACGTGGAACCGGGCCTTGT CAGGGAGTGGTACGCAAGTGGCCTCGGAATTGCGACCGGCACGAGGCATCTGGCTCGCATATCGAAGCAACTTGT CCATAGGAACCCTCACATGCATATTCTCGAGGTTGTCGCCGACATTGGAGCCGCAACTGCGGCCATCCGGGATGA GATTGGCCGTGAATCGGCCTCGTACACCATCACCGGCCAGGCTCGTGCCGCGCAGGATTCAGCACCACTGCCGTC CGAGGCAGGCGACCACGTGATAGCCTCGGATCTCTCCAAGGACCTCCGGGATCAGGGCCTCTCCGAGGGGGCATA CGATCTGGTCATCGTAACCCTAGCCCTGTCGACCACCCCAGCCGTCGAGGGCGCCCTGCGCAATCTACGACGTCT GCTGACGTCTGGCGGCTACCTCGTAGTGCTTGCCGCACCGCCACTGCCTCGGAGTCAATTTCTAA |