Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|7364
Gene name
LocationContig_424:4270..9060
Strand+
Gene length (bp)4790
Transcript length (bp)4521
Coding sequence length (bp)4521
Protein length (aa) 1507

Overview

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PFAM Domains

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 hits

[Show all]
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
[Show all]
[Show less]
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
[Show less]

GO

(None)

Deeploc

[Help with interpreting the results of Deeploc 2.0]
Localizations Signals Cytoplasm Nucleus Extracellular Cell membrane Mitochondrion Plastid Endoplasmic reticulum Lysosome vacuole Golgi apparatus Peroxisome
Cytoplasm 0.637 0.3307 0.086 0.1111 0.1313 0.005 0.1196 0.0946 0.0673 0.0045

SignalP

(None)

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

Gene cluster ID Type of secondary metabolism gene
Cluster 34 PKS

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup78
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|4899
Ophiocordyceps australis map64 (Brazil) OphauB2|5634
Ophiocordyceps kimflemingae Ophio5|8256
Ophiocordyceps subramaniannii Hirsu2|9925
Ophiocordyceps subramaniannii Hirsu2|9186
Ophiocordyceps subramaniannii Hirsu2|8479
Ophiocordyceps subramaniannii Hirsu2|7364 (this protein)
Ophiocordyceps subramaniannii Hirsu2|6703
Ophiocordyceps subramaniannii Hirsu2|6204
Ophiocordyceps subramaniannii Hirsu2|11185
Ophiocordyceps subramaniannii Hirsu2|4298
Ophiocordyceps subramaniannii Hirsu2|3326
Ophiocordyceps subramaniannii Hirsu2|3276
Ophiocordyceps subramaniannii Hirsu2|3122
Ophiocordyceps subramaniannii Hirsu2|24
Ophiocordyceps subramaniannii Hirsu2|1531
Ophiocordyceps subramaniannii Hirsu2|5152
Ophiocordyceps subramaniannii Hirsu2|5593

Sequences

Type of sequenceSequence
Locus Download genbank file of locus Download genbank file of locus (reverse complement)
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded.
Protein >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

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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