Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauB2|2015
Gene name
LocationContig_16:100627..103672
Strand+
Gene length (bp)3045
Transcript length (bp)3045
Coding sequence length (bp)3045
Protein length (aa) 1015

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF04408 HA2 Helicase associated domain (HA2) 3.6E-18 765 839
PF07717 OB_NTP_bind Oligonucleotide/oligosaccharide-binding (OB)-fold 1.8E-15 917 995
PF00271 Helicase_C Helicase conserved C-terminal domain 8.3E-14 576 703
PF13401 AAA_22 AAA domain 4.4E-06 388 505
PF00270 DEAD DEAD/DEAH box helicase 2.9E-06 378 531

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|Q10752|CDC28_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase-like protein cdc28 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=cdc28 PE=3 SV=2 169 1005 0.0E+00
sp|Q8VY00|ESP3_ARATH Pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH1 OS=Arabidopsis thaliana GN=ESP3 PE=1 SV=1 133 1011 0.0E+00
sp|Q7YR39|DHX16_PANTR Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Pan troglodytes GN=DHX16 PE=3 SV=1 116 1011 0.0E+00
sp|O60231|DHX16_HUMAN Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Homo sapiens GN=DHX16 PE=1 SV=2 116 1011 0.0E+00
sp|F4IJV4|DEAH6_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH6 OS=Arabidopsis thaliana GN=MEE29 PE=2 SV=1 121 1012 0.0E+00
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|Q10752|CDC28_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase-like protein cdc28 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=cdc28 PE=3 SV=2 169 1005 0.0E+00
sp|Q8VY00|ESP3_ARATH Pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH1 OS=Arabidopsis thaliana GN=ESP3 PE=1 SV=1 133 1011 0.0E+00
sp|Q7YR39|DHX16_PANTR Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Pan troglodytes GN=DHX16 PE=3 SV=1 116 1011 0.0E+00
sp|O60231|DHX16_HUMAN Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Homo sapiens GN=DHX16 PE=1 SV=2 116 1011 0.0E+00
sp|F4IJV4|DEAH6_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH6 OS=Arabidopsis thaliana GN=MEE29 PE=2 SV=1 121 1012 0.0E+00
sp|Q767K6|DHX16_PIG Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Sus scrofa GN=DHX16 PE=3 SV=1 116 1011 0.0E+00
sp|O45244|DHX16_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-4 OS=Caenorhabditis elegans GN=mog-4 PE=1 SV=2 136 1013 0.0E+00
sp|Q54MH3|DHX16_DICDI Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 OS=Dictyostelium discoideum GN=dhx16 PE=3 SV=1 138 1012 0.0E+00
sp|F4JMJ3|DEAH8_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH8 OS=Arabidopsis thaliana GN=At4g16680 PE=2 SV=2 220 1008 0.0E+00
sp|Q14562|DHX8_HUMAN ATP-dependent RNA helicase DHX8 OS=Homo sapiens GN=DHX8 PE=1 SV=1 358 1008 0.0E+00
sp|Q38953|DEAH5_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH5 OS=Arabidopsis thaliana GN=At3g26560 PE=1 SV=2 358 1008 0.0E+00
sp|Q54F05|DHX8_DICDI ATP-dependent RNA helicase dhx8 OS=Dictyostelium discoideum GN=dhx8 PE=3 SV=1 336 1008 0.0E+00
sp|A2A4P0|DHX8_MOUSE ATP-dependent RNA helicase DHX8 OS=Mus musculus GN=Dhx8 PE=2 SV=1 358 1008 0.0E+00
sp|Q09530|MOG5_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-5 OS=Caenorhabditis elegans GN=mog-5 PE=1 SV=1 360 1008 0.0E+00
sp|P20095|PRP2_YEAST Pre-mRNA-splicing factor ATP-dependent RNA helicase-like protein PRP2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PRP2 PE=1 SV=1 315 997 0.0E+00
sp|O42643|PRP22_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase prp22 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp22 PE=1 SV=1 325 1012 0.0E+00
sp|P24384|PRP22_YEAST Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP22 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PRP22 PE=1 SV=1 351 1008 0.0E+00
sp|P34498|MOG1_CAEEL Probable pre-mRNA-splicing factor ATP-dependent RNA helicase mog-1 OS=Caenorhabditis elegans GN=mog-1 PE=1 SV=2 364 996 0.0E+00
sp|Q17R09|PRP16_BOVIN Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 OS=Bos taurus GN=DHX38 PE=2 SV=1 299 1014 0.0E+00
sp|Q92620|PRP16_HUMAN Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 OS=Homo sapiens GN=DHX38 PE=1 SV=2 352 1014 0.0E+00
sp|Q9LZQ9|DEAH2_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH2 OS=Arabidopsis thaliana GN=At3g62310 PE=2 SV=1 360 1009 0.0E+00
sp|F4K2E9|PRP16_ARATH Pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH7 OS=Arabidopsis thaliana GN=CUV PE=1 SV=1 364 1002 0.0E+00
sp|O22899|PRP43_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH3 OS=Arabidopsis thaliana GN=At2g47250 PE=2 SV=1 360 1008 0.0E+00
sp|Q9H5Z1|DHX35_HUMAN Probable ATP-dependent RNA helicase DHX35 OS=Homo sapiens GN=DHX35 PE=1 SV=2 363 997 0.0E+00
sp|Q5RBD4|DHX35_PONAB Probable ATP-dependent RNA helicase DHX35 OS=Pongo abelii GN=DHX35 PE=2 SV=1 363 997 0.0E+00
sp|O43143|DHX15_HUMAN Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Homo sapiens GN=DHX15 PE=1 SV=2 361 1008 0.0E+00
sp|O35286|DHX15_MOUSE Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Mus musculus GN=Dhx15 PE=1 SV=2 361 1008 0.0E+00
sp|Q5RAZ4|DHX15_PONAB Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 OS=Pongo abelii GN=DHX15 PE=2 SV=2 361 1008 0.0E+00
sp|Q9P774|PRP16_SCHPO Pre-mRNA-splicing factor ATP-dependent RNA helicase prp16 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp16 PE=3 SV=2 332 996 0.0E+00
sp|Q54NJ4|DHX15_DICDI Putative pre-mRNA-splicing factor ATP-dependent RNA helicase dhx15 OS=Dictyostelium discoideum GN=dhx15 PE=3 SV=1 346 997 0.0E+00
sp|O42945|DHX15_SCHPO Probable pre-mRNA-splicing factor ATP-dependent RNA helicase prp43 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prp43 PE=3 SV=1 363 1008 0.0E+00
sp|Q20875|DHX15_CAEEL Pre-mRNA-splicing factor ATP-dependent RNA helicase ddx-15 OS=Caenorhabditis elegans GN=ddx-15 PE=3 SV=1 360 1004 0.0E+00
sp|P53131|PRP43_YEAST Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP43 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PRP43 PE=1 SV=1 363 1007 0.0E+00
sp|F4JRJ6|DEAH9_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH9 OS=Arabidopsis thaliana GN=At4g18465 PE=3 SV=1 364 997 0.0E+00
sp|F4IE66|PRP22_ARATH Pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH10 OS=Arabidopsis thaliana GN=RID1 PE=1 SV=1 365 997 0.0E+00
sp|Q93Y16|DEAH4_ARATH Probable pre-mRNA-splicing factor ATP-dependent RNA helicase DEAH4 OS=Arabidopsis thaliana GN=At1g27900 PE=1 SV=1 371 1009 1.0E-180
sp|P15938|PRP16_YEAST Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PRP16 PE=1 SV=2 344 996 4.0E-171
sp|Q80VY9|DHX33_MOUSE Putative ATP-dependent RNA helicase DHX33 OS=Mus musculus GN=Dhx33 PE=1 SV=1 364 997 1.0E-167
sp|Q03319|PRH1_SCHPO Probable ATP-dependent RNA helicase prh1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prh1 PE=3 SV=2 365 995 2.0E-165
sp|Q9BKQ8|DHX35_CAEEL Probable ATP-dependent RNA helicase DHX35 homolog OS=Caenorhabditis elegans GN=Y67D2.6 PE=3 SV=1 363 1009 8.0E-165
sp|Q9H6R0|DHX33_HUMAN Putative ATP-dependent RNA helicase DHX33 OS=Homo sapiens GN=DHX33 PE=1 SV=2 364 997 1.0E-162
sp|Q5R864|DHX40_PONAB Probable ATP-dependent RNA helicase DHX40 OS=Pongo abelii GN=DHX40 PE=2 SV=1 355 1004 2.0E-146
sp|Q8IX18|DHX40_HUMAN Probable ATP-dependent RNA helicase DHX40 OS=Homo sapiens GN=DHX40 PE=1 SV=2 355 1004 3.0E-146
sp|Q5XI69|DHX40_RAT Probable ATP-dependent RNA helicase DHX40 OS=Rattus norvegicus GN=Dhx40 PE=2 SV=1 353 1009 9.0E-146
sp|Q6PE54|DHX40_MOUSE Probable ATP-dependent RNA helicase DHX40 OS=Mus musculus GN=Dhx40 PE=1 SV=1 353 1009 9.0E-145
sp|O17438|DHX15_STRPU Putative pre-mRNA-splicing factor ATP-dependent RNA helicase PRP1 (Fragment) OS=Strongylocentrotus purpuratus GN=PRP1 PE=2 SV=1 466 906 7.0E-140
sp|Q9HE06|YK99_SCHPO Putative pre-mRNA-splicing factor ATP-dependent RNA helicase C20H4.09 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC20H4.09 PE=3 SV=1 363 960 3.0E-131
sp|P36009|DHR2_YEAST Probable ATP-dependent RNA helicase DHR2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DHR2 PE=1 SV=1 369 994 1.0E-129
sp|P45018|HRPA_HAEIN ATP-dependent RNA helicase HrpA homolog OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=hrpA PE=3 SV=2 337 997 8.0E-111
sp|P43329|HRPA_ECOLI ATP-dependent RNA helicase HrpA OS=Escherichia coli (strain K12) GN=hrpA PE=3 SV=3 371 997 6.0E-106
sp|F4KGU4|DEAHC_ARATH ATP-dependent RNA helicase DEAH12, chloroplastic OS=Arabidopsis thaliana GN=At5g10370 PE=3 SV=1 315 1009 4.0E-103
sp|Q14147|DHX34_HUMAN Probable ATP-dependent RNA helicase DHX34 OS=Homo sapiens GN=DHX34 PE=1 SV=2 339 897 1.0E-102
sp|Q9DBV3|DHX34_MOUSE Probable ATP-dependent RNA helicase DHX34 OS=Mus musculus GN=Dhx34 PE=1 SV=2 339 897 3.0E-101
sp|Q9HDY4|YK16_SCHPO Putative ATP-dependent RNA helicase PB1A10.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAPB1A10.06c PE=3 SV=1 365 898 1.0E-99
sp|P0CE10|DEAHB_ARATH ATP-dependent RNA helicase DEAH11, chloroplastic OS=Arabidopsis thaliana GN=At4g01020 PE=3 SV=1 363 1009 2.0E-99
sp|Q5XH12|DHX32_XENLA Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Xenopus laevis GN=dhx32 PE=2 SV=1 369 996 3.0E-94
sp|Q8BZS9|DHX32_MOUSE Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Mus musculus GN=Dhx32 PE=1 SV=2 369 996 9.0E-91
sp|Q7L7V1|DHX32_HUMAN Putative pre-mRNA-splicing factor ATP-dependent RNA helicase DHX32 OS=Homo sapiens GN=DHX32 PE=1 SV=1 369 996 1.0E-88
sp|Q7L2E3|DHX30_HUMAN Putative ATP-dependent RNA helicase DHX30 OS=Homo sapiens GN=DHX30 PE=1 SV=1 347 882 7.0E-86
sp|Q5ZI74|DHX30_CHICK Putative ATP-dependent RNA helicase DHX30 OS=Gallus gallus GN=DHX30 PE=2 SV=1 347 878 1.0E-85
sp|Q2NKY8|DHX30_BOVIN Putative ATP-dependent RNA helicase DHX30 OS=Bos taurus GN=DHX30 PE=2 SV=1 347 882 2.0E-85
sp|Q99PU8|DHX30_MOUSE Putative ATP-dependent RNA helicase DHX30 OS=Mus musculus GN=Dhx30 PE=1 SV=1 347 882 2.0E-85
sp|Q5BJS0|DHX30_RAT Putative ATP-dependent RNA helicase DHX30 OS=Rattus norvegicus GN=Dhx30 PE=1 SV=1 347 882 3.0E-85
sp|Q5R607|DHX30_PONAB Putative ATP-dependent RNA helicase DHX30 OS=Pongo abelii GN=DHX30 PE=2 SV=1 347 882 1.0E-84
sp|Q924H9|DQX1_MOUSE ATP-dependent RNA helicase DQX1 OS=Mus musculus GN=Dqx1 PE=2 SV=1 365 996 2.0E-78
sp|O94536|UCP12_SCHPO Putative ATP-dependent RNA helicase ucp12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ucp12 PE=3 SV=1 369 984 1.0E-77
sp|Q3ZBE0|DQX1_BOVIN ATP-dependent RNA helicase DQX1 OS=Bos taurus GN=DQX1 PE=2 SV=1 365 996 3.0E-77
sp|Q8TE96|DQX1_HUMAN ATP-dependent RNA helicase DQX1 OS=Homo sapiens GN=DQX1 PE=2 SV=2 369 996 3.0E-67
sp|P0C7L7|YUM14_USTMA Putative DEAH-box ATP-dependent helicase UM11114 OS=Ustilago maydis (strain 521 / FGSC 9021) GN=UMAG_11114 PE=3 SV=1 365 844 2.0E-65
sp|P37024|HRPB_ECOLI ATP-dependent RNA helicase HrpB OS=Escherichia coli (strain K12) GN=hrpB PE=3 SV=3 371 804 2.0E-64
sp|Q06698|YL419_YEAST Putative ATP-dependent RNA helicase YLR419W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YLR419W PE=1 SV=1 364 945 1.0E-62
sp|B0XDC4|SPNE_CULQU Probable ATP-dependent RNA helicase spindle-E OS=Culex quinquefasciatus GN=spn-E PE=3 SV=1 369 928 5.0E-62
sp|Q16JS8|SPNE_AEDAE Probable ATP-dependent RNA helicase spindle-E OS=Aedes aegypti GN=spn-E PE=3 SV=1 336 862 6.0E-62
sp|B8A4F4|TDRD9_DANRE Putative ATP-dependent RNA helicase TDRD9 OS=Danio rerio GN=tdrd9 PE=2 SV=1 372 899 2.0E-61
sp|Q296Q5|SPNE_DROPS Probable ATP-dependent RNA helicase spindle-E OS=Drosophila pseudoobscura pseudoobscura GN=spn-E PE=3 SV=2 370 901 5.0E-61
sp|B4HLH4|SPNE_DROSE Probable ATP-dependent RNA helicase spindle-E OS=Drosophila sechellia GN=spn-E PE=3 SV=1 370 935 8.0E-60
sp|B4JT42|SPNE_DROGR Probable ATP-dependent RNA helicase spindle-E OS=Drosophila grimshawi GN=spn-E PE=3 SV=1 370 901 1.0E-59
sp|B4GEU5|SPNE_DROPE Probable ATP-dependent RNA helicase spindle-E OS=Drosophila persimilis GN=spn-E PE=3 SV=1 370 901 1.0E-59
sp|B4LX81|SPNE_DROVI Probable ATP-dependent RNA helicase spindle-E OS=Drosophila virilis GN=spn-E PE=3 SV=1 370 907 2.0E-58
sp|Q9VF26|SPNE_DROME Probable ATP-dependent RNA helicase spindle-E OS=Drosophila melanogaster GN=spn-E PE=2 SV=1 370 904 2.0E-58
sp|Q7QCW2|SPNE_ANOGA Probable ATP-dependent RNA helicase spindle-E OS=Anopheles gambiae GN=spn-E PE=3 SV=5 368 862 2.0E-58
sp|Q8NDG6|TDRD9_HUMAN Putative ATP-dependent RNA helicase TDRD9 OS=Homo sapiens GN=TDRD9 PE=2 SV=3 372 899 1.0E-57
sp|B3P3W1|SPNE_DROER Probable ATP-dependent RNA helicase spindle-E OS=Drosophila erecta GN=spn-E PE=3 SV=1 370 906 3.0E-57
sp|B3M383|SPNE_DROAN Probable ATP-dependent RNA helicase spindle-E OS=Drosophila ananassae GN=spn-E PE=3 SV=1 370 905 1.0E-56
sp|B4NBB0|SPNE_DROWI Probable ATP-dependent RNA helicase spindle-E OS=Drosophila willistoni GN=spn-E PE=3 SV=1 370 926 1.0E-56
sp|B4PRJ9|SPNE_DROYA Probable ATP-dependent RNA helicase spindle-E OS=Drosophila yakuba GN=spn-E PE=3 SV=1 370 906 6.0E-56
sp|Q14BI7|TDRD9_MOUSE Putative ATP-dependent RNA helicase TDRD9 OS=Mus musculus GN=Tdrd9 PE=1 SV=3 372 899 1.0E-55
sp|F4ILR7|DEXH1_ARATH DExH-box ATP-dependent RNA helicase DExH1 OS=Arabidopsis thaliana GN=At2g35920 PE=2 SV=1 571 988 2.0E-55
sp|Q3MHU3|TDRD9_RAT Putative ATP-dependent RNA helicase TDRD9 OS=Rattus norvegicus GN=Tdrd9 PE=2 SV=3 372 899 2.0E-55
sp|Q5UQ96|YL540_MIMIV Putative ATP-dependent RNA helicase L540 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_L540 PE=1 SV=1 371 874 1.0E-53
sp|B4K5R2|SPNE_DROMO Probable ATP-dependent RNA helicase spindle-E OS=Drosophila mojavensis GN=spn-E PE=3 SV=1 370 895 3.0E-52
sp|Q04217|DHR1_YEAST Probable ATP-dependent RNA helicase DHR1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ECM16 PE=1 SV=1 365 594 3.0E-50
sp|Q8IY37|DHX37_HUMAN Probable ATP-dependent RNA helicase DHX37 OS=Homo sapiens GN=DHX37 PE=1 SV=1 615 995 1.0E-49
sp|Q9C813|DEAHD_ARATH ATP-dependent RNA helicase DEAH13 OS=Arabidopsis thaliana GN=FAS4 PE=2 SV=1 361 608 4.0E-49
sp|O46072|KZ_DROME Probable ATP-dependent RNA helicase kurz OS=Drosophila melanogaster GN=kz PE=1 SV=1 361 604 4.0E-49
sp|Q8IY37|DHX37_HUMAN Probable ATP-dependent RNA helicase DHX37 OS=Homo sapiens GN=DHX37 PE=1 SV=1 361 601 2.0E-47
sp|Q6P158|DHX57_HUMAN Putative ATP-dependent RNA helicase DHX57 OS=Homo sapiens GN=DHX57 PE=1 SV=2 317 562 2.0E-47
sp|F4I9Q5|DEXH7_ARATH DExH-box ATP-dependent RNA helicase DExH7, chloroplastic OS=Arabidopsis thaliana GN=At1g58060 PE=2 SV=1 574 988 6.0E-47
sp|F4HYJ7|DEXH3_ARATH DExH-box ATP-dependent RNA helicase DExH3 OS=Arabidopsis thaliana GN=At1g48650 PE=2 SV=1 520 978 5.0E-46
sp|Q6P158|DHX57_HUMAN Putative ATP-dependent RNA helicase DHX57 OS=Homo sapiens GN=DHX57 PE=1 SV=2 582 983 6.0E-46
sp|F4ILR7|DEXH1_ARATH DExH-box ATP-dependent RNA helicase DExH1 OS=Arabidopsis thaliana GN=At2g35920 PE=2 SV=1 364 552 1.0E-45
sp|F4IM84|DEXH5_ARATH DExH-box ATP-dependent RNA helicase DExH5, mitochondrial OS=Arabidopsis thaliana GN=At2g01130 PE=3 SV=1 575 923 3.0E-45
sp|Q6P5D3|DHX57_MOUSE Putative ATP-dependent RNA helicase DHX57 OS=Mus musculus GN=Dhx57 PE=1 SV=2 582 983 9.0E-45
sp|F4IM84|DEXH5_ARATH DExH-box ATP-dependent RNA helicase DExH5, mitochondrial OS=Arabidopsis thaliana GN=At2g01130 PE=3 SV=1 367 552 2.0E-44
sp|Q8VHK9|DHX36_MOUSE ATP-dependent RNA helicase DHX36 OS=Mus musculus GN=Dhx36 PE=1 SV=2 582 959 2.0E-44
sp|P34305|RHA2_CAEEL Putative ATP-dependent RNA helicase rha-2 OS=Caenorhabditis elegans GN=rha-2 PE=3 SV=2 361 595 3.0E-44
sp|Q7Z478|DHX29_HUMAN ATP-dependent RNA helicase DHX29 OS=Homo sapiens GN=DHX29 PE=1 SV=2 581 978 5.0E-44
sp|A3KMI0|DHX29_XENLA ATP-dependent RNA helicase DHX29 OS=Xenopus laevis GN=dhx29 PE=2 SV=1 581 978 6.0E-44
sp|Q6PGC1|DHX29_MOUSE ATP-dependent RNA helicase Dhx29 OS=Mus musculus GN=Dhx29 PE=1 SV=1 581 978 1.0E-43
sp|F4HYJ7|DEXH3_ARATH DExH-box ATP-dependent RNA helicase DExH3 OS=Arabidopsis thaliana GN=At1g48650 PE=2 SV=1 369 552 2.0E-43
sp|Q9H2U1|DHX36_HUMAN ATP-dependent RNA helicase DHX36 OS=Homo sapiens GN=DHX36 PE=1 SV=2 582 977 2.0E-43
sp|B2RR83|YTDC2_MOUSE Probable ATP-dependent RNA helicase YTHDC2 OS=Mus musculus GN=Ythdc2 PE=1 SV=1 573 955 3.0E-43
sp|Q6P5D3|DHX57_MOUSE Putative ATP-dependent RNA helicase DHX57 OS=Mus musculus GN=Dhx57 PE=1 SV=2 348 555 7.0E-43
sp|A3KMI0|DHX29_XENLA ATP-dependent RNA helicase DHX29 OS=Xenopus laevis GN=dhx29 PE=2 SV=1 369 556 1.0E-42
sp|Q9H6S0|YTDC2_HUMAN Probable ATP-dependent RNA helicase YTHDC2 OS=Homo sapiens GN=YTHDC2 PE=1 SV=2 573 955 1.0E-42
sp|Q04217|DHR1_YEAST Probable ATP-dependent RNA helicase DHR1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ECM16 PE=1 SV=1 615 821 2.0E-42
sp|O46072|KZ_DROME Probable ATP-dependent RNA helicase kurz OS=Drosophila melanogaster GN=kz PE=1 SV=1 615 1013 1.0E-41
sp|F4INY4|HVT1_ARATH DExH-box ATP-dependent RNA helicase DExH6 OS=Arabidopsis thaliana GN=HVT1 PE=2 SV=1 353 552 2.0E-41
sp|F4IDQ6|NIH_ARATH DExH-box ATP-dependent RNA helicase DExH2 OS=Arabidopsis thaliana GN=NIH PE=1 SV=1 365 555 3.0E-41
sp|Q9H2U1|DHX36_HUMAN ATP-dependent RNA helicase DHX36 OS=Homo sapiens GN=DHX36 PE=1 SV=2 342 552 4.0E-41
sp|O60114|YG65_SCHPO Uncharacterized helicase C15C4.05 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC15C4.05 PE=3 SV=1 584 925 5.0E-41
sp|Q7Z478|DHX29_HUMAN ATP-dependent RNA helicase DHX29 OS=Homo sapiens GN=DHX29 PE=1 SV=2 369 556 8.0E-41
sp|B2RR83|YTDC2_MOUSE Probable ATP-dependent RNA helicase YTHDC2 OS=Mus musculus GN=Ythdc2 PE=1 SV=1 369 552 8.0E-41
sp|Q9H6S0|YTDC2_HUMAN Probable ATP-dependent RNA helicase YTHDC2 OS=Homo sapiens GN=YTHDC2 PE=1 SV=2 369 552 9.0E-41
sp|Q6PGC1|DHX29_MOUSE ATP-dependent RNA helicase Dhx29 OS=Mus musculus GN=Dhx29 PE=1 SV=1 325 556 3.0E-40
sp|Q68FK8|DHX9_XENLA ATP-dependent RNA helicase A-like protein OS=Xenopus laevis GN=dhx9 PE=2 SV=1 325 555 4.0E-40
sp|Q9C6G0|DEXH4_ARATH DExH-box ATP-dependent RNA helicase DExH4, chloroplastic OS=Arabidopsis thaliana GN=At1g58050 PE=3 SV=1 553 834 4.0E-40
sp|Q8VHK9|DHX36_MOUSE ATP-dependent RNA helicase DHX36 OS=Mus musculus GN=Dhx36 PE=1 SV=2 352 552 5.0E-40
sp|Q68FK8|DHX9_XENLA ATP-dependent RNA helicase A-like protein OS=Xenopus laevis GN=dhx9 PE=2 SV=1 575 988 3.0E-39
sp|O70133|DHX9_MOUSE ATP-dependent RNA helicase A OS=Mus musculus GN=Dhx9 PE=1 SV=2 575 988 6.0E-39
sp|Q9C813|DEAHD_ARATH ATP-dependent RNA helicase DEAH13 OS=Arabidopsis thaliana GN=FAS4 PE=2 SV=1 614 979 1.0E-38
sp|Q28141|DHX9_BOVIN ATP-dependent RNA helicase A OS=Bos taurus GN=DHX9 PE=2 SV=1 325 555 4.0E-38
sp|Q5R874|DHX9_PONAB ATP-dependent RNA helicase A OS=Pongo abelii GN=DHX9 PE=2 SV=1 325 555 7.0E-38
sp|Q08211|DHX9_HUMAN ATP-dependent RNA helicase A OS=Homo sapiens GN=DHX9 PE=1 SV=4 325 555 7.0E-38
sp|P34305|RHA2_CAEEL Putative ATP-dependent RNA helicase rha-2 OS=Caenorhabditis elegans GN=rha-2 PE=3 SV=2 615 995 2.0E-37
sp|P24785|MLE_DROME Dosage compensation regulator OS=Drosophila melanogaster GN=mle PE=1 SV=2 367 552 2.0E-37
sp|P0C9A4|H962L_ASFK5 Putative RNA Helicase B962L OS=African swine fever virus (isolate Pig/Kenya/KEN-50/1950) GN=Ken-084 PE=3 SV=1 389 791 7.0E-37
sp|Q1EHT7|C3H4_ORYSJ Zinc finger CCCH domain-containing protein 4 OS=Oryza sativa subsp. japonica GN=Os01g0256800 PE=2 SV=1 355 776 8.0E-37
sp|F4IDQ6|NIH_ARATH DExH-box ATP-dependent RNA helicase DExH2 OS=Arabidopsis thaliana GN=NIH PE=1 SV=1 574 868 9.0E-37
sp|F4INY4|HVT1_ARATH DExH-box ATP-dependent RNA helicase DExH6 OS=Arabidopsis thaliana GN=HVT1 PE=2 SV=1 582 933 1.0E-36
sp|Q28141|DHX9_BOVIN ATP-dependent RNA helicase A OS=Bos taurus GN=DHX9 PE=2 SV=1 575 988 2.0E-36
sp|Q5R874|DHX9_PONAB ATP-dependent RNA helicase A OS=Pongo abelii GN=DHX9 PE=2 SV=1 575 988 2.0E-36
sp|Q08211|DHX9_HUMAN ATP-dependent RNA helicase A OS=Homo sapiens GN=DHX9 PE=1 SV=4 575 988 2.0E-36
sp|Q89443|H962L_ASFB7 Putative RNA helicase B962L OS=African swine fever virus (strain Badajoz 1971 Vero-adapted) GN=Ba71V-072 PE=3 SV=1 389 791 2.0E-36
sp|Q8V9U2|H962L_ASFM2 Putative RNA Helicase B962L OS=African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) GN=Mal-080 PE=3 SV=1 389 791 3.0E-36
sp|P0C9A3|H962L_ASFWA Putative RNA Helicase B962L OS=African swine fever virus (isolate Warthog/Namibia/Wart80/1980) GN=War-082 PE=3 SV=1 389 791 4.0E-36
sp|P0C9A2|H962L_ASFP4 Putative RNA Helicase B962L OS=African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) GN=Pret-084 PE=3 SV=1 389 791 4.0E-36
sp|O60114|YG65_SCHPO Uncharacterized helicase C15C4.05 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC15C4.05 PE=3 SV=1 369 552 8.0E-36
sp|O70133|DHX9_MOUSE ATP-dependent RNA helicase A OS=Mus musculus GN=Dhx9 PE=1 SV=2 325 555 3.0E-34
sp|F4I9Q5|DEXH7_ARATH DExH-box ATP-dependent RNA helicase DExH7, chloroplastic OS=Arabidopsis thaliana GN=At1g58060 PE=2 SV=1 367 567 2.0E-33
sp|O22243|C3H31_ARATH DExH-box ATP-dependent RNA helicase DExH8 OS=Arabidopsis thaliana GN=At2g47680 PE=2 SV=2 371 803 2.0E-33
sp|P24785|MLE_DROME Dosage compensation regulator OS=Drosophila melanogaster GN=mle PE=1 SV=2 573 827 8.0E-33
sp|Q5UR20|YR366_MIMIV Putative ATP-dependent RNA helicase R366 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R366 PE=3 SV=1 389 741 1.0E-32
sp|Q9C6G0|DEXH4_ARATH DExH-box ATP-dependent RNA helicase DExH4, chloroplastic OS=Arabidopsis thaliana GN=At1g58050 PE=3 SV=1 367 555 2.0E-32
sp|Q22307|DHX9_CAEEL Probable ATP-dependent RNA helicase A OS=Caenorhabditis elegans GN=rha-1 PE=2 SV=3 309 555 4.0E-31
sp|Q22307|DHX9_CAEEL Probable ATP-dependent RNA helicase A OS=Caenorhabditis elegans GN=rha-1 PE=2 SV=3 582 858 2.0E-21
sp|Q5R746|YTDC2_PONAB YTH domain-containing protein 2 OS=Pongo abelii GN=YTHDC2 PE=2 SV=1 720 955 1.0E-10
sp|P90245|POL1_BAMMN Genome polyprotein 1 OS=Barley mild mosaic virus (strain Na1) PE=3 SV=1 393 705 4.0E-10
sp|Q9Q8Q2|NPH2_MYXVL RNA helicase NPH-II OS=Myxoma virus (strain Lausanne) GN=NPH2 PE=3 SV=1 391 711 8.0E-10
sp|Q9W1I2|BGCN_DROME Benign gonial cell neoplasm protein OS=Drosophila melanogaster GN=bgcn PE=1 SV=2 582 960 3.0E-09
sp|Q9Q927|NPH2_RFVKA RNA helicase NPH-II OS=Rabbit fibroma virus (strain Kasza) GN=NPH2 PE=2 SV=1 391 711 7.0E-09
sp|Q9W1I2|BGCN_DROME Benign gonial cell neoplasm protein OS=Drosophila melanogaster GN=bgcn PE=1 SV=2 380 538 1.0E-08
sp|P21231|POLG_SBMVN Genome polyprotein OS=Soybean mosaic virus (strain N) PE=1 SV=2 344 710 4.0E-07
sp|O36979|POLG_ZYMVS Genome polyprotein OS=Zucchini yellow mosaic virus (strain Singapore) PE=3 SV=2 340 710 4.0E-06
sp|Q98218|NPH2_MCV1 RNA helicase NPH-II OS=Molluscum contagiosum virus subtype 1 GN=NPH2 PE=3 SV=1 479 711 7.0E-06
[Show less]

GO

GO Term Description Terminal node
GO:0003676 nucleic acid binding Yes
GO:0005524 ATP binding Yes
GO:0004386 helicase activity Yes
GO:0017076 purine nucleotide binding No
GO:0005488 binding No
GO:0003674 molecular_function No
GO:0035639 purine ribonucleoside triphosphate binding No
GO:0000166 nucleotide binding No
GO:0043167 ion binding No
GO:0140640 catalytic activity, acting on a nucleic acid No
GO:0032553 ribonucleotide binding No
GO:0097367 carbohydrate derivative binding No
GO:0003824 catalytic activity No
GO:0043168 anion binding No
GO:0097159 organic cyclic compound binding No
GO:1901265 nucleoside phosphate binding No
GO:0032555 purine ribonucleotide binding No
GO:1901363 heterocyclic compound binding No
GO:0032559 adenyl ribonucleotide binding No
GO:0036094 small molecule binding No
GO:0140657 ATP-dependent activity No
GO:0030554 adenyl nucleotide binding No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 42 0.45

Transmembrane Domains

(None)

Transcription Factor Class

(None)

Expression data

No expression data available for this genome

Sequences

Type of sequenceSequence
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 >OphauB2|2015
MKKYAFVPMDDDEVGPQKISKENKHRRRHRSTDGDGDISKRSTSKRHRSRSKSPSDPKSSSHRSKRNRTYRHRHV
EADFDDRWGDEEPPSEPDQEYDGGEPEESASKRVKLSHRDEAPREEDLSDGAKEERARQKDIEERETFAKRLKEK
DGSNSRRQSAEGAATSSRRKLATDAIAREAALPDLRLRSRQEYLGKRGAENLALFRKQVAAETAELQSGVRLSKR
EKARFAENRETLRLAEEHLKIDDYRDGYKMPEEYVTDQGKIDLKKKEEALHKRYVERDEMGQEKFVTEHELFERE
QIAKVKAQVKLAQAGSDNYSYVLDEEQYSKWVKDSTLAGVGEGKTKEQIALDAQIEEAEKRDLSIQETRRSLPMY
KYRQEILDAIEKYQILVIVGETGSGKTTQLPQYLHEAGYTKNGMKVGCTQPRRVAAMSIAARVAQEVGVKLGNEV
GYSVRFEDNTNDKTVLKYMTDGMLLRELMTEPQLEGYSALMIDEAHERTVHTDILLALVKDLARARPELKLLISS
ATMDAEKFSDYFGRAPIFNIPGRRFPVDIYNTPEPVANYLTAAVTTTFQIHTTQGKGDILIFLTGQEEIEAAERE
ITETSRKLGNRIKELVICPIYANLPSELQSKIFEPTPEGARKVVLATNIAETSLTIDGIVYVIDPGFVKENVYDS
ATGMSNLVVVPCSRASANQRSGRAGRVGPGKCFRLYTKFSYNDEMQQSTTPEIQRTNLNGVILQLMCLGVSNIFQ
FDYLDRPSAESMKGAFNQLYALEAINHKGQLTKVGRQMAEFPTDPMLAKVLIVAHAQGCVDEALSVVAMLAESAA
LFFRPKDRKVHADSARARFTVREGGDHATLLNIWTQWVDADYSPVWARENYLQQRSLTRARDVRDQLAKLCERVE
LDAFSTCGAANGNLRPLKRALTAGFFLNAARLAKDGYRTLKKRTGVWIHPSSVLNDVHPPERLVVYYELVQTSKE
YMRGVFPIDVALLREVAPHYYKPVDLDELEVKKMPKNRQ*
Coding >OphauB2|2015
ATGAAAAAGTACGCCTTTGTACCCATGGACGATGACGAAGTCGGGCCCCAAAAAATATCAAAAGAAAACAAGCAC
AGACGTCGGCATCGCTCCACTGACGGCGACGGCGACATCTCAAAGCGCTCAACCTCGAAACGCCATCGCTCCCGC
TCCAAGTCCCCTTCCGACCCGAAATCTTCCAGTCACCGCTCAAAACGTAACAGAACCTATCGCCACCGACATGTA
GAGGCCGACTTCGACGACCGGTGGGGGGATGAGGAGCCTCCATCAGAGCCTGATCAGGAGTATGACGGCGGCGAG
CCAGAAGAATCTGCAAGCAAGCGCGTCAAGCTCAGTCACCGTGATGAGGCGCCACGAGAAGAGGATTTGTCAGAC
GGCGCCAAGGAGGAACGTGCCAGGCAAAAGGATATTGAAGAGCGCGAGACCTTTGCCAAGCGACTAAAGGAAAAG
GACGGCTCCAATTCGAGAAGACAGAGTGCCGAGGGGGCTGCCACTTCTTCCAGACGAAAGCTCGCCACAGATGCC
ATTGCACGAGAGGCCGCGTTGCCAGACTTGCGACTGCGGTCACGGCAAGAGTATCTGGGCAAGCGTGGAGCAGAG
AACCTGGCTCTCTTTCGGAAGCAAGTCGCTGCAGAAACGGCCGAGCTGCAGAGTGGCGTCCGCCTCTCCAAGAGA
GAAAAGGCCAGATTTGCGGAAAACAGGGAGACGTTGCGTCTGGCTGAAGAGCACCTGAAAATCGACGACTACCGC
GATGGCTACAAGATGCCCGAGGAGTATGTGACGGACCAGGGCAAGATTGACCTCAAAAAGAAGGAGGAGGCGCTT
CACAAGCGATATGTCGAGCGCGACGAAATGGGCCAGGAGAAGTTTGTGACTGAGCATGAATTGTTTGAGAGAGAG
CAAATAGCCAAAGTCAAGGCCCAAGTCAAGCTTGCACAAGCCGGAAGCGACAACTACTCGTACGTGCTCGACGAG
GAACAATACTCCAAGTGGGTCAAGGACTCAACACTGGCGGGTGTGGGCGAGGGCAAGACCAAGGAGCAGATTGCC
TTGGACGCGCAAATCGAAGAAGCCGAAAAGAGGGACTTGTCAATACAGGAGACGCGGCGAAGCCTACCCATGTAC
AAGTATCGACAAGAGATACTGGATGCCATTGAAAAGTATCAGATTCTTGTCATTGTCGGCGAGACGGGAAGCGGC
AAGACGACGCAGCTGCCGCAGTATCTGCACGAAGCAGGATACACCAAGAATGGCATGAAGGTTGGGTGCACGCAG
CCACGGCGAGTGGCTGCCATGAGCATAGCGGCTCGAGTAGCCCAAGAGGTTGGCGTCAAGTTGGGCAACGAGGTG
GGATACTCTGTGCGCTTCGAGGACAATACAAACGACAAGACGGTGCTCAAGTACATGACGGACGGCATGCTGCTG
CGAGAGCTCATGACGGAGCCACAGCTCGAGGGATACTCGGCCCTCATGATTGACGAGGCTCACGAGCGCACAGTG
CACACTGATATTCTGCTGGCCTTGGTCAAGGACCTGGCGCGTGCGCGGCCCGAGCTGAAGCTCCTGATATCCTCG
GCCACGATGGACGCGGAAAAGTTTTCAGACTACTTTGGCAGAGCGCCCATTTTCAACATTCCCGGCCGCAGATTT
CCAGTCGACATATACAATACACCAGAACCAGTGGCGAATTACCTGACAGCGGCCGTGACGACGACGTTTCAAATC
CACACGACCCAAGGCAAAGGGGACATCCTAATCTTCCTCACCGGACAAGAGGAAATCGAAGCGGCAGAGCGCGAA
ATCACGGAAACATCTCGCAAACTCGGCAACCGCATCAAGGAGCTCGTTATATGTCCCATTTATGCCAACTTGCCG
TCGGAACTGCAGTCCAAGATTTTTGAGCCGACGCCCGAGGGCGCGCGCAAAGTGGTGCTGGCCACCAACATTGCC
GAGACGAGTCTGACGATTGACGGCATCGTCTATGTCATTGATCCTGGCTTTGTCAAGGAGAATGTCTATGACTCG
GCCACGGGCATGTCCAACCTGGTGGTGGTGCCGTGCTCGCGCGCGTCGGCCAACCAGCGCTCGGGACGTGCTGGG
CGTGTCGGCCCTGGCAAATGCTTCCGACTGTATACCAAGTTCTCGTACAATGACGAGATGCAGCAGTCCACCACG
CCCGAGATTCAACGCACCAATCTCAACGGCGTCATCTTGCAGCTCATGTGCCTGGGCGTCTCCAACATCTTCCAG
TTTGACTACTTGGATCGCCCGTCGGCCGAATCCATGAAGGGCGCCTTTAACCAGCTCTATGCGCTCGAGGCCATC
AACCACAAAGGTCAGCTGACCAAGGTTGGGCGGCAAATGGCAGAGTTTCCCACCGATCCCATGCTGGCCAAGGTG
TTGATTGTGGCCCATGCACAAGGCTGCGTCGACGAGGCGCTGTCCGTTGTTGCCATGCTGGCCGAATCGGCAGCC
CTTTTTTTCCGGCCCAAGGACCGCAAAGTACACGCCGACAGTGCTCGGGCGCGCTTCACGGTGCGCGAGGGCGGC
GACCATGCAACCTTGCTCAATATCTGGACGCAATGGGTCGATGCCGACTACTCGCCCGTATGGGCCCGCGAAAAC
TATTTGCAGCAGCGGTCCCTGACGAGGGCCCGCGACGTGCGCGACCAATTGGCCAAGCTATGCGAGCGCGTCGAG
CTCGATGCCTTTTCAACCTGTGGCGCGGCAAACGGCAACCTGAGGCCGCTTAAGCGAGCCCTGACGGCCGGCTTC
TTCCTCAACGCGGCGCGGCTGGCCAAGGATGGATACCGCACGCTCAAGAAGAGGACGGGCGTGTGGATTCATCCC
AGTAGTGTCTTGAACGACGTGCACCCCCCAGAGAGGCTGGTGGTGTACTATGAGCTGGTGCAGACGTCAAAGGAG
TACATGAGGGGCGTCTTTCCCATTGATGTGGCCTTGCTGAGGGAGGTGGCGCCGCATTACTACAAGCCAGTAGAC
TTGGACGAGCTCGAGGTGAAGAAGATGCCAAAGAATAGGCAATAG
Transcript >OphauB2|2015
ATGAAAAAGTACGCCTTTGTACCCATGGACGATGACGAAGTCGGGCCCCAAAAAATATCAAAAGAAAACAAGCAC
AGACGTCGGCATCGCTCCACTGACGGCGACGGCGACATCTCAAAGCGCTCAACCTCGAAACGCCATCGCTCCCGC
TCCAAGTCCCCTTCCGACCCGAAATCTTCCAGTCACCGCTCAAAACGTAACAGAACCTATCGCCACCGACATGTA
GAGGCCGACTTCGACGACCGGTGGGGGGATGAGGAGCCTCCATCAGAGCCTGATCAGGAGTATGACGGCGGCGAG
CCAGAAGAATCTGCAAGCAAGCGCGTCAAGCTCAGTCACCGTGATGAGGCGCCACGAGAAGAGGATTTGTCAGAC
GGCGCCAAGGAGGAACGTGCCAGGCAAAAGGATATTGAAGAGCGCGAGACCTTTGCCAAGCGACTAAAGGAAAAG
GACGGCTCCAATTCGAGAAGACAGAGTGCCGAGGGGGCTGCCACTTCTTCCAGACGAAAGCTCGCCACAGATGCC
ATTGCACGAGAGGCCGCGTTGCCAGACTTGCGACTGCGGTCACGGCAAGAGTATCTGGGCAAGCGTGGAGCAGAG
AACCTGGCTCTCTTTCGGAAGCAAGTCGCTGCAGAAACGGCCGAGCTGCAGAGTGGCGTCCGCCTCTCCAAGAGA
GAAAAGGCCAGATTTGCGGAAAACAGGGAGACGTTGCGTCTGGCTGAAGAGCACCTGAAAATCGACGACTACCGC
GATGGCTACAAGATGCCCGAGGAGTATGTGACGGACCAGGGCAAGATTGACCTCAAAAAGAAGGAGGAGGCGCTT
CACAAGCGATATGTCGAGCGCGACGAAATGGGCCAGGAGAAGTTTGTGACTGAGCATGAATTGTTTGAGAGAGAG
CAAATAGCCAAAGTCAAGGCCCAAGTCAAGCTTGCACAAGCCGGAAGCGACAACTACTCGTACGTGCTCGACGAG
GAACAATACTCCAAGTGGGTCAAGGACTCAACACTGGCGGGTGTGGGCGAGGGCAAGACCAAGGAGCAGATTGCC
TTGGACGCGCAAATCGAAGAAGCCGAAAAGAGGGACTTGTCAATACAGGAGACGCGGCGAAGCCTACCCATGTAC
AAGTATCGACAAGAGATACTGGATGCCATTGAAAAGTATCAGATTCTTGTCATTGTCGGCGAGACGGGAAGCGGC
AAGACGACGCAGCTGCCGCAGTATCTGCACGAAGCAGGATACACCAAGAATGGCATGAAGGTTGGGTGCACGCAG
CCACGGCGAGTGGCTGCCATGAGCATAGCGGCTCGAGTAGCCCAAGAGGTTGGCGTCAAGTTGGGCAACGAGGTG
GGATACTCTGTGCGCTTCGAGGACAATACAAACGACAAGACGGTGCTCAAGTACATGACGGACGGCATGCTGCTG
CGAGAGCTCATGACGGAGCCACAGCTCGAGGGATACTCGGCCCTCATGATTGACGAGGCTCACGAGCGCACAGTG
CACACTGATATTCTGCTGGCCTTGGTCAAGGACCTGGCGCGTGCGCGGCCCGAGCTGAAGCTCCTGATATCCTCG
GCCACGATGGACGCGGAAAAGTTTTCAGACTACTTTGGCAGAGCGCCCATTTTCAACATTCCCGGCCGCAGATTT
CCAGTCGACATATACAATACACCAGAACCAGTGGCGAATTACCTGACAGCGGCCGTGACGACGACGTTTCAAATC
CACACGACCCAAGGCAAAGGGGACATCCTAATCTTCCTCACCGGACAAGAGGAAATCGAAGCGGCAGAGCGCGAA
ATCACGGAAACATCTCGCAAACTCGGCAACCGCATCAAGGAGCTCGTTATATGTCCCATTTATGCCAACTTGCCG
TCGGAACTGCAGTCCAAGATTTTTGAGCCGACGCCCGAGGGCGCGCGCAAAGTGGTGCTGGCCACCAACATTGCC
GAGACGAGTCTGACGATTGACGGCATCGTCTATGTCATTGATCCTGGCTTTGTCAAGGAGAATGTCTATGACTCG
GCCACGGGCATGTCCAACCTGGTGGTGGTGCCGTGCTCGCGCGCGTCGGCCAACCAGCGCTCGGGACGTGCTGGG
CGTGTCGGCCCTGGCAAATGCTTCCGACTGTATACCAAGTTCTCGTACAATGACGAGATGCAGCAGTCCACCACG
CCCGAGATTCAACGCACCAATCTCAACGGCGTCATCTTGCAGCTCATGTGCCTGGGCGTCTCCAACATCTTCCAG
TTTGACTACTTGGATCGCCCGTCGGCCGAATCCATGAAGGGCGCCTTTAACCAGCTCTATGCGCTCGAGGCCATC
AACCACAAAGGTCAGCTGACCAAGGTTGGGCGGCAAATGGCAGAGTTTCCCACCGATCCCATGCTGGCCAAGGTG
TTGATTGTGGCCCATGCACAAGGCTGCGTCGACGAGGCGCTGTCCGTTGTTGCCATGCTGGCCGAATCGGCAGCC
CTTTTTTTCCGGCCCAAGGACCGCAAAGTACACGCCGACAGTGCTCGGGCGCGCTTCACGGTGCGCGAGGGCGGC
GACCATGCAACCTTGCTCAATATCTGGACGCAATGGGTCGATGCCGACTACTCGCCCGTATGGGCCCGCGAAAAC
TATTTGCAGCAGCGGTCCCTGACGAGGGCCCGCGACGTGCGCGACCAATTGGCCAAGCTATGCGAGCGCGTCGAG
CTCGATGCCTTTTCAACCTGTGGCGCGGCAAACGGCAACCTGAGGCCGCTTAAGCGAGCCCTGACGGCCGGCTTC
TTCCTCAACGCGGCGCGGCTGGCCAAGGATGGATACCGCACGCTCAAGAAGAGGACGGGCGTGTGGATTCATCCC
AGTAGTGTCTTGAACGACGTGCACCCCCCAGAGAGGCTGGTGGTGTACTATGAGCTGGTGCAGACGTCAAAGGAG
TACATGAGGGGCGTCTTTCCCATTGATGTGGCCTTGCTGAGGGAGGTGGCGCCGCATTACTACAAGCCAGTAGAC
TTGGACGAGCTCGAGGTGAAGAAGATGCCAAAGAATAGGCAATAG
Gene >OphauB2|2015
ATGAAAAAGTACGCCTTTGTACCCATGGACGATGACGAAGTCGGGCCCCAAAAAATATCAAAAGAAAACAAGCAC
AGACGTCGGCATCGCTCCACTGACGGCGACGGCGACATCTCAAAGCGCTCAACCTCGAAACGCCATCGCTCCCGC
TCCAAGTCCCCTTCCGACCCGAAATCTTCCAGTCACCGCTCAAAACGTAACAGAACCTATCGCCACCGACATGTA
GAGGCCGACTTCGACGACCGGTGGGGGGATGAGGAGCCTCCATCAGAGCCTGATCAGGAGTATGACGGCGGCGAG
CCAGAAGAATCTGCAAGCAAGCGCGTCAAGCTCAGTCACCGTGATGAGGCGCCACGAGAAGAGGATTTGTCAGAC
GGCGCCAAGGAGGAACGTGCCAGGCAAAAGGATATTGAAGAGCGCGAGACCTTTGCCAAGCGACTAAAGGAAAAG
GACGGCTCCAATTCGAGAAGACAGAGTGCCGAGGGGGCTGCCACTTCTTCCAGACGAAAGCTCGCCACAGATGCC
ATTGCACGAGAGGCCGCGTTGCCAGACTTGCGACTGCGGTCACGGCAAGAGTATCTGGGCAAGCGTGGAGCAGAG
AACCTGGCTCTCTTTCGGAAGCAAGTCGCTGCAGAAACGGCCGAGCTGCAGAGTGGCGTCCGCCTCTCCAAGAGA
GAAAAGGCCAGATTTGCGGAAAACAGGGAGACGTTGCGTCTGGCTGAAGAGCACCTGAAAATCGACGACTACCGC
GATGGCTACAAGATGCCCGAGGAGTATGTGACGGACCAGGGCAAGATTGACCTCAAAAAGAAGGAGGAGGCGCTT
CACAAGCGATATGTCGAGCGCGACGAAATGGGCCAGGAGAAGTTTGTGACTGAGCATGAATTGTTTGAGAGAGAG
CAAATAGCCAAAGTCAAGGCCCAAGTCAAGCTTGCACAAGCCGGAAGCGACAACTACTCGTACGTGCTCGACGAG
GAACAATACTCCAAGTGGGTCAAGGACTCAACACTGGCGGGTGTGGGCGAGGGCAAGACCAAGGAGCAGATTGCC
TTGGACGCGCAAATCGAAGAAGCCGAAAAGAGGGACTTGTCAATACAGGAGACGCGGCGAAGCCTACCCATGTAC
AAGTATCGACAAGAGATACTGGATGCCATTGAAAAGTATCAGATTCTTGTCATTGTCGGCGAGACGGGAAGCGGC
AAGACGACGCAGCTGCCGCAGTATCTGCACGAAGCAGGATACACCAAGAATGGCATGAAGGTTGGGTGCACGCAG
CCACGGCGAGTGGCTGCCATGAGCATAGCGGCTCGAGTAGCCCAAGAGGTTGGCGTCAAGTTGGGCAACGAGGTG
GGATACTCTGTGCGCTTCGAGGACAATACAAACGACAAGACGGTGCTCAAGTACATGACGGACGGCATGCTGCTG
CGAGAGCTCATGACGGAGCCACAGCTCGAGGGATACTCGGCCCTCATGATTGACGAGGCTCACGAGCGCACAGTG
CACACTGATATTCTGCTGGCCTTGGTCAAGGACCTGGCGCGTGCGCGGCCCGAGCTGAAGCTCCTGATATCCTCG
GCCACGATGGACGCGGAAAAGTTTTCAGACTACTTTGGCAGAGCGCCCATTTTCAACATTCCCGGCCGCAGATTT
CCAGTCGACATATACAATACACCAGAACCAGTGGCGAATTACCTGACAGCGGCCGTGACGACGACGTTTCAAATC
CACACGACCCAAGGCAAAGGGGACATCCTAATCTTCCTCACCGGACAAGAGGAAATCGAAGCGGCAGAGCGCGAA
ATCACGGAAACATCTCGCAAACTCGGCAACCGCATCAAGGAGCTCGTTATATGTCCCATTTATGCCAACTTGCCG
TCGGAACTGCAGTCCAAGATTTTTGAGCCGACGCCCGAGGGCGCGCGCAAAGTGGTGCTGGCCACCAACATTGCC
GAGACGAGTCTGACGATTGACGGCATCGTCTATGTCATTGATCCTGGCTTTGTCAAGGAGAATGTCTATGACTCG
GCCACGGGCATGTCCAACCTGGTGGTGGTGCCGTGCTCGCGCGCGTCGGCCAACCAGCGCTCGGGACGTGCTGGG
CGTGTCGGCCCTGGCAAATGCTTCCGACTGTATACCAAGTTCTCGTACAATGACGAGATGCAGCAGTCCACCACG
CCCGAGATTCAACGCACCAATCTCAACGGCGTCATCTTGCAGCTCATGTGCCTGGGCGTCTCCAACATCTTCCAG
TTTGACTACTTGGATCGCCCGTCGGCCGAATCCATGAAGGGCGCCTTTAACCAGCTCTATGCGCTCGAGGCCATC
AACCACAAAGGTCAGCTGACCAAGGTTGGGCGGCAAATGGCAGAGTTTCCCACCGATCCCATGCTGGCCAAGGTG
TTGATTGTGGCCCATGCACAAGGCTGCGTCGACGAGGCGCTGTCCGTTGTTGCCATGCTGGCCGAATCGGCAGCC
CTTTTTTTCCGGCCCAAGGACCGCAAAGTACACGCCGACAGTGCTCGGGCGCGCTTCACGGTGCGCGAGGGCGGC
GACCATGCAACCTTGCTCAATATCTGGACGCAATGGGTCGATGCCGACTACTCGCCCGTATGGGCCCGCGAAAAC
TATTTGCAGCAGCGGTCCCTGACGAGGGCCCGCGACGTGCGCGACCAATTGGCCAAGCTATGCGAGCGCGTCGAG
CTCGATGCCTTTTCAACCTGTGGCGCGGCAAACGGCAACCTGAGGCCGCTTAAGCGAGCCCTGACGGCCGGCTTC
TTCCTCAACGCGGCGCGGCTGGCCAAGGATGGATACCGCACGCTCAAGAAGAGGACGGGCGTGTGGATTCATCCC
AGTAGTGTCTTGAACGACGTGCACCCCCCAGAGAGGCTGGTGGTGTACTATGAGCTGGTGCAGACGTCAAAGGAG
TACATGAGGGGCGTCTTTCCCATTGATGTGGCCTTGCTGAGGGAGGTGGCGCCGCATTACTACAAGCCAGTAGAC
TTGGACGAGCTCGAGGTGAAGAAGATGCCAAAGAATAGGCAATAG

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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