Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|3355
Gene name
LocationContig_187:7125..8917
Strand-
Gene length (bp)1792
Transcript length (bp)1704
Coding sequence length (bp)1704
Protein length (aa) 568

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF07731 Cu-oxidase_2 Multicopper oxidase 1.3E-38 410 531
PF07732 Cu-oxidase_3 Multicopper oxidase 3.5E-36 76 192
PF00394 Cu-oxidase Multicopper oxidase 1.3E-30 203 346

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|Q96WM9|LAC2_BOTFU Laccase-2 OS=Botryotinia fuckeliana GN=lcc2 PE=2 SV=1 14 567 9.0E-160
sp|Q12570|LAC1_BOTFU Laccase-1 OS=Botryotinia fuckeliana GN=lcc1 PE=2 SV=3 13 567 4.0E-155
sp|P06811|LAC1_NEUCR Laccase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=lacc PE=1 SV=3 7 567 1.0E-125
sp|Q70KY3|LAC1_MELAO Laccase-1 OS=Melanocarpus albomyces GN=LAC1 PE=1 SV=1 7 567 1.0E-123
sp|Q96UM2|LAC3_BOTFU Laccase-3 (Fragment) OS=Botryotinia fuckeliana GN=lcc3 PE=3 SV=1 98 528 5.0E-123
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|Q96WM9|LAC2_BOTFU Laccase-2 OS=Botryotinia fuckeliana GN=lcc2 PE=2 SV=1 14 567 9.0E-160
sp|Q12570|LAC1_BOTFU Laccase-1 OS=Botryotinia fuckeliana GN=lcc1 PE=2 SV=3 13 567 4.0E-155
sp|P06811|LAC1_NEUCR Laccase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=lacc PE=1 SV=3 7 567 1.0E-125
sp|Q70KY3|LAC1_MELAO Laccase-1 OS=Melanocarpus albomyces GN=LAC1 PE=1 SV=1 7 567 1.0E-123
sp|Q96UM2|LAC3_BOTFU Laccase-3 (Fragment) OS=Botryotinia fuckeliana GN=lcc3 PE=3 SV=1 98 528 5.0E-123
sp|Q03966|LAC1_CRYPA Laccase OS=Cryphonectria parasitica GN=LAC-1 PE=3 SV=1 6 567 7.0E-123
sp|P78722|LAC2_PODAS Laccase-2 OS=Podospora anserina GN=LAC2 PE=2 SV=1 42 567 3.0E-114
sp|D4APX3|LAC1_ARTBC Laccase ARB_05828 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_05828 PE=1 SV=1 52 555 8.0E-91
sp|Q02081|LAC4_THACU Laccase-4 OS=Thanatephorus cucumeris GN=LCC4 PE=1 SV=1 64 516 1.0E-59
sp|Q01679|LAC1_PHLRA Laccase OS=Phlebia radiata GN=LAC PE=1 SV=2 76 538 3.0E-55
sp|Q12719|LAC4_TRAVE Laccase-4 OS=Trametes versicolor GN=LCC4 PE=3 SV=1 74 536 3.0E-54
sp|Q99055|LAC4_TRAVI Laccase-4 OS=Trametes villosa GN=LCC4 PE=3 SV=1 74 536 5.0E-53
sp|Q09920|FIO1_SCHPO Iron transport multicopper oxidase fio1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=fio1 PE=3 SV=1 70 548 1.0E-52
sp|Q12542|LAC2_AGABI Laccase-2 OS=Agaricus bisporus GN=lcc2 PE=1 SV=1 69 530 9.0E-52
sp|Q12717|LAC5_TRAVE Laccase-5 OS=Trametes versicolor GN=LCC5 PE=2 SV=1 74 530 2.0E-51
sp|Q12541|LAC1_AGABI Laccase-1 OS=Agaricus bisporus GN=lcc1 PE=1 SV=1 69 530 1.0E-50
sp|P14133|ASO_CUCSA L-ascorbate oxidase OS=Cucumis sativus PE=1 SV=1 70 530 1.0E-50
sp|Q99056|LAC5_TRAVI Laccase-5 OS=Trametes villosa GN=LCC5 PE=3 SV=2 74 530 2.0E-50
sp|Q99044|LAC1_TRAVI Laccase-1 OS=Trametes villosa GN=LCC1 PE=3 SV=1 74 536 9.0E-50
sp|Q2QUN2|LAC24_ORYSJ Laccase-24 OS=Oryza sativa subsp. japonica GN=LAC24 PE=2 SV=1 92 528 2.0E-49
sp|P37064|ASO_CUCPM L-ascorbate oxidase OS=Cucurbita pepo var. melopepo PE=1 SV=1 70 536 2.0E-49
sp|Q40588|ASO_TOBAC L-ascorbate oxidase OS=Nicotiana tabacum GN=AAO PE=2 SV=1 69 530 5.0E-49
sp|P24792|ASO_CUCMA L-ascorbate oxidase OS=Cucurbita maxima GN=AAO PE=1 SV=2 70 536 2.0E-48
sp|D0VWU3|LAC1_TRAMX Laccase OS=Trametes maxima PE=1 SV=1 76 526 4.0E-48
sp|O59896|LAC1_PYCCI Laccase OS=Pycnoporus cinnabarinus GN=LCC3-1 PE=1 SV=1 74 530 2.0E-47
sp|O80434|LAC4_ARATH Laccase-4 OS=Arabidopsis thaliana GN=IRX12 PE=2 SV=2 50 529 3.0E-47
sp|Q9SR40|LAC7_ARATH Laccase-7 OS=Arabidopsis thaliana GN=LAC7 PE=2 SV=1 71 531 7.0E-47
sp|Q12718|LAC2_TRAVE Laccase-2 OS=Trametes versicolor GN=LCC2 PE=1 SV=1 74 552 6.0E-46
sp|Q99046|LAC2_TRAVI Laccase-2 OS=Trametes villosa GN=LCC2 PE=3 SV=1 74 552 1.0E-45
sp|Q9FLB5|LAC12_ARATH Laccase-12 OS=Arabidopsis thaliana GN=LAC12 PE=2 SV=1 88 529 4.0E-45
sp|Q8RYM9|LAC2_ORYSJ Laccase-2 OS=Oryza sativa subsp. japonica GN=LAC2 PE=2 SV=1 70 544 4.0E-44
sp|Q12739|LAC2_PLEOS Laccase-2 OS=Pleurotus ostreatus GN=POX2 PE=1 SV=1 81 556 7.0E-44
sp|Q02497|LAC1_TRAHI Laccase OS=Trametes hirsuta PE=1 SV=1 74 536 2.0E-43
sp|Q99049|LAC3_TRAVI Laccase-3 OS=Trametes villosa GN=LCC3 PE=3 SV=1 74 558 2.0E-41
sp|Q69L99|LAC14_ORYSJ Laccase-14 OS=Oryza sativa subsp. japonica GN=LAC14 PE=3 SV=1 71 528 2.0E-41
sp|Q12729|LAC1_PLEOS Laccase-1 OS=Pleurotus ostreatus GN=POX1 PE=2 SV=1 81 557 4.0E-41
sp|Q9ZPY2|LAC6_ARATH Laccase-6 OS=Arabidopsis thaliana GN=LAC6 PE=2 SV=1 67 531 7.0E-41
sp|Q6ID18|LAC10_ARATH Laccase-10 OS=Arabidopsis thaliana GN=LAC10 PE=2 SV=1 67 529 8.0E-41
sp|Q8VZA1|LAC11_ARATH Laccase-11 OS=Arabidopsis thaliana GN=LAC11 PE=2 SV=1 63 538 9.0E-40
sp|Q5N9W4|LAC5_ORYSJ Putative laccase-5 OS=Oryza sativa subsp. japonica GN=LAC5 PE=3 SV=1 67 544 1.0E-39
sp|P43561|FET5_YEAST Iron transport multicopper oxidase FET5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FET5 PE=1 SV=1 79 530 5.0E-39
sp|P56193|LAC1_THACU Laccase-1 OS=Thanatephorus cucumeris GN=LCC1 PE=1 SV=1 69 324 7.0E-39
sp|Q6CII3|FET3_KLULA Iron transport multicopper oxidase FET3 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=FET3 PE=3 SV=1 88 535 1.0E-38
sp|O81081|LAC2_ARATH Laccase-2 OS=Arabidopsis thaliana GN=LAC2 PE=2 SV=1 52 529 6.0E-38
sp|Q96WT3|FET3_CANGA Iron transport multicopper oxidase FET3 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=FET3 PE=3 SV=1 84 530 1.0E-37
sp|Q02075|LAC2_THACU Laccase-2 OS=Thanatephorus cucumeris GN=LCC2 PE=2 SV=1 71 347 2.0E-37
sp|P78591|FET3_CANAX Iron transport multicopper oxidase FET3 OS=Candida albicans GN=FET3 PE=3 SV=1 83 549 3.0E-37
sp|Q02079|LAC3_THACU Laccase-3 OS=Thanatephorus cucumeris GN=LCC3 PE=2 SV=1 69 333 7.0E-37
sp|Q9LMS3|LAC1_ARATH Laccase-1 OS=Arabidopsis thaliana GN=LAC1 PE=2 SV=1 88 531 2.0E-35
sp|Q9FY79|LAC14_ARATH Laccase-14 OS=Arabidopsis thaliana GN=LAC14 PE=2 SV=1 91 531 1.0E-34
sp|Q0DHL2|LAC12_ORYSJ Laccase-12/13 OS=Oryza sativa subsp. japonica GN=LAC12 PE=2 SV=1 68 353 3.0E-34
sp|P38993|FET3_YEAST Iron transport multicopper oxidase FET3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FET3 PE=1 SV=2 84 519 5.0E-34
sp|Q84J37|LAC15_ARATH Laccase-15 OS=Arabidopsis thaliana GN=TT10 PE=1 SV=1 68 531 6.0E-34
sp|Q9FJD5|LAC17_ARATH Laccase-17 OS=Arabidopsis thaliana GN=LAC17 PE=2 SV=1 64 345 4.0E-30
sp|I6WZK7|MMCO_MYCTU Multicopper oxidase MmcO OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mmcO PE=1 SV=1 96 528 5.0E-30
sp|Q5N9X2|LAC4_ORYSJ Laccase-4 OS=Oryza sativa subsp. japonica GN=LAC4 PE=2 SV=1 67 357 3.0E-29
sp|Q9LFD1|LAC9_ARATH Laccase-9 OS=Arabidopsis thaliana GN=LAC9 PE=2 SV=1 71 313 9.0E-28
sp|Q9LFD2|LAC8_ARATH Laccase-8 OS=Arabidopsis thaliana GN=LAC8 PE=2 SV=1 52 326 7.0E-27
sp|Q5N7A3|LAC6_ORYSJ Laccase-6 OS=Oryza sativa subsp. japonica GN=LAC6 PE=2 SV=1 92 351 4.0E-26
sp|Q9SIY8|LAC5_ARATH Laccase-5 OS=Arabidopsis thaliana GN=LAC5 PE=2 SV=1 90 313 5.0E-26
sp|Q2QYS3|LAC23_ORYSJ Laccase-23 OS=Oryza sativa subsp. japonica GN=LAC23 PE=3 SV=1 88 313 1.0E-25
sp|Q2RBK2|LAC17_ORYSJ Putative laccase-17 OS=Oryza sativa subsp. japonica GN=LAC17 PE=3 SV=1 91 313 3.0E-25
sp|Q941X2|LAC3_ORYSJ Laccase-3 OS=Oryza sativa subsp. japonica GN=LAC3 PE=2 SV=1 91 314 2.0E-24
sp|Q47452|PCOA_ECOLX Copper resistance protein A OS=Escherichia coli GN=pcoA PE=3 SV=1 71 309 4.0E-24
sp|A2XCN6|LAC18_ORYSI Putative laccase-18 OS=Oryza sativa subsp. indica GN=LAC18 PE=3 SV=1 93 312 1.0E-23
sp|A2Y9C2|LAC20_ORYSI Laccase-20 OS=Oryza sativa subsp. indica GN=LAC20 PE=3 SV=1 91 312 1.0E-23
sp|Q2R0L0|LAC20_ORYSJ Laccase-20 OS=Oryza sativa subsp. japonica GN=LAC20 PE=2 SV=1 91 312 2.0E-23
sp|Q2R0L2|LAC19_ORYSJ Laccase-19 OS=Oryza sativa subsp. japonica GN=LAC19 PE=2 SV=1 92 312 2.0E-23
sp|Q53LU4|LAC18_ORYSJ Laccase-18 OS=Oryza sativa subsp. japonica GN=LAC18 PE=2 SV=1 93 312 2.0E-23
sp|Q0IP28|LAC25_ORYSJ Laccase-25 OS=Oryza sativa subsp. japonica GN=LAC25 PE=3 SV=1 87 327 2.0E-23
sp|P12374|COPA_PSEUB Copper resistance protein A OS=Pseudomonas syringae pv. tomato GN=copA PE=1 SV=1 71 309 3.0E-23
sp|Q56YT0|LAC3_ARATH Laccase-3 OS=Arabidopsis thaliana GN=LAC3 PE=2 SV=2 76 350 3.0E-23
sp|Q1PDH6|LAC16_ARATH Laccase-16 OS=Arabidopsis thaliana GN=LAC16 PE=2 SV=2 88 354 3.0E-23
sp|A2Y9C5|LAC19_ORYSI Putative laccase-19 OS=Oryza sativa subsp. indica GN=LAC19 PE=3 SV=1 92 312 3.0E-23
sp|Q0DHL5|LAC11_ORYSJ Putative laccase-11 OS=Oryza sativa subsp. japonica GN=LAC11 PE=5 SV=2 86 353 5.0E-23
sp|P59571|COPA_PSESM Copper resistance protein A homolog OS=Pseudomonas syringae pv. tomato (strain DC3000) GN=copA PE=3 SV=1 64 315 2.0E-22
sp|Q9LYQ2|LAC13_ARATH Laccase-13 OS=Arabidopsis thaliana GN=LAC13 PE=2 SV=1 90 313 2.0E-22
sp|Q0IQU1|LAC22_ORYSJ Laccase-22 OS=Oryza sativa subsp. japonica GN=LAC22 PE=2 SV=2 67 351 7.0E-22
sp|Q9SU40|SKU5_ARATH Monocopper oxidase-like protein SKU5 OS=Arabidopsis thaliana GN=SKU5 PE=1 SV=1 72 515 8.0E-22
sp|Q7XE50|LAC16_ORYSJ Putative laccase-16 OS=Oryza sativa subsp. japonica GN=LAC16 PE=5 SV=1 128 531 2.0E-21
sp|Q0JHP8|LAC8_ORYSJ Laccase-8 OS=Oryza sativa subsp. japonica GN=LAC8 PE=3 SV=2 94 309 2.0E-21
sp|Q6Z8L2|LAC9_ORYSJ Putative laccase-9 OS=Oryza sativa subsp. japonica GN=LAC9 PE=3 SV=1 69 348 3.0E-19
sp|Q5N7B4|LAC7_ORYSJ Laccase-7 OS=Oryza sativa subsp. japonica GN=LAC7 PE=2 SV=1 91 345 1.0E-18
sp|Q941X2|LAC3_ORYSJ Laccase-3 OS=Oryza sativa subsp. japonica GN=LAC3 PE=2 SV=1 442 529 2.0E-18
sp|Q339K6|LAC15_ORYSJ Laccase-15 OS=Oryza sativa subsp. japonica GN=LAC15 PE=2 SV=1 93 326 4.0E-18
sp|Q2QYS3|LAC23_ORYSJ Laccase-23 OS=Oryza sativa subsp. japonica GN=LAC23 PE=3 SV=1 454 529 1.0E-17
sp|Q2RBK2|LAC17_ORYSJ Putative laccase-17 OS=Oryza sativa subsp. japonica GN=LAC17 PE=3 SV=1 454 529 2.0E-17
sp|Q339K6|LAC15_ORYSJ Laccase-15 OS=Oryza sativa subsp. japonica GN=LAC15 PE=2 SV=1 455 529 3.0E-17
sp|Q2QZ80|LAC21_ORYSJ Laccase-21 OS=Oryza sativa subsp. japonica GN=LAC21 PE=2 SV=1 88 352 3.0E-17
sp|Q10ND7|LAC10_ORYSJ Laccase-10 OS=Oryza sativa subsp. japonica GN=LAC10 PE=2 SV=1 88 312 3.0E-17
sp|Q5ZCW1|LAC1_ORYSJ Putative laccase-1 OS=Oryza sativa subsp. japonica GN=LAC1 PE=3 SV=1 69 348 9.0E-17
sp|Q0IQU1|LAC22_ORYSJ Laccase-22 OS=Oryza sativa subsp. japonica GN=LAC22 PE=2 SV=2 451 529 1.0E-16
sp|Q02075|LAC2_THACU Laccase-2 OS=Thanatephorus cucumeris GN=LCC2 PE=2 SV=1 381 535 2.0E-16
sp|Q9SIY8|LAC5_ARATH Laccase-5 OS=Arabidopsis thaliana GN=LAC5 PE=2 SV=1 444 529 2.0E-16
sp|Q9LYQ2|LAC13_ARATH Laccase-13 OS=Arabidopsis thaliana GN=LAC13 PE=2 SV=1 454 534 3.0E-16
sp|Q5N7B4|LAC7_ORYSJ Laccase-7 OS=Oryza sativa subsp. japonica GN=LAC7 PE=2 SV=1 439 528 3.0E-16
sp|Q10ND7|LAC10_ORYSJ Laccase-10 OS=Oryza sativa subsp. japonica GN=LAC10 PE=2 SV=1 428 544 3.0E-16
sp|Q9FHN6|SKS2_ARATH Monocopper oxidase-like protein SKS2 OS=Arabidopsis thaliana GN=SKS2 PE=1 SV=1 72 510 3.0E-16
sp|Q5N7A3|LAC6_ORYSJ Laccase-6 OS=Oryza sativa subsp. japonica GN=LAC6 PE=2 SV=1 439 528 4.0E-16
sp|Q0IP28|LAC25_ORYSJ Laccase-25 OS=Oryza sativa subsp. japonica GN=LAC25 PE=3 SV=1 439 526 4.0E-16
sp|Q5N9X2|LAC4_ORYSJ Laccase-4 OS=Oryza sativa subsp. japonica GN=LAC4 PE=2 SV=1 454 529 2.0E-15
sp|A2XCN6|LAC18_ORYSI Putative laccase-18 OS=Oryza sativa subsp. indica GN=LAC18 PE=3 SV=1 455 529 2.0E-15
sp|Q2R0L2|LAC19_ORYSJ Laccase-19 OS=Oryza sativa subsp. japonica GN=LAC19 PE=2 SV=1 455 529 2.0E-15
sp|A2Y9C5|LAC19_ORYSI Putative laccase-19 OS=Oryza sativa subsp. indica GN=LAC19 PE=3 SV=1 455 529 2.0E-15
sp|Q8VXX5|SKS1_ARATH Monocopper oxidase-like protein SKS1 OS=Arabidopsis thaliana GN=SKS1 PE=1 SV=1 72 510 3.0E-15
sp|Q0JHP8|LAC8_ORYSJ Laccase-8 OS=Oryza sativa subsp. japonica GN=LAC8 PE=3 SV=2 454 528 6.0E-15
sp|Q53LU4|LAC18_ORYSJ Laccase-18 OS=Oryza sativa subsp. japonica GN=LAC18 PE=2 SV=1 455 529 7.0E-15
sp|Q56YT0|LAC3_ARATH Laccase-3 OS=Arabidopsis thaliana GN=LAC3 PE=2 SV=2 443 529 8.0E-15
sp|Q1PDH6|LAC16_ARATH Laccase-16 OS=Arabidopsis thaliana GN=LAC16 PE=2 SV=2 439 529 8.0E-15
sp|A2Y9C2|LAC20_ORYSI Laccase-20 OS=Oryza sativa subsp. indica GN=LAC20 PE=3 SV=1 455 529 9.0E-15
sp|Q2R0L0|LAC20_ORYSJ Laccase-20 OS=Oryza sativa subsp. japonica GN=LAC20 PE=2 SV=1 455 529 9.0E-15
sp|Q00624|ASOL_BRANA L-ascorbate oxidase homolog OS=Brassica napus GN=Bp10 PE=2 SV=1 75 325 1.0E-14
sp|Q9LFD1|LAC9_ARATH Laccase-9 OS=Arabidopsis thaliana GN=LAC9 PE=2 SV=1 439 529 4.0E-14
sp|Q0DHL2|LAC12_ORYSJ Laccase-12/13 OS=Oryza sativa subsp. japonica GN=LAC12 PE=2 SV=1 454 529 6.0E-14
sp|Q9LFD2|LAC8_ARATH Laccase-8 OS=Arabidopsis thaliana GN=LAC8 PE=2 SV=1 439 529 8.0E-14
sp|Q9FJD5|LAC17_ARATH Laccase-17 OS=Arabidopsis thaliana GN=LAC17 PE=2 SV=1 454 529 2.0E-13
sp|Q0DHL5|LAC11_ORYSJ Putative laccase-11 OS=Oryza sativa subsp. japonica GN=LAC11 PE=5 SV=2 454 543 2.0E-13
sp|P17489|LAC1_EMENI Laccase-1 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=yA PE=2 SV=3 85 189 2.0E-13
sp|P56193|LAC1_THACU Laccase-1 OS=Thanatephorus cucumeris GN=LCC1 PE=1 SV=1 414 530 4.0E-12
sp|Q02079|LAC3_THACU Laccase-3 OS=Thanatephorus cucumeris GN=LCC3 PE=2 SV=1 414 558 6.0E-12
sp|Q2QZ80|LAC21_ORYSJ Laccase-21 OS=Oryza sativa subsp. japonica GN=LAC21 PE=2 SV=1 431 531 3.0E-11
sp|Q6Z8L2|LAC9_ORYSJ Putative laccase-9 OS=Oryza sativa subsp. japonica GN=LAC9 PE=3 SV=1 454 531 7.0E-11
sp|Q5ZCW1|LAC1_ORYSJ Putative laccase-1 OS=Oryza sativa subsp. japonica GN=LAC1 PE=3 SV=1 409 531 9.0E-11
sp|P29162|ASOL_TOBAC L-ascorbate oxidase homolog OS=Nicotiana tabacum PE=2 SV=1 75 547 1.0E-09
sp|Q04399|GMC1_YEAST Putative multicopper oxidase GMC1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GMC1 PE=1 SV=1 439 528 6.0E-09
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GO

GO Term Description Terminal node
GO:0016491 oxidoreductase activity Yes
GO:0005507 copper ion binding Yes
GO:0003824 catalytic activity No
GO:0046872 metal ion binding No
GO:0005488 binding No
GO:0043167 ion binding No
GO:0046914 transition metal ion binding No
GO:0003674 molecular_function No
GO:0043169 cation binding No

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
Extracellular Signal peptide 0.1485 0.0881 0.8131 0.175 0.0871 0.0209 0.2379 0.1604 0.0933 0.0138

SignalP

SignalP signal predicted Location Score
Yes 1 - 18 0.999696

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

CAZyme category E-value Start End
AA1_3 7.0E-127 57 363

Secondary Metabolism

(None)

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup416
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|7396
Ophiocordyceps australis map64 (Brazil) OphauB2|7897
Ophiocordyceps camponoti-floridani Ophcf2|03021
Ophiocordyceps camponoti-floridani Ophcf2|07232
Ophiocordyceps camponoti-rufipedis Ophun1|2520
Ophiocordyceps camponoti-rufipedis Ophun1|3408
Ophiocordyceps camponoti-rufipedis Ophun1|3926
Ophiocordyceps kimflemingae Ophio5|2677
Ophiocordyceps subramaniannii Hirsu2|3355 (this protein)
Ophiocordyceps subramaniannii Hirsu2|9622

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|3355
MLSQHWLLPALLISSGAALPGQRPKSPSQAESCSSSEACAGNTPLTRSDWCSFSVDTDYTEVAPDTGVTREYWLD
VTDVVVAPDGVPRTAMAVNGSIPGPTLFADWGDTVVVHVTNSLHTSRNGTSIHFHGIRQNYTNQNDGVSSITECP
TVPGNTKTYTWRAVQYGSSWYHSHFALQSWQGVFGGIVINGPATANYDEDLGVVFLNDWDPQTVDELYPEAETQG
PPFLATGLINGTNVSNVGGQRLNISFTPGRSHRMRLVNAAVDTHFKFTLDNHTMTVIAADFIPVEPYTTTVLDIG
MGQRYDVVIAADQAHVADSFWLRALPQTVCSNNNNSQNIRAVVHYGDSPSTPATVGYNYTDACDDENRNLIPRVA
KKLEAADITTSTFANLTTIDGLFKWTLNSTTMVVDWGNPTLNQIMDRVTTFEVSNAVIALPEPNKLFSMVIQTTL
PIPHPIHLHGHDFFVLAQGVGNYSSATALNWDNPPRRDTAMLPGGGFLVIAFETDNPGAWLMHCHIGWHTTEGFG
LQFIERYDEIAPLIDEKVLRDECRAWNTFQDTFAIVQTDSGI*
Coding >Hirsu2|3355
ATGCTTTCCCAACACTGGCTCCTACCAGCTCTGCTGATCTCGTCAGGGGCCGCTCTGCCCGGGCAGCGCCCCAAG
AGTCCGAGTCAGGCCGAGTCGTGCTCCTCCTCGGAGGCCTGCGCGGGAAACACGCCCCTGACTCGCTCGGATTGG
TGTAGTTTCTCGGTAGACACCGATTACACTGAGGTGGCGCCCGACACGGGCGTGACCAGAGAGTACTGGCTGGAC
GTCACCGACGTTGTCGTTGCCCCTGATGGCGTGCCGCGAACCGCGATGGCCGTCAATGGCAGCATCCCCGGCCCA
ACTCTCTTCGCCGACTGGGGCGATACTGTCGTCGTTCATGTCACCAACTCGCTCCACACCTCCAGGAACGGGACC
AGCATCCACTTCCACGGCATCCGGCAAAACTACACGAACCAGAACGACGGCGTCTCTTCCATCACCGAATGCCCT
ACTGTGCCGGGAAACACCAAGACCTACACCTGGCGGGCCGTCCAGTACGGCTCCAGCTGGTACCACTCCCATTTC
GCTCTCCAGTCGTGGCAGGGCGTGTTCGGCGGCATCGTCATCAACGGCCCGGCGACGGCAAACTACGACGAGGAT
CTCGGCGTCGTCTTTCTCAACGACTGGGACCCCCAGACGGTCGACGAGCTCTATCCGGAGGCTGAAACCCAAGGC
CCCCCATTCCTGGCCACCGGTTTGATCAACGGCACCAACGTATCCAACGTCGGCGGCCAGCGACTGAACATCTCT
TTTACCCCGGGGCGTTCTCATCGCATGCGCCTTGTCAACGCTGCGGTCGATACTCATTTCAAGTTTACTCTCGAC
AACCACACCATGACCGTTATCGCTGCCGATTTCATACCCGTCGAGCCCTATACCACGACGGTCCTGGACATTGGC
ATGGGCCAGCGTTACGACGTGGTCATCGCAGCGGACCAGGCCCATGTGGCCGACAGCTTCTGGCTGCGAGCTCTC
CCTCAGACCGTCTGCTCCAACAACAACAATTCGCAGAACATCCGCGCCGTCGTCCACTACGGCGATTCTCCTTCG
ACGCCAGCCACGGTGGGCTACAACTACACGGACGCCTGCGACGACGAGAACAGGAACCTTATCCCTCGTGTTGCC
AAGAAACTGGAAGCCGCCGATATCACAACGTCGACCTTTGCCAACCTCACCACCATCGACGGCCTATTCAAATGG
ACCCTCAACAGCACGACCATGGTCGTGGACTGGGGGAACCCGACACTGAACCAGATCATGGACAGGGTCACGACT
TTCGAGGTCTCCAACGCCGTCATCGCGCTGCCCGAGCCCAACAAGCTCTTCTCCATGGTCATCCAGACGACGCTG
CCCATCCCGCACCCTATCCACCTGCACGGCCACGATTTCTTCGTCCTCGCCCAGGGGGTCGGCAACTATTCGTCC
GCAACCGCCCTCAACTGGGACAACCCGCCGAGACGGGACACCGCCATGCTGCCCGGGGGCGGCTTCCTGGTCATC
GCGTTCGAGACGGACAATCCGGGCGCTTGGCTGATGCATTGCCATATCGGCTGGCATACGACCGAGGGGTTTGGC
CTGCAGTTCATCGAGCGGTACGACGAAATCGCCCCCTTGATCGACGAGAAGGTTCTCCGAGACGAATGCAGGGCT
TGGAATACGTTCCAGGATACATTTGCGATTGTACAAACCGACTCCGGAATCTGA
Transcript >Hirsu2|3355
ATGCTTTCCCAACACTGGCTCCTACCAGCTCTGCTGATCTCGTCAGGGGCCGCTCTGCCCGGGCAGCGCCCCAAG
AGTCCGAGTCAGGCCGAGTCGTGCTCCTCCTCGGAGGCCTGCGCGGGAAACACGCCCCTGACTCGCTCGGATTGG
TGTAGTTTCTCGGTAGACACCGATTACACTGAGGTGGCGCCCGACACGGGCGTGACCAGAGAGTACTGGCTGGAC
GTCACCGACGTTGTCGTTGCCCCTGATGGCGTGCCGCGAACCGCGATGGCCGTCAATGGCAGCATCCCCGGCCCA
ACTCTCTTCGCCGACTGGGGCGATACTGTCGTCGTTCATGTCACCAACTCGCTCCACACCTCCAGGAACGGGACC
AGCATCCACTTCCACGGCATCCGGCAAAACTACACGAACCAGAACGACGGCGTCTCTTCCATCACCGAATGCCCT
ACTGTGCCGGGAAACACCAAGACCTACACCTGGCGGGCCGTCCAGTACGGCTCCAGCTGGTACCACTCCCATTTC
GCTCTCCAGTCGTGGCAGGGCGTGTTCGGCGGCATCGTCATCAACGGCCCGGCGACGGCAAACTACGACGAGGAT
CTCGGCGTCGTCTTTCTCAACGACTGGGACCCCCAGACGGTCGACGAGCTCTATCCGGAGGCTGAAACCCAAGGC
CCCCCATTCCTGGCCACCGGTTTGATCAACGGCACCAACGTATCCAACGTCGGCGGCCAGCGACTGAACATCTCT
TTTACCCCGGGGCGTTCTCATCGCATGCGCCTTGTCAACGCTGCGGTCGATACTCATTTCAAGTTTACTCTCGAC
AACCACACCATGACCGTTATCGCTGCCGATTTCATACCCGTCGAGCCCTATACCACGACGGTCCTGGACATTGGC
ATGGGCCAGCGTTACGACGTGGTCATCGCAGCGGACCAGGCCCATGTGGCCGACAGCTTCTGGCTGCGAGCTCTC
CCTCAGACCGTCTGCTCCAACAACAACAATTCGCAGAACATCCGCGCCGTCGTCCACTACGGCGATTCTCCTTCG
ACGCCAGCCACGGTGGGCTACAACTACACGGACGCCTGCGACGACGAGAACAGGAACCTTATCCCTCGTGTTGCC
AAGAAACTGGAAGCCGCCGATATCACAACGTCGACCTTTGCCAACCTCACCACCATCGACGGCCTATTCAAATGG
ACCCTCAACAGCACGACCATGGTCGTGGACTGGGGGAACCCGACACTGAACCAGATCATGGACAGGGTCACGACT
TTCGAGGTCTCCAACGCCGTCATCGCGCTGCCCGAGCCCAACAAGCTCTTCTCCATGGTCATCCAGACGACGCTG
CCCATCCCGCACCCTATCCACCTGCACGGCCACGATTTCTTCGTCCTCGCCCAGGGGGTCGGCAACTATTCGTCC
GCAACCGCCCTCAACTGGGACAACCCGCCGAGACGGGACACCGCCATGCTGCCCGGGGGCGGCTTCCTGGTCATC
GCGTTCGAGACGGACAATCCGGGCGCTTGGCTGATGCATTGCCATATCGGCTGGCATACGACCGAGGGGTTTGGC
CTGCAGTTCATCGAGCGGTACGACGAAATCGCCCCCTTGATCGACGAGAAGGTTCTCCGAGACGAATGCAGGGCT
TGGAATACGTTCCAGGATACATTTGCGATTGTACAAACCGACTCCGGAATCTGA
Gene >Hirsu2|3355
ATGCTTTCCCAACACTGGCTCCTACCAGCTCTGCTGATCTCGTCAGGGGCCGCTCTGCCCGGGCAGCGCCCCAAG
AGTCCGAGTCAGGCCGAGTCGTGCTCCTCCTCGGAGGCCTGCGCGGGAAACACGCCCCTGACTCGCTCGGATTGG
TGTAGTTTCTCGGTAGACACCGATTACACTGAGGTGGCGCCCGACACGGGCGTGACCAGAGAGTACTGGCTGGAC
GTCACCGACGTTGTCGTTGCCCCTGATGGCGTGCCGCGAACCGCGATGGGTACGTCTGCCACTGCTCCTGACTCG
ACGAAAGTCTTCGACCCGCTCTATACGAAGACGGTGCGCTAATGCCCGTTCCTCCTCCGTAGCCGTCAATGGCAG
CATCCCCGGCCCAACTCTCTTCGCCGACTGGGGCGATACTGTCGTCGTTCATGTCACCAACTCGCTCCACACCTC
CAGGAACGGGACCAGCATCCACTTCCACGGCATCCGGCAAAACTACACGAACCAGAACGACGGCGTCTCTTCCAT
CACCGAATGCCCTACTGTGCCGGGAAACACCAAGACCTACACCTGGCGGGCCGTCCAGTACGGCTCCAGCTGGTA
CCACTCCCATTTCGCTCTCCAGTCGTGGCAGGGCGTGTTCGGCGGCATCGTCATCAACGGCCCGGCGACGGCAAA
CTACGACGAGGATCTCGGCGTCGTCTTTCTCAACGACTGGGACCCCCAGACGGTCGACGAGCTCTATCCGGAGGC
TGAAACCCAAGGCCCCCCATTCCTGGCCACCGGTTTGATCAACGGCACCAACGTATCCAACGTCGGCGGCCAGCG
ACTGAACATCTCTTTTACCCCGGGGCGTTCTCATCGCATGCGCCTTGTCAACGCTGCGGTCGATACTCATTTCAA
GTTTACTCTCGACAACCACACCATGACCGTTATCGCTGCCGATTTCATACCCGTCGAGCCCTATACCACGACGGT
CCTGGACATTGGCATGGGCCAGCGTTACGACGTGGTCATCGCAGCGGACCAGGCCCATGTGGCCGACAGCTTCTG
GCTGCGAGCTCTCCCTCAGACCGTCTGCTCCAACAACAACAATTCGCAGAACATCCGCGCCGTCGTCCACTACGG
CGATTCTCCTTCGACGCCAGCCACGGTGGGCTACAACTACACGGACGCCTGCGACGACGAGAACAGGAACCTTAT
CCCTCGTGTTGCCAAGAAACTGGAAGCCGCCGATATCACAACGTCGACCTTTGCCAACCTCACCACCATCGACGG
CCTATTCAAATGGACCCTCAACAGCACGACCATGGTCGTGGACTGGGGGAACCCGACACTGAACCAGATCATGGA
CAGGGTCACGACTTTCGAGGTCTCCAACGCCGTCATCGCGCTGCCCGAGCCCAACAAGCTCTTCTCCATGGTCAT
CCAGACGACGCTGCCCATCCCGCACCCTATCCACCTGCACGGCCACGATTTCTTCGTCCTCGCCCAGGGGGTCGG
CAACTATTCGTCCGCAACCGCCCTCAACTGGGACAACCCGCCGAGACGGGACACCGCCATGCTGCCCGGGGGCGG
CTTCCTGGTCATCGCGTTCGAGACGGACAATCCGGGCGCTTGGCTGATGCATTGCCATATCGGCTGGCATACGAC
CGAGGGGTTTGGCCTGCAGTTCATCGAGCGGTACGACGAAATCGCCCCCTTGATCGACGAGAAGGTTCTCCGAGA
CGAATGCAGGGCTTGGAATACGTTCCAGGATACATTTGCGATTGTACAAACCGACTCCGGAATCTGA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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