© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|5821 |
| Gene name | |
| Location | Contig_294:13033..18629 |
| Strand | + |
| Gene length (bp) | 5596 |
| Transcript length (bp) | 5379 |
| Coding sequence length (bp) | 5379 |
| Protein length (aa) | 1793 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00109 | ketoacyl-synt | Beta-ketoacyl synthase, N-terminal domain | 1.1E-72 | 407 | 657 |
| PF16073 | SAT | Starter unit:ACP transacylase in aflatoxin biosynthesis | 6.3E-48 | 37 | 265 |
| PF00698 | Acyl_transf_1 | Acyl transferase domain | 8.6E-47 | 941 | 1261 |
| PF02801 | Ketoacyl-synt_C | Beta-ketoacyl synthase, C-terminal domain | 1.9E-32 | 666 | 785 |
| PF16197 | KAsynt_C_assoc | Ketoacyl-synthetase C-terminal extension | 5.3E-09 | 797 | 903 |
| PF00550 | PP-binding | Phosphopantetheine attachment site | 5.0E-09 | 1725 | 1786 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| 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 | 37 | 1789 | 0.0E+00 |
| sp|Q12053|PKSL1_ASPPA | Noranthrone synthase OS=Aspergillus parasiticus GN=pksL1 PE=1 SV=1 | 31 | 1787 | 0.0E+00 |
| 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 | 32 | 1787 | 0.0E+00 |
| sp|Q7TXL7|PPSD_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsD PE=3 SV=1 | 408 | 1292 | 5.0E-107 |
| sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 408 | 1292 | 5.0E-107 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| 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 | 37 | 1789 | 0.0E+00 |
| sp|Q12053|PKSL1_ASPPA | Noranthrone synthase OS=Aspergillus parasiticus GN=pksL1 PE=1 SV=1 | 31 | 1787 | 0.0E+00 |
| 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 | 32 | 1787 | 0.0E+00 |
| sp|Q7TXL7|PPSD_MYCBO | Phthiocerol/phenolphthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ppsD PE=3 SV=1 | 408 | 1292 | 5.0E-107 |
| sp|P9WQE3|PPSD_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsD PE=1 SV=1 | 408 | 1292 | 5.0E-107 |
| sp|P9WQE2|PPSD_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsD OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsD PE=3 SV=1 | 408 | 1292 | 5.0E-107 |
| sp|P9WQE9|PHAS_MYCTU | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=pks2 PE=1 SV=1 | 403 | 1296 | 5.0E-107 |
| sp|P9WQE8|PHAS_MYCTO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=pks2 PE=3 SV=1 | 403 | 1296 | 5.0E-107 |
| sp|A5U9F4|PHAS_MYCTA | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=pks2 PE=3 SV=1 | 403 | 1296 | 5.0E-107 |
| sp|Q7TVK8|PHAS_MYCBO | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=pks2 PE=3 SV=1 | 403 | 1296 | 5.0E-107 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 396 | 1292 | 6.0E-107 |
| sp|A1KQG0|PHAS_MYCBP | Phthioceranic/hydroxyphthioceranic acid synthase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=pks2 PE=3 SV=1 | 403 | 1296 | 4.0E-106 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 408 | 1293 | 2.0E-105 |
| 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 | 404 | 1291 | 2.0E-105 |
| 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 | 404 | 1291 | 3.0E-102 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 408 | 1291 | 9.0E-102 |
| sp|Q869W9|PKS16_DICDI | Probable polyketide synthase 16 OS=Dictyostelium discoideum GN=pks16 PE=2 SV=1 | 408 | 1325 | 1.0E-101 |
| sp|Q03132|ERYA2_SACER | Erythronolide synthase, modules 3 and 4 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=3 | 408 | 1293 | 6.0E-101 |
| sp|Q869X2|PKS17_DICDI | Probable polyketide synthase 17 OS=Dictyostelium discoideum GN=pks17 PE=3 SV=1 | 408 | 1321 | 2.0E-100 |
| sp|B4XYB8|AZIB_STREG | 5-methyl-1-naphthoate synthase OS=Streptomyces sahachiroi GN=aziB PE=1 SV=1 | 401 | 1292 | 3.0E-99 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 404 | 1292 | 1.0E-97 |
| sp|Q02251|MCAS_MYCBO | Mycocerosic acid synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mas PE=1 SV=2 | 406 | 1296 | 2.0E-97 |
| sp|P9WQE7|PPSA_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsA PE=1 SV=1 | 394 | 1221 | 9.0E-96 |
| sp|P9WQE6|PPSA_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsA PE=3 SV=1 | 394 | 1221 | 1.0E-95 |
| sp|P96202|PPSC_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsC OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsC PE=1 SV=2 | 408 | 1221 | 4.0E-95 |
| 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 | 408 | 1221 | 4.0E-95 |
| 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 | 408 | 1292 | 2.0E-94 |
| sp|P9WQE5|PPSB_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsB PE=1 SV=1 | 408 | 1292 | 3.0E-94 |
| sp|P9WQE4|PPSB_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsB OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsB PE=3 SV=1 | 408 | 1292 | 3.0E-94 |
| sp|Q0C8M3|LNKS_ASPTN | Lovastatin nonaketide synthase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lovB PE=3 SV=2 | 395 | 1293 | 3.0E-94 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 404 | 1292 | 5.0E-94 |
| 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 | 394 | 1221 | 8.0E-94 |
| sp|Q03133|ERYA3_SACER | Erythronolide synthase, modules 5 and 6 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=4 | 390 | 1298 | 1.0E-93 |
| sp|Q07017|OL56_STRAT | Oleandomycin polyketide synthase, modules 5 and 6 OS=Streptomyces antibioticus GN=orfB PE=3 SV=1 | 404 | 1292 | 2.0E-93 |
| sp|Q55E72|PKS1_DICDI | Probable polyketide synthase 1 OS=Dictyostelium discoideum GN=stlA PE=1 SV=1 | 397 | 1291 | 2.0E-93 |
| sp|Q9Y8A5|LNKS_ASPTE | Lovastatin nonaketide synthase OS=Aspergillus terreus GN=lovB PE=1 SV=1 | 395 | 1293 | 2.0E-93 |
| sp|Q9Y7D5|LOVF_ASPTE | Lovastatin diketide synthase LovF OS=Aspergillus terreus GN=lovF PE=1 SV=1 | 399 | 1291 | 1.0E-92 |
| 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 | 399 | 1289 | 1.0E-90 |
| 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 | 408 | 1291 | 3.0E-88 |
| sp|Q54IX3|PKS26_DICDI | Probable polyketide synthase 26 OS=Dictyostelium discoideum GN=pks26 PE=3 SV=1 | 405 | 1291 | 2.0E-87 |
| sp|Q55CN6|PKS3_DICDI | Probable polyketide synthase 3 OS=Dictyostelium discoideum GN=pks3 PE=3 SV=1 | 416 | 1291 | 1.0E-86 |
| sp|Q54KU5|PKS24_DICDI | Probable polyketide synthase 24 OS=Dictyostelium discoideum GN=pks24 PE=3 SV=1 | 408 | 1293 | 7.0E-85 |
| sp|B0G100|PKS7_DICDI | Probable polyketide synthase 7 OS=Dictyostelium discoideum GN=pks7 PE=3 SV=1 | 408 | 1293 | 8.0E-85 |
| sp|Q54KU3|PKS25_DICDI | Probable polyketide synthase 25 OS=Dictyostelium discoideum GN=pks25 PE=3 SV=1 | 408 | 1293 | 8.0E-85 |
| sp|Q559A9|PKS13_DICDI | Probable polyketide synthase 13 OS=Dictyostelium discoideum GN=pks13 PE=3 SV=1 | 405 | 1291 | 1.0E-84 |
| sp|Q86AE3|PKS9_DICDI | Probable polyketide synthase 9/36 OS=Dictyostelium discoideum GN=pks9 PE=2 SV=1 | 408 | 1293 | 4.0E-83 |
| sp|B0G0Z9|PKS6_DICDI | Probable polyketide synthase 6 OS=Dictyostelium discoideum GN=pks6 PE=3 SV=1 | 408 | 1293 | 6.0E-83 |
| sp|P22367|MSAS_PENPA | 6-methylsalicylic acid synthase OS=Penicillium patulum PE=1 SV=1 | 406 | 1291 | 6.0E-82 |
| sp|Q558Y6|PKS14_DICDI | Probable polyketide synthase 14 OS=Dictyostelium discoideum GN=pks14 PE=3 SV=2 | 399 | 1291 | 2.0E-81 |
| sp|Q54QD3|PKS22_DICDI | Probable polyketide synthase 22 OS=Dictyostelium discoideum GN=pks22 PE=3 SV=1 | 406 | 1291 | 7.0E-81 |
| sp|Q54QD1|PKS23_DICDI | Probable polyketide synthase 23 OS=Dictyostelium discoideum GN=pks23 PE=3 SV=1 | 406 | 1291 | 1.0E-80 |
| sp|B0G101|PKS8_DICDI | Probable polyketide synthase 8/35 OS=Dictyostelium discoideum GN=pks8 PE=3 SV=1 | 408 | 1293 | 1.0E-80 |
| sp|Q54FI3|PKS37_DICDI | Probable polyketide synthase 37 OS=Dictyostelium discoideum GN=stlB PE=2 SV=1 | 408 | 1293 | 3.0E-80 |
| sp|Q54ED6|PKS41_DICDI | Probable polyketide synthase 41 OS=Dictyostelium discoideum GN=pks41 PE=3 SV=1 | 406 | 1291 | 7.0E-79 |
| sp|Q86JI5|PKS5_DICDI | Probable polyketide synthase 5 OS=Dictyostelium discoideum GN=pks5 PE=2 SV=1 | 408 | 1293 | 5.0E-78 |
| sp|Q55DM7|PKS2_DICDI | Probable polyketide synthase 2 OS=Dictyostelium discoideum GN=pks2 PE=3 SV=1 | 408 | 1291 | 4.0E-77 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 408 | 924 | 5.0E-77 |
| sp|B0G103|PKS10_DICDI | Probable polyketide synthase 10 OS=Dictyostelium discoideum GN=pks10 PE=3 SV=1 | 408 | 1291 | 9.0E-77 |
| sp|B0G138|PKS21_DICDI | Probable polyketide synthase 21 OS=Dictyostelium discoideum GN=pks21 PE=3 SV=1 | 407 | 1291 | 4.0E-76 |
| sp|P9WQE1|PPSE_MYCTU | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ppsE PE=1 SV=1 | 405 | 1340 | 3.0E-75 |
| sp|P9WQE0|PPSE_MYCTO | Phthiocerol synthesis polyketide synthase type I PpsE OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ppsE PE=3 SV=1 | 405 | 1340 | 3.0E-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 | 405 | 1340 | 3.0E-75 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 408 | 928 | 6.0E-75 |
| sp|Q54T36|PKS19_DICDI | Probable polyketide synthase 19 OS=Dictyostelium discoideum GN=pks19 PE=3 SV=1 | 407 | 1291 | 7.0E-75 |
| sp|Q54ED7|PKS40_DICDI | Probable polyketide synthase 40 OS=Dictyostelium discoideum GN=pks40 PE=3 SV=1 | 406 | 1291 | 2.0E-74 |
| sp|Q54FN7|PKS33_DICDI | Probable polyketide synthase 33 OS=Dictyostelium discoideum GN=pks33 PE=3 SV=2 | 408 | 1291 | 5.0E-74 |
| sp|Q54G30|PKS27_DICDI | Probable polyketide synthase 27 OS=Dictyostelium discoideum GN=pks27 PE=3 SV=1 | 476 | 1291 | 1.0E-73 |
| sp|Q54FD2|PKS38_DICDI | Probable polyketide synthase 38 OS=Dictyostelium discoideum GN=pks38 PE=3 SV=1 | 408 | 1293 | 3.0E-73 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 383 | 918 | 5.0E-73 |
| sp|Q54FQ3|PKS29_DICDI | Probable polyketide synthase 29 OS=Dictyostelium discoideum GN=pks29 PE=3 SV=1 | 408 | 1291 | 1.0E-72 |
| sp|Q54FQ2|PKS30_DICDI | Probable polyketide synthase 30 OS=Dictyostelium discoideum GN=pks30 PE=3 SV=1 | 408 | 1291 | 3.0E-72 |
| sp|Q54B49|PKS45_DICDI | Probable polyketide synthase 45 OS=Dictyostelium discoideum GN=pks45 PE=3 SV=2 | 408 | 1291 | 3.0E-72 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 401 | 927 | 5.0E-72 |
| sp|P12785|FAS_RAT | Fatty acid synthase OS=Rattus norvegicus GN=Fasn PE=1 SV=3 | 407 | 1291 | 7.0E-72 |
| sp|Q54FC8|PKS39_DICDI | Probable polyketide synthase 39 OS=Dictyostelium discoideum GN=pks39 PE=3 SV=1 | 408 | 1291 | 9.0E-72 |
| sp|Q54B51|PKS44_DICDI | Probable polyketide synthase 44 OS=Dictyostelium discoideum GN=pks44 PE=3 SV=1 | 408 | 1291 | 9.0E-72 |
| sp|B0G170|PKS28_DICDI | Probable polyketide synthase 28 OS=Dictyostelium discoideum GN=pks28 PE=3 SV=1 | 476 | 1224 | 3.0E-71 |
| sp|P19096|FAS_MOUSE | Fatty acid synthase OS=Mus musculus GN=Fasn PE=1 SV=2 | 407 | 1291 | 4.0E-71 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 389 | 928 | 1.0E-70 |
| sp|Q71SP7|FAS_BOVIN | Fatty acid synthase OS=Bos taurus GN=FASN PE=2 SV=1 | 407 | 1291 | 1.0E-70 |
| sp|Q54FQ1|PKS31_DICDI | Probable polyketide synthase 31 OS=Dictyostelium discoideum GN=pks31 PE=3 SV=1 | 409 | 1291 | 2.0E-70 |
| sp|Q54FN2|PKS34_DICDI | Probable polyketide synthase 34 OS=Dictyostelium discoideum GN=pks34 PE=3 SV=1 | 408 | 1291 | 2.0E-69 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 404 | 918 | 2.0E-68 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 408 | 918 | 3.0E-68 |
| sp|Q54FP8|PKS32_DICDI | Probable polyketide synthase 32 OS=Dictyostelium discoideum GN=pks32 PE=3 SV=1 | 408 | 1291 | 3.0E-68 |
| sp|P49327|FAS_HUMAN | Fatty acid synthase OS=Homo sapiens GN=FASN PE=1 SV=3 | 407 | 1272 | 2.0E-67 |
| 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 | 404 | 837 | 5.0E-67 |
| sp|P12276|FAS_CHICK | Fatty acid synthase OS=Gallus gallus GN=FASN PE=1 SV=5 | 408 | 1291 | 1.0E-66 |
| sp|Q54D44|PKS42_DICDI | Probable polyketide synthase 42 OS=Dictyostelium discoideum GN=pks42 PE=3 SV=2 | 476 | 1291 | 7.0E-66 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 408 | 924 | 1.0E-62 |
| sp|P40872|PKSM_BACSU | Polyketide synthase PksM OS=Bacillus subtilis (strain 168) GN=pksM PE=1 SV=4 | 393 | 933 | 7.0E-62 |
| sp|Q9R9J1|MYCA_BACIU | Mycosubtilin synthase subunit A OS=Bacillus subtilis GN=mycA PE=3 SV=1 | 397 | 924 | 1.0E-60 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 389 | 969 | 1.0E-55 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 408 | 924 | 3.0E-53 |
| sp|P36189|FAS_ANSAN | Fatty acid synthase (Fragment) OS=Anser anser anser GN=FASN PE=1 SV=1 | 408 | 776 | 5.0E-53 |
| sp|O31782|PKSN_BACSU | Polyketide synthase PksN OS=Bacillus subtilis (strain 168) GN=pksN PE=1 SV=3 | 408 | 924 | 9.0E-50 |
| sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 404 | 839 | 7.0E-48 |
| sp|O31784|PKSR_BACSU | Polyketide synthase PksR OS=Bacillus subtilis (strain 168) GN=pksR PE=1 SV=2 | 408 | 920 | 1.0E-45 |
| sp|P40806|PKSJ_BACSU | Polyketide synthase PksJ OS=Bacillus subtilis (strain 168) GN=pksJ PE=1 SV=3 | 383 | 871 | 5.0E-43 |
| sp|Q05470|PKSL_BACSU | Polyketide synthase PksL OS=Bacillus subtilis (strain 168) GN=pksL PE=1 SV=3 | 366 | 838 | 2.0E-42 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 407 | 839 | 3.0E-40 |
| 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 | 859 | 1291 | 5.0E-31 |
| sp|P39525|CEM1_YEAST | 3-oxoacyl-[acyl-carrier-protein] synthase homolog OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CEM1 PE=1 SV=1 | 495 | 839 | 3.0E-28 |
| 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 | 405 | 837 | 2.0E-25 |
| 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 | 404 | 838 | 3.0E-25 |
| sp|P52410|KASC1_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Arabidopsis thaliana GN=KAS1 PE=2 SV=2 | 383 | 837 | 4.0E-25 |
| sp|P55338|FABF_VIBHA | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Vibrio harveyi GN=fabF PE=3 SV=2 | 404 | 839 | 7.0E-25 |
| sp|P23902|KASC1_HORVU | 3-oxoacyl-[acyl-carrier-protein] synthase I, chloroplastic OS=Hordeum vulgare GN=KAS12 PE=1 SV=1 | 405 | 837 | 2.0E-24 |
| sp|Q558W4|PKS15_DICDI | Probable polyketide synthase 15 OS=Dictyostelium discoideum GN=pks15 PE=3 SV=2 | 934 | 1229 | 3.0E-24 |
| sp|P0AAI8|FABF_SHIFL | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Shigella flexneri GN=fabF PE=3 SV=2 | 483 | 839 | 4.0E-24 |
| sp|P0AAI5|FABF_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli (strain K12) GN=fabF PE=1 SV=2 | 483 | 839 | 4.0E-24 |
| 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 | 483 | 839 | 4.0E-24 |
| sp|P0AAI7|FABF_ECO57 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Escherichia coli O157:H7 GN=fabF PE=3 SV=2 | 483 | 839 | 4.0E-24 |
| sp|P56902|FABF_RHIME | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Rhizobium meliloti (strain 1021) GN=fabF PE=3 SV=2 | 474 | 837 | 2.0E-23 |
| sp|Q54TW0|PKS18_DICDI | Probable polyketide synthase 18 OS=Dictyostelium discoideum GN=pks18 PE=2 SV=1 | 937 | 1291 | 8.0E-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 | 938 | 1230 | 4.0E-22 |
| sp|O34877|PKSD_BACSU | Polyketide biosynthesis acyltransferase homolog PksD OS=Bacillus subtilis (strain 168) GN=pksD PE=1 SV=2 | 938 | 1229 | 9.0E-22 |
| sp|Q9D404|OXSM_MOUSE | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Mus musculus GN=Oxsm PE=1 SV=1 | 542 | 837 | 1.0E-21 |
| sp|Q03131|ERYA1_SACER | Erythronolide synthase, modules 1 and 2 OS=Saccharopolyspora erythraea GN=eryA PE=1 SV=1 | 893 | 1264 | 2.0E-21 |
| 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 | 405 | 787 | 2.0E-21 |
| sp|P71019|FABD_BACSU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis (strain 168) GN=fabD PE=3 SV=2 | 939 | 1225 | 8.0E-21 |
| sp|O34340|FABF_BACSU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Bacillus subtilis (strain 168) GN=fabF PE=1 SV=1 | 483 | 839 | 1.0E-20 |
| sp|Q9NWU1|OXSM_HUMAN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Homo sapiens GN=OXSM PE=1 SV=1 | 542 | 837 | 2.0E-20 |
| sp|Q7A6F8|FABF_STAAN | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain N315) GN=fabF PE=1 SV=1 | 405 | 842 | 4.0E-19 |
| sp|Q99VA6|FABF_STAAM | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabF PE=3 SV=1 | 405 | 842 | 4.0E-19 |
| sp|P16538|KAS1_STRGA | Tetracenomycin C polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces glaucescens GN=tcmK PE=3 SV=1 | 404 | 781 | 6.0E-19 |
| sp|Q0VCA7|OXSM_BOVIN | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Bos taurus GN=OXSM PE=2 SV=1 | 543 | 837 | 1.0E-18 |
| sp|Q8L3X9|KASM_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial OS=Arabidopsis thaliana GN=KAS PE=1 SV=1 | 542 | 837 | 1.0E-18 |
| sp|Q5TKS0|FABF_STAAU | 3-oxoacyl-[acyl-carrier-protein] synthase 2 (Fragment) OS=Staphylococcus aureus GN=fabF PE=3 SV=1 | 482 | 783 | 1.0E-18 |
| sp|Q8NXE1|FABF_STAAW | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MW2) GN=fabF PE=1 SV=1 | 405 | 842 | 2.0E-18 |
| sp|Q6GAU2|FABF_STAAS | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MSSA476) GN=fabF PE=3 SV=1 | 405 | 842 | 2.0E-18 |
| sp|Q5HHA1|FABF_STAAC | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain COL) GN=fabF PE=1 SV=1 | 405 | 842 | 2.0E-18 |
| sp|P72331|NODE_RHIS3 | Nodulation protein E OS=Rhizobium sp. (strain N33) GN=nodE PE=3 SV=1 | 479 | 839 | 2.0E-18 |
| sp|Q6GIA3|FABF_STAAR | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Staphylococcus aureus (strain MRSA252) GN=fabF PE=3 SV=1 | 407 | 842 | 2.0E-18 |
| 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 | 496 | 839 | 2.0E-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 | 576 | 837 | 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 | 576 | 837 | 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 | 576 | 837 | 7.0E-18 |
| sp|P41175|KAS1_STRCM | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cinnamonensis PE=3 SV=1 | 405 | 787 | 1.0E-17 |
| sp|P06230|NODE_RHIME | Nodulation protein E OS=Rhizobium meliloti (strain 1021) GN=nodE PE=3 SV=1 | 479 | 839 | 3.0E-17 |
| sp|P06231|NOE4_RHIML | Nodulation protein E OS=Rhizobium meliloti GN=nodE PE=3 SV=1 | 479 | 839 | 3.0E-17 |
| sp|P04684|NODE_RHILT | Nodulation protein E OS=Rhizobium leguminosarum bv. trifolii GN=nodE PE=3 SV=2 | 485 | 836 | 5.0E-17 |
| sp|O69473|FAB2_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Mycobacterium leprae (strain TN) GN=kasB PE=3 SV=2 | 576 | 837 | 8.0E-17 |
| sp|Q9C9P4|KASC2_ARATH | 3-oxoacyl-[acyl-carrier-protein] synthase II, chloroplastic OS=Arabidopsis thaliana GN=KAS2 PE=1 SV=1 | 483 | 837 | 1.0E-16 |
| sp|P16540|KAS1_STRVN | Granaticin polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces violaceoruber GN=gra-orf1 PE=3 SV=1 | 407 | 787 | 7.0E-16 |
| sp|Q02578|KAS1_STRCN | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces cyaneus GN=curA PE=3 SV=1 | 407 | 787 | 1.0E-15 |
| sp|Q05356|KAS1_STRHA | Putative polyketide beta-ketoacyl synthase 1 OS=Streptomyces halstedii GN=sch1 PE=3 SV=1 | 407 | 808 | 4.0E-15 |
| sp|P0A953|FABB_ECOLI | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Escherichia coli (strain K12) GN=fabB PE=1 SV=1 | 565 | 839 | 4.0E-15 |
| sp|P0A954|FABB_ECOL6 | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=fabB PE=3 SV=1 | 565 | 839 | 4.0E-15 |
| 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 | 498 | 838 | 5.0E-15 |
| sp|P73283|FABF_SYNY3 | 3-oxoacyl-[acyl-carrier-protein] synthase 2 OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabF PE=1 SV=1 | 405 | 839 | 6.0E-15 |
| sp|P40804|PKSF_BACSU | Polyketide biosynthesis malonyl-ACP decarboxylase PksF OS=Bacillus subtilis (strain 168) GN=pksF PE=1 SV=3 | 496 | 793 | 1.0E-14 |
| sp|P0AAI9|FABD_ECOLI | Malonyl CoA-acyl carrier protein transacylase OS=Escherichia coli (strain K12) GN=fabD PE=1 SV=2 | 940 | 1228 | 2.0E-14 |
| 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 | 940 | 1228 | 2.0E-14 |
| sp|O85140|FABD_SALTY | Malonyl CoA-acyl carrier protein transacylase OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=fabD PE=1 SV=3 | 940 | 1228 | 3.0E-14 |
| sp|P73242|FABD_SYNY3 | Malonyl CoA-acyl carrier protein transacylase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=fabD PE=1 SV=1 | 940 | 1233 | 3.0E-14 |
| 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 | 496 | 839 | 5.0E-14 |
| sp|P04683|NODE_RHILV | Nodulation protein E OS=Rhizobium leguminosarum bv. viciae GN=nodE PE=3 SV=2 | 479 | 841 | 5.0E-14 |
| 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 | 405 | 808 | 6.0E-14 |
| sp|Q8X8I7|FABD_ECO57 | Malonyl CoA-acyl carrier protein transacylase OS=Escherichia coli O157:H7 GN=fabD PE=3 SV=3 | 940 | 1228 | 1.0E-13 |
| sp|Q6GHK5|FABD_STAAR | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MRSA252) GN=fabD PE=3 SV=1 | 940 | 1225 | 1.0E-13 |
| sp|Q6G9Y3|FABD_STAAS | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MSSA476) GN=fabD PE=3 SV=1 | 1012 | 1225 | 3.0E-13 |
| sp|Q93QD4|FABD_STAAU | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus GN=fabD PE=3 SV=1 | 1012 | 1225 | 4.0E-13 |
| sp|Q5HGK3|FABD_STAAC | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain COL) GN=fabD PE=3 SV=1 | 1012 | 1225 | 4.0E-13 |
| sp|Q7A124|FABD_STAAW | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain MW2) GN=fabD PE=3 SV=1 | 1012 | 1225 | 4.0E-13 |
| sp|Q7A5Z3|FABD_STAAN | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain N315) GN=fabD PE=1 SV=1 | 1012 | 1225 | 4.0E-13 |
| sp|Q99UN8|FABD_STAAM | Malonyl CoA-acyl carrier protein transacylase OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=fabD PE=1 SV=1 | 1012 | 1225 | 4.0E-13 |
| sp|Q89AY4|FABB_BUCBP | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) GN=fabB PE=3 SV=1 | 495 | 839 | 2.0E-11 |
| sp|O34825|PKSC_BACSU | Polyketide biosynthesis malonyl CoA-acyl carrier protein transacylase PksC OS=Bacillus subtilis (strain 168) GN=pksC PE=1 SV=1 | 939 | 1169 | 2.0E-11 |
| sp|Q02K94|FABB_PSEAB | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Pseudomonas aeruginosa (strain UCBPP-PA14) GN=fabB PE=1 SV=1 | 565 | 838 | 3.0E-11 |
| 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 | 940 | 1228 | 5.0E-11 |
| sp|A7Z4Y0|BAEE_BACMF | Polyketide biosynthesis protein BaeE OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=baeE PE=1 SV=1 | 939 | 1278 | 1.0E-10 |
| sp|P43678|KAS1_STRRM | Oxytetracycline polyketide putative beta-ketoacyl synthase 1 OS=Streptomyces rimosus PE=3 SV=2 | 407 | 797 | 1.0E-10 |
| 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 | 561 | 839 | 6.0E-10 |
| sp|P9WQD9|FAB1_MYCTU | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kasA PE=1 SV=1 | 576 | 837 | 9.0E-10 |
| sp|P9WQD8|FAB1_MYCTO | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=kasA PE=3 SV=1 | 576 | 837 | 9.0E-10 |
| 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 | 576 | 837 | 9.0E-10 |
| 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 | 576 | 837 | 9.0E-10 |
| sp|Q8K9J6|FABD_BUCAP | Malonyl CoA-acyl carrier protein transacylase OS=Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) GN=fabD PE=3 SV=1 | 940 | 1248 | 2.0E-09 |
| 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 | 939 | 1164 | 2.0E-09 |
| sp|Q9R9J2|FENF_BACIU | Malonyl CoA-acyl carrier protein transacylase OS=Bacillus subtilis GN=fenF PE=1 SV=1 | 939 | 1164 | 8.0E-09 |
| sp|Q9CBS7|FAB1_MYCLE | 3-oxoacyl-[acyl-carrier-protein] synthase 1 OS=Mycobacterium leprae (strain TN) GN=kasA PE=3 SV=1 | 576 | 837 | 8.0E-09 |
| sp|O34787|PKSE_BACSU | Polyketide biosynthesis protein PksE OS=Bacillus subtilis (strain 168) GN=pksE PE=1 SV=3 | 939 | 1224 | 3.0E-07 |
| sp|P0C842|CJ052_HUMAN | Putative uncharacterized protein encoded by LINC00614 OS=Homo sapiens GN=LINC00614 PE=5 SV=1 | 433 | 535 | 2.0E-06 |
| 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 | 997 | 1171 | 5.0E-06 |
| sp|P16539|KAS2_STRGA | Tetracenomycin C polyketide putative beta-ketoacyl synthase 2 OS=Streptomyces glaucescens GN=tcmL PE=3 SV=2 | 542 | 837 | 5.0E-06 |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 57 | 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|5821 MPMYTPITSSDSDEDSRAMKLVYFSNEFPKDDLRDLFRRLHNRSKARRHPLLAQFLSEATWAAKDEVRRLPAGLK QLVPPFQTVLSWAEDAEFRQGPLCGAVDGVLLVVAQLATYIGYAEHSAGELDDFSNTCLAGLGIGLLASTAVALS KTTAGLPLAGADAVRLAFRLGVHVKNVSENLETGEASERPDTWAYVVHDADLDTVRKELDALHKRSAAPDTAKVF VSAVSRTSVTVSGPPARLKALLARSDLFRASRSAALPVYGGLCHAPHVYGPQDTRWVVHGGGLGVLGEEHRLVAL PVYSTSTGLPYTATDAAGLLEAVVSELLTEPICWNRVVRSVVDRAEHAAAAEAVLYCFGNSAPLNDVSAGLAGRM PRLSVSVRSLIPWLQQAPAAASSAPRGPAQSKLAIVGMACRLPGGADTTDRFWEVLDKGLDVSRRVPSDRFDVDS HYDASGRQLNKSMTQYGCFIDAPGLFDAPFFNMSPREAQVVDPQMRLALVTAYEALERAGFVGDRTAASRLQRVG TFYGQAADDYREVNQGQEVSTYYIPGGCRAFGPGRINYFFKFAGPSYSIDTACSSGLAAIEVACQALWSGEVDTA VAGGVNILTNPDGFAGLCQGHFLTHGHNACKTWDATADGYCRADGIGSVVLKRLEDAEADNDRILGLILGAGTNH SAEAVSITHPHAGHQGQLSRQVLRQAGVDPLDVSYVELHGTGTKAGDREEMQGILDVYAPLAGRRHKDRPLHIGA VKANVGHGESVAGTTALIKVLLMLQNSAIPPHVGIKTEINPGFPRDFDRRNLHIPLDVTPWPRVPGRPRLAAVNN FGAAGGNTTMVLEEAPALLAAEIADPRPIHAVAVSAKTRRSLAANVERLIAHLDAYPDVSMADLSYTTTARRLHH AYRVAVAASDVTQLRKQLAIRLGGLDSVGPIGKSGPPPVAFAFTGQGASHKSMSLELYRDVPAFREHLVHLDSLA RGQGFPSFLPALDGSQPRDHAHPPVVAQLALVCAEMALAKHWSSLGVRPDIVVGHSLGEYAAMHAAGVIMANDAI SMVGRRAQLLSERCSAGSHVMMAVRASLAQIAESAGGRTYTIACVNGPSDTVLSGTTAQMDGLTAPLEAAGYRCF KLDVAFAFHSEQMDPILEDFEAAAKAGVVFQEPRLPFISPLLGKVVFDGKTLNAGYVRRATRDAVDFLAAVQSAR KMSAIGDETVWVEIGPHPVCTGFVKSAIPSTGLVVPSLRRGEDSWKTMAEAMAALHLAGIAVGWDEFHRPMESKL RLLDLPTYAWNDKNYWLQYNGDWCLTKGNTFYGAQKEATGTREALLAGGNAICTSTVQQIVDEALDGYAGTVAMQ SDLMQPDFLAAAHGHRMNNCGVVTSSIHADIAYTLGDYLHRKLRPEAGGADMNIANLVVTKGLVAQSNDRTPQVI RVTAATADIRSGLVDLTWQNVDGDGKAHEPFATASVLYGDASDWLSSWVPLAHLVRGRIEALEQLAAEGKASRFS QGMAYTLFAGNLVDYAEKYRGMQSVVLHQLEGFADVQLAGEGGGGVWTVPPHFIDSVAHLAGFIMNCSDAVDTKN NYCVTPGWSSMRFAKPLEPGARYRSYVKMIPTAEDPAVYLGDVYVLQGDTIVGLVGGIRFRRYPRILLARFFSPP DKMAAMEAGPSAGPAPNPAPKAKSAVPGPTGRDSPNGATPTDHVPSSARGGKGAVGAASAQLATGPDSTTAKAFA LIAREAGLEVSDLEDDACFSNLGIDSLLSLVIAEKFRVELDVKVGGSLFLDYPTIGDLRRWLDEYYS* |
| Coding | >Hirsu2|5821 ATGCCTATGTACACCCCTATTACAAGTTCTGATTCGGACGAGGACTCGCGCGCTATGAAGTTGGTCTACTTCAGC AACGAGTTTCCCAAGGATGACCTGAGGGACCTCTTCCGCCGCCTACACAACCGCAGCAAGGCCAGGCGCCACCCG CTCCTGGCCCAGTTCTTGAGTGAGGCCACCTGGGCGGCCAAGGACGAGGTTCGGCGGCTGCCAGCGGGGCTTAAG CAGCTGGTACCGCCATTCCAGACAGTCTTGAGCTGGGCCGAGGACGCCGAGTTTCGCCAAGGCCCCCTTTGCGGC GCAGTGGACGGAGTGCTGCTTGTCGTCGCCCAGCTGGCGACCTATATAGGGTATGCCGAACACAGTGCCGGAGAG CTGGACGACTTCTCAAACACCTGCCTTGCCGGTTTGGGCATCGGCCTGCTGGCGTCGACCGCCGTCGCGCTATCG AAGACGACGGCTGGCCTCCCCCTGGCGGGCGCGGATGCCGTCCGGCTGGCCTTCCGCTTGGGAGTCCACGTTAAG AATGTTTCGGAGAACCTCGAGACCGGCGAGGCGTCGGAGCGTCCCGACACGTGGGCCTACGTCGTCCACGATGCC GACCTCGATACCGTCCGGAAGGAGCTCGACGCCCTGCACAAGCGGTCGGCCGCGCCGGATACCGCTAAGGTCTTC GTCAGCGCCGTCAGCCGGACGTCGGTCACGGTCAGCGGGCCACCGGCTCGGCTGAAGGCGCTATTGGCCAGGTCC GACCTGTTCCGCGCGTCCAGATCCGCCGCGCTGCCTGTTTATGGCGGCCTGTGCCACGCGCCGCATGTCTACGGA CCGCAGGATACGCGCTGGGTCGTCCACGGCGGCGGGCTGGGCGTGCTCGGAGAGGAGCACCGGCTGGTGGCGTTG CCCGTCTACTCCACTAGCACCGGCCTGCCGTATACGGCCACGGACGCGGCGGGGCTGCTCGAGGCCGTCGTCTCG GAGCTCCTCACCGAGCCCATTTGCTGGAACCGCGTCGTGCGCAGCGTGGTCGACCGGGCCGAGCATGCAGCCGCC GCGGAGGCGGTGCTGTACTGCTTCGGCAACTCGGCCCCGCTCAACGACGTTAGCGCGGGGCTCGCGGGCCGCATG CCCCGCCTCTCCGTCTCCGTCCGTAGTCTCATCCCGTGGCTCCAGCAGGCGCCGGCGGCGGCGAGCTCGGCGCCC CGCGGCCCGGCCCAGTCCAAGCTCGCCATCGTCGGCATGGCCTGCCGACTCCCGGGCGGCGCGGACACGACGGAC CGGTTCTGGGAGGTCCTGGACAAGGGTCTGGATGTGTCGCGGCGCGTGCCGTCGGACCGGTTCGACGTCGACTCG CACTACGATGCGTCCGGGCGGCAGCTGAACAAGAGCATGACGCAATATGGCTGTTTCATCGATGCGCCCGGCCTG TTCGACGCGCCATTCTTCAACATGTCGCCGCGCGAGGCTCAGGTCGTCGACCCGCAGATGCGCCTGGCCCTCGTC ACGGCCTACGAGGCGCTAGAACGAGCGGGCTTCGTCGGCGACCGCACGGCCGCCTCGCGACTGCAGCGCGTTGGC ACCTTCTACGGCCAGGCGGCCGACGACTATCGCGAGGTCAACCAGGGCCAGGAGGTCAGCACCTACTACATCCCA GGCGGATGCCGGGCCTTTGGGCCGGGCCGCATCAACTACTTCTTCAAGTTCGCCGGCCCCAGCTATAGCATTGAT ACCGCCTGCTCGTCCGGGCTGGCGGCGATTGAGGTCGCCTGCCAAGCCCTCTGGAGCGGCGAGGTCGACACGGCC GTGGCCGGCGGCGTCAACATACTGACCAACCCGGACGGCTTCGCTGGCCTCTGCCAGGGCCACTTCCTCACGCAC GGCCATAATGCATGCAAGACGTGGGACGCCACGGCCGACGGGTACTGCCGGGCTGACGGCATCGGGTCCGTGGTG CTAAAGCGGCTCGAGGACGCCGAGGCCGATAACGACCGCATCCTCGGCCTCATCCTCGGGGCCGGCACCAACCAC TCGGCCGAGGCCGTGTCCATCACGCATCCCCACGCCGGCCACCAGGGCCAGCTTTCGCGCCAGGTGCTGCGCCAG GCCGGCGTCGACCCGCTCGACGTCTCGTACGTCGAGCTCCACGGCACCGGCACCAAGGCCGGCGACCGCGAGGAG ATGCAGGGCATCCTGGACGTCTACGCCCCGCTGGCCGGCCGTCGCCACAAGGACCGGCCGCTGCATATCGGCGCC GTCAAGGCCAACGTCGGCCACGGCGAGTCCGTTGCCGGCACAACCGCTCTCATCAAGGTGCTCTTAATGCTCCAG AACAGCGCCATCCCGCCCCACGTCGGCATCAAGACCGAGATCAACCCCGGCTTCCCCCGCGACTTCGACCGGCGC AACCTCCACATCCCGCTGGACGTGACGCCCTGGCCCCGAGTGCCCGGCCGCCCGCGGCTCGCGGCCGTTAACAAC TTCGGTGCGGCCGGCGGCAACACGACCATGGTCCTAGAGGAGGCCCCGGCCCTCCTCGCCGCCGAGATCGCCGAC CCGCGACCTATCCACGCCGTCGCTGTCTCGGCCAAGACGCGGCGGTCGCTGGCTGCCAACGTGGAACGCCTGATC GCCCACCTCGACGCCTATCCGGACGTCAGCATGGCTGACCTCTCATACACAACGACGGCCCGCCGCCTTCACCAC GCTTACCGCGTGGCCGTCGCCGCCTCGGACGTGACCCAGCTCCGGAAGCAGCTGGCAATCCGGCTGGGCGGGCTG GACTCAGTTGGGCCCATCGGCAAGTCGGGCCCGCCGCCGGTCGCCTTCGCCTTCACCGGCCAAGGCGCCTCGCAC AAGTCGATGAGCCTGGAGCTGTACCGCGACGTGCCGGCGTTCCGCGAGCACCTCGTGCATCTCGATTCGCTCGCC CGCGGCCAGGGCTTCCCGTCCTTCTTACCCGCCCTCGACGGGTCACAGCCGCGGGACCACGCGCACCCGCCCGTC GTCGCCCAGCTGGCCTTAGTGTGCGCCGAGATGGCCTTGGCCAAGCACTGGTCCTCGCTCGGGGTCCGGCCCGAC ATCGTCGTTGGCCACAGCCTAGGCGAGTACGCGGCGATGCACGCGGCTGGCGTCATCATGGCCAACGACGCCATC TCTATGGTCGGCCGCAGAGCCCAGCTGCTATCAGAGCGGTGCTCGGCCGGCAGTCACGTTATGATGGCCGTCCGG GCCTCGCTGGCGCAGATCGCCGAGAGCGCCGGCGGCCGCACGTATACCATCGCCTGCGTCAACGGGCCTTCGGAC ACGGTGCTCAGCGGCACCACGGCGCAGATGGACGGCCTGACTGCGCCGCTCGAGGCAGCCGGCTACCGCTGCTTC AAGCTAGACGTCGCCTTCGCCTTTCACTCGGAACAGATGGACCCCATCCTGGAAGACTTTGAGGCCGCGGCCAAG GCCGGCGTCGTCTTTCAGGAGCCCAGGCTGCCCTTCATCTCGCCGCTGCTGGGCAAGGTCGTATTCGACGGCAAG ACGCTCAACGCCGGATACGTGCGCCGGGCCACCCGCGACGCCGTCGACTTCCTGGCGGCCGTGCAAAGCGCTCGG AAGATGTCCGCCATCGGCGACGAGACGGTCTGGGTCGAGATCGGGCCGCATCCCGTGTGCACGGGCTTCGTCAAG TCCGCCATTCCGTCCACCGGGTTGGTCGTCCCGTCCCTCCGCCGCGGCGAAGACAGCTGGAAGACCATGGCCGAG GCCATGGCCGCCCTGCACCTCGCCGGCATTGCTGTCGGCTGGGACGAGTTCCACCGGCCGATGGAGAGCAAGCTG CGTCTCCTTGACTTGCCGACGTATGCCTGGAACGACAAGAATTACTGGCTGCAGTACAACGGCGACTGGTGCCTT ACAAAGGGCAACACCTTCTACGGAGCCCAAAAGGAGGCCACAGGGACTCGGGAAGCGCTACTTGCCGGCGGCAAC GCTATCTGTACGTCTACCGTGCAGCAAATTGTCGACGAGGCCTTGGATGGATATGCCGGCACCGTTGCCATGCAG TCCGACCTCATGCAGCCGGACTTCCTCGCCGCCGCCCATGGGCACCGTATGAACAACTGTGGCGTCGTCACGTCG TCCATCCACGCCGACATCGCTTACACCCTCGGCGACTATCTCCATCGCAAGCTGCGCCCCGAAGCCGGGGGCGCG GACATGAATATCGCAAACCTGGTTGTCACCAAGGGTCTCGTGGCCCAGAGCAACGACCGGACGCCCCAGGTGATC CGCGTCACGGCCGCCACGGCCGACATACGCTCCGGCTTAGTCGACCTGACGTGGCAGAATGTGGACGGCGACGGC AAGGCCCACGAGCCTTTTGCCACCGCCAGCGTCCTCTATGGCGACGCGTCCGATTGGCTCTCCTCCTGGGTGCCG CTGGCCCATCTCGTGCGCGGCCGCATCGAGGCGCTTGAGCAGCTGGCCGCCGAGGGCAAGGCCAGCCGCTTCTCG CAGGGCATGGCGTATACGCTCTTCGCTGGAAACCTGGTAGACTATGCAGAGAAGTACCGAGGAATGCAGTCCGTT GTGCTGCACCAGCTCGAGGGCTTCGCCGATGTGCAGCTCGCCGGCGAGGGGGGCGGTGGCGTCTGGACCGTCCCG CCACACTTTATCGACAGCGTCGCCCACCTGGCCGGCTTCATCATGAACTGTTCCGACGCCGTCGACACCAAGAAT AACTACTGCGTCACGCCGGGCTGGAGCTCCATGCGGTTCGCCAAGCCCCTCGAGCCGGGGGCCAGGTATCGATCG TACGTCAAGATGATCCCCACGGCCGAGGACCCGGCCGTCTACCTGGGCGACGTGTACGTCCTGCAGGGCGACACT ATCGTCGGCCTGGTCGGCGGCATCCGGTTCCGCCGCTACCCGCGCATCCTGCTCGCCCGCTTCTTCTCGCCGCCG GACAAGATGGCTGCTATGGAAGCCGGGCCGAGTGCCGGTCCCGCACCGAACCCCGCACCGAAGGCCAAGTCGGCA GTCCCCGGCCCCACTGGCCGGGACAGCCCGAACGGGGCCACCCCCACAGACCATGTTCCCTCTTCGGCACGAGGC GGCAAGGGTGCCGTCGGCGCGGCATCCGCCCAACTGGCGACCGGCCCCGACAGCACGACAGCCAAGGCATTCGCG CTCATTGCCAGGGAGGCCGGCCTGGAGGTTTCCGACCTTGAGGACGACGCCTGCTTCTCTAACCTGGGCATCGAC AGCCTGCTGTCACTGGTGATTGCGGAGAAGTTCCGGGTGGAGCTGGACGTCAAGGTTGGCGGCAGCCTCTTCCTG GACTATCCGACAATCGGGGACTTGCGGAGGTGGCTGGACGAGTATTACAGCTAG |
| Transcript | >Hirsu2|5821 ATGCCTATGTACACCCCTATTACAAGTTCTGATTCGGACGAGGACTCGCGCGCTATGAAGTTGGTCTACTTCAGC AACGAGTTTCCCAAGGATGACCTGAGGGACCTCTTCCGCCGCCTACACAACCGCAGCAAGGCCAGGCGCCACCCG CTCCTGGCCCAGTTCTTGAGTGAGGCCACCTGGGCGGCCAAGGACGAGGTTCGGCGGCTGCCAGCGGGGCTTAAG CAGCTGGTACCGCCATTCCAGACAGTCTTGAGCTGGGCCGAGGACGCCGAGTTTCGCCAAGGCCCCCTTTGCGGC GCAGTGGACGGAGTGCTGCTTGTCGTCGCCCAGCTGGCGACCTATATAGGGTATGCCGAACACAGTGCCGGAGAG CTGGACGACTTCTCAAACACCTGCCTTGCCGGTTTGGGCATCGGCCTGCTGGCGTCGACCGCCGTCGCGCTATCG AAGACGACGGCTGGCCTCCCCCTGGCGGGCGCGGATGCCGTCCGGCTGGCCTTCCGCTTGGGAGTCCACGTTAAG AATGTTTCGGAGAACCTCGAGACCGGCGAGGCGTCGGAGCGTCCCGACACGTGGGCCTACGTCGTCCACGATGCC GACCTCGATACCGTCCGGAAGGAGCTCGACGCCCTGCACAAGCGGTCGGCCGCGCCGGATACCGCTAAGGTCTTC GTCAGCGCCGTCAGCCGGACGTCGGTCACGGTCAGCGGGCCACCGGCTCGGCTGAAGGCGCTATTGGCCAGGTCC GACCTGTTCCGCGCGTCCAGATCCGCCGCGCTGCCTGTTTATGGCGGCCTGTGCCACGCGCCGCATGTCTACGGA CCGCAGGATACGCGCTGGGTCGTCCACGGCGGCGGGCTGGGCGTGCTCGGAGAGGAGCACCGGCTGGTGGCGTTG CCCGTCTACTCCACTAGCACCGGCCTGCCGTATACGGCCACGGACGCGGCGGGGCTGCTCGAGGCCGTCGTCTCG GAGCTCCTCACCGAGCCCATTTGCTGGAACCGCGTCGTGCGCAGCGTGGTCGACCGGGCCGAGCATGCAGCCGCC GCGGAGGCGGTGCTGTACTGCTTCGGCAACTCGGCCCCGCTCAACGACGTTAGCGCGGGGCTCGCGGGCCGCATG CCCCGCCTCTCCGTCTCCGTCCGTAGTCTCATCCCGTGGCTCCAGCAGGCGCCGGCGGCGGCGAGCTCGGCGCCC CGCGGCCCGGCCCAGTCCAAGCTCGCCATCGTCGGCATGGCCTGCCGACTCCCGGGCGGCGCGGACACGACGGAC CGGTTCTGGGAGGTCCTGGACAAGGGTCTGGATGTGTCGCGGCGCGTGCCGTCGGACCGGTTCGACGTCGACTCG CACTACGATGCGTCCGGGCGGCAGCTGAACAAGAGCATGACGCAATATGGCTGTTTCATCGATGCGCCCGGCCTG TTCGACGCGCCATTCTTCAACATGTCGCCGCGCGAGGCTCAGGTCGTCGACCCGCAGATGCGCCTGGCCCTCGTC ACGGCCTACGAGGCGCTAGAACGAGCGGGCTTCGTCGGCGACCGCACGGCCGCCTCGCGACTGCAGCGCGTTGGC ACCTTCTACGGCCAGGCGGCCGACGACTATCGCGAGGTCAACCAGGGCCAGGAGGTCAGCACCTACTACATCCCA GGCGGATGCCGGGCCTTTGGGCCGGGCCGCATCAACTACTTCTTCAAGTTCGCCGGCCCCAGCTATAGCATTGAT ACCGCCTGCTCGTCCGGGCTGGCGGCGATTGAGGTCGCCTGCCAAGCCCTCTGGAGCGGCGAGGTCGACACGGCC GTGGCCGGCGGCGTCAACATACTGACCAACCCGGACGGCTTCGCTGGCCTCTGCCAGGGCCACTTCCTCACGCAC GGCCATAATGCATGCAAGACGTGGGACGCCACGGCCGACGGGTACTGCCGGGCTGACGGCATCGGGTCCGTGGTG CTAAAGCGGCTCGAGGACGCCGAGGCCGATAACGACCGCATCCTCGGCCTCATCCTCGGGGCCGGCACCAACCAC TCGGCCGAGGCCGTGTCCATCACGCATCCCCACGCCGGCCACCAGGGCCAGCTTTCGCGCCAGGTGCTGCGCCAG GCCGGCGTCGACCCGCTCGACGTCTCGTACGTCGAGCTCCACGGCACCGGCACCAAGGCCGGCGACCGCGAGGAG ATGCAGGGCATCCTGGACGTCTACGCCCCGCTGGCCGGCCGTCGCCACAAGGACCGGCCGCTGCATATCGGCGCC GTCAAGGCCAACGTCGGCCACGGCGAGTCCGTTGCCGGCACAACCGCTCTCATCAAGGTGCTCTTAATGCTCCAG AACAGCGCCATCCCGCCCCACGTCGGCATCAAGACCGAGATCAACCCCGGCTTCCCCCGCGACTTCGACCGGCGC AACCTCCACATCCCGCTGGACGTGACGCCCTGGCCCCGAGTGCCCGGCCGCCCGCGGCTCGCGGCCGTTAACAAC TTCGGTGCGGCCGGCGGCAACACGACCATGGTCCTAGAGGAGGCCCCGGCCCTCCTCGCCGCCGAGATCGCCGAC CCGCGACCTATCCACGCCGTCGCTGTCTCGGCCAAGACGCGGCGGTCGCTGGCTGCCAACGTGGAACGCCTGATC GCCCACCTCGACGCCTATCCGGACGTCAGCATGGCTGACCTCTCATACACAACGACGGCCCGCCGCCTTCACCAC GCTTACCGCGTGGCCGTCGCCGCCTCGGACGTGACCCAGCTCCGGAAGCAGCTGGCAATCCGGCTGGGCGGGCTG GACTCAGTTGGGCCCATCGGCAAGTCGGGCCCGCCGCCGGTCGCCTTCGCCTTCACCGGCCAAGGCGCCTCGCAC AAGTCGATGAGCCTGGAGCTGTACCGCGACGTGCCGGCGTTCCGCGAGCACCTCGTGCATCTCGATTCGCTCGCC CGCGGCCAGGGCTTCCCGTCCTTCTTACCCGCCCTCGACGGGTCACAGCCGCGGGACCACGCGCACCCGCCCGTC GTCGCCCAGCTGGCCTTAGTGTGCGCCGAGATGGCCTTGGCCAAGCACTGGTCCTCGCTCGGGGTCCGGCCCGAC ATCGTCGTTGGCCACAGCCTAGGCGAGTACGCGGCGATGCACGCGGCTGGCGTCATCATGGCCAACGACGCCATC TCTATGGTCGGCCGCAGAGCCCAGCTGCTATCAGAGCGGTGCTCGGCCGGCAGTCACGTTATGATGGCCGTCCGG GCCTCGCTGGCGCAGATCGCCGAGAGCGCCGGCGGCCGCACGTATACCATCGCCTGCGTCAACGGGCCTTCGGAC ACGGTGCTCAGCGGCACCACGGCGCAGATGGACGGCCTGACTGCGCCGCTCGAGGCAGCCGGCTACCGCTGCTTC AAGCTAGACGTCGCCTTCGCCTTTCACTCGGAACAGATGGACCCCATCCTGGAAGACTTTGAGGCCGCGGCCAAG GCCGGCGTCGTCTTTCAGGAGCCCAGGCTGCCCTTCATCTCGCCGCTGCTGGGCAAGGTCGTATTCGACGGCAAG ACGCTCAACGCCGGATACGTGCGCCGGGCCACCCGCGACGCCGTCGACTTCCTGGCGGCCGTGCAAAGCGCTCGG AAGATGTCCGCCATCGGCGACGAGACGGTCTGGGTCGAGATCGGGCCGCATCCCGTGTGCACGGGCTTCGTCAAG TCCGCCATTCCGTCCACCGGGTTGGTCGTCCCGTCCCTCCGCCGCGGCGAAGACAGCTGGAAGACCATGGCCGAG GCCATGGCCGCCCTGCACCTCGCCGGCATTGCTGTCGGCTGGGACGAGTTCCACCGGCCGATGGAGAGCAAGCTG CGTCTCCTTGACTTGCCGACGTATGCCTGGAACGACAAGAATTACTGGCTGCAGTACAACGGCGACTGGTGCCTT ACAAAGGGCAACACCTTCTACGGAGCCCAAAAGGAGGCCACAGGGACTCGGGAAGCGCTACTTGCCGGCGGCAAC GCTATCTGTACGTCTACCGTGCAGCAAATTGTCGACGAGGCCTTGGATGGATATGCCGGCACCGTTGCCATGCAG TCCGACCTCATGCAGCCGGACTTCCTCGCCGCCGCCCATGGGCACCGTATGAACAACTGTGGCGTCGTCACGTCG TCCATCCACGCCGACATCGCTTACACCCTCGGCGACTATCTCCATCGCAAGCTGCGCCCCGAAGCCGGGGGCGCG GACATGAATATCGCAAACCTGGTTGTCACCAAGGGTCTCGTGGCCCAGAGCAACGACCGGACGCCCCAGGTGATC CGCGTCACGGCCGCCACGGCCGACATACGCTCCGGCTTAGTCGACCTGACGTGGCAGAATGTGGACGGCGACGGC AAGGCCCACGAGCCTTTTGCCACCGCCAGCGTCCTCTATGGCGACGCGTCCGATTGGCTCTCCTCCTGGGTGCCG CTGGCCCATCTCGTGCGCGGCCGCATCGAGGCGCTTGAGCAGCTGGCCGCCGAGGGCAAGGCCAGCCGCTTCTCG CAGGGCATGGCGTATACGCTCTTCGCTGGAAACCTGGTAGACTATGCAGAGAAGTACCGAGGAATGCAGTCCGTT GTGCTGCACCAGCTCGAGGGCTTCGCCGATGTGCAGCTCGCCGGCGAGGGGGGCGGTGGCGTCTGGACCGTCCCG CCACACTTTATCGACAGCGTCGCCCACCTGGCCGGCTTCATCATGAACTGTTCCGACGCCGTCGACACCAAGAAT AACTACTGCGTCACGCCGGGCTGGAGCTCCATGCGGTTCGCCAAGCCCCTCGAGCCGGGGGCCAGGTATCGATCG TACGTCAAGATGATCCCCACGGCCGAGGACCCGGCCGTCTACCTGGGCGACGTGTACGTCCTGCAGGGCGACACT ATCGTCGGCCTGGTCGGCGGCATCCGGTTCCGCCGCTACCCGCGCATCCTGCTCGCCCGCTTCTTCTCGCCGCCG GACAAGATGGCTGCTATGGAAGCCGGGCCGAGTGCCGGTCCCGCACCGAACCCCGCACCGAAGGCCAAGTCGGCA GTCCCCGGCCCCACTGGCCGGGACAGCCCGAACGGGGCCACCCCCACAGACCATGTTCCCTCTTCGGCACGAGGC GGCAAGGGTGCCGTCGGCGCGGCATCCGCCCAACTGGCGACCGGCCCCGACAGCACGACAGCCAAGGCATTCGCG CTCATTGCCAGGGAGGCCGGCCTGGAGGTTTCCGACCTTGAGGACGACGCCTGCTTCTCTAACCTGGGCATCGAC AGCCTGCTGTCACTGGTGATTGCGGAGAAGTTCCGGGTGGAGCTGGACGTCAAGGTTGGCGGCAGCCTCTTCCTG GACTATCCGACAATCGGGGACTTGCGGAGGTGGCTGGACGAGTATTACAGCTAG |
| Gene | >Hirsu2|5821 ATGCCTATGTACACCCCTATTACAAGTTCTGATTCGGACGAGGACTCGCGCGCTATGAAGTTGGTCTACTTCAGC AACGAGTTTCCCAAGGATGACCTGAGGGACCTCTTCCGCCGCCTACACAACCGCAGCAAGGCCAGGCGCCACCCG CTCCTGGCCCAGTTCTTGAGTGAGGCCACCTGGGCGGCCAAGGACGAGGTTCGGCGGCTGCCAGCGGGGCTTAAG CAGCTGGTACCGCCATTCCAGACAGTCTTGAGCTGGGCCGAGGACGCCGAGTTTCGCCAAGGCCCCCTTTGCGGC GCAGTGGACGGAGTGCTGCTTGTCGTCGCCCAGCTGGCGACCTATATAGGGTGAGCGTTCTGCCTCAGTCGGAAA TTGGGTTTTGAGAGGACGAGCGCTGACCTGGGCCGGTAGGTATGCCGAACACAGTGCCGGAGAGCTGGACGACTT CTCAAACACCTGCCTTGCCGGTTTGGGCATCGGCCTGCTGGCGTCGACCGCCGTCGCGCTATCGAAGACGACGGC TGGCCTCCCCCTGGCGGGCGCGGATGCCGTCCGGCTGGCCTTCCGCTTGGGAGTCCACGTTAAGAATGTTTCGGA GAACCTCGAGACCGGCGAGGCGTCGGAGCGTCCCGACACGTGGGCCTACGTCGTCCACGATGCCGACCTCGATAC CGTCCGGAAGGAGCTCGACGCCCTGCACAAGCGGTCGGCCGCGCCGGATACCGCTAAGGTCTTCGTCAGCGCCGT CAGCCGGACGTCGGTCACGGTCAGCGGGCCACCGGCTCGGCTGAAGGCGCTATTGGCCAGGTCCGACCTGTTCCG CGCGTCCAGATCCGCCGCGCTGCCTGTTTATGGCGGCCTGTGCCACGCGCCGCATGTCTACGGACCGCAGGATAC GCGCTGGGTCGTCCACGGCGGCGGGCTGGGCGTGCTCGGAGAGGAGCACCGGCTGGTGGCGTTGCCCGTCTACTC CACTAGCACCGGCCTGCCGTATACGGCCACGGACGCGGCGGGGCTGCTCGAGGCCGTCGTCTCGGAGCTCCTCAC CGAGCCCATTTGCTGGAACCGCGTCGTGCGCAGCGTGGTCGACCGGGCCGAGCATGCAGCCGCCGCGGAGGCGGT GCTGTACTGCTTCGGCAACTCGGCCCCGCTCAACGACGTTAGCGCGGGGCTCGCGGGCCGCATGCCCCGCCTCTC CGTCTCCGTCCGTAGTCTCATCCCGTGGCTCCAGCAGGCGCCGGCGGCGGCGAGCTCGGCGCCCCGCGGCCCGGC CCAGTCCAAGCTCGCCATCGTCGGCATGGCCTGCCGACTCCCGGGCGGCGCGGACACGACGGACCGGTTCTGGGA GGTCCTGGACAAGGGTCTGGATGTGTCGCGGCGCGTGCCGTCGGACCGGTTCGACGTCGACTCGCACTACGATGC GTCCGGGCGGCAGCTGAACAAGAGCATGACGCAATATGGCTGTTTCATCGATGCGCCCGGCCTGTTCGACGCGCC ATTCTTCAACATGTCGCCGCGCGAGGCTCAGGTCGTCGACCCGCAGATGCGCCTGGCCCTCGTCACGGCCTACGA GGCGCTAGAACGAGCGGGCTTCGTCGGCGACCGCACGGCCGCCTCGCGACTGCAGCGCGTTGGCACCTTCTACGG CCAGGCGGCCGACGACTATCGCGAGGTCAACCAGGGCCAGGAGGTCAGCACCTACTACATCCCAGGCGGATGCCG GGCCTTTGGGCCGGGCCGCATCAACTACTTCTTCAAGTTCGCCGGCCCCAGCTATAGCATTGATACCGCCTGCTC GTCCGGGCTGGCGGCGATTGAGGTAGGCATTAGACGGCCGCTGAGAGCCGTGCTCGTACCATCGTGACGCCGGCT GACCTCCCCTTGCCCCAGGTCGCCTGCCAAGCCCTCTGGAGCGGCGAGGTCGACACGGCCGTGGCCGGCGGCGTC AACATACTGACCAACCCGGACGGCTTCGCTGGCCTCTGCCAGGGCCACTTCCTCACGCACGGCCATAATGCATGC AAGACGTGGGACGCCACGGCCGACGGGTACTGCCGGGCTGACGGCATCGGGTCCGTGGTGCTAAAGCGGCTCGAG GACGCCGAGGCCGATAACGACCGCATCCTCGGCCTCATCCTCGGGGCCGGCACCAACCACTCGGCCGAGGCCGTG TCCATCACGCATCCCCACGCCGGCCACCAGGGCCAGCTTTCGCGCCAGGTGCTGCGCCAGGCCGGCGTCGACCCG CTCGACGTCTCGTACGTCGAGCTCCACGGCACCGGCACCAAGGCCGGCGACCGCGAGGAGATGCAGGGCATCCTG GACGTCTACGCCCCGCTGGCCGGCCGTCGCCACAAGGACCGGCCGCTGCATATCGGCGCCGTCAAGGCCAACGTC GGCCACGGCGAGTCCGTTGCCGGCACAACCGCTCTCATCAAGGTGCTCTTAATGCTCCAGAACAGCGCCATCCCG CCCCACGTCGGCATCAAGACCGAGATCAACCCCGGCTTCCCCCGCGACTTCGACCGGCGCAACCTCCACATCCCG CTGGACGTGACGCCCTGGCCCCGAGTGCCCGGCCGCCCGCGGCTCGCGGCCGTTAACAACTTCGGTGCGGCCGGC GGCAACACGACCATGGTCCTAGAGGAGGCCCCGGCCCTCCTCGCCGCCGAGATCGCCGACCCGCGACCTATCCAC GCCGTCGCTGTCTCGGCCAAGACGCGGCGGTCGCTGGCTGCCAACGTGGAACGCCTGATCGCCCACCTCGACGCC TATCCGGACGTCAGCATGGCTGACCTCTCATACACAACGACGGCCCGCCGCCTTCACCACGCTTACCGCGTGGCC GTCGCCGCCTCGGACGTGACCCAGCTCCGGAAGCAGCTGGCAATCCGGCTGGGCGGGCTGGACTCAGTTGGGCCC ATCGGCAAGTCGGGCCCGCCGCCGGTCGCCTTCGCCTTCACCGGCCAAGGCGCCTCGCACAAGTCGATGAGCCTG GAGCTGTACCGCGACGTGCCGGCGTTCCGCGAGCACCTCGTGCATCTCGATTCGCTCGCCCGCGGCCAGGGCTTC CCGTCCTTCTTACCCGCCCTCGACGGGTCACAGCCGCGGGACCACGCGCACCCGCCCGTCGTCGCCCAGCTGGCC TTAGTGTGCGCCGAGATGGCCTTGGCCAAGCACTGGTCCTCGCTCGGGGTCCGGCCCGACATCGTCGTTGGCCAC AGCCTAGGCGAGTACGCGGCGATGCACGCGGCTGGCGTCATCATGGCCAACGACGCCATCTCTATGGTCGGCCGC AGAGCCCAGCTGCTATCAGAGCGGTGCTCGGCCGGCAGTCACGTTATGATGGCCGTCCGGGCCTCGCTGGCGCAG ATCGCCGAGAGCGCCGGCGGCCGCACGTATACCATCGCCTGCGTCAACGGGCCTTCGGACACGGTGCTCAGCGGC ACCACGGCGCAGATGGACGGCCTGACTGCGCCGCTCGAGGCAGCCGGCTACCGCTGCTTCAAGCTAGACGTCGCC TTCGCCTTTCACTCGGAACAGATGGACCCCATCCTGGAAGACTTTGAGGCCGCGGCCAAGGCCGGCGTCGTCTTT CAGGAGCCCAGGCTGCCCTTCATCTCGCCGCTGCTGGGCAAGGTCGTATTCGACGGCAAGACGCTCAACGCCGGA TACGTGCGCCGGGCCACCCGCGACGCCGTCGACTTCCTGGCGGCCGTGCAAAGCGCTCGGAAGATGTCCGCCATC GGCGACGAGACGGTCTGGGTCGAGATCGGGCCGCATCCCGTGTGCACGGGCTTCGTCAAGTCCGCCATTCCGTCC ACCGGGTTGGTCGTCCCGTCCCTCCGCCGCGGCGAAGACAGCTGGAAGACCATGGCCGAGGCCATGGCCGCCCTG CACCTCGCCGGCATTGCTGTCGGCTGGGACGAGTTCCACCGGCCGATGGAGAGCAAGCTGCGTCTCCTTGACTTG CCGACGTATGCCTGGAACGACAAGAATTACTGGCTGCAGTACAACGGCGACTGGTGCCTTACAAAGGGCAACACC TTCTACGGAGCCCAAAAGGAGGCCACAGGGACTCGGGAAGCGCTACTTGCCGGCGGCAACGCTATCTGTACGTCT ACCGTGCAGCAAATTGTCGACGAGGCCTTGGATGGATATGCCGGCACCGTTGCCATGCAGTCCGACCTCATGCAG CCGGACTTCCTCGCCGCCGCCCATGGGCACCGTATGAACAACTGTGGCGTCGTCACGTCGGTAAGTCCAGATCCG TCTCCCCTTTCCTCCCGACAGCTGCGTTGTCGATTCTCGACGGTATGCTCACCACCGAGCGGTGCAGTCCATCCA CGCCGACATCGCTTACACCCTCGGCGACTATCTCCATCGCAAGCTGCGCCCCGAAGCCGGGGGCGCGGACATGAA TATCGCAAACCTGGTTGTCACCAAGGGTCTCGTGGCCCAGAGCAACGACCGGACGCCCCAGGTGATCCGCGTCAC GGCCGCCACGGCCGACATACGCTCCGGCTTAGTCGACCTGACGTGGCAGAATGTGGACGGCGACGGCAAGGCCCA CGAGCCTTTTGCCACCGCCAGCGTCCTCTATGGCGACGCGTCCGATTGGCTCTCCTCCTGGGTGCCGCTGGCCCA TCTCGTGCGCGGCCGCATCGAGGCGCTTGAGCAGCTGGCCGCCGAGGGCAAGGCCAGCCGCTTCTCGCAGGGCAT GGCGTATACGCTCTTCGCTGGAAACCTGGTAGACTATGCAGAGAAGTACCGAGGAATGCAGTCCGTTGTGCTGCA CCAGCTCGAGGGCTTCGCCGATGTGCAGCTCGCCGGCGAGGGGGGCGGTGGCGTCTGGACCGTCCCGCCACACTT TATCGACAGCGTCGCCCACCTGGCCGGCTTCATCATGAACTGTTCCGACGCCGTCGACACCAAGAATAACTACTG CGTCACGCCGGGCTGGAGCTCCATGCGGTTCGCCAAGCCCCTCGAGCCGGGGGCCAGGTATCGATCGTACGTCAA GATGATCCCCACGGCCGAGGACCCGGCCGTCTACCTGGGCGACGTGTACGTCCTGCAGGGCGACACTATCGTCGG CCTGGTCGGCGGCATCCGGTTCCGCCGCTACCCGCGCATCCTGCTCGCCCGCTTCTTCTCGCCGCCGGACAAGAT GGCTGCTATGGAAGCCGGGCCGAGTGCCGGTCCCGCACCGAACCCCGCACCGAAGGCCAAGTCGGCAGTCCCCGG CCCCACTGGCCGGGACAGCCCGAACGGGGCCACCCCCACAGACCATGTTCCCTCTTCGGCACGAGGCGGCAAGGG TGCCGTCGGCGCGGCATCCGCCCAACTGGCGACCGGCCCCGACAGCACGACAGCCAAGGCATTCGCGCTCATTGC CAGGGAGGCCGGCCTGGAGGTTTCCGACCTTGAGGACGACGCCTGCTTCTCTAACCTGGGCATCGACAGCCTGCT GTCACTGGTGATTGCGGAGAAGTTCCGGGTGGAGCTGGACGTCAAGGTTGGCGGCAGCCTCTTCCTGGACTATCC GACAATCGGGGACTTGCGGAGGTGGCTGGACGAGTATTACAGCTAG |