Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|5669
Gene name
Locationscaffold_47:38768..40366
Strand-
Gene length (bp)1598
Transcript length (bp)1272
Coding sequence length (bp)1269
Protein length (aa) 423

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00083 Sugar_tr Sugar (and other) transporter 6.2E-28 177 412

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|P45598|ARAE_KLEOX Arabinose-proton symporter OS=Klebsiella oxytoca GN=araE PE=3 SV=1 174 361 3.0E-13
sp|P0AE24|ARAE_ECOLI Arabinose-proton symporter OS=Escherichia coli (strain K12) GN=araE PE=1 SV=1 174 361 2.0E-12
sp|P0AE25|ARAE_ECO57 Arabinose-proton symporter OS=Escherichia coli O157:H7 GN=araE PE=3 SV=1 174 361 2.0E-12
sp|C0SPB2|YWTG_BACSU Putative metabolite transport protein YwtG OS=Bacillus subtilis (strain 168) GN=ywtG PE=3 SV=1 174 368 1.0E-10
sp|Q9XIH6|PLT2_ARATH Putative polyol transporter 2 OS=Arabidopsis thaliana GN=PLT2 PE=3 SV=1 180 355 5.0E-10
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Swissprot ID Swissprot Description Start End E-value
sp|P45598|ARAE_KLEOX Arabinose-proton symporter OS=Klebsiella oxytoca GN=araE PE=3 SV=1 174 361 3.0E-13
sp|P0AE24|ARAE_ECOLI Arabinose-proton symporter OS=Escherichia coli (strain K12) GN=araE PE=1 SV=1 174 361 2.0E-12
sp|P0AE25|ARAE_ECO57 Arabinose-proton symporter OS=Escherichia coli O157:H7 GN=araE PE=3 SV=1 174 361 2.0E-12
sp|C0SPB2|YWTG_BACSU Putative metabolite transport protein YwtG OS=Bacillus subtilis (strain 168) GN=ywtG PE=3 SV=1 174 368 1.0E-10
sp|Q9XIH6|PLT2_ARATH Putative polyol transporter 2 OS=Arabidopsis thaliana GN=PLT2 PE=3 SV=1 180 355 5.0E-10
sp|Q9XIH7|PLT1_ARATH Putative polyol transporter 1 OS=Arabidopsis thaliana GN=PLT1 PE=3 SV=1 180 355 2.0E-09
sp|Q92253|RCO3_NEUCR Probable glucose transporter rco-3 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=rco-3 PE=3 SV=2 182 412 3.0E-09
sp|P54862|HXT11_YEAST Hexose transporter HXT11 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT11 PE=1 SV=1 194 375 3.0E-09
sp|Q9SD00|MSSP3_ARATH Monosaccharide-sensing protein 3 OS=Arabidopsis thaliana GN=MSSP3 PE=2 SV=1 180 341 4.0E-09
sp|P40885|HXT9_YEAST Hexose transporter HXT9 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT9 PE=1 SV=1 194 375 5.0E-09
sp|P38695|HXT5_YEAST Probable glucose transporter HXT5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT5 PE=1 SV=1 194 375 5.0E-09
sp|P30606|ITR2_YEAST Myo-inositol transporter 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ITR2 PE=1 SV=2 194 412 6.0E-09
sp|O74849|GHT6_SCHPO High-affinity fructose transporter ght6 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ght6 PE=1 SV=1 182 412 7.0E-09
sp|Q41144|STC_RICCO Sugar carrier protein C OS=Ricinus communis GN=STC PE=2 SV=1 173 371 1.0E-08
sp|Q8GXR2|PLT6_ARATH Probable polyol transporter 6 OS=Arabidopsis thaliana GN=PLT6 PE=2 SV=2 180 344 1.0E-08
sp|P18631|RAG1_KLULA Low-affinity glucose transporter OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=RAG1 PE=1 SV=1 217 375 3.0E-08
sp|P13181|GAL2_YEAST Galactose transporter OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GAL2 PE=1 SV=3 194 412 3.0E-08
sp|P15325|QUTD_EMENI Quinate permease OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=qutD PE=1 SV=2 179 366 4.0E-08
sp|P32467|HXT4_YEAST Low-affinity glucose transporter HXT4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT4 PE=1 SV=1 218 412 4.0E-08
sp|P53387|KHT2_KLULC Hexose transporter 2 OS=Kluyveromyces lactis GN=KHT2 PE=3 SV=1 194 412 4.0E-08
sp|A6ZT02|HXT4_YEAS7 Low-affinity glucose transporter HXT4 OS=Saccharomyces cerevisiae (strain YJM789) GN=HXT4 PE=3 SV=1 218 412 5.0E-08
sp|C7GWV6|HXT4_YEAS2 Low-affinity glucose transporter HXT4 OS=Saccharomyces cerevisiae (strain JAY291) GN=HXT4 PE=3 SV=1 218 412 5.0E-08
sp|Q9LNV3|STP2_ARATH Sugar transport protein 2 OS=Arabidopsis thaliana GN=STP2 PE=1 SV=3 173 341 5.0E-08
sp|O74969|GHT2_SCHPO High-affinity glucose transporter ght2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ght2 PE=1 SV=1 179 412 5.0E-08
sp|P40886|HXT8_YEAST Hexose transporter HXT8 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT8 PE=1 SV=1 182 412 5.0E-08
sp|Q8TFG1|GHT7_SCHPO Probable high-affinity hexose transporter ght7 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ght7 PE=3 SV=1 179 416 7.0E-08
sp|Q9ZNS0|PLT3_ARATH Probable polyol transporter 3 OS=Arabidopsis thaliana GN=PLT3 PE=3 SV=1 180 348 1.0E-07
sp|P32466|HXT3_YEAST Low-affinity glucose transporter HXT3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT3 PE=1 SV=1 218 375 2.0E-07
sp|P43581|HXT10_YEAST Hexose transporter HXT10 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT10 PE=1 SV=1 194 359 2.0E-07
sp|P0AEP1|GALP_ECOLI Galactose-proton symporter OS=Escherichia coli (strain K12) GN=galP PE=1 SV=1 174 361 3.0E-07
sp|P0AEP2|GALP_ECOL6 Galactose-proton symporter OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=galP PE=3 SV=1 174 361 3.0E-07
sp|P30605|ITR1_YEAST Myo-inositol transporter 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ITR1 PE=1 SV=2 194 336 3.0E-07
sp|P23585|HXT2_YEAST High-affinity glucose transporter HXT2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT2 PE=1 SV=1 194 360 3.0E-07
sp|Q96290|MSSP1_ARATH Monosaccharide-sensing protein 1 OS=Arabidopsis thaliana GN=MSSP1 PE=1 SV=2 177 341 4.0E-07
sp|O34718|IOLT_BACSU Major myo-inositol transporter IolT OS=Bacillus subtilis (strain 168) GN=iolT PE=2 SV=1 159 358 5.0E-07
sp|P39003|HXT6_YEAST High-affinity hexose transporter HXT6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT6 PE=1 SV=2 218 412 5.0E-07
sp|P39004|HXT7_YEAST High-affinity hexose transporter HXT6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT7 PE=1 SV=1 218 412 5.0E-07
sp|P87110|ITR2_SCHPO Myo-inositol transporter 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=itr2 PE=2 SV=1 178 412 1.0E-06
sp|Q96QE2|MYCT_HUMAN Proton myo-inositol cotransporter OS=Homo sapiens GN=SLC2A13 PE=1 SV=3 190 341 1.0E-06
sp|A1D2R3|QUTD_NEOFI Probable quinate permease OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=qutD PE=3 SV=1 179 366 1.0E-06
sp|Q6NWF1|GTR12_DANRE Solute carrier family 2, facilitated glucose transporter member 12 OS=Danio rerio GN=slc2a12 PE=2 SV=2 194 360 1.0E-06
sp|Q9FMX3|STP11_ARATH Sugar transport protein 11 OS=Arabidopsis thaliana GN=STP11 PE=1 SV=1 173 340 2.0E-06
sp|P23586|STP1_ARATH Sugar transport protein 1 OS=Arabidopsis thaliana GN=STP1 PE=1 SV=2 173 417 2.0E-06
sp|Q0D135|QUTD_ASPTN Probable quinate permease OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=qutD PE=3 SV=1 189 359 2.0E-06
sp|Q01440|GTR1_LEIDO Membrane transporter D1 OS=Leishmania donovani PE=3 SV=1 179 322 2.0E-06
sp|Q9LT15|STP10_ARATH Sugar transport protein 10 OS=Arabidopsis thaliana GN=STP10 PE=2 SV=1 173 357 3.0E-06
sp|Q2U2Y9|QUTD_ASPOR Probable quinate permease OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=qutD PE=3 SV=1 189 366 3.0E-06
sp|B8NIM7|QUTD_ASPFN Probable quinate permease OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=qutD PE=3 SV=1 189 366 3.0E-06
sp|P15686|HUP1_PARKE H(+)/hexose cotransporter 1 OS=Parachlorella kessleri GN=HUP1 PE=2 SV=2 174 341 3.0E-06
sp|P32465|HXT1_YEAST Low-affinity glucose transporter HXT1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HXT1 PE=1 SV=1 194 375 3.0E-06
sp|Q9P3U7|GHT8_SCHPO Probable high-affinity hexose transporter ght8, mitochondrial OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ght8 PE=1 SV=1 179 361 4.0E-06
sp|A2QQV6|QUTD_ASPNC Probable quinate permease OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=qutD PE=3 SV=1 189 366 4.0E-06
sp|Q39525|HUP3_PARKE H(+)/hexose cotransporter 3 OS=Parachlorella kessleri GN=HUP3 PE=2 SV=1 174 341 5.0E-06
sp|Q32NG5|GTR12_XENLA Solute carrier family 2, facilitated glucose transporter member 12 OS=Xenopus laevis GN=slc2a12 PE=2 SV=1 179 347 5.0E-06
sp|P11636|QAY_NEUCR Quinate permease OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=qa-y PE=3 SV=2 179 370 8.0E-06
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GO

GO Term Description Terminal node
GO:0016021 integral component of membrane Yes
GO:0022857 transmembrane transporter activity Yes
GO:0055085 transmembrane transport Yes
GO:0009987 cellular process No
GO:0051234 establishment of localization No
GO:0110165 cellular anatomical entity No
GO:0031224 intrinsic component of membrane No
GO:0008150 biological_process No
GO:0005215 transporter activity No
GO:0005575 cellular_component No
GO:0003674 molecular_function No
GO:0051179 localization No
GO:0006810 transport No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 15 0.45

Transmembrane Domains

Domain # Start End Length
1 173 195 22
2 200 217 17
3 258 280 22
4 287 309 22

Transcription Factor Class

(None)

Expression data

Analysis 1: Expression analysis during behavioral modification. Published in De Bekker et al., 2017.

Click here for more information

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 >Ophio5|5669
MPNEAASRGYRDRFAAQARSRRANDGAVIENPLATDVRIFAENHLPDVPYDRVLRAARVAKDIRLYDEIARRTRI
DGSHLPVRLTDREKDALCREKDVTFSEKGMRIVIATVSLAALLQGRVLCFPLLDEIYYRFVQSSFNGASLYASVW
KLRLEEGGDGVPLDVWLLGAANASPWFFAALVGCPLSLPINYWFGRRGAIAVAAFLILASSIGAIFVSDWKQMFG
VRVVNGLGMGIKAVSTPILASETAVGFWRGSAILAWQLWVAFGIMAGFAFNMIFSQARDEQMILRLIQGAPLVPS
LALLVLSLGFCPESPRYHLMKGPNYSVQKAYEVLKRVRNTELQALRDLYMVHKALEQERVGVSWDPHVSMSPGFF
WVIRDFLSQYGQLFRRRRLYNALLSACTVNLAQQLCGGETHVLLSNWG
Coding >Ophio5|5669
ATGCCTAACGAGGCTGCTTCTCGCGGATACCGCGACAGGTTTGCTGCTCAGGCCCGAAGCAGGAGAGCCAACGAT
GGCGCCGTCATTGAGAATCCCCTTGCGACGGACGTCAGGATCTTCGCCGAAAATCACCTGCCCGATGTTCCTTAC
GATCGTGTTCTTCGCGCCGCGCGGGTTGCCAAGGATATCCGCCTATACGATGAAATAGCTCGGAGGACGCGTATT
GACGGAAGCCATTTGCCCGTGCGTCTTACCGATAGAGAAAAGGATGCCCTGTGCAGAGAAAAGGATGTTACGTTT
AGCGAAAAGGGCATGCGCATTGTCATTGCCACCGTGTCCTTGGCCGCTCTTTTGCAAGGTCGAGTCTTGTGTTTT
CCTCTCCTTGACGAGATATACTATCGCTTTGTGCAGTCATCATTCAACGGGGCATCTTTGTACGCTTCAGTCTGG
AAACTACGCTTGGAAGAAGGGGGAGACGGCGTGCCCCTTGACGTCTGGCTTCTTGGAGCCGCCAATGCCTCGCCC
TGGTTCTTCGCCGCCTTGGTGGGCTGTCCGCTCTCGCTGCCCATCAACTACTGGTTCGGCAGACGAGGAGCCATC
GCCGTCGCAGCCTTCCTGATCCTAGCGAGCTCCATCGGCGCCATATTCGTCTCCGATTGGAAGCAGATGTTTGGT
GTCCGAGTCGTCAATGGCCTGGGCATGGGCATCAAGGCCGTGAGCACTCCCATCTTGGCTTCCGAGACGGCGGTG
GGCTTCTGGCGCGGGTCGGCAATCCTTGCCTGGCAACTTTGGGTCGCCTTCGGTATCATGGCAGGCTTCGCCTTT
AACATGATCTTCAGCCAAGCCCGCGACGAACAAATGATCCTGCGTCTGATACAGGGCGCCCCTCTCGTTCCCAGT
CTCGCCCTGCTCGTCCTTAGCTTGGGCTTCTGCCCCGAGTCCCCCCGTTACCACCTCATGAAGGGGCCAAACTAC
AGTGTCCAAAAGGCGTACGAGGTTTTGAAAAGGGTCCGAAATACCGAGTTGCAAGCCTTGCGCGACCTGTACATG
GTTCACAAGGCGCTCGAGCAAGAGCGTGTCGGCGTCAGCTGGGATCCTCACGTCTCCATGTCCCCGGGCTTCTTC
TGGGTCATTCGCGATTTCCTCTCGCAGTACGGGCAGCTTTTCCGGCGCCGGCGGCTGTACAATGCCCTTCTATCC
GCATGCACGGTCAATCTAGCGCAGCAGCTCTGTGGAGGTGAGACCCATGTCTTATTGAGCAACTGGGGC
Transcript >Ophio5|5669
ATGCCTAACGAGGCTGCTTCTCGCGGATACCGCGACAGGTTTGCTGCTCAGGCCCGAAGCAGGAGAGCCAACGAT
GGCGCCGTCATTGAGAATCCCCTTGCGACGGACGTCAGGATCTTCGCCGAAAATCACCTGCCCGATGTTCCTTAC
GATCGTGTTCTTCGCGCCGCGCGGGTTGCCAAGGATATCCGCCTATACGATGAAATAGCTCGGAGGACGCGTATT
GACGGAAGCCATTTGCCCGTGCGTCTTACCGATAGAGAAAAGGATGCCCTGTGCAGAGAAAAGGATGTTACGTTT
AGCGAAAAGGGCATGCGCATTGTCATTGCCACCGTGTCCTTGGCCGCTCTTTTGCAAGGTCGAGTCTTGTGTTTT
CCTCTCCTTGACGAGATATACTATCGCTTTGTGCAGTCATCATTCAACGGGGCATCTTTGTACGCTTCAGTCTGG
AAACTACGCTTGGAAGAAGGGGGAGACGGCGTGCCCCTTGACGTCTGGCTTCTTGGAGCCGCCAATGCCTCGCCC
TGGTTCTTCGCCGCCTTGGTGGGCTGTCCGCTCTCGCTGCCCATCAACTACTGGTTCGGCAGACGAGGAGCCATC
GCCGTCGCAGCCTTCCTGATCCTAGCGAGCTCCATCGGCGCCATATTCGTCTCCGATTGGAAGCAGATGTTTGGT
GTCCGAGTCGTCAATGGCCTGGGCATGGGCATCAAGGCCGTGAGCACTCCCATCTTGGCTTCCGAGACGGCGGTG
GGCTTCTGGCGCGGGTCGGCAATCCTTGCCTGGCAACTTTGGGTCGCCTTCGGTATCATGGCAGGCTTCGCCTTT
AACATGATCTTCAGCCAAGCCCGCGACGAACAAATGATCCTGCGTCTGATACAGGGCGCCCCTCTCGTTCCCAGT
CTCGCCCTGCTCGTCCTTAGCTTGGGCTTCTGCCCCGAGTCCCCCCGTTACCACCTCATGAAGGGGCCAAACTAC
AGTGTCCAAAAGGCGTACGAGGTTTTGAAAAGGGTCCGAAATACCGAGTTGCAAGCCTTGCGCGACCTGTACATG
GTTCACAAGGCGCTCGAGCAAGAGCGTGTCGGCGTCAGCTGGGATCCTCACGTCTCCATGTCCCCGGGCTTCTTC
TGGGTCATTCGCGATTTCCTCTCGCAGTACGGGCAGCTTTTCCGGCGCCGGCGGCTGTACAATGCCCTTCTATCC
GCATGCACGGTCAATCTAGCGCAGCAGCTCTGTGGAGGTGAGACCCATGTCTTATTGAGCAACTGGGGCTGA
Gene >Ophio5|5669
ATGCCTAACGAGGCTGCTTCTCGCGGATACCGCGACAGGTTTGCTGCTCAGGCCCGAAGCAGGAGAGCCAACGAT
GGCGCCGTCATTGAGAATCCCCTTGGTACGGCCTCTCCGAGAGGCCGTGGTAGTCAAGGGCTGACATGAGAGAGG
ACGATGCAGCACATATGACGGACGCGGACCTAGCGACGGACGTCAGGATCTTCGCCGAAAATCACCTGCCCGATG
TTCCTTACGATCGTGTTCTTCGCGCCGCGCGGGTTGCCAAGGATATCCGCCTATACGATGAAATAGCTCGGAGGA
CGCGTATTGACGGAAGCCATTTGCCCGTGCGTCTTACCGATAGAGAAAAGGATGCCCTGTGCAGAGAAAAGGATG
TTACGTTTAGCGAAAAGGGCATGCGCATTGTCATTGCCACCGTGTCCTTGGCCGCTCTTTTGCAAGGTCGAGTCT
TGTGTTTTCCTCTCCTTGACGAGATATACTATCGTCGGACCACGAACCCTTGGGGTCAACGTATGCCTTGACGCG
TGCTGACCGTCTCCTAGGCTTTGTGCAGTCATCATTCAACGGGGCATCTTTGTACGCTTCAGTCTGGAAACTACG
CTTGGAAGAAGGGGGAGACGGCGTGCCCCTTGACGTCTGGCTTCTTGGAGCCGCCAATGCCTCGCCCTGGTTCTT
CGCCGCCTTGGTGGGCTGTCCGCTCTCGCTGCCCATCAACTACTGGTTCGGCAGACGAGGAGCCATCGCCGTCGC
AGCCTTCCTGATCCTAGCGAGCTCCATCGGCGCCATATTCGTCTCCGATTGGAAGCAGATGTTTGGTGTCCGAGT
CGTCAATGGCCTGGGTTCGTCTTTCCTTTCGACGACGGTCCGTTTCGAGCCTACTAATAATGACTTCTTCCCTCG
ACAGGCATGGGCATCAAGGCCGTGAGCACTCCCATCTTGGCTTCCGAGACGGCGGTGGGCTTCTGGCGCGGGTCG
GCAATCCTTGCCTGGCAACTTTGGTATGGCAATTGATGAACACATGGAGGCACAAGCTGATGACGCACACTCGTG
AAAAAGGGTCGCCTTCGGTATCATGGCAGGCTTCGCCTTTAACATGATCTTCAGCCAAGCCCGCGACGAACAAAT
GATCCTGCGTCTGATACAGGGCGCCCCTCTCGTTCCCAGTCTCGCCCTGCTCGTCCTTAGCTTGGGCTTCTGCCC
CGAGTCCCCCCGTTACCACCTCATGAAGGGGCCAAACTACAGTGTCCAAAAGGCGTACGAGGTTTTGAAAAGGGT
CCGAAATACCGAGGTATGTGTTCCAAGTTGTATTCTCGCAAGCCGTGCTTCACGTCTGATGCGCAATCACGCAGT
TGCAAGCCTTGCGCGACCTGTACATGGTTCACAAGGCGCTCGAGCAAGAGCGTGTCGGCGTCAGCTGGGATCCTC
ACGTCTCCATGTCCCCGGGCTTCTTCTGGGTCATTCGCGATTTCCTCTCGCAGTACGGGCAGCTTTTCCGGCGCC
GGCGGCTGTACAATGCCCTTCTATCCGCATGCACGGTCAATCTAGCGCAGCAGCTCTGTGGAGGTGAGACCCATG
TCTTATTGAGCAACTGGGGCTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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