Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauB2|8171
Gene name
LocationContig_99:63226..65738
Strand+
Gene length (bp)2512
Transcript length (bp)2064
Coding sequence length (bp)2064
Protein length (aa) 688

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF03169 OPT OPT oligopeptide transporter protein 8.3E-142 16 679

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|P53134|YGL4_YEAST Putative oligopeptide transporter YGL114W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YGL114W PE=1 SV=1 2 686 1.0E-177
sp|Q7XRV2|YSL6_ORYSJ Probable metal-nicotianamine transporter YSL6 OS=Oryza sativa subsp. japonica GN=YSL6 PE=2 SV=1 297 680 1.0E-23
sp|Q6H3Z6|YSL2_ORYSJ Metal-nicotianamine transporter YSL2 OS=Oryza sativa subsp. japonica GN=YSL2 PE=2 SV=2 246 670 1.0E-21
sp|Q941V3|YSL18_ORYSJ Probable metal-nicotianamine transporter YSL18 OS=Oryza sativa subsp. japonica GN=YSL18 PE=2 SV=1 278 684 1.0E-21
sp|Q6AVD0|YSL3_ORYSJ Probable metal-nicotianamine transporter YSL3 OS=Oryza sativa subsp. japonica GN=YSL3 PE=2 SV=2 276 684 2.0E-20
[Show all]
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Swissprot ID Swissprot Description Start End E-value
sp|P53134|YGL4_YEAST Putative oligopeptide transporter YGL114W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YGL114W PE=1 SV=1 2 686 1.0E-177
sp|Q7XRV2|YSL6_ORYSJ Probable metal-nicotianamine transporter YSL6 OS=Oryza sativa subsp. japonica GN=YSL6 PE=2 SV=1 297 680 1.0E-23
sp|Q6H3Z6|YSL2_ORYSJ Metal-nicotianamine transporter YSL2 OS=Oryza sativa subsp. japonica GN=YSL2 PE=2 SV=2 246 670 1.0E-21
sp|Q941V3|YSL18_ORYSJ Probable metal-nicotianamine transporter YSL18 OS=Oryza sativa subsp. japonica GN=YSL18 PE=2 SV=1 278 684 1.0E-21
sp|Q6AVD0|YSL3_ORYSJ Probable metal-nicotianamine transporter YSL3 OS=Oryza sativa subsp. japonica GN=YSL3 PE=2 SV=2 276 684 2.0E-20
sp|Q6R3K9|YSL2_ARATH Metal-nicotianamine transporter YSL2 OS=Arabidopsis thaliana GN=YSL2 PE=1 SV=1 276 670 8.0E-20
sp|Q6ZGM7|YSL7_ORYSJ Probable metal-nicotianamine transporter YSL7 OS=Oryza sativa subsp. japonica GN=YSL7 PE=2 SV=1 276 685 1.0E-19
sp|Q7XN54|YSL16_ORYSJ Probable metal-nicotianamine transporter YSL16 OS=Oryza sativa subsp. japonica GN=YSL16 PE=2 SV=2 246 670 2.0E-19
sp|Q7XRV1|YSL5_ORYSJ Probable metal-nicotianamine transporter YSL5 OS=Oryza sativa subsp. japonica GN=YSL5 PE=2 SV=3 276 680 2.0E-19
sp|Q0E4J6|YSL8_ORYSJ Probable metal-nicotianamine transporter YSL8 OS=Oryza sativa subsp. japonica GN=YSL8 PE=2 SV=1 234 684 1.0E-18
sp|Q6H3Z3|YSL15_ORYSJ Iron-phytosiderophore transporter YSL15 OS=Oryza sativa subsp. japonica GN=YSL15 PE=2 SV=1 278 670 4.0E-18
sp|Q9SHY2|YSL7_ARATH Probable metal-nicotianamine transporter YSL7 OS=Arabidopsis thaliana GN=YSL7 PE=2 SV=1 278 685 6.0E-18
sp|Q6H7J6|YSL14_ORYSJ Probable metal-nicotianamine transporter YSL14 OS=Oryza sativa subsp. japonica GN=YSL14 PE=2 SV=1 276 670 1.0E-17
sp|Q7XUJ2|YSL9_ORYSJ Probable metal-nicotianamine transporter YSL9 OS=Oryza sativa subsp. japonica GN=YSL9 PE=2 SV=2 276 670 1.0E-17
sp|Q7X660|YSL11_ORYSJ Probable metal-nicotianamine transporter YSL11 OS=Oryza sativa subsp. japonica GN=YSL11 PE=2 SV=1 276 684 2.0E-17
sp|Q5JQD7|YSL12_ORYSJ Probable metal-nicotianamine transporter YSL12 OS=Oryza sativa subsp. japonica GN=YSL12 PE=2 SV=2 276 670 4.0E-17
sp|Q0J932|YSL10_ORYSJ Probable metal-nicotianamine transporter YSL10 OS=Oryza sativa subsp. japonica GN=YSL10 PE=2 SV=2 297 679 5.0E-17
sp|Q6R3K6|YSL6_ARATH Probable metal-nicotianamine transporter YSL6 OS=Arabidopsis thaliana GN=YSL6 PE=2 SV=2 297 680 7.0E-16
sp|Q2EF88|YSL3_ARATH Metal-nicotianamine transporter YSL3 OS=Arabidopsis thaliana GN=YSL3 PE=2 SV=1 278 670 1.0E-15
sp|Q7XKF4|YSL13_ORYSJ Probable metal-nicotianamine transporter YSL13 OS=Oryza sativa subsp. japonica GN=YSL13 PE=2 SV=2 297 670 1.0E-15
sp|Q6R3K4|YSL8_ARATH Probable metal-nicotianamine transporter YSL8 OS=Arabidopsis thaliana GN=YSL8 PE=1 SV=2 276 679 2.0E-15
sp|Q6R3L0|YSL1_ARATH Metal-nicotianamine transporter YSL1 OS=Arabidopsis thaliana GN=YSL1 PE=2 SV=2 278 670 5.0E-15
sp|Q688S6|YSL4_ORYSJ Probable metal-nicotianamine transporter YSL4 OS=Oryza sativa subsp. japonica GN=YSL4 PE=2 SV=1 292 684 6.0E-15
sp|Q9AY27|YS1_MAIZE Iron-phytosiderophore transporter yellow stripe 1 OS=Zea mays GN=YS1 PE=2 SV=1 241 679 3.0E-14
sp|Q9LUN2|YSL5_ARATH Probable metal-nicotianamine transporter YSL5 OS=Arabidopsis thaliana GN=YSL5 PE=1 SV=1 276 685 1.0E-13
sp|Q6R3K8|YSL4_ARATH Probable metal-nicotianamine transporter YSL4 OS=Arabidopsis thaliana GN=YSL4 PE=2 SV=1 297 680 7.0E-13
sp|Q6ZCX1|YSL17_ORYSJ Probable metal-nicotianamine transporter YSL17 OS=Oryza sativa subsp. japonica GN=YSL17 PE=2 SV=1 279 679 1.0E-12
sp|Q941V3|YSL18_ORYSJ Probable metal-nicotianamine transporter YSL18 OS=Oryza sativa subsp. japonica GN=YSL18 PE=2 SV=1 17 190 6.0E-09
sp|Q6R3L0|YSL1_ARATH Metal-nicotianamine transporter YSL1 OS=Arabidopsis thaliana GN=YSL1 PE=2 SV=2 14 175 5.0E-08
sp|Q7XUJ2|YSL9_ORYSJ Probable metal-nicotianamine transporter YSL9 OS=Oryza sativa subsp. japonica GN=YSL9 PE=2 SV=2 13 165 2.0E-07
sp|Q6ZCX1|YSL17_ORYSJ Probable metal-nicotianamine transporter YSL17 OS=Oryza sativa subsp. japonica GN=YSL17 PE=2 SV=1 17 165 2.0E-06
sp|Q6R3K9|YSL2_ARATH Metal-nicotianamine transporter YSL2 OS=Arabidopsis thaliana GN=YSL2 PE=1 SV=1 13 176 2.0E-06
sp|Q2EF88|YSL3_ARATH Metal-nicotianamine transporter YSL3 OS=Arabidopsis thaliana GN=YSL3 PE=2 SV=1 13 165 3.0E-06
sp|Q7X660|YSL11_ORYSJ Probable metal-nicotianamine transporter YSL11 OS=Oryza sativa subsp. japonica GN=YSL11 PE=2 SV=1 13 165 3.0E-06
sp|Q9AY27|YS1_MAIZE Iron-phytosiderophore transporter yellow stripe 1 OS=Zea mays GN=YS1 PE=2 SV=1 13 185 8.0E-06
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GO

GO Term Description Terminal node
GO:0035673 oligopeptide transmembrane transporter activity Yes
GO:0042887 amide transmembrane transporter activity No
GO:0003674 molecular_function No
GO:0005215 transporter activity No
GO:1904680 peptide transmembrane transporter activity No
GO:0022857 transmembrane transporter activity No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 20 0.5

Transmembrane Domains

Domain # Start End Length
1 21 40 19
2 44 63 19
3 76 98 22
4 118 140 22
5 255 277 22
6 350 372 22
7 414 436 22
8 441 463 22
9 476 498 22
10 531 548 17
11 555 577 22
12 587 609 22
13 616 638 22
14 658 680 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|8171
MTPASEAVQMDHQRHFTVRSVLAGLAVGTVICAANVYFGLQTGWVSIMSMPASLMGFGLFRLLRAHLRFPFSPVE
NVLLQSVACGMAIMPLGCGLVGVMPAMEYLLTGEEQGPLAMSMAQLMVWSIGLCYFGVVFAVPLRRQVIIRERLR
FPSGFSTAILISVLHGQIEPGTQQEHDSLEAAARGGFASLAMPPSLPRQPEREARHEEWHETGHEADHEADDEAD
DETGRGVEHEPLLSTESGHQDQDSWSNMRLLLLCFAASGLFTICTYFVPVLRELPVFGSVAASTWLWTLNPSPAY
IGQGIIMGTETTLHMTLGALVGWAMLSPWAKMQGWAPGPVDDWERGSKGWILWVSLAIMLVDAVVSLGYIALRPA
VLHLMRRRAAFGMNYGQAEPNADLDDKNDAPPEQRISGRVVIVGLVLSVLLCIVTVRLVFGDLVPLYATVTAVLM
ALVLSIMGVRALGETDLNPVSGISKLAQLFFALIIPQSNPASVLINLVAGAISEAGALQAGDLMQDLKTGHLLGA
APRAQFWGQIIGASFGAIVSALLYRLYTTVYTIPGPLFQVPTAYVWIFTARLVTGRGLPPMAGQWAAAAGLLFAF
ITLARSVSVGKSWRKWLPGGIAVAIGMYNVPSFTLARALGGLFNWYWIHRLKRSSTPLIILASGFILGEGFLSIV
NLVLQGFNVPHV*
Coding >OphauB2|8171
ATGACGCCCGCGAGCGAGGCAGTACAAATGGACCACCAGCGCCACTTTACGGTGCGCAGTGTTTTGGCAGGCCTC
GCCGTCGGGACTGTCATTTGCGCGGCCAATGTCTACTTTGGACTGCAGACGGGCTGGGTGTCCATCATGTCCATG
CCTGCCAGCCTCATGGGCTTTGGGCTGTTCCGGCTGCTGCGCGCACACCTGCGATTTCCGTTTAGCCCGGTGGAA
AACGTGCTGCTGCAGAGCGTTGCTTGTGGCATGGCCATTATGCCTCTGGGCTGCGGCCTGGTTGGGGTGATGCCA
GCCATGGAGTATCTCTTGACGGGCGAGGAGCAGGGCCCGCTGGCCATGAGCATGGCGCAGCTCATGGTTTGGTCC
ATTGGCTTGTGCTATTTTGGCGTCGTCTTTGCCGTGCCACTACGGCGGCAGGTGATTATCCGGGAGCGGTTGAGG
TTTCCCAGCGGCTTCAGCACTGCCATATTGATTTCGGTCCTGCACGGCCAGATTGAGCCGGGCACGCAGCAGGAG
CATGATAGTCTAGAGGCAGCGGCGCGAGGGGGGTTTGCCAGTCTGGCTATGCCGCCGAGTCTGCCACGGCAGCCA
GAGCGCGAGGCGAGGCACGAAGAATGGCACGAGACGGGGCACGAGGCGGATCACGAGGCCGACGACGAAGCCGAC
GACGAGACGGGACGCGGAGTAGAGCACGAGCCGCTGCTGTCCACGGAATCTGGCCATCAAGACCAAGACTCGTGG
TCCAACATGCGCCTCCTGCTGCTTTGCTTTGCCGCCTCGGGCCTCTTTACCATTTGCACCTACTTTGTGCCCGTG
CTGCGCGAGCTGCCCGTCTTTGGCTCTGTTGCCGCAAGCACATGGCTCTGGACTCTGAATCCGAGCCCGGCATAC
ATTGGCCAGGGCATCATCATGGGCACCGAGACGACGCTTCACATGACTCTGGGCGCGCTGGTTGGCTGGGCCATG
CTCAGCCCCTGGGCCAAGATGCAGGGCTGGGCGCCGGGCCCAGTGGACGACTGGGAGCGCGGCAGCAAGGGCTGG
ATTCTCTGGGTCTCGCTGGCCATTATGCTTGTTGATGCCGTTGTCAGCCTCGGCTACATTGCCCTGCGCCCTGCC
GTTTTGCATTTGATGCGTCGGCGCGCAGCCTTTGGCATGAATTACGGGCAGGCGGAGCCCAATGCCGACTTGGAC
GACAAGAATGATGCCCCCCCGGAGCAGCGCATCAGTGGCCGCGTCGTCATTGTCGGCCTCGTCTTGTCCGTCTTG
CTCTGCATTGTGACGGTGCGTCTCGTCTTTGGCGACTTGGTGCCTCTGTACGCCACCGTTACCGCCGTCTTGATG
GCCCTTGTTCTCAGCATCATGGGGGTTCGCGCGCTGGGAGAGACGGACCTCAACCCCGTCTCAGGCATCAGCAAG
CTGGCCCAGCTCTTCTTTGCCCTTATTATTCCCCAATCGAACCCTGCCAGCGTGCTCATCAATCTTGTTGCCGGC
GCCATTTCTGAAGCTGGGGCGCTCCAAGCTGGAGATCTCATGCAAGACCTCAAGACGGGCCATTTACTTGGCGCC
GCGCCACGAGCGCAGTTTTGGGGCCAGATTATCGGAGCAAGCTTTGGAGCTATCGTCAGTGCGCTTCTCTACCGC
CTTTACACCACCGTCTACACGATACCCGGTCCCCTCTTCCAGGTCCCGACGGCATATGTATGGATATTTACTGCC
AGGCTTGTGACGGGGCGCGGCTTGCCGCCCATGGCTGGGCAGTGGGCAGCCGCTGCAGGGCTCCTCTTTGCCTTT
ATTACTCTGGCCAGGTCTGTCAGTGTGGGCAAGTCGTGGCGCAAATGGCTTCCTGGCGGCATCGCCGTCGCCATT
GGCATGTACAATGTGCCCTCTTTCACCTTGGCCCGGGCTCTGGGGGGACTGTTCAACTGGTACTGGATCCACCGG
CTCAAACGCTCCAGCACACCCCTTATTATTCTGGCATCTGGCTTCATCCTGGGGGAAGGCTTCCTCAGCATTGTC
AATCTCGTCTTGCAGGGATTCAACGTTCCACATGTTTGA
Transcript >OphauB2|8171
ATGACGCCCGCGAGCGAGGCAGTACAAATGGACCACCAGCGCCACTTTACGGTGCGCAGTGTTTTGGCAGGCCTC
GCCGTCGGGACTGTCATTTGCGCGGCCAATGTCTACTTTGGACTGCAGACGGGCTGGGTGTCCATCATGTCCATG
CCTGCCAGCCTCATGGGCTTTGGGCTGTTCCGGCTGCTGCGCGCACACCTGCGATTTCCGTTTAGCCCGGTGGAA
AACGTGCTGCTGCAGAGCGTTGCTTGTGGCATGGCCATTATGCCTCTGGGCTGCGGCCTGGTTGGGGTGATGCCA
GCCATGGAGTATCTCTTGACGGGCGAGGAGCAGGGCCCGCTGGCCATGAGCATGGCGCAGCTCATGGTTTGGTCC
ATTGGCTTGTGCTATTTTGGCGTCGTCTTTGCCGTGCCACTACGGCGGCAGGTGATTATCCGGGAGCGGTTGAGG
TTTCCCAGCGGCTTCAGCACTGCCATATTGATTTCGGTCCTGCACGGCCAGATTGAGCCGGGCACGCAGCAGGAG
CATGATAGTCTAGAGGCAGCGGCGCGAGGGGGGTTTGCCAGTCTGGCTATGCCGCCGAGTCTGCCACGGCAGCCA
GAGCGCGAGGCGAGGCACGAAGAATGGCACGAGACGGGGCACGAGGCGGATCACGAGGCCGACGACGAAGCCGAC
GACGAGACGGGACGCGGAGTAGAGCACGAGCCGCTGCTGTCCACGGAATCTGGCCATCAAGACCAAGACTCGTGG
TCCAACATGCGCCTCCTGCTGCTTTGCTTTGCCGCCTCGGGCCTCTTTACCATTTGCACCTACTTTGTGCCCGTG
CTGCGCGAGCTGCCCGTCTTTGGCTCTGTTGCCGCAAGCACATGGCTCTGGACTCTGAATCCGAGCCCGGCATAC
ATTGGCCAGGGCATCATCATGGGCACCGAGACGACGCTTCACATGACTCTGGGCGCGCTGGTTGGCTGGGCCATG
CTCAGCCCCTGGGCCAAGATGCAGGGCTGGGCGCCGGGCCCAGTGGACGACTGGGAGCGCGGCAGCAAGGGCTGG
ATTCTCTGGGTCTCGCTGGCCATTATGCTTGTTGATGCCGTTGTCAGCCTCGGCTACATTGCCCTGCGCCCTGCC
GTTTTGCATTTGATGCGTCGGCGCGCAGCCTTTGGCATGAATTACGGGCAGGCGGAGCCCAATGCCGACTTGGAC
GACAAGAATGATGCCCCCCCGGAGCAGCGCATCAGTGGCCGCGTCGTCATTGTCGGCCTCGTCTTGTCCGTCTTG
CTCTGCATTGTGACGGTGCGTCTCGTCTTTGGCGACTTGGTGCCTCTGTACGCCACCGTTACCGCCGTCTTGATG
GCCCTTGTTCTCAGCATCATGGGGGTTCGCGCGCTGGGAGAGACGGACCTCAACCCCGTCTCAGGCATCAGCAAG
CTGGCCCAGCTCTTCTTTGCCCTTATTATTCCCCAATCGAACCCTGCCAGCGTGCTCATCAATCTTGTTGCCGGC
GCCATTTCTGAAGCTGGGGCGCTCCAAGCTGGAGATCTCATGCAAGACCTCAAGACGGGCCATTTACTTGGCGCC
GCGCCACGAGCGCAGTTTTGGGGCCAGATTATCGGAGCAAGCTTTGGAGCTATCGTCAGTGCGCTTCTCTACCGC
CTTTACACCACCGTCTACACGATACCCGGTCCCCTCTTCCAGGTCCCGACGGCATATGTATGGATATTTACTGCC
AGGCTTGTGACGGGGCGCGGCTTGCCGCCCATGGCTGGGCAGTGGGCAGCCGCTGCAGGGCTCCTCTTTGCCTTT
ATTACTCTGGCCAGGTCTGTCAGTGTGGGCAAGTCGTGGCGCAAATGGCTTCCTGGCGGCATCGCCGTCGCCATT
GGCATGTACAATGTGCCCTCTTTCACCTTGGCCCGGGCTCTGGGGGGACTGTTCAACTGGTACTGGATCCACCGG
CTCAAACGCTCCAGCACACCCCTTATTATTCTGGCATCTGGCTTCATCCTGGGGGAAGGCTTCCTCAGCATTGTC
AATCTCGTCTTGCAGGGATTCAACGTTCCACATGTTTGA
Gene >OphauB2|8171
ATGACGCCCGCGAGCGAGGCAGTACAAATGGACCACCAGCGCCACTTTACGGTGCGCAGTGTTTTGGCAGGCCTC
GCCGTCGGGACTGTCATTTGCGCGGCCAATGTCTACTTTGGACTGCAGACGGGCTGGGTGTCCATCATGTCCATG
CCTGCCAGCCTCATGGGCTTTGGGCTGTTCCGGCTGCTGCGCGCACACCTGCGATTTCCGTTTAGCCCGGTGGAA
AACGTGCTGCTGCAGAGCGTTGCTTGTGGCATGGCCATTATGCCTCTGGGCTGCGGCCTGGTTGGGGTGGTTAGT
GTCTCATGGGCCAATTTTGGCAGAGCGAGTCTGGGCTGATTAAAGGGGAGGGGAGTCCAGATGCCAGCCATGGAG
TATCTCTTGACGGGCGAGGAGCAGGGCCCGCTGGCCATGAGCATGGCGCAGCTCATGGTTTGGTCCATTGGCTTG
TGCTATTTTGGCGTCGTCTTTGCCGTGCCACTGTGAGGAGAAGGAAGAGCCAGGCCCACGAGGACGCGAGAGCTG
CACCTGCTAATTGCAAGGCCAGACGGCGGCAGGTGATTATCCGGGAGCGGTTGAGGTTTCCCAGCGGCTTCAGCA
CTGCCATATTGATTTCGGTCCTGCACGGCCAGATTGAGCCGGGCACGCAGCAGGAGCATGATAGTCTAGAGGCAG
CGGCGCGAGGGGGGTTTGCCAGTCTGGCTATGCCGCCGAGTCTGCCACGGCAGCCAGAGCGCGAGGCGAGGCACG
AAGAATGGCACGAGACGGGGCACGAGGCGGATCACGAGGCCGACGACGAAGCCGACGACGAGACGGGACGCGGAG
TAGAGCACGAGCCGCTGCTGTCCACGGAATCTGGCCATCAAGACCAAGACTCGTGGTCCAACATGCGCCTCCTGC
TGCTTTGCTTTGCCGCCTCGGGCCTCTTTACCATTTGCACCTACTTTGTGCCCGTGCTGCGCGAGCTGCCCGTCT
TTGGCTCTGTTGCCGCAAGCACATGGCTCTGGACTCTGAATCCGAGCCCGGCATACATTGGCCAGGGCATCATCA
TGGGCACCGAGACGACGCTTCACATGACTCTGGGCGCGCTGGTTGGCTGGGCCATGCTCAGCCCCTGGGCCAAGA
TGCAGGGCTGGGCGCCGGGCCCAGTGGACGACTGGGAGCGCGGCAGCAAGGGCTGGATTCTCTGGGTCTCGCTGG
CCATTATGCTTGTTGATGCCGTTGTCAGCCTCGGCTACATTGCCCTGCGCCCTGCCGTTTTGCATTTGATGCGTC
GGCGCGCAGCCTTTGGCATGAATTACGGGCAGGCGGAGCCCAATGCCGACTTGGACGACAAGAATGATGCCCCCC
CGGAGCAGCGCATCAGTGGCCGCGTCGTCATTGTCGGCCTCGTCTTGTCCGTCTTGCTCTGCATTGTGACGGTGC
GTCTCGTCTTTGGCGACTTGGTGCCTCTGTACGCCACCGTTACCGCCGTCTTGATGGCCCTTGTTCTCAGCATCA
TGGGGGTTCGCGCGCTGGGAGAGACGGACCTCAACCCCGTCTCAGGCATCAGCAAGCTGGCCCAGCTCTTCTTTG
CCCTTATTATTCCCCAATCGAACCCTGCCAGCGTGCTCATCAATCTTGTTGCCGGCGCCATTGTAAGACCAAGCC
GAATATATTCTCGTCGGAGGCGTCATGCTAACGAGGAGCGGCCCTAGTCTGAAGCTGTTGGTGGCACCGGGACCC
CGTCTCTTGCTGCCCCTTTGCTAACCTTGATAGGGGGCGCTCCAAGCTGGAGATCTCATGCAAGACCTCAAGACG
GGCCATTTACTTGGCGCCGCGCCACGAGCGCAGTTTTGGGGCCAGATTATCGGAGCAAGCTTTGGAGCTATCGTC
AGTGCGCTTCTCTACCGCCTTTACACCACGTGAGCGCTCCCTCTTTTTTTTTTTGATTTCCTTCCTCTTTTCTGC
AAAGCCAGGGCTAACGACGTGTGACGCACAGCGTCTACACGATACCCGGTCCCCTCTTCCAGGTCCCGACGGCAT
ATGTATGGATATTTACTGCCAGGCTTGTGACGGGGCGCGGCTTGCCGCCCATGGCTGGGCAGTGGGCAGCCGCTG
CAGGGCTCCTCTTTGCCTTTATTACTCTGGCCAGGTCTGTCAGTGTGGGCAAGTCGTGGCGCAAATGGCTTCCTG
GCGGCATCGCCGTCGCCATTGGTAATCTTCTTCATTTGTCTTGTGTCTTTTGTCGTCACATCTTGCTCCGCTAAC
TACTAGGTAGGCATGTACAATGTGCCCTCTTTCACCTTGGCCCGGGCTCTGGGGGGACTGTTCAACTGGTACTGG
ATCCACCGGCTCAAACGCTCCAGCACACCCCTTATTATTCTGGCATCTGTAGGTGTATTCCTGCACGCACGACAG
CTTCCAAGACACAGCACTTGCTGACCAATGTTACCAGGGCTTCATCCTGGGGGAAGGCTTCCTCAGCATTGTCAA
TCTCGTCTTGCAGGGATTCAACGTTCCACATGTTTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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