Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauB2|748
Gene name
LocationContig_115:31189..32813
Strand+
Gene length (bp)1624
Transcript length (bp)1509
Coding sequence length (bp)1509
Protein length (aa) 503

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF03155 Alg6_Alg8 ALG6, ALG8 glycosyltransferase family 9.4E-176 17 494

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q7RXP5|ALG8_NEUCR Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=alg-8 PE=3 SV=2 6 502 0.0E+00
sp|Q4IJT0|ALG8_GIBZE Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=ALG8 PE=3 SV=1 6 502 0.0E+00
sp|Q5AWM9|ALG8_EMENI Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=alg8 PE=3 SV=1 6 476 0.0E+00
sp|Q1DJR8|ALG8_COCIM Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Coccidioides immitis (strain RS) GN=ALG8 PE=3 SV=1 6 502 0.0E+00
sp|Q2UB20|ALG8_ASPOR Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=alg8 PE=3 SV=1 1 502 0.0E+00
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Swissprot ID Swissprot Description Start End E-value
sp|Q7RXP5|ALG8_NEUCR Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=alg-8 PE=3 SV=2 6 502 0.0E+00
sp|Q4IJT0|ALG8_GIBZE Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=ALG8 PE=3 SV=1 6 502 0.0E+00
sp|Q5AWM9|ALG8_EMENI Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=alg8 PE=3 SV=1 6 476 0.0E+00
sp|Q1DJR8|ALG8_COCIM Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Coccidioides immitis (strain RS) GN=ALG8 PE=3 SV=1 6 502 0.0E+00
sp|Q2UB20|ALG8_ASPOR Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=alg8 PE=3 SV=1 1 502 0.0E+00
sp|Q2HA14|ALG8_CHAGB Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=ALG8 PE=3 SV=1 6 502 0.0E+00
sp|Q10479|ALG8_SCHPO Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg8 PE=3 SV=1 9 502 3.0E-179
sp|Q5AJD2|ALG8_CANAL Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=ALG8 PE=3 SV=1 8 502 8.0E-153
sp|Q6CJR2|ALG8_KLULA Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=ALG8 PE=3 SV=1 12 494 7.0E-149
sp|Q6FKM3|ALG8_CANGA Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=ALG8 PE=3 SV=1 25 494 2.0E-146
sp|Q759R3|ALG8_ASHGO Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=ALG8 PE=3 SV=2 14 494 2.0E-146
sp|P40351|ALG8_YEAST Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG8 PE=1 SV=1 20 492 3.0E-145
sp|Q6BRE5|ALG8_DEBHA Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=ALG8 PE=3 SV=1 26 502 5.0E-145
sp|Q9BVK2|ALG8_HUMAN Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG8 PE=1 SV=2 20 492 2.0E-112
sp|O80505|ALG8_ARATH Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At2g44660 PE=2 SV=3 15 492 6.0E-111
sp|Q9W3V8|ALG8_DROME Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=xit PE=2 SV=1 15 495 2.0E-110
sp|Q0P5D9|ALG8_BOVIN Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Bos taurus GN=ALG8 PE=2 SV=1 20 492 8.0E-110
sp|Q6P8H8|ALG8_MOUSE Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg8 PE=2 SV=2 20 493 1.0E-105
sp|Q554E2|ALG8_DICDI Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 140 489 3.0E-74
sp|P52887|ALG8_CAEEL Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08H9.3 PE=3 SV=3 18 490 2.0E-70
sp|Q54QG6|ALG6_DICDI Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg6 PE=3 SV=1 31 407 2.0E-34
sp|Q802T2|ALG6_CHICK Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gallus gallus GN=ALG6 PE=2 SV=1 31 377 1.0E-33
sp|Q9Y672|ALG6_HUMAN Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG6 PE=1 SV=1 31 377 3.0E-33
sp|Q5NVS8|ALG6_PONAB Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Pongo abelii GN=ALG6 PE=2 SV=1 31 377 1.0E-32
sp|O43053|ALG6_SCHPO Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg6 PE=3 SV=1 31 377 8.0E-30
sp|Q3T1L5|ALG6_RAT Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Rattus norvegicus GN=Alg6 PE=2 SV=1 31 377 1.0E-29
sp|Q3TAE8|ALG6_MOUSE Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg6 PE=2 SV=1 31 377 1.0E-29
sp|Q9FF17|ALG6_ARATH Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At5g38460 PE=2 SV=1 28 403 3.0E-29
sp|Q554E2|ALG8_DICDI Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 14 125 3.0E-28
sp|Q09226|ALG6_CAEEL Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08B11.8 PE=3 SV=1 31 367 3.0E-26
sp|Q12001|ALG6_YEAST Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG6 PE=1 SV=1 31 365 5.0E-25
sp|Q9VKX7|ALG6_DROME Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=gny PE=2 SV=2 31 373 1.0E-23
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GO

GO Term Description Terminal node
GO:0016758 hexosyltransferase activity Yes
GO:0003824 catalytic activity No
GO:0016757 glycosyltransferase activity No
GO:0003674 molecular_function No
GO:0016740 transferase activity No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 24 0.45

Transmembrane Domains

Domain # Start End Length
1 149 168 19
2 175 197 22
3 225 244 19
4 319 341 22
5 356 378 22
6 385 404 19
7 414 433 19
8 445 467 22
9 477 499 22

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|748
MADPSYPTLTQCAVVSAAFKVLLFPAYKSTDFEVHRNWLAITYSLPLSEWYFEQTSQWTLDYPPFFAYFEWLLSL
VGHIVDPAMVKLYSLNHESWATVCFQRGSVLVSELVLAWALQLFIESTPLPCRRAAQVAALSVLLSPGLLIIDHI
HFQYNGFMYGILILSLVLARCKGTLLLSGLVFAALLCFKHIYLYLAPAYFVFLLRTYCLAEESIFGIRLTNCVKL
GAGIAAIFAAALGPFAALGQMPQLLSRLFPFSRGLCHAYWAPNVWALYSMADRVLIHVAPRLGLAVKSEALQSVT
RGLVGDTAFAVLPEVSPRLCFALTLLFQALPLGKLMLQPTWDNFIGAVTLCGYASFLFGWHVHEKAILLVIIPFS
LIALRDRRHLSAFRPLAVAGYVSLFPLLFTPAEFPIKTVYTVFWLVLFLMAFDRLAPASNKPRFFLLDRFSTLYI
AVSIPLIVYTSLLHAVMFGKRYEFLPLMFTSSYSAIGVVGSWAGYMVVYFTS*
Coding >OphauB2|748
ATGGCCGACCCGTCCTATCCCACTCTGACGCAATGCGCCGTCGTGTCTGCTGCCTTCAAGGTGCTGCTGTTTCCT
GCATACAAATCCACCGACTTTGAGGTGCATCGCAACTGGCTGGCCATTACATACAGCCTGCCACTGTCGGAATGG
TACTTTGAGCAGACCTCGCAATGGACCCTCGACTATCCTCCGTTTTTTGCCTACTTTGAGTGGCTGCTCTCCCTC
GTTGGCCACATTGTCGACCCAGCCATGGTGAAGCTGTACAGCCTCAACCACGAAAGCTGGGCCACGGTGTGCTTT
CAGCGTGGCTCCGTGCTCGTGTCGGAACTGGTGCTGGCCTGGGCACTCCAGCTCTTTATAGAGTCAACGCCGCTA
CCTTGTCGCCGCGCTGCTCAGGTGGCTGCCTTGTCGGTCCTTTTGTCACCCGGCCTGCTCATCATTGACCACATC
CACTTCCAGTATAACGGCTTCATGTATGGCATTTTGATTCTCTCGCTTGTTCTTGCTCGGTGCAAGGGGACACTG
CTGCTCAGCGGCCTAGTCTTTGCTGCCCTGCTATGCTTCAAGCACATCTATCTCTATCTGGCGCCCGCCTACTTT
GTCTTTCTGCTGCGTACATACTGTCTTGCCGAAGAGTCCATCTTTGGCATCAGACTGACAAATTGCGTCAAGCTG
GGGGCTGGCATTGCTGCCATCTTTGCCGCTGCTTTGGGACCCTTTGCCGCTTTGGGACAGATGCCGCAATTACTC
AGCCGTCTTTTCCCGTTTTCGCGTGGTCTGTGTCACGCATACTGGGCTCCTAATGTCTGGGCCCTCTATTCAATG
GCTGACCGCGTGCTGATTCATGTGGCACCTCGACTTGGTTTGGCCGTCAAAAGCGAGGCCCTGCAGAGCGTTACA
CGGGGGCTTGTCGGCGATACAGCTTTTGCGGTGCTGCCCGAAGTATCTCCTCGGTTGTGCTTTGCCCTGACGCTG
CTATTCCAGGCACTGCCTCTAGGCAAGCTGATGCTACAGCCAACATGGGATAATTTTATCGGAGCAGTCACGCTA
TGTGGATATGCCTCGTTTTTATTTGGGTGGCATGTGCATGAAAAGGCCATTTTGCTCGTCATTATTCCCTTTAGC
CTCATTGCGCTCAGGGACCGGCGACACTTGAGCGCATTCCGCCCGCTTGCCGTGGCAGGCTACGTGTCCTTGTTT
CCGCTGCTTTTTACGCCCGCAGAGTTTCCCATAAAGACGGTCTATACAGTGTTTTGGCTCGTCTTATTTCTCATG
GCCTTTGACCGGCTGGCTCCAGCATCCAACAAGCCACGATTTTTCCTCCTGGACCGCTTCAGCACACTCTACATT
GCCGTGAGCATACCGCTCATAGTCTACACGTCGCTGCTTCATGCCGTCATGTTTGGCAAGCGGTATGAGTTTCTG
CCCCTCATGTTCACCAGCTCGTACTCGGCAATAGGGGTTGTCGGTAGCTGGGCAGGATACATGGTTGTTTATTTC
ACGTCTTGA
Transcript >OphauB2|748
ATGGCCGACCCGTCCTATCCCACTCTGACGCAATGCGCCGTCGTGTCTGCTGCCTTCAAGGTGCTGCTGTTTCCT
GCATACAAATCCACCGACTTTGAGGTGCATCGCAACTGGCTGGCCATTACATACAGCCTGCCACTGTCGGAATGG
TACTTTGAGCAGACCTCGCAATGGACCCTCGACTATCCTCCGTTTTTTGCCTACTTTGAGTGGCTGCTCTCCCTC
GTTGGCCACATTGTCGACCCAGCCATGGTGAAGCTGTACAGCCTCAACCACGAAAGCTGGGCCACGGTGTGCTTT
CAGCGTGGCTCCGTGCTCGTGTCGGAACTGGTGCTGGCCTGGGCACTCCAGCTCTTTATAGAGTCAACGCCGCTA
CCTTGTCGCCGCGCTGCTCAGGTGGCTGCCTTGTCGGTCCTTTTGTCACCCGGCCTGCTCATCATTGACCACATC
CACTTCCAGTATAACGGCTTCATGTATGGCATTTTGATTCTCTCGCTTGTTCTTGCTCGGTGCAAGGGGACACTG
CTGCTCAGCGGCCTAGTCTTTGCTGCCCTGCTATGCTTCAAGCACATCTATCTCTATCTGGCGCCCGCCTACTTT
GTCTTTCTGCTGCGTACATACTGTCTTGCCGAAGAGTCCATCTTTGGCATCAGACTGACAAATTGCGTCAAGCTG
GGGGCTGGCATTGCTGCCATCTTTGCCGCTGCTTTGGGACCCTTTGCCGCTTTGGGACAGATGCCGCAATTACTC
AGCCGTCTTTTCCCGTTTTCGCGTGGTCTGTGTCACGCATACTGGGCTCCTAATGTCTGGGCCCTCTATTCAATG
GCTGACCGCGTGCTGATTCATGTGGCACCTCGACTTGGTTTGGCCGTCAAAAGCGAGGCCCTGCAGAGCGTTACA
CGGGGGCTTGTCGGCGATACAGCTTTTGCGGTGCTGCCCGAAGTATCTCCTCGGTTGTGCTTTGCCCTGACGCTG
CTATTCCAGGCACTGCCTCTAGGCAAGCTGATGCTACAGCCAACATGGGATAATTTTATCGGAGCAGTCACGCTA
TGTGGATATGCCTCGTTTTTATTTGGGTGGCATGTGCATGAAAAGGCCATTTTGCTCGTCATTATTCCCTTTAGC
CTCATTGCGCTCAGGGACCGGCGACACTTGAGCGCATTCCGCCCGCTTGCCGTGGCAGGCTACGTGTCCTTGTTT
CCGCTGCTTTTTACGCCCGCAGAGTTTCCCATAAAGACGGTCTATACAGTGTTTTGGCTCGTCTTATTTCTCATG
GCCTTTGACCGGCTGGCTCCAGCATCCAACAAGCCACGATTTTTCCTCCTGGACCGCTTCAGCACACTCTACATT
GCCGTGAGCATACCGCTCATAGTCTACACGTCGCTGCTTCATGCCGTCATGTTTGGCAAGCGGTATGAGTTTCTG
CCCCTCATGTTCACCAGCTCGTACTCGGCAATAGGGGTTGTCGGTAGCTGGGCAGGATACATGGTTGTTTATTTC
ACGTCTTGA
Gene >OphauB2|748
ATGGCCGACCCGTCCTATCCCACTCTGACGCAATGCGCCGTCGTGTCTGCTGCCTTCAAGGTGCTGCTGTTTCCT
GCATAGTAAGTCTGATCTGCTTGATTCTTCAACTCTAGAGATGCCAATGCCACCAATAGCAAATCCACCGACTTT
GAGGTGCATCGCAACTGGCTGGCCATTACATACAGCCTGCCACTGTCGGAATGGTACTTTGAGCAGACCTCGCAA
TGGACCCTCGACTATCCTCCGTTTTTTGCCTACTTTGAGTGGCTGCTCTCCCTCGTTGGCCACATTGTCGACCCA
GCCATGGTGAAGCTGTACAGCCTCAACCACGAAAGCTGGGCCACGGTGTGCTTTCAGCGTGGCTCCGTGCTCGTG
TCGGAACTGGTGCTGGCCTGGGCACTCCAGCTCTTTATAGAGTCAACGCCGCTACCTTGTCGCCGCGCTGCTCAG
GTGGCTGCCTTGTCGGTCCTTTTGTCACCCGGCCTGCTCATCATTGACCACATCCACTTCCAGTATAACGGCTTC
ATGTATGGCATTTTGATTCTCTCGCTTGTTCTTGCTCGGTGCAAGGGGACACTGCTGCTCAGCGGCCTAGTCTTT
GCTGCCCTGCTATGCTTCAAGCACATCTATCTCTATCTGGCGCCCGCCTACTTTGTCTTTCTGCTGCGTACATAC
TGTCTTGCCGAAGAGTCCATCTTTGGCATCAGACTGACAAATTGCGTCAAGCTGGGGGCTGGCATTGCTGCCATC
TTTGCCGCTGCTTTGGGACCCTTTGCCGCTTTGGGACAGATGCCGCAATTACTCAGCCGTCTTTTCCCGTTTTCG
CGTGGTCTGTGTCACGCATACTGGGCTCCTAATGTCTGGGCCCTCTATTCAATGGCTGACCGCGTGCTGATTCAT
GGTGAGGTGCCGATGTGATTTTCTCAAACTCTAGTCTTGTGAGCTAATCTCTGCGACCATAGTGGCACCTCGACT
TGGTTTGGCCGTCAAAAGCGAGGCCCTGCAGAGCGTTACACGGGGGCTTGTCGGCGATACAGCTTTTGCGGTGCT
GCCCGAAGTATCTCCTCGGTTGTGCTTTGCCCTGACGCTGCTATTCCAGGCACTGCCTCTAGGCAAGCTGATGCT
ACAGCCAACATGGGATAATTTTATCGGAGCAGTCACGCTATGTGGATATGCCTCGTTTTTATTTGGGTGGCATGT
GCATGAAAAGGCCATTTTGCTCGTCATTATTCCCTTTAGCCTCATTGCGCTCAGGGACCGGCGACACTTGAGCGC
ATTCCGCCCGCTTGCCGTGGCAGGCTACGTGTCCTTGTTTCCGCTGCTTTTTACGCCCGCAGAGTTTCCCATAAA
GACGGTCTATACAGTGTTTTGGCTCGTCTTATTTCTCATGGCCTTTGACCGGCTGGCTCCAGCATCCAACAAGCC
ACGATTTTTCCTCCTGGACCGCTTCAGCACACTCTACATTGCCGTGAGCATACCGCTCATAGTCTACACGTCGCT
GCTTCATGCCGTCATGTTTGGCAAGCGGTATGAGTTTCTGCCCCTCATGTTCACCAGCTCGTACTCGGCAATAGG
GGTTGTCGGTAGCTGGGCAGGATACATGGTTGTTTATTTCACGTCTTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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