Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|2126
Gene name
LocationContig_1498:2757..4625
Strand+
Gene length (bp)1868
Transcript length (bp)1626
Coding sequence length (bp)1626
Protein length (aa) 542

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF13520 AA_permease_2 Amino acid permease 8.8E-89 46 476
PF00324 AA_permease Amino acid permease 5.5E-17 59 451

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|P50276|MUP1_YEAST High-affinity methionine permease OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MUP1 PE=1 SV=1 23 534 1.0E-178
sp|P38734|MUP3_YEAST Low-affinity methionine permease OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MUP3 PE=1 SV=1 16 522 2.0E-68
sp|Q9WTR6|XCT_MOUSE Cystine/glutamate transporter OS=Mus musculus GN=Slc7a11 PE=1 SV=1 43 450 4.0E-36
sp|P82251|BAT1_HUMAN b(0,+)-type amino acid transporter 1 OS=Homo sapiens GN=SLC7A9 PE=1 SV=1 14 489 1.0E-35
sp|Q9N1R6|BAT1_RABIT b(0,+)-type amino acid transporter 1 OS=Oryctolagus cuniculus GN=SLC7A9 PE=1 SV=1 20 352 2.0E-35
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Swissprot ID Swissprot Description Start End E-value
sp|P50276|MUP1_YEAST High-affinity methionine permease OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MUP1 PE=1 SV=1 23 534 1.0E-178
sp|P38734|MUP3_YEAST Low-affinity methionine permease OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MUP3 PE=1 SV=1 16 522 2.0E-68
sp|Q9WTR6|XCT_MOUSE Cystine/glutamate transporter OS=Mus musculus GN=Slc7a11 PE=1 SV=1 43 450 4.0E-36
sp|P82251|BAT1_HUMAN b(0,+)-type amino acid transporter 1 OS=Homo sapiens GN=SLC7A9 PE=1 SV=1 14 489 1.0E-35
sp|Q9N1R6|BAT1_RABIT b(0,+)-type amino acid transporter 1 OS=Oryctolagus cuniculus GN=SLC7A9 PE=1 SV=1 20 352 2.0E-35
sp|Q9QXA6|BAT1_MOUSE b(0,+)-type amino acid transporter 1 OS=Mus musculus GN=Slc7a9 PE=1 SV=1 14 352 3.0E-34
sp|P82252|BAT1_RAT b(0,+)-type amino acid transporter 1 OS=Rattus norvegicus GN=Slc7a9 PE=1 SV=1 14 352 2.0E-32
sp|Q8BGK6|YLAT2_MOUSE Y+L amino acid transporter 2 OS=Mus musculus GN=Slc7a6 PE=1 SV=1 12 503 3.0E-32
sp|Q92536|YLAT2_HUMAN Y+L amino acid transporter 2 OS=Homo sapiens GN=SLC7A6 PE=1 SV=3 19 518 2.0E-31
sp|Q28I80|YLAT2_XENTR Y+L amino acid transporter 2 OS=Xenopus tropicalis GN=slc7a6 PE=2 SV=1 18 452 4.0E-31
sp|Q9Z1K8|YLAT1_MOUSE Y+L amino acid transporter 1 OS=Mus musculus GN=Slc7a7 PE=1 SV=1 22 452 8.0E-31
sp|Q59I64|YLAT2_DANRE Y+L amino acid transporter 2 OS=Danio rerio GN=slc7a6 PE=2 SV=1 41 452 8.0E-31
sp|A1L3M3|YLAT2_XENLA Y+L amino acid transporter 2 OS=Xenopus laevis GN=slc7a6 PE=2 SV=1 23 452 1.0E-30
sp|Q9R0S5|YLAT1_RAT Y+L amino acid transporter 1 OS=Rattus norvegicus GN=Slc7a7 PE=1 SV=1 11 531 1.0E-30
sp|Q9UM01|YLAT1_HUMAN Y+L amino acid transporter 1 OS=Homo sapiens GN=SLC7A7 PE=1 SV=2 43 452 1.0E-29
sp|Q9UPY5|XCT_HUMAN Cystine/glutamate transporter OS=Homo sapiens GN=SLC7A11 PE=1 SV=1 67 449 5.0E-29
sp|Q5RAG7|XCT_PONAB Cystine/glutamate transporter OS=Pongo abelii GN=SLC7A11 PE=2 SV=1 67 449 5.0E-29
sp|Q01650|LAT1_HUMAN Large neutral amino acids transporter small subunit 1 OS=Homo sapiens GN=SLC7A5 PE=1 SV=2 20 486 5.0E-25
sp|Q9WVR6|LAT2_RAT Large neutral amino acids transporter small subunit 2 OS=Rattus norvegicus GN=Slc7a8 PE=1 SV=1 20 525 1.0E-24
sp|Q9QXW9|LAT2_MOUSE Large neutral amino acids transporter small subunit 2 OS=Mus musculus GN=Slc7a8 PE=1 SV=1 21 529 7.0E-24
sp|Q5RAE3|LAT2_PONAB Large neutral amino acids transporter small subunit 2 OS=Pongo abelii GN=SLC7A8 PE=2 SV=2 21 355 1.0E-23
sp|Q9UHI5|LAT2_HUMAN Large neutral amino acids transporter small subunit 2 OS=Homo sapiens GN=SLC7A8 PE=1 SV=1 21 355 1.0E-23
sp|P63116|AAA1_RAT Asc-type amino acid transporter 1 OS=Rattus norvegicus GN=Slc7a10 PE=2 SV=1 43 462 4.0E-23
sp|P63115|AAA1_MOUSE Asc-type amino acid transporter 1 OS=Mus musculus GN=Slc7a10 PE=1 SV=1 43 462 4.0E-23
sp|Q9NS82|AAA1_HUMAN Asc-type amino acid transporter 1 OS=Homo sapiens GN=SLC7A10 PE=2 SV=1 20 538 4.0E-23
sp|Q9N1Q4|LAT2_RABIT Large neutral amino acids transporter small subunit 2 OS=Oryctolagus cuniculus GN=SLC7A8 PE=1 SV=1 43 486 7.0E-23
sp|Q7YQK4|LAT1_RABIT Large neutral amino acids transporter small subunit 1 OS=Oryctolagus cuniculus GN=SLC7A5 PE=1 SV=1 43 486 1.0E-22
sp|Q9Z127|LAT1_MOUSE Large neutral amino acids transporter small subunit 1 OS=Mus musculus GN=Slc7a5 PE=1 SV=2 43 491 2.0E-20
sp|Q63016|LAT1_RAT Large neutral amino acids transporter small subunit 1 OS=Rattus norvegicus GN=Slc7a5 PE=1 SV=2 43 486 4.0E-20
sp|O34739|STET_BACSU Serine/threonine exchanger SteT OS=Bacillus subtilis (strain 168) GN=steT PE=1 SV=1 43 369 2.0E-14
sp|Q91WN3|S7A13_MOUSE Solute carrier family 7 member 13 OS=Mus musculus GN=Slc7a13 PE=1 SV=1 43 463 6.0E-14
sp|Q8TCU3|S7A13_HUMAN Solute carrier family 7 member 13 OS=Homo sapiens GN=SLC7A13 PE=2 SV=1 60 454 5.0E-13
sp|Q5RKI7|S7A13_RAT Solute carrier family 7 member 13 OS=Rattus norvegicus GN=Slc7a13 PE=2 SV=1 43 463 2.0E-12
sp|Q8X845|FRLA_ECO57 Putative fructoselysine transporter FrlA OS=Escherichia coli O157:H7 GN=frlA PE=3 SV=2 39 369 2.0E-10
sp|P45539|FRLA_ECOLI Putative fructoselysine transporter FrlA OS=Escherichia coli (strain K12) GN=frlA PE=3 SV=2 39 369 2.0E-10
sp|Q8MH63|LAT1N_HUMAN Putative L-type amino acid transporter 1-like protein MLAS OS=Homo sapiens GN=SLC7A5P1 PE=5 SV=1 20 126 2.0E-08
sp|P60066|ADIC_SALTY Arginine/agmatine antiporter OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=adiC PE=1 SV=1 39 374 6.0E-06
sp|P60065|ADIC_SALTI Arginine/agmatine antiporter OS=Salmonella typhi GN=adiC PE=3 SV=1 39 374 6.0E-06
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GO

GO Term Description Terminal node
GO:0055085 transmembrane transport Yes
GO:0022857 transmembrane transporter activity Yes
GO:0016020 membrane Yes
GO:0009987 cellular process No
GO:0110165 cellular anatomical entity No
GO:0051179 localization No
GO:0005215 transporter activity No
GO:0005575 cellular_component No
GO:0008150 biological_process No
GO:0051234 establishment of localization No
GO:0003674 molecular_function No
GO:0006810 transport 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
Lysosome/Vacuole Signal peptide|Transmembrane domain 0.12 0.0771 0.0349 0.3399 0.0771 0.0046 0.3654 0.6218 0.5743 0.0316

SignalP

(None)

Transmembrane Domains

Domain # Start End Length
1 50 72 22
2 82 104 22
3 125 147 22
4 167 184 17
5 191 213 22
6 228 250 22
7 271 293 22
8 321 340 19
9 365 387 22
10 397 419 22
11 431 453 22
12 468 490 22

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

(None)

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup1961
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|5512
Ophiocordyceps australis map64 (Brazil) OphauB2|2181
Ophiocordyceps camponoti-floridani Ophcf2|05533
Ophiocordyceps camponoti-rufipedis Ophun1|3776
Ophiocordyceps kimflemingae Ophio5|5388
Ophiocordyceps subramaniannii Hirsu2|2126 (this protein)

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|2126
MDRVLAGLRVTKADEGVTVKGSDSASASHDTETGQLEVARENKRQIGIPSAALLIFNRTIGTAIFATPGTILSLS
GSVGLSLFMWIAGMLIAVAGTAVYMELGTGLPRNGGEKNYLEYVYRRPRFLTTCLYTGYVLLLGWAAGNSVIFGE
YILHAARVEVTRWNQRGIALACLTGAFLVHGVALKWGIRIQNFLGILKILVIVIIIIAPLFNLSKVRQNNNFSRP
FDGTTASAYSVVTALYNVIWSFVGYSNANYALSETKNPTRTLKYAAPLGIGTISVLYILANVSYFAAVPREEILE
SKRLVAASLFRNMFGEPAERALSVFVALSALGNVMSVIFSQGRLVQELGREGILPFSRLWASNRPFNAPLAGLFE
HWLVTAITVLAPPAGDAYNFVLNLISYPLAIINVFVAGALIHLYRNRQSWNWNPPLKATLPVTIFFLLSNIYLVI
APFVPPEEGNGIYENLPYWIHCVVGFGVIFAGGLYWLVWAVILPKIGRYELVRETTVDEIDGWERNVFYKRPLGD
APRDGPLPSPADDSGK*
Coding >Hirsu2|2126
ATGGATCGCGTCCTCGCAGGCTTGCGGGTCACCAAGGCCGACGAGGGCGTCACTGTCAAGGGCAGCGACTCGGCC
TCGGCCAGCCACGACACCGAAACCGGACAGCTTGAAGTCGCGCGCGAGAACAAGCGCCAGATCGGCATCCCCTCC
GCCGCCCTGCTCATCTTCAACCGCACCATCGGCACCGCCATCTTCGCCACGCCCGGCACCATCCTCTCGCTGTCC
GGCAGCGTGGGCCTGTCGCTCTTCATGTGGATCGCCGGTATGCTCATCGCCGTCGCCGGCACCGCCGTCTACATG
GAGCTCGGCACCGGTCTGCCGCGCAACGGCGGCGAGAAGAACTACCTCGAGTACGTCTACCGCCGGCCGCGCTTC
CTCACCACCTGCCTCTACACCGGATACGTCCTCCTGCTCGGCTGGGCCGCCGGCAACTCCGTCATCTTCGGCGAG
TACATCCTCCACGCCGCCCGCGTCGAAGTCACCCGATGGAACCAGCGCGGCATCGCCCTCGCCTGTCTTACCGGC
GCCTTCCTCGTCCACGGCGTCGCTCTCAAGTGGGGCATCCGCATCCAGAACTTCCTCGGCATCCTCAAGATCCTC
GTCATCGTCATCATCATCATCGCGCCCCTCTTCAACCTCTCCAAGGTCCGCCAGAACAACAACTTCTCCCGGCCC
TTCGACGGCACCACCGCCAGCGCCTACAGCGTCGTCACCGCCCTCTACAACGTCATCTGGAGCTTCGTCGGCTAC
AGCAACGCAAACTACGCCCTTAGCGAGACCAAGAACCCGACGCGCACCCTCAAGTATGCCGCCCCGCTCGGCATC
GGCACCATCTCCGTCCTCTACATCCTCGCCAACGTCTCCTACTTCGCTGCCGTGCCCAGGGAGGAGATTCTCGAG
TCCAAGCGCCTCGTCGCCGCCTCCCTCTTCCGCAACATGTTTGGCGAGCCGGCCGAGCGTGCCCTGTCCGTCTTC
GTCGCCCTCTCCGCCCTGGGCAACGTCATGAGCGTCATCTTCTCCCAGGGCCGCCTGGTCCAGGAGCTGGGCCGC
GAGGGCATTCTGCCCTTCTCCCGCCTCTGGGCCAGCAACCGACCCTTCAACGCCCCCTTGGCCGGCCTCTTCGAG
CACTGGCTCGTGACCGCCATCACCGTCCTGGCACCGCCGGCCGGCGATGCGTACAACTTCGTCCTGAATCTCATC
TCCTATCCTCTGGCCATCATCAACGTCTTCGTCGCTGGTGCTCTTATTCACCTGTACCGCAACCGGCAGAGCTGG
AATTGGAACCCCCCACTGAAGGCCACCCTGCCCGTCACCATCTTCTTCCTTCTCAGCAACATCTATCTCGTCATC
GCCCCCTTCGTCCCTCCCGAGGAAGGCAACGGAATCTATGAGAATCTGCCGTACTGGATCCACTGCGTGGTGGGC
TTCGGCGTCATCTTTGCCGGCGGTCTCTACTGGCTGGTTTGGGCCGTCATCTTGCCCAAGATTGGGCGGTACGAG
CTGGTGCGCGAGACGACCGTGGATGAGATCGACGGCTGGGAACGGAATGTCTTCTACAAGCGGCCGCTCGGAGAT
GCCCCTCGCGACGGCCCGCTGCCCTCGCCGGCTGACGACAGCGGAAAATAA
Transcript >Hirsu2|2126
ATGGATCGCGTCCTCGCAGGCTTGCGGGTCACCAAGGCCGACGAGGGCGTCACTGTCAAGGGCAGCGACTCGGCC
TCGGCCAGCCACGACACCGAAACCGGACAGCTTGAAGTCGCGCGCGAGAACAAGCGCCAGATCGGCATCCCCTCC
GCCGCCCTGCTCATCTTCAACCGCACCATCGGCACCGCCATCTTCGCCACGCCCGGCACCATCCTCTCGCTGTCC
GGCAGCGTGGGCCTGTCGCTCTTCATGTGGATCGCCGGTATGCTCATCGCCGTCGCCGGCACCGCCGTCTACATG
GAGCTCGGCACCGGTCTGCCGCGCAACGGCGGCGAGAAGAACTACCTCGAGTACGTCTACCGCCGGCCGCGCTTC
CTCACCACCTGCCTCTACACCGGATACGTCCTCCTGCTCGGCTGGGCCGCCGGCAACTCCGTCATCTTCGGCGAG
TACATCCTCCACGCCGCCCGCGTCGAAGTCACCCGATGGAACCAGCGCGGCATCGCCCTCGCCTGTCTTACCGGC
GCCTTCCTCGTCCACGGCGTCGCTCTCAAGTGGGGCATCCGCATCCAGAACTTCCTCGGCATCCTCAAGATCCTC
GTCATCGTCATCATCATCATCGCGCCCCTCTTCAACCTCTCCAAGGTCCGCCAGAACAACAACTTCTCCCGGCCC
TTCGACGGCACCACCGCCAGCGCCTACAGCGTCGTCACCGCCCTCTACAACGTCATCTGGAGCTTCGTCGGCTAC
AGCAACGCAAACTACGCCCTTAGCGAGACCAAGAACCCGACGCGCACCCTCAAGTATGCCGCCCCGCTCGGCATC
GGCACCATCTCCGTCCTCTACATCCTCGCCAACGTCTCCTACTTCGCTGCCGTGCCCAGGGAGGAGATTCTCGAG
TCCAAGCGCCTCGTCGCCGCCTCCCTCTTCCGCAACATGTTTGGCGAGCCGGCCGAGCGTGCCCTGTCCGTCTTC
GTCGCCCTCTCCGCCCTGGGCAACGTCATGAGCGTCATCTTCTCCCAGGGCCGCCTGGTCCAGGAGCTGGGCCGC
GAGGGCATTCTGCCCTTCTCCCGCCTCTGGGCCAGCAACCGACCCTTCAACGCCCCCTTGGCCGGCCTCTTCGAG
CACTGGCTCGTGACCGCCATCACCGTCCTGGCACCGCCGGCCGGCGATGCGTACAACTTCGTCCTGAATCTCATC
TCCTATCCTCTGGCCATCATCAACGTCTTCGTCGCTGGTGCTCTTATTCACCTGTACCGCAACCGGCAGAGCTGG
AATTGGAACCCCCCACTGAAGGCCACCCTGCCCGTCACCATCTTCTTCCTTCTCAGCAACATCTATCTCGTCATC
GCCCCCTTCGTCCCTCCCGAGGAAGGCAACGGAATCTATGAGAATCTGCCGTACTGGATCCACTGCGTGGTGGGC
TTCGGCGTCATCTTTGCCGGCGGTCTCTACTGGCTGGTTTGGGCCGTCATCTTGCCCAAGATTGGGCGGTACGAG
CTGGTGCGCGAGACGACCGTGGATGAGATCGACGGCTGGGAACGGAATGTCTTCTACAAGCGGCCGCTCGGAGAT
GCCCCTCGCGACGGCCCGCTGCCCTCGCCGGCTGACGACAGCGGAAAATAA
Gene >Hirsu2|2126
ATGGATCGCGTCCTCGCAGGCTTGCGGGTCACCAAGGCCGACGAGGGCGTCACTGTCAAGGGCAGCGACTCGGCC
TCGGCCAGCCACGACACCGAAACCGGTCAGTTTTGCCTTGCTCCCGCTCCCGCTCCCGCTCCCGCTCCCTGCGCC
CTCTCGTACGCCTCAAGGCAGGCGGACCGGTGCGACAGCGTTGCTTTTCCTCTCGTGCTCCGAGACCCTCCCGCT
GACGCTCGACTCCAGGACAGCTTGAAGTCGCGCGCGAGAACAAGCGCCAGATCGGCATCCCCTCCGCCGCCCTGC
TCATCTTCAACCGCACCATCGGCACCGCCATCTTCGCCACGCCCGGCACCATCCTCTCGCTGTCCGGCAGCGTGG
GCCTGTCGCTCTTCATGTGGATCGCCGGTATGCTCATCGCCGTCGCCGGCACCGCCGTCTACATGGAGCTCGGCA
CCGGTCTGCCGCGCAACGGCGGCGAGAAGAACTACCTCGAGTACGTCTACCGCCGGCCGCGCTTCCTCACCACCT
GCCTCTACACCGGATACGTCCTCCTGCTCGGCTGGGCCGCCGGCAACTCCGTCATCTTCGGCGAGTACATCCTCC
ACGCCGCCCGCGTCGAAGTCACCCGATGGAACCAGCGCGGCATCGCCCTCGCCTGTCTTACCGGCGCCTTCCTCG
TCCACGGCGTCGCTCTCAAGTGGGGCATCCGCATCCAGAACTTCCTCGGCATCCTCAAGATCCTCGTCATCGTCA
TCATCATCATCGCGCCCCTCTTCAACCTCTCCAAGGTCCGCCAGAACAACAACTTCTCCCGGCCCTTCGACGGCA
CCACCGCCAGCGCCTACAGCGTCGTCACCGCCCTCTACAACGTCATCTGGAGCTTCGTCGGCTACAGCAACGCAA
ACTACGCCCTTAGCGAGACCAAGAACCCGACGCGCACCCTCAAGTATGCCGCCCCGCTCGGCATCGGCACCATCT
CCGTCCTCTACATCCTCGCCAACGTCTCCTACTTCGCTGCCGTGCCCAGGGAGGAGATTCTCGAGTCCAAGCGCC
TCGTCGCCGCCTCCCTCTTCCGCAACATGTTTGGCGAGCCGGCCGAGCGTGCCCTGTCCGTCTTCGTCGCCCTCT
CCGCCCTGGGCAACGTCATGAGCGTCATCTTCTCCCAGGGCCGCCTGGTCCAGGAGCTGGGCCGCGAGGGCATTC
TGCCCTTCTCCCGCCTCTGGGCCAGCAACCGACCCTTCAACGCCCCCTTGGCCGGCCTCTTCGAGCACTGGCTCG
TGACCGCCATCACCGTCCTGGCACCGCCGGCCGGCGATGCGTACAACTTCGTCCTGAAGTGAGTCTCGTCCTCCT
TCCCTACCCTTCTGATGGGCCCTCTCCGCTACCATGTCGGGCCAGCGGCCCGTTATCATCAGCTAACGTCTGCAC
CTCTTTTTAGTCTCATCTCCTATCCTCTGGCCATCATCAACGTCTTCGTCGCTGGTGCTCTTATTCACCTGTACC
GCAACCGGCAGAGCTGGAATTGGAACCCCCCACTGAAGGCCACCCTGCCCGTCACCATCTTCTTCCTTCTCAGCA
ACATCTATCTCGTCATCGCCCCCTTCGTCCCTCCCGAGGAAGGCAACGGAATCTATGAGAATCTGCCGTACTGGA
TCCACTGCGTGGTGGGCTTCGGCGTCATCTTTGCCGGCGGTCTCTACTGGCTGGTTTGGGCCGTCATCTTGCCCA
AGATTGGGCGGTACGAGCTGGTGCGCGAGACGACCGTGGATGAGATCGACGGCTGGGAACGGAATGTCTTCTACA
AGCGGCCGCTCGGAGATGCCCCTCGCGACGGCCCGCTGCCCTCGCCGGCTGACGACAGCGGAAAATAA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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