Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauG2|4876
Gene name
LocationContig_422:7062..8707
Strand+
Gene length (bp)1645
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 1.2E-174 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-178
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 3.0E-151
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 5.0E-149
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-146
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-145
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 6.0E-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 4.0E-143
sp|Q9BVK2|ALG8_HUMAN Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG8 PE=1 SV=2 20 492 3.0E-110
sp|Q9W3V8|ALG8_DROME Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=xit PE=2 SV=1 15 489 4.0E-110
sp|O80505|ALG8_ARATH Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At2g44660 PE=2 SV=3 15 493 2.0E-108
sp|Q0P5D9|ALG8_BOVIN Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Bos taurus GN=ALG8 PE=2 SV=1 20 493 9.0E-107
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-103
sp|Q554E2|ALG8_DICDI Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 140 489 2.0E-68
sp|P52887|ALG8_CAEEL Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08H9.3 PE=3 SV=3 18 490 1.0E-67
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-36
sp|Q802T2|ALG6_CHICK Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gallus gallus GN=ALG6 PE=2 SV=1 31 377 2.0E-35
sp|Q9Y672|ALG6_HUMAN Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG6 PE=1 SV=1 31 377 2.0E-33
sp|Q5NVS8|ALG6_PONAB Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Pongo abelii GN=ALG6 PE=2 SV=1 31 377 8.0E-33
sp|Q9FF17|ALG6_ARATH Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At5g38460 PE=2 SV=1 28 403 1.0E-30
sp|Q3T1L5|ALG6_RAT Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Rattus norvegicus GN=Alg6 PE=2 SV=1 31 377 4.0E-30
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 1.0E-29
sp|Q554E2|ALG8_DICDI Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 14 125 2.0E-29
sp|Q3TAE8|ALG6_MOUSE Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg6 PE=2 SV=1 31 377 3.0E-29
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 2.0E-27
sp|Q09226|ALG6_CAEEL Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08B11.8 PE=3 SV=1 31 367 8.0E-27
sp|Q9VKX7|ALG6_DROME Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=gny PE=2 SV=2 31 373 3.0E-23
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GO

GO Term Description Terminal node
GO:0016758 hexosyltransferase activity Yes
GO:0003674 molecular_function No
GO:0016740 transferase activity No
GO:0016757 glycosyltransferase activity No
GO:0003824 catalytic 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 68 90 22
2 103 120 17
3 130 147 17
4 154 171 17
5 181 203 22
6 223 245 22
7 356 378 22
8 385 404 19
9 414 433 19
10 445 467 22
11 477 499 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 >OphauG2|4876
MADPSYPTLTQCAVVSAAFKVLLFPAYKSTDFEVHRNWLAITYSLPLSEWYFEHTSQWTLDYPPFFAYFEWLLSL
VAHLVDPAMVRLYSLNHESWATVCFQRATVLVSDLVLAWALQLFIKSTPLPCRRAAQVAALSVLLSPGLLIIDHI
HFQYNGFMYGILILSLVLARCKPTLLLSGLVFAALLCFKHIHLYLAPAYFVFLLRTYCLAPESIFRIRPMNCLKL
GAGITAIFAAAFAPFAALGQMPQLLSRLFPFSRGLCHAYWAPNVWALYSMADRILIHVAPRLGLVVKTEALQSVT
RGLVGDTAFAVLPEPSPRLCFVLTLLFQALPLGKLMLQPTWDNFIGAVTLCGYASFLFGWHVHEKAVLLVIIPFS
LIALRDRRHLSAFRPLAVAGYVSLFPLLFTPAEFPIKTVYTVFWLVLFLMAFDRLAPASNKPRFFLLDRFSTLYI
AVSIPLILYTSLLHAVMFGKRYEFLPLMFTSSYSAVGVVGSWVGYMVVYFTS*
Coding >OphauG2|4876
ATGGCCGACCCGTCCTATCCCACGTTGACCCAATGCGCCGTCGTCTCCGCTGCCTTTAAAGTCCTGCTGTTTCCT
GCATACAAATCTACCGACTTTGAGGTCCATCGCAACTGGCTGGCCATTACATACAGCCTGCCCCTGTCGGAATGG
TACTTTGAGCACACCTCGCAATGGACCCTCGACTATCCTCCCTTTTTTGCCTACTTTGAATGGCTGCTCTCCCTC
GTCGCCCACCTCGTCGACCCAGCCATGGTGAGGCTCTACAGCCTCAACCACGAATCCTGGGCCACCGTATGCTTC
CAGCGTGCCACCGTGCTCGTGTCCGATCTGGTGCTGGCCTGGGCTCTGCAGCTCTTCATAAAGTCAACCCCGCTG
CCTTGTCGCCGTGCCGCTCAGGTGGCCGCCCTGTCGGTGCTCCTGTCACCCGGCCTGCTCATCATTGATCACATT
CACTTCCAGTACAACGGCTTCATGTATGGCATTCTCATTCTCTCCCTTGTTCTTGCTCGCTGCAAGCCGACACTG
TTGCTCAGCGGCCTTGTCTTTGCTGCCCTGCTATGCTTCAAGCACATCCATCTCTATCTGGCGCCTGCCTACTTT
GTCTTTCTGCTGCGCACCTACTGCCTTGCCCCAGAGTCCATCTTTCGCATCAGACCCATGAATTGCCTCAAGTTG
GGCGCTGGCATTACTGCCATCTTTGCCGCCGCCTTTGCACCCTTTGCCGCCCTGGGACAGATGCCACAGCTACTC
AGCCGTCTCTTTCCCTTTTCCCGTGGCCTATGCCACGCATACTGGGCTCCTAATGTCTGGGCTCTCTATTCAATG
GCTGATCGCATCCTGATTCATGTCGCACCTCGCCTTGGTTTAGTCGTCAAGACAGAGGCCCTGCAGAGCGTTACC
CGCGGACTTGTCGGCGATACGGCTTTTGCTGTGCTGCCCGAGCCATCTCCCAGGCTGTGCTTTGTCCTGACGCTG
CTATTCCAGGCACTGCCTCTAGGCAAGCTGATGCTACAGCCAACATGGGATAACTTTATCGGAGCAGTCACGCTA
TGTGGATATGCCTCGTTTCTTTTTGGCTGGCATGTACATGAAAAGGCCGTTTTGCTCGTCATTATCCCCTTTAGT
CTCATTGCCCTCAGGGACCGACGACACTTGAGCGCCTTCCGCCCGCTGGCCGTGGCAGGCTACGTGTCCTTATTC
CCCCTGCTTTTTACGCCCGCAGAGTTTCCCATCAAGACGGTGTATACAGTGTTTTGGCTCGTCTTATTTCTCATG
GCCTTTGACCGGCTGGCCCCAGCGTCCAACAAGCCACGTTTTTTCCTGCTGGACCGCTTCAGCACGCTCTACATT
GCCGTGAGCATCCCGCTCATACTCTACACGTCACTGCTTCATGCCGTCATGTTTGGCAAGCGGTACGAGTTTCTG
CCCCTCATGTTCACCAGCTCGTACTCGGCAGTAGGAGTTGTCGGTAGCTGGGTAGGATACATGGTTGTTTATTTC
ACGTCTTGA
Transcript >OphauG2|4876
ATGGCCGACCCGTCCTATCCCACGTTGACCCAATGCGCCGTCGTCTCCGCTGCCTTTAAAGTCCTGCTGTTTCCT
GCATACAAATCTACCGACTTTGAGGTCCATCGCAACTGGCTGGCCATTACATACAGCCTGCCCCTGTCGGAATGG
TACTTTGAGCACACCTCGCAATGGACCCTCGACTATCCTCCCTTTTTTGCCTACTTTGAATGGCTGCTCTCCCTC
GTCGCCCACCTCGTCGACCCAGCCATGGTGAGGCTCTACAGCCTCAACCACGAATCCTGGGCCACCGTATGCTTC
CAGCGTGCCACCGTGCTCGTGTCCGATCTGGTGCTGGCCTGGGCTCTGCAGCTCTTCATAAAGTCAACCCCGCTG
CCTTGTCGCCGTGCCGCTCAGGTGGCCGCCCTGTCGGTGCTCCTGTCACCCGGCCTGCTCATCATTGATCACATT
CACTTCCAGTACAACGGCTTCATGTATGGCATTCTCATTCTCTCCCTTGTTCTTGCTCGCTGCAAGCCGACACTG
TTGCTCAGCGGCCTTGTCTTTGCTGCCCTGCTATGCTTCAAGCACATCCATCTCTATCTGGCGCCTGCCTACTTT
GTCTTTCTGCTGCGCACCTACTGCCTTGCCCCAGAGTCCATCTTTCGCATCAGACCCATGAATTGCCTCAAGTTG
GGCGCTGGCATTACTGCCATCTTTGCCGCCGCCTTTGCACCCTTTGCCGCCCTGGGACAGATGCCACAGCTACTC
AGCCGTCTCTTTCCCTTTTCCCGTGGCCTATGCCACGCATACTGGGCTCCTAATGTCTGGGCTCTCTATTCAATG
GCTGATCGCATCCTGATTCATGTCGCACCTCGCCTTGGTTTAGTCGTCAAGACAGAGGCCCTGCAGAGCGTTACC
CGCGGACTTGTCGGCGATACGGCTTTTGCTGTGCTGCCCGAGCCATCTCCCAGGCTGTGCTTTGTCCTGACGCTG
CTATTCCAGGCACTGCCTCTAGGCAAGCTGATGCTACAGCCAACATGGGATAACTTTATCGGAGCAGTCACGCTA
TGTGGATATGCCTCGTTTCTTTTTGGCTGGCATGTACATGAAAAGGCCGTTTTGCTCGTCATTATCCCCTTTAGT
CTCATTGCCCTCAGGGACCGACGACACTTGAGCGCCTTCCGCCCGCTGGCCGTGGCAGGCTACGTGTCCTTATTC
CCCCTGCTTTTTACGCCCGCAGAGTTTCCCATCAAGACGGTGTATACAGTGTTTTGGCTCGTCTTATTTCTCATG
GCCTTTGACCGGCTGGCCCCAGCGTCCAACAAGCCACGTTTTTTCCTGCTGGACCGCTTCAGCACGCTCTACATT
GCCGTGAGCATCCCGCTCATACTCTACACGTCACTGCTTCATGCCGTCATGTTTGGCAAGCGGTACGAGTTTCTG
CCCCTCATGTTCACCAGCTCGTACTCGGCAGTAGGAGTTGTCGGTAGCTGGGTAGGATACATGGTTGTTTATTTC
ACGTCTTGA
Gene >OphauG2|4876
ATGGCCGACCCGTCCTATCCCACGTTGACCCAATGCGCCGTCGTCTCCGCTGCCTTTAAAGTCCTGCTGTTTCCT
GCATAGTAAGCCAAGCTCCTATCCTCCTGTCCTTGATTCCTCGGCCCCAGAGATGCCAATCCCACAAACAGCAAA
TCTACCGACTTTGAGGTCCATCGCAACTGGCTGGCCATTACATACAGCCTGCCCCTGTCGGAATGGTACTTTGAG
CACACCTCGCAATGGACCCTCGACTATCCTCCCTTTTTTGCCTACTTTGAATGGCTGCTCTCCCTCGTCGCCCAC
CTCGTCGACCCAGCCATGGTGAGGCTCTACAGCCTCAACCACGAATCCTGGGCCACCGTATGCTTCCAGCGTGCC
ACCGTGCTCGTGTCCGATCTGGTGCTGGCCTGGGCTCTGCAGCTCTTCATAAAGTCAACCCCGCTGCCTTGTCGC
CGTGCCGCTCAGGTGGCCGCCCTGTCGGTGCTCCTGTCACCCGGCCTGCTCATCATTGATCACATTCACTTCCAG
TACAACGGCTTCATGTATGGCATTCTCATTCTCTCCCTTGTTCTTGCTCGCTGCAAGCCGACACTGTTGCTCAGC
GGCCTTGTCTTTGCTGCCCTGCTATGCTTCAAGCACATCCATCTCTATCTGGCGCCTGCCTACTTTGTCTTTCTG
CTGCGCACCTACTGCCTTGCCCCAGAGTCCATCTTTCGCATCAGACCCATGAATTGCCTCAAGTTGGGCGCTGGC
ATTACTGCCATCTTTGCCGCCGCCTTTGCACCCTTTGCCGCCCTGGGACAGATGCCACAGCTACTCAGCCGTCTC
TTTCCCTTTTCCCGTGGCCTATGCCACGCATACTGGGCTCCTAATGTCTGGGCTCTCTATTCAATGGCTGATCGC
ATCCTGATTCATGGTGAGCCTGTTGTTCGTGATTTTCTCGAGCCTAGTCTTGGAAGCTAATAAATAATACCTGCC
CACCACAGTCGCACCTCGCCTTGGTTTAGTCGTCAAGACAGAGGCCCTGCAGAGCGTTACCCGCGGACTTGTCGG
CGATACGGCTTTTGCTGTGCTGCCCGAGCCATCTCCCAGGCTGTGCTTTGTCCTGACGCTGCTATTCCAGGCACT
GCCTCTAGGCAAGCTGATGCTACAGCCAACATGGGATAACTTTATCGGAGCAGTCACGCTATGTGGATATGCCTC
GTTTCTTTTTGGCTGGCATGTACATGAAAAGGCCGTTTTGCTCGTCATTATCCCCTTTAGTCTCATTGCCCTCAG
GGACCGACGACACTTGAGCGCCTTCCGCCCGCTGGCCGTGGCAGGCTACGTGTCCTTATTCCCCCTGCTTTTTAC
GCCCGCAGAGTTTCCCATCAAGACGGTGTATACAGTGTTTTGGCTCGTCTTATTTCTCATGGCCTTTGACCGGCT
GGCCCCAGCGTCCAACAAGCCACGTTTTTTCCTGCTGGACCGCTTCAGCACGCTCTACATTGCCGTGAGCATCCC
GCTCATACTCTACACGTCACTGCTTCATGCCGTCATGTTTGGCAAGCGGTACGAGTTTCTGCCCCTCATGTTCAC
CAGCTCGTACTCGGCAGTAGGAGTTGTCGGTAGCTGGGTAGGATACATGGTTGTTTATTTCACGTCTTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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