Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauB2|5500
Gene name
LocationContig_43:16380..18478
Strand+
Gene length (bp)2098
Transcript length (bp)2034
Coding sequence length (bp)2034
Protein length (aa) 678

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF07992 Pyr_redox_2 Pyridine nucleotide-disulphide oxidoreductase 8.5E-45 154 474
PF00070 Pyr_redox Pyridine nucleotide-disulphide oxidoreductase 1.6E-09 315 397
PF00036 EF-hand_1 EF hand 1.5E-06 528 553

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q1JPL4|NDB1_ARATH External alternative NAD(P)H-ubiquinone oxidoreductase B1, mitochondrial OS=Arabidopsis thaliana GN=NDB1 PE=1 SV=1 155 673 3.0E-107
sp|Q9ST62|NDB1_SOLTU External alternative NAD(P)H-ubiquinone oxidoreductase B1, mitochondrial OS=Solanum tuberosum GN=NDB1 PE=1 SV=1 91 673 3.0E-104
sp|M1BYJ7|ENDB1_SOLTU External alternative NAD(P)H-ubiquinone oxidoreductase B1, mitochondrial OS=Solanum tuberosum GN=NDB1 PE=3 SV=1 91 673 3.0E-103
sp|F4JJJ3|NDB3_ARATH External alternative NAD(P)H-ubiquinone oxidoreductase B3, mitochondrial OS=Arabidopsis thaliana GN=NDB3 PE=2 SV=1 148 673 3.0E-101
sp|Q94BV7|NDB2_ARATH External alternative NAD(P)H-ubiquinone oxidoreductase B2, mitochondrial OS=Arabidopsis thaliana GN=NDB2 PE=1 SV=1 152 676 1.0E-98
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Swissprot ID Swissprot Description Start End E-value
sp|Q1JPL4|NDB1_ARATH External alternative NAD(P)H-ubiquinone oxidoreductase B1, mitochondrial OS=Arabidopsis thaliana GN=NDB1 PE=1 SV=1 155 673 3.0E-107
sp|Q9ST62|NDB1_SOLTU External alternative NAD(P)H-ubiquinone oxidoreductase B1, mitochondrial OS=Solanum tuberosum GN=NDB1 PE=1 SV=1 91 673 3.0E-104
sp|M1BYJ7|ENDB1_SOLTU External alternative NAD(P)H-ubiquinone oxidoreductase B1, mitochondrial OS=Solanum tuberosum GN=NDB1 PE=3 SV=1 91 673 3.0E-103
sp|F4JJJ3|NDB3_ARATH External alternative NAD(P)H-ubiquinone oxidoreductase B3, mitochondrial OS=Arabidopsis thaliana GN=NDB3 PE=2 SV=1 148 673 3.0E-101
sp|Q94BV7|NDB2_ARATH External alternative NAD(P)H-ubiquinone oxidoreductase B2, mitochondrial OS=Arabidopsis thaliana GN=NDB2 PE=1 SV=1 152 676 1.0E-98
sp|Q9SKT7|NDB4_ARATH External alternative NAD(P)H-ubiquinone oxidoreductase B4, mitochondrial OS=Arabidopsis thaliana GN=NDB4 PE=1 SV=1 132 676 6.0E-92
sp|P40215|NDH1_YEAST External NADH-ubiquinone oxidoreductase 1, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NDE1 PE=1 SV=1 124 673 1.0E-70
sp|F2Z699|NDH2_YARLI External alternative NADH-ubiquinone oxidoreductase, mitochondrial OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=NDH2 PE=1 SV=1 151 674 2.0E-69
sp|Q07500|NDH2_YEAST External NADH-ubiquinone oxidoreductase 2, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NDE2 PE=1 SV=1 32 472 3.0E-66
sp|Q55CD9|NDH_DICDI Probable NADH dehydrogenase OS=Dictyostelium discoideum GN=DDB_G0270104 PE=3 SV=2 154 476 5.0E-64
sp|O43090|NDH2_SCHPO Probable NADH-ubiquinone oxidoreductase C947.15c, mitochondrial OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC947.15c PE=3 SV=1 152 472 4.0E-59
sp|O14121|NDH1_SCHPO Probable NADH-ubiquinone oxidoreductase C3A11.07, mitochondrial OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC3A11.07 PE=3 SV=1 151 472 7.0E-57
sp|M0ZYF3|INDA1_SOLTU Internal alternative NAD(P)H-ubiquinone oxidoreductase A1, mitochondrial OS=Solanum tuberosum GN=NDA1 PE=3 SV=1 148 495 3.0E-51
sp|Q8GWA1|NDA1_ARATH Internal alternative NAD(P)H-ubiquinone oxidoreductase A1, mitochondrial OS=Arabidopsis thaliana GN=NDA1 PE=2 SV=1 145 495 5.0E-51
sp|Q9ST63|NDA1_SOLTU Internal alternative NAD(P)H-ubiquinone oxidoreductase A1, mitochondrial OS=Solanum tuberosum GN=NDA1 PE=1 SV=1 148 495 8.0E-51
sp|P32340|NDI1_YEAST Rotenone-insensitive NADH-ubiquinone oxidoreductase, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NDI1 PE=1 SV=1 151 472 5.0E-50
sp|O80874|NDA2_ARATH Internal alternative NAD(P)H-ubiquinone oxidoreductase A2, mitochondrial OS=Arabidopsis thaliana GN=NDA2 PE=2 SV=1 148 495 1.0E-48
sp|O05267|YUMB_BACSU NADH dehydrogenase-like protein YumB OS=Bacillus subtilis (strain 168) GN=yumB PE=3 SV=1 151 494 1.0E-19
sp|Q2FZV7|Y878_STAA8 NADH dehydrogenase-like protein SAOUHSC_00878 OS=Staphylococcus aureus (strain NCTC 8325) GN=SAOUHSC_00878 PE=1 SV=1 150 516 4.0E-19
sp|Q6GIE7|Y903_STAAR NADH dehydrogenase-like protein SAR0903 OS=Staphylococcus aureus (strain MRSA252) GN=SAR0903 PE=3 SV=1 150 516 4.0E-19
sp|Q99VE0|Y941_STAAM NADH dehydrogenase-like protein SAV0941 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=SAV0941 PE=3 SV=1 150 516 4.0E-19
sp|Q5HHE4|Y944_STAAC NADH dehydrogenase-like protein SACOL0944 OS=Staphylococcus aureus (strain COL) GN=SACOL0944 PE=3 SV=1 150 516 4.0E-19
sp|Q2FID4|Y844_STAA3 NADH dehydrogenase-like protein SAUSA300_0844 OS=Staphylococcus aureus (strain USA300) GN=SAUSA300_0844 PE=3 SV=1 150 516 4.0E-19
sp|Q7A6J4|Y802_STAAN NADH dehydrogenase-like protein SA0802 OS=Staphylococcus aureus (strain N315) GN=SA0802 PE=1 SV=1 150 516 4.0E-19
sp|Q6GAY5|Y811_STAAS NADH dehydrogenase-like protein SAS0811 OS=Staphylococcus aureus (strain MSSA476) GN=SAS0811 PE=3 SV=1 150 516 5.0E-19
sp|Q2YWP9|Y807_STAAB NADH dehydrogenase-like protein SAB0807 OS=Staphylococcus aureus (strain bovine RF122 / ET3-1) GN=SAB0807 PE=3 SV=1 150 516 5.0E-19
sp|Q8NXG0|Y823_STAAW NADH dehydrogenase-like protein MW0823 OS=Staphylococcus aureus (strain MW2) GN=MW0823 PE=3 SV=1 150 516 5.0E-19
sp|Q4L4V6|Y2010_STAHJ NADH dehydrogenase-like protein SH2010 OS=Staphylococcus haemolyticus (strain JCSC1435) GN=SH2010 PE=3 SV=1 150 472 1.0E-18
sp|Q49W80|Y1834_STAS1 NADH dehydrogenase-like protein SSP1834 OS=Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229) GN=SSP1834 PE=3 SV=1 150 472 3.0E-16
sp|Q8CPV5|Y635_STAES NADH dehydrogenase-like protein SE_0635 OS=Staphylococcus epidermidis (strain ATCC 12228) GN=SE_0635 PE=3 SV=1 150 472 4.0E-16
sp|P00393|DHNA_ECOLI NADH dehydrogenase OS=Escherichia coli (strain K12) GN=ndh PE=1 SV=2 178 474 5.0E-16
sp|Q5HQM1|Y527_STAEQ NADH dehydrogenase-like protein SERP0527 OS=Staphylococcus epidermidis (strain ATCC 35984 / RP62A) GN=SERP0527 PE=3 SV=1 150 472 7.0E-16
sp|P32340|NDI1_YEAST Rotenone-insensitive NADH-ubiquinone oxidoreductase, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NDI1 PE=1 SV=1 488 674 3.0E-14
sp|P44856|DHNA_HAEIN NADH dehydrogenase OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=ndh PE=3 SV=1 178 477 7.0E-14
sp|Q07500|NDH2_YEAST External NADH-ubiquinone oxidoreductase 2, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NDE2 PE=1 SV=1 565 673 8.0E-14
sp|Q8GWA1|NDA1_ARATH Internal alternative NAD(P)H-ubiquinone oxidoreductase A1, mitochondrial OS=Arabidopsis thaliana GN=NDA1 PE=2 SV=1 560 674 2.0E-13
sp|O14121|NDH1_SCHPO Probable NADH-ubiquinone oxidoreductase C3A11.07, mitochondrial OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC3A11.07 PE=3 SV=1 556 677 9.0E-13
sp|O80874|NDA2_ARATH Internal alternative NAD(P)H-ubiquinone oxidoreductase A2, mitochondrial OS=Arabidopsis thaliana GN=NDA2 PE=2 SV=1 561 674 1.0E-10
sp|Q9ST63|NDA1_SOLTU Internal alternative NAD(P)H-ubiquinone oxidoreductase A1, mitochondrial OS=Solanum tuberosum GN=NDA1 PE=1 SV=1 562 674 1.0E-10
sp|M0ZYF3|INDA1_SOLTU Internal alternative NAD(P)H-ubiquinone oxidoreductase A1, mitochondrial OS=Solanum tuberosum GN=NDA1 PE=3 SV=1 562 674 1.0E-10
sp|Q55CD9|NDH_DICDI Probable NADH dehydrogenase OS=Dictyostelium discoideum GN=DDB_G0270104 PE=3 SV=2 537 677 1.0E-10
sp|Q8GXR9|DHNA_ARATH Alternative NAD(P)H-ubiquinone oxidoreductase C1, chloroplastic/mitochondrial OS=Arabidopsis thaliana GN=NDC1 PE=1 SV=2 92 477 4.0E-09
sp|O32117|YUTJ_BACSU NADH dehydrogenase-like protein YutJ OS=Bacillus subtilis (strain 168) GN=yutJ PE=3 SV=2 154 474 9.0E-09
sp|O43090|NDH2_SCHPO Probable NADH-ubiquinone oxidoreductase C947.15c, mitochondrial OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC947.15c PE=3 SV=1 556 672 2.0E-08
sp|B7JBP8|SQRD_ACIF2 Sulfide-quinone reductase OS=Acidithiobacillus ferrooxidans (strain ATCC 23270 / DSM 14882 / CIP 104768 / NCIMB 8455) GN=AFE_1792 PE=1 SV=1 155 262 2.0E-07
sp|P80861|YJLD_BACSU NADH dehydrogenase-like protein YjlD OS=Bacillus subtilis (strain 168) GN=yjlD PE=1 SV=3 155 399 5.0E-07
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GO

GO Term Description Terminal node
GO:0005509 calcium ion binding Yes
GO:0016491 oxidoreductase activity Yes
GO:0003824 catalytic activity No
GO:0046872 metal ion binding No
GO:0003674 molecular_function No
GO:0005488 binding No
GO:0043167 ion binding No
GO:0043169 cation binding No

SignalP

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

Transmembrane Domains

Domain # Start End Length
1 79 101 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|5500
MRAPSRLPWAAVASARQGQRPKIVSLIHKRSLLTQLSTARTRRALYVQRPPPFHVSLRRLSGKPLPQGKSRLVNF
CYRAAAWVGISITVVGVGILAFFIYDATTYKEHAVLSDIDVSQLALQPRRGGPKNLPIADVFIDDDDCDAKKRTR
NKPKLVVLGGGWGGVALLKELSAQDYHVTVISPTNYFLFTPMLPSATVGTLELRSLVEPIRRILGRVHGHFIRAK
AEDVDFAGKLVEVSQLDPQGNEVHFYVPYDKLVIAVGSVTNPHGVKGLENAFFLKDIDDARKIRNKVVHNLELAC
LPTTGDDERKRLLSFVISGGGPTGVEFAAELYDLLNEDLTRHYPRLLRNEISVHLIQSRSHILNTYDETVSQYAE
SRFARDQVEVLTNSRVKEVQPDKIVFTQKQPDGTLLTKELPIGFCLWSTGVAPTNICRKLSHKLGTFQTNRRALE
TDTYLRVNGTPLGEVYAIGDCSTVQNNVADHVITFLRTLAWKQGKDPETLQLHFNDWRRVAQDVKKRFPQAVSHL
KRLDKLFAEFDKDQSGTLDFGELRELLNQIDSRLTSLPATAQRAHQQGTYLAKKFNKMARLAEGLTVNEIREGDL
DAAVYKAFEYRHLGSLAYIGNSAVFDLGDGWSFSGGLWAVYAWRSVYFAQSVSFRTRSLMAMDWAKRAIFGRDLV
SF*
Coding >OphauB2|5500
ATGCGGGCGCCTTCCCGTCTGCCATGGGCCGCGGTGGCTTCGGCTCGCCAAGGCCAACGCCCGAAAATCGTCTCT
TTAATACACAAACGCTCCCTCTTGACGCAATTGTCTACTGCTCGCACTCGTCGCGCTCTCTACGTGCAAAGGCCA
CCGCCCTTTCACGTGTCCCTTCGCCGTCTCTCTGGCAAGCCGCTTCCCCAAGGCAAATCGCGCTTGGTCAACTTC
TGCTACCGTGCTGCGGCCTGGGTGGGCATCTCAATCACTGTCGTGGGCGTCGGCATCCTGGCCTTCTTCATCTAC
GACGCTACCACCTACAAAGAGCATGCAGTCCTCAGCGACATTGATGTTTCTCAGCTGGCCTTGCAGCCTCGCCGC
GGTGGCCCCAAGAACCTGCCCATCGCCGACGTTTTCATCGACGACGACGACTGCGATGCCAAGAAGCGAACAAGA
AACAAGCCCAAGCTCGTGGTCCTGGGCGGGGGCTGGGGTGGCGTCGCTCTTCTCAAAGAGCTCAGTGCCCAAGAC
TATCATGTTACCGTCATCTCCCCCACGAATTATTTTCTCTTTACACCAATGCTGCCATCGGCCACGGTGGGCACT
CTTGAGCTGCGTTCTCTAGTTGAGCCTATTCGCCGCATTCTTGGCCGTGTCCATGGCCATTTTATACGTGCAAAA
GCAGAAGATGTCGACTTTGCAGGCAAGCTCGTCGAGGTTTCCCAATTGGACCCCCAAGGCAACGAGGTGCACTTC
TACGTGCCATACGATAAGCTCGTCATTGCTGTTGGCTCCGTCACCAATCCTCACGGTGTCAAAGGCCTGGAAAAC
GCCTTTTTCCTCAAGGACATTGATGATGCCCGCAAAATTCGCAACAAGGTTGTCCACAATCTCGAGCTTGCCTGC
CTCCCGACAACGGGAGACGACGAGCGCAAGCGTTTGCTTTCCTTTGTCATCAGCGGCGGCGGCCCTACAGGCGTT
GAGTTTGCTGCTGAGCTCTATGATCTCCTCAATGAAGATCTCACCCGTCACTATCCACGCCTTCTGCGTAACGAG
ATTTCGGTCCACCTTATTCAGAGCCGAAGCCACATACTCAACACCTATGATGAAACTGTATCACAATATGCAGAG
AGTCGCTTTGCTCGCGATCAGGTCGAGGTTCTCACCAACTCCAGGGTCAAGGAAGTTCAGCCCGACAAGATAGTC
TTCACACAAAAGCAGCCGGATGGGACCCTTCTGACAAAGGAGCTCCCCATAGGCTTCTGCCTGTGGTCTACCGGT
GTCGCACCAACAAATATCTGCCGCAAACTATCGCACAAACTGGGCACTTTTCAGACGAACCGCCGAGCACTTGAA
ACGGATACCTATTTACGCGTAAACGGCACTCCTCTGGGAGAAGTCTACGCCATTGGAGACTGCTCCACTGTACAG
AACAACGTGGCGGATCATGTCATCACCTTTCTGCGCACTCTGGCCTGGAAACAAGGCAAGGATCCTGAAACCCTG
CAGCTACACTTCAACGATTGGCGAAGGGTGGCCCAGGACGTCAAGAAACGGTTTCCTCAGGCCGTTAGCCACCTC
AAGCGCCTTGACAAACTGTTTGCAGAGTTTGACAAGGACCAGTCTGGCACTCTTGACTTTGGCGAGCTGCGAGAG
CTCCTCAATCAGATAGACAGCAGATTGACTTCGCTGCCTGCGACGGCGCAGCGCGCCCACCAACAAGGAACTTAT
CTCGCCAAAAAGTTTAACAAAATGGCCCGTCTCGCCGAGGGTCTGACGGTCAACGAAATACGCGAGGGCGACCTT
GACGCGGCCGTTTACAAGGCGTTCGAGTATCGTCACCTTGGAAGTCTGGCCTACATTGGAAATTCTGCCGTCTTT
GACCTGGGTGATGGTTGGAGCTTCAGCGGCGGCCTGTGGGCCGTCTATGCTTGGCGGTCAGTCTATTTTGCGCAA
AGCGTAAGCTTCCGGACGCGCAGTCTCATGGCCATGGATTGGGCGAAAAGAGCCATATTCGGACGTGATTTGGTT
AGTTTCTAG
Transcript >OphauB2|5500
ATGCGGGCGCCTTCCCGTCTGCCATGGGCCGCGGTGGCTTCGGCTCGCCAAGGCCAACGCCCGAAAATCGTCTCT
TTAATACACAAACGCTCCCTCTTGACGCAATTGTCTACTGCTCGCACTCGTCGCGCTCTCTACGTGCAAAGGCCA
CCGCCCTTTCACGTGTCCCTTCGCCGTCTCTCTGGCAAGCCGCTTCCCCAAGGCAAATCGCGCTTGGTCAACTTC
TGCTACCGTGCTGCGGCCTGGGTGGGCATCTCAATCACTGTCGTGGGCGTCGGCATCCTGGCCTTCTTCATCTAC
GACGCTACCACCTACAAAGAGCATGCAGTCCTCAGCGACATTGATGTTTCTCAGCTGGCCTTGCAGCCTCGCCGC
GGTGGCCCCAAGAACCTGCCCATCGCCGACGTTTTCATCGACGACGACGACTGCGATGCCAAGAAGCGAACAAGA
AACAAGCCCAAGCTCGTGGTCCTGGGCGGGGGCTGGGGTGGCGTCGCTCTTCTCAAAGAGCTCAGTGCCCAAGAC
TATCATGTTACCGTCATCTCCCCCACGAATTATTTTCTCTTTACACCAATGCTGCCATCGGCCACGGTGGGCACT
CTTGAGCTGCGTTCTCTAGTTGAGCCTATTCGCCGCATTCTTGGCCGTGTCCATGGCCATTTTATACGTGCAAAA
GCAGAAGATGTCGACTTTGCAGGCAAGCTCGTCGAGGTTTCCCAATTGGACCCCCAAGGCAACGAGGTGCACTTC
TACGTGCCATACGATAAGCTCGTCATTGCTGTTGGCTCCGTCACCAATCCTCACGGTGTCAAAGGCCTGGAAAAC
GCCTTTTTCCTCAAGGACATTGATGATGCCCGCAAAATTCGCAACAAGGTTGTCCACAATCTCGAGCTTGCCTGC
CTCCCGACAACGGGAGACGACGAGCGCAAGCGTTTGCTTTCCTTTGTCATCAGCGGCGGCGGCCCTACAGGCGTT
GAGTTTGCTGCTGAGCTCTATGATCTCCTCAATGAAGATCTCACCCGTCACTATCCACGCCTTCTGCGTAACGAG
ATTTCGGTCCACCTTATTCAGAGCCGAAGCCACATACTCAACACCTATGATGAAACTGTATCACAATATGCAGAG
AGTCGCTTTGCTCGCGATCAGGTCGAGGTTCTCACCAACTCCAGGGTCAAGGAAGTTCAGCCCGACAAGATAGTC
TTCACACAAAAGCAGCCGGATGGGACCCTTCTGACAAAGGAGCTCCCCATAGGCTTCTGCCTGTGGTCTACCGGT
GTCGCACCAACAAATATCTGCCGCAAACTATCGCACAAACTGGGCACTTTTCAGACGAACCGCCGAGCACTTGAA
ACGGATACCTATTTACGCGTAAACGGCACTCCTCTGGGAGAAGTCTACGCCATTGGAGACTGCTCCACTGTACAG
AACAACGTGGCGGATCATGTCATCACCTTTCTGCGCACTCTGGCCTGGAAACAAGGCAAGGATCCTGAAACCCTG
CAGCTACACTTCAACGATTGGCGAAGGGTGGCCCAGGACGTCAAGAAACGGTTTCCTCAGGCCGTTAGCCACCTC
AAGCGCCTTGACAAACTGTTTGCAGAGTTTGACAAGGACCAGTCTGGCACTCTTGACTTTGGCGAGCTGCGAGAG
CTCCTCAATCAGATAGACAGCAGATTGACTTCGCTGCCTGCGACGGCGCAGCGCGCCCACCAACAAGGAACTTAT
CTCGCCAAAAAGTTTAACAAAATGGCCCGTCTCGCCGAGGGTCTGACGGTCAACGAAATACGCGAGGGCGACCTT
GACGCGGCCGTTTACAAGGCGTTCGAGTATCGTCACCTTGGAAGTCTGGCCTACATTGGAAATTCTGCCGTCTTT
GACCTGGGTGATGGTTGGAGCTTCAGCGGCGGCCTGTGGGCCGTCTATGCTTGGCGGTCAGTCTATTTTGCGCAA
AGCGTAAGCTTCCGGACGCGCAGTCTCATGGCCATGGATTGGGCGAAAAGAGCCATATTCGGACGTGATTTGGTT
AGTTTCTAG
Gene >OphauB2|5500
ATGCGGGCGCCTTCCCGTCTGCCATGGGCCGCGGTGGCTTCGGCTCGCCAAGGCCAACGCCCGAAAATCGTCTCT
TTAATACACAAACGCTCCCTCTTGACGCAATTGTCTACTGCTCGCACTCGTCGCGCTCTCTACGTGCAAAGGCCA
CCGCCCTTTCACGTGTCCCTTCGCCGTCTCTCTGGCAAGCCGCTTCCCCAAGGCAAATCGCGCTTGGTCAACTTC
TGCTACCGTGCTGCGGCCTGGGTGGGCATCTCAATCACTGTCGTGGGCGTCGGCATCCTGGCCTTCTTCATCTAC
GACGCTACCACCTACAAAGAGCATGCAGTCCTCAGCGACATTGATGTTTCTCAGCTGGCCTTGCAGCCTCGCCGC
GGTGGCCCCAAGAACCTGCCCATCGCCGACGTTTTCATCGACGACGACGACTGCGATGCCAAGAAGCGAACAAGA
AACAAGCCCAAGCTCGTGGTCCTGGGCGGGGGCTGGGGTGGCGTCGCTCTTCTCAAAGAGCTCAGTGCCCAAGAC
TATCATGTTACCGTCATCTCCCCCACGAATTATTTTCTCTTTACACCAATGCTGCCATCGGCCACGGTGGGCACT
CTTGAGCTGCGTTCTCTAGTTGAGCCTATTCGCCGCATTCTTGGCCGTGTCCATGGCCATTTTATACGTGCAAAA
GCAGAAGATGTCGACTTTGCAGGCAAGCTCGTCGAGGTTTCCCAATTGGACCCCCAAGGCAACGAGGTGCACTTC
TACGTGCCATACGATAAGCTCGTCATTGCTGTTGGCTCCGTCACCAATCCTCACGGTGTCAAAGGCCTGGAAAAC
GCCTTTTTCCTCAAGGACATTGATGATGCCCGCAAAATTCGCAACAAGGTTGTCCACAATCTCGAGCTTGCCTGC
CTCCCGACAACGGGAGACGACGAGCGCAAGCGTTTGCTTTCCTTTGTCATCAGCGGCGGCGGCCCTACAGGCGTT
GAGTTTGCTGCTGAGCTCTATGATCTCCTCAATGAAGATCTCACCCGTCACTATCCACGCCTTCTGCGTAACGAG
ATTTCGGTCCACCTTATTCAGAGCCGAAGCCACATACTCAACACCTATGATGAAACTGTATCACAATATGCAGAG
AGTCGCTTTGCTCGCGATCAGGTCGAGGTTCTCACCAACTCCAGGGTCAAGGAAGTTCAGCCCGACAAGATAGTC
TTCACACAAAAGCAGCCGGATGGGACCCTTCTGACAAAGGAGCTCCCCATAGGCTTCTGCCTGTGGTCTACCGGT
GTCGCACCAACAAATATCTGCCGCAAACTATCGCACAAACTGGGCACTTTTCAGACGAACCGCCGAGCACTTGAA
ACGGATACCTATTTACGCGTAAACGGCACTCCTCTGGGAGAAGTCTACGCCATTGGAGACTGCTCCACTGTACAG
AACAACGTGGCGGATCATGTCATCACCTTTCTGCGCACTCTGGCCTGGAAACAAGGCAAGGATCCTGAAACCCTG
CAGCTACACTTCAACGATTGGCGAAGGGTGGCCCAGGACGTCAAGAAACGGTTTCCTCAGGCCGTTAGCCACCTC
AAGCGCCTTGACAAACTGTTTGCAGAGTTTGACAAGGACCAGTCTGGCACTCTTGACTTTGGCGAGCTGCGAGAG
CTCCTCAATCAGATAGACAGCAGATTGACTTCGCTGCCTGCGACGGCGCAGCGCGCCCACCAACAAGGAACTTAT
CTCGCCAAAAAGTTTAACAAAATGGCCCGTCTCGCCGAGGGTCTGACGGTCAACGAAATACGCGAGGGCGACCTT
GACGCGGCCGTTTACAAGGCGTTCGAGTATCGTCACCTTGGAAGTCTGGCCTACATTGGAAATTCTGCCGTCTTT
GACCTGGGTGATGGTTGGAGCTTCAGCGGCGGCCTGTGGGCCGTCTATGCTTGGCGGTCAGTCTATTTTGCGCAA
AGCGTAAGCTTCCGGACGCGCAGTCTCATGGCCATGGATTGGGCGAAAAGAGCCATATTCGGACGTGGTACGTTT
ATCCCTTGATGTGCCGATGAATCAGTATGACTTTGTGTGCTGACTCCAAAATGCAGATTTGGTTAGTTTCTAG

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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