Fungal Genomics

at Utrecht University

General Properties

Protein IDOphun1|3487
Gene name
LocationContig_31:27064..28894
Strand+
Gene length (bp)1830
Transcript length (bp)1761
Coding sequence length (bp)1761
Protein length (aa) 587

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF03155 Alg6_Alg8 ALG6, ALG8 glycosyltransferase family 4.6E-79 64 292
PF03155 Alg6_Alg8 ALG6, ALG8 glycosyltransferase family 8.4E-48 335 566

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
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 44 584 3.0E-132
sp|Q12001|ALG6_YEAST Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG6 PE=1 SV=1 39 568 6.0E-122
sp|Q9VKX7|ALG6_DROME Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=gny PE=2 SV=2 64 571 8.0E-84
sp|Q9Y672|ALG6_HUMAN Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG6 PE=1 SV=1 48 441 3.0E-82
sp|Q5NVS8|ALG6_PONAB Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Pongo abelii GN=ALG6 PE=2 SV=1 48 441 3.0E-81
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Swissprot ID Swissprot Description Start End E-value
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 44 584 3.0E-132
sp|Q12001|ALG6_YEAST Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG6 PE=1 SV=1 39 568 6.0E-122
sp|Q9VKX7|ALG6_DROME Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=gny PE=2 SV=2 64 571 8.0E-84
sp|Q9Y672|ALG6_HUMAN Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG6 PE=1 SV=1 48 441 3.0E-82
sp|Q5NVS8|ALG6_PONAB Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Pongo abelii GN=ALG6 PE=2 SV=1 48 441 3.0E-81
sp|Q3TAE8|ALG6_MOUSE Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg6 PE=2 SV=1 56 441 6.0E-79
sp|Q3T1L5|ALG6_RAT Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Rattus norvegicus GN=Alg6 PE=2 SV=1 56 441 3.0E-78
sp|Q54QG6|ALG6_DICDI Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg6 PE=3 SV=1 46 485 2.0E-77
sp|Q9FF17|ALG6_ARATH Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At5g38460 PE=2 SV=1 11 492 5.0E-73
sp|Q09226|ALG6_CAEEL Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08B11.8 PE=3 SV=1 56 429 4.0E-66
sp|Q802T2|ALG6_CHICK Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gallus gallus GN=ALG6 PE=2 SV=1 48 260 1.0E-49
sp|Q9BVK2|ALG8_HUMAN Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG8 PE=1 SV=2 83 469 4.0E-31
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 83 469 1.0E-28
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 83 485 2.0E-28
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 83 523 2.0E-27
sp|Q0P5D9|ALG8_BOVIN Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Bos taurus GN=ALG8 PE=2 SV=1 83 443 5.0E-27
sp|Q6P8H8|ALG8_MOUSE Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg8 PE=2 SV=2 83 469 8.0E-27
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 1 486 1.0E-26
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 83 485 9.0E-26
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 83 504 9.0E-25
sp|Q802T2|ALG6_CHICK Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gallus gallus GN=ALG6 PE=2 SV=1 335 557 9.0E-25
sp|Q9W3V8|ALG8_DROME Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=xit PE=2 SV=1 83 477 1.0E-23
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 83 469 3.0E-22
sp|P40351|ALG8_YEAST Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG8 PE=1 SV=1 83 471 5.0E-22
sp|Q10479|ALG8_SCHPO Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg8 PE=3 SV=1 83 439 1.0E-21
sp|Q1DJR8|ALG8_COCIM Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Coccidioides immitis (strain RS) GN=ALG8 PE=3 SV=1 83 485 5.0E-21
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 78 471 6.0E-21
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 83 440 2.0E-20
sp|O80505|ALG8_ARATH Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At2g44660 PE=2 SV=3 83 471 9.0E-20
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 83 266 1.0E-19
sp|P52887|ALG8_CAEEL Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08H9.3 PE=3 SV=3 83 495 3.0E-19
sp|Q554E2|ALG8_DICDI Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 83 164 2.0E-09
sp|Q554E2|ALG8_DICDI Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 197 489 1.0E-08
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GO

GO Term Description Terminal node
GO:0016758 hexosyltransferase activity Yes
GO:0016757 glycosyltransferase activity No
GO:0003674 molecular_function No
GO:0016740 transferase 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 - 49 0.5

Transmembrane Domains

Domain # Start End Length
1 52 74 22
2 152 174 22
3 181 203 22
4 208 227 19
5 234 256 22
6 271 293 22
7 406 425 19
8 450 469 19
9 474 496 22
10 509 531 22
11 544 566 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 >Ophun1|3487
MATASPSTRKPRRKPRRSGPGPDGAGPLIRAPSFALAAFLWPARCASSQWEVLPLVLIAVGLFRWAAGLWGYSGF
ESPPMYGDYEAQRHWMELTTNLPVSQWYFHDLQWWGLDYPPLTAYHSWLMGKLGAFINPAWFALFSSRGSDDPDL
KIFMRASVIVSEYLIYIPAAVVFVRRFGRLNGVVSWTSSIALVAFLMQPATMLIDHVHFQYNTVMLGLVVASMNS
MLAERYKSAAFFFVAALGFKQMALYYALTVFSYLLSKCLLPTLNLTRLVSVALITLLSLAALLLPLVLGTLYDRY
RGIELWPDMDVRPPLPLFPSLGNYLDDRSVSYAIVEQLLQMVHRVFPFARGLFEDKVANFWCAANVFVKLRDLPP
STLQKASLAATLISILPPNIILFFRPRKTTLPLAFAATAWGFFLFSYQVHEKSVLLPLMPMTLLLAGRHGLSGEV
RAWVGFANLLGAWTLFPLLHRVSLGVPYAVLTLLWAYLLGLPPFSWDAVWEAPDGQSGLVRWATILIHGVFYGAM
GLWHILDASFRPPLDKPDLWVVANVGIGAAGFGICYLWCLWKLAQESDLLPKGRTGKKKTS*
Coding >Ophun1|3487
ATGGCCACAGCGAGTCCCTCGACGCGCAAGCCCCGGCGCAAACCCCGACGGTCAGGCCCCGGTCCCGACGGCGCC
GGGCCTCTGATCCGCGCGCCGTCGTTCGCGCTGGCCGCCTTTCTCTGGCCCGCGCGCTGCGCCTCTTCGCAATGG
GAGGTTCTGCCTCTTGTACTCATAGCTGTAGGCCTGTTTCGCTGGGCGGCTGGTCTATGGGGCTACTCTGGCTTT
GAGTCGCCGCCCATGTATGGCGATTATGAGGCGCAGCGTCACTGGATGGAGCTGACGACGAATCTACCCGTGTCG
CAATGGTATTTTCACGATCTTCAGTGGTGGGGGCTCGACTATCCGCCCTTGACGGCCTATCATAGCTGGCTGATG
GGCAAGCTCGGTGCCTTTATCAACCCAGCATGGTTCGCCCTCTTCTCCTCGCGCGGATCCGACGATCCGGATCTC
AAGATCTTCATGAGAGCCTCCGTCATCGTCTCCGAATACCTCATCTATATTCCCGCCGCTGTCGTCTTCGTTCGT
CGCTTCGGCCGGCTAAACGGCGTCGTCTCCTGGACGAGTTCCATTGCCCTCGTCGCCTTTCTCATGCAGCCGGCT
ACCATGCTTATCGATCATGTTCACTTTCAGTACAATACCGTCATGCTCGGTCTCGTCGTTGCCAGCATGAACAGC
ATGCTGGCAGAGAGGTATAAAAGCGCCGCCTTCTTCTTCGTCGCTGCTCTCGGCTTCAAGCAGATGGCCCTCTAC
TATGCCTTGACCGTCTTCTCATATCTCTTGTCCAAGTGTCTGCTCCCGACACTTAACCTGACGAGACTGGTTTCC
GTCGCTCTAATCACTCTATTATCCTTGGCCGCCTTGCTTCTTCCTCTCGTCTTGGGAACCTTGTATGACAGATAC
CGAGGCATCGAGTTGTGGCCCGACATGGACGTCCGCCCTCCGCTACCCCTTTTCCCCTCTCTCGGCAACTACCTC
GATGACCGATCCGTCTCTTACGCCATCGTCGAGCAACTGCTTCAGATGGTCCATCGCGTCTTTCCCTTTGCAAGA
GGCCTGTTCGAGGACAAGGTGGCCAATTTCTGGTGCGCCGCCAACGTCTTCGTCAAGCTCCGCGACCTCCCCCCC
TCGACGCTGCAAAAGGCATCGCTGGCCGCCACGCTCATCTCCATCCTACCGCCCAACATCATCCTGTTCTTTCGG
CCGCGGAAGACGACGCTACCCCTGGCCTTTGCCGCCACGGCATGGGGATTCTTCCTCTTCAGCTATCAGGTTCAC
GAGAAGAGCGTCCTGCTGCCTTTGATGCCCATGACGCTCTTGCTCGCCGGGAGGCACGGCCTGAGCGGAGAGGTG
CGTGCTTGGGTGGGCTTCGCCAATCTTCTGGGAGCGTGGACGCTGTTTCCGTTGCTGCATCGCGTCAGTCTGGGC
GTGCCATACGCCGTCTTGACCCTTCTTTGGGCCTATCTGCTCGGCCTCCCGCCCTTTTCGTGGGACGCCGTCTGG
GAAGCGCCGGACGGGCAATCGGGGTTGGTCCGGTGGGCGACGATTCTGATACACGGAGTCTTTTACGGTGCCATG
GGGCTATGGCATATCCTCGACGCCTCGTTTCGCCCGCCCCTCGACAAGCCAGATCTGTGGGTCGTGGCAAACGTT
GGTATCGGTGCTGCGGGTTTCGGCATCTGTTACCTCTGGTGTCTGTGGAAGCTGGCGCAAGAAAGCGACCTTTTG
CCCAAGGGGCGGACGGGAAAGAAAAAGACGAGTTGA
Transcript >Ophun1|3487
ATGGCCACAGCGAGTCCCTCGACGCGCAAGCCCCGGCGCAAACCCCGACGGTCAGGCCCCGGTCCCGACGGCGCC
GGGCCTCTGATCCGCGCGCCGTCGTTCGCGCTGGCCGCCTTTCTCTGGCCCGCGCGCTGCGCCTCTTCGCAATGG
GAGGTTCTGCCTCTTGTACTCATAGCTGTAGGCCTGTTTCGCTGGGCGGCTGGTCTATGGGGCTACTCTGGCTTT
GAGTCGCCGCCCATGTATGGCGATTATGAGGCGCAGCGTCACTGGATGGAGCTGACGACGAATCTACCCGTGTCG
CAATGGTATTTTCACGATCTTCAGTGGTGGGGGCTCGACTATCCGCCCTTGACGGCCTATCATAGCTGGCTGATG
GGCAAGCTCGGTGCCTTTATCAACCCAGCATGGTTCGCCCTCTTCTCCTCGCGCGGATCCGACGATCCGGATCTC
AAGATCTTCATGAGAGCCTCCGTCATCGTCTCCGAATACCTCATCTATATTCCCGCCGCTGTCGTCTTCGTTCGT
CGCTTCGGCCGGCTAAACGGCGTCGTCTCCTGGACGAGTTCCATTGCCCTCGTCGCCTTTCTCATGCAGCCGGCT
ACCATGCTTATCGATCATGTTCACTTTCAGTACAATACCGTCATGCTCGGTCTCGTCGTTGCCAGCATGAACAGC
ATGCTGGCAGAGAGGTATAAAAGCGCCGCCTTCTTCTTCGTCGCTGCTCTCGGCTTCAAGCAGATGGCCCTCTAC
TATGCCTTGACCGTCTTCTCATATCTCTTGTCCAAGTGTCTGCTCCCGACACTTAACCTGACGAGACTGGTTTCC
GTCGCTCTAATCACTCTATTATCCTTGGCCGCCTTGCTTCTTCCTCTCGTCTTGGGAACCTTGTATGACAGATAC
CGAGGCATCGAGTTGTGGCCCGACATGGACGTCCGCCCTCCGCTACCCCTTTTCCCCTCTCTCGGCAACTACCTC
GATGACCGATCCGTCTCTTACGCCATCGTCGAGCAACTGCTTCAGATGGTCCATCGCGTCTTTCCCTTTGCAAGA
GGCCTGTTCGAGGACAAGGTGGCCAATTTCTGGTGCGCCGCCAACGTCTTCGTCAAGCTCCGCGACCTCCCCCCC
TCGACGCTGCAAAAGGCATCGCTGGCCGCCACGCTCATCTCCATCCTACCGCCCAACATCATCCTGTTCTTTCGG
CCGCGGAAGACGACGCTACCCCTGGCCTTTGCCGCCACGGCATGGGGATTCTTCCTCTTCAGCTATCAGGTTCAC
GAGAAGAGCGTCCTGCTGCCTTTGATGCCCATGACGCTCTTGCTCGCCGGGAGGCACGGCCTGAGCGGAGAGGTG
CGTGCTTGGGTGGGCTTCGCCAATCTTCTGGGAGCGTGGACGCTGTTTCCGTTGCTGCATCGCGTCAGTCTGGGC
GTGCCATACGCCGTCTTGACCCTTCTTTGGGCCTATCTGCTCGGCCTCCCGCCCTTTTCGTGGGACGCCGTCTGG
GAAGCGCCGGACGGGCAATCGGGGTTGGTCCGGTGGGCGACGATTCTGATACACGGAGTCTTTTACGGTGCCATG
GGGCTATGGCATATCCTCGACGCCTCGTTTCGCCCGCCCCTCGACAAGCCAGATCTGTGGGTCGTGGCAAACGTT
GGTATCGGTGCTGCGGGTTTCGGCATCTGTTACCTCTGGTGTCTGTGGAAGCTGGCGCAAGAAAGCGACCTTTTG
CCCAAGGGGCGGACGGGAAAGAAAAAGACGAGTTGA
Gene >Ophun1|3487
ATGGCCACAGCGAGTCCCTCGACGCGCAAGCCCCGGCGCAAACCCCGACGGTCAGGCCCCGGTCCCGACGGCGCC
GGGCCTCTGATCCGCGCGCCGTCGTTCGCGCTGGCCGCCTTTCTCTGGCCCGCGCGCTGCGCCTCTTCGCAATGG
GAGGTTCTGCCTCTTGTACTCATAGCTGTAGGCCTGTTTCGCTGGGCGGCTGGTCTATGGGGCTACTCTGGTGAA
TATTCGCCGCCTTGTTTTTCTCGGGCCTGCTGGGGCTGACGACGTCGTCTTGGGGGTTGGGTAGGCTTTGAGTCG
CCGCCCATGTATGGCGATTATGAGGCGCAGCGTCACTGGATGGAGCTGACGACGAATCTACCCGTGTCGCAATGG
TATTTTCACGATCTTCAGTGGTGGGGGCTCGACTATCCGCCCTTGACGGCCTATCATAGCTGGCTGATGGGCAAG
CTCGGTGCCTTTATCAACCCAGCATGGTTCGCCCTCTTCTCCTCGCGCGGATCCGACGATCCGGATCTCAAGATC
TTCATGAGAGCCTCCGTCATCGTCTCCGAATACCTCATCTATATTCCCGCCGCTGTCGTCTTCGTTCGTCGCTTC
GGCCGGCTAAACGGCGTCGTCTCCTGGACGAGTTCCATTGCCCTCGTCGCCTTTCTCATGCAGCCGGCTACCATG
CTTATCGATCATGTTCACTTTCAGTACAATACCGTCATGCTCGGTCTCGTCGTTGCCAGCATGAACAGCATGCTG
GCAGAGAGGTATAAAAGCGCCGCCTTCTTCTTCGTCGCTGCTCTCGGCTTCAAGCAGATGGCCCTCTACTATGCC
TTGACCGTCTTCTCATATCTCTTGTCCAAGTGTCTGCTCCCGACACTTAACCTGACGAGACTGGTTTCCGTCGCT
CTAATCACTCTATTATCCTTGGCCGCCTTGCTTCTTCCTCTCGTCTTGGGAACCTTGTATGACAGATACCGAGGC
ATCGAGTTGTGGCCCGACATGGACGTCCGCCCTCCGCTACCCCTTTTCCCCTCTCTCGGCAACTACCTCGATGAC
CGATCCGTCTCTTACGCCATCGTCGAGCAACTGCTTCAGATGGTCCATCGCGTCTTTCCCTTTGCAAGAGGCCTG
TTCGAGGACAAGGTGGCCAATTTCTGGTGCGCCGCCAACGTCTTCGTCAAGCTCCGCGACCTCCCCCCCTCGACG
CTGCAAAAGGCATCGCTGGCCGCCACGCTCATCTCCATCCTACCGCCCAACATCATCCTGTTCTTTCGGCCGCGG
AAGACGACGCTACCCCTGGCCTTTGCCGCCACGGCATGGGGATTCTTCCTCTTCAGCTATCAGGTTCACGAGAAG
AGCGTCCTGCTGCCTTTGATGCCCATGACGCTCTTGCTCGCCGGGAGGCACGGCCTGAGCGGAGAGGTGCGTGCT
TGGGTGGGCTTCGCCAATCTTCTGGGAGCGTGGACGCTGTTTCCGTTGCTGCATCGCGTCAGTCTGGGCGTGCCA
TACGCCGTCTTGACCCTTCTTTGGGCCTATCTGCTCGGCCTCCCGCCCTTTTCGTGGGACGCCGTCTGGGAAGCG
CCGGACGGGCAATCGGGGTTGGTCCGGTGGGCGACGATTCTGATACACGGAGTCTTTTACGGTGCCATGGGGCTA
TGGCATATCCTCGACGCCTCGTTTCGCCCGCCCCTCGACAAGCCAGATCTGTGGGTCGTGGCAAACGTTGGTATC
GGTGCTGCGGGTTTCGGCATCTGTTACCTCTGGTGTCTGTGGAAGCTGGCGCAAGAAAGCGACCTTTTGCCCAAG
GGGCGGACGGGAAAGAAAAAGACGAGTTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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