Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|318
Gene name
Locationscaffold_107:25790..28614
Strand-
Gene length (bp)2824
Transcript length (bp)2583
Coding sequence length (bp)2580
Protein length (aa) 860

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00443 UCH Ubiquitin carboxyl-terminal hydrolase 8.1E-44 414 773

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|O94269|UBP3_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp3 PE=3 SV=1 386 773 1.0E-88
sp|Q6DIJ4|UBP10_XENTR Ubiquitin carboxyl-terminal hydrolase 10 OS=Xenopus tropicalis GN=usp10 PE=2 SV=1 316 779 3.0E-61
sp|Q5ZJN4|UBP10_CHICK Ubiquitin carboxyl-terminal hydrolase 10 OS=Gallus gallus GN=USP10 PE=2 SV=1 303 779 5.0E-60
sp|Q2NL57|UB10A_XENLA Ubiquitin carboxyl-terminal hydrolase 10-A OS=Xenopus laevis GN=usp10-a PE=2 SV=1 410 779 7.0E-60
sp|Q7ZXR7|UB10B_XENLA Ubiquitin carboxyl-terminal hydrolase 10-B OS=Xenopus laevis GN=usp10-b PE=2 SV=1 303 779 7.0E-60
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|O94269|UBP3_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp3 PE=3 SV=1 386 773 1.0E-88
sp|Q6DIJ4|UBP10_XENTR Ubiquitin carboxyl-terminal hydrolase 10 OS=Xenopus tropicalis GN=usp10 PE=2 SV=1 316 779 3.0E-61
sp|Q5ZJN4|UBP10_CHICK Ubiquitin carboxyl-terminal hydrolase 10 OS=Gallus gallus GN=USP10 PE=2 SV=1 303 779 5.0E-60
sp|Q2NL57|UB10A_XENLA Ubiquitin carboxyl-terminal hydrolase 10-A OS=Xenopus laevis GN=usp10-a PE=2 SV=1 410 779 7.0E-60
sp|Q7ZXR7|UB10B_XENLA Ubiquitin carboxyl-terminal hydrolase 10-B OS=Xenopus laevis GN=usp10-b PE=2 SV=1 303 779 7.0E-60
sp|Q14694|UBP10_HUMAN Ubiquitin carboxyl-terminal hydrolase 10 OS=Homo sapiens GN=USP10 PE=1 SV=2 287 779 2.0E-58
sp|Q3KR59|UBP10_RAT Ubiquitin carboxyl-terminal hydrolase 10 OS=Rattus norvegicus GN=Usp10 PE=1 SV=1 410 774 4.0E-58
sp|P52479|UBP10_MOUSE Ubiquitin carboxyl-terminal hydrolase 10 OS=Mus musculus GN=Usp10 PE=1 SV=3 303 775 5.0E-58
sp|A5PJS6|UBP10_BOVIN Ubiquitin carboxyl-terminal hydrolase 10 OS=Bos taurus GN=USP10 PE=2 SV=1 410 762 2.0E-57
sp|Q9FPS3|UBP24_ARATH Ubiquitin carboxyl-terminal hydrolase 24 OS=Arabidopsis thaliana GN=UBP24 PE=1 SV=1 412 762 3.0E-52
sp|Q01477|UBP3_YEAST Ubiquitin carboxyl-terminal hydrolase 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP3 PE=1 SV=1 390 786 9.0E-52
sp|O96612|UBPB_DICDI Ubiquitin hydrolase B OS=Dictyostelium discoideum GN=ubpB PE=1 SV=1 520 773 3.0E-39
sp|B4QIS3|UBP36_DROSI Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila simulans GN=Usp36 PE=3 SV=1 414 774 3.0E-24
sp|B3NC86|UBP36_DROER Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila erecta GN=Usp36 PE=3 SV=1 414 774 7.0E-24
sp|B4PIW8|UBP36_DROYA Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila yakuba GN=Usp36 PE=3 SV=1 414 774 2.0E-23
sp|B4IXE0|UBP36_DROGR Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila grimshawi GN=Usp36 PE=3 SV=1 414 774 9.0E-23
sp|B2RQC2|UBP42_MOUSE Ubiquitin carboxyl-terminal hydrolase 42 OS=Mus musculus GN=Usp42 PE=1 SV=1 318 777 1.0E-22
sp|Q9VRP5|UBP36_DROME Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila melanogaster GN=scny PE=1 SV=3 414 774 2.0E-22
sp|A5D9H7|UBP12_BOVIN Ubiquitin carboxyl-terminal hydrolase 12 OS=Bos taurus GN=USP12 PE=2 SV=1 414 775 3.0E-22
sp|E1B9W9|UBP42_BOVIN Ubiquitin carboxyl-terminal hydrolase 42 OS=Bos taurus GN=USP42 PE=3 SV=1 292 777 4.0E-22
sp|Q9D9M2|UBP12_MOUSE Ubiquitin carboxyl-terminal hydrolase 12 OS=Mus musculus GN=Usp12 PE=2 SV=2 414 775 4.0E-22
sp|B1AQJ2|UBP36_MOUSE Ubiquitin carboxyl-terminal hydrolase 36 OS=Mus musculus GN=Usp36 PE=1 SV=1 397 765 4.0E-22
sp|A4FUN7|UBP12_DANRE Ubiquitin carboxyl-terminal hydrolase 12A OS=Danio rerio GN=usp12a PE=2 SV=1 414 775 1.0E-21
sp|Q9H9J4|UBP42_HUMAN Ubiquitin carboxyl-terminal hydrolase 42 OS=Homo sapiens GN=USP42 PE=1 SV=3 292 777 1.0E-21
sp|Q9P275|UBP36_HUMAN Ubiquitin carboxyl-terminal hydrolase 36 OS=Homo sapiens GN=USP36 PE=1 SV=3 397 765 2.0E-21
sp|Q2LZB1|UBP36_DROPS Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila pseudoobscura pseudoobscura GN=Usp36 PE=3 SV=2 414 774 3.0E-21
sp|B4KXJ5|UBP36_DROMO Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila mojavensis GN=Usp36 PE=3 SV=1 414 774 3.0E-21
sp|B4LG38|UBP36_DROVI Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila virilis GN=Usp36 PE=3 SV=1 414 774 3.0E-21
sp|O75317|UBP12_HUMAN Ubiquitin carboxyl-terminal hydrolase 12 OS=Homo sapiens GN=USP12 PE=1 SV=2 414 775 5.0E-21
sp|B3M3M6|UBP36_DROAN Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila ananassae GN=Usp36 PE=3 SV=1 414 774 6.0E-21
sp|C0HB46|UBP12_SALSA Ubiquitin carboxyl-terminal hydrolase 12 OS=Salmo salar GN=usp12 PE=2 SV=1 414 775 1.0E-20
sp|B4MLR8|UBP36_DROWI Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila willistoni GN=Usp36 PE=3 SV=1 414 778 1.0E-20
sp|Q5M981|UB12B_XENLA Ubiquitin carboxyl-terminal hydrolase 12-B OS=Xenopus laevis GN=usp12-b PE=2 SV=2 414 775 3.0E-20
sp|Q52KZ6|UB12A_XENLA Ubiquitin carboxyl-terminal hydrolase 12-A OS=Xenopus laevis GN=usp12-a PE=2 SV=1 414 775 4.0E-20
sp|Q5RBQ4|UBP46_PONAB Ubiquitin carboxyl-terminal hydrolase 46 OS=Pongo abelii GN=USP46 PE=2 SV=1 414 775 1.0E-19
sp|P62069|UBP46_MOUSE Ubiquitin carboxyl-terminal hydrolase 46 OS=Mus musculus GN=Usp46 PE=1 SV=1 414 775 1.0E-19
sp|P62068|UBP46_HUMAN Ubiquitin carboxyl-terminal hydrolase 46 OS=Homo sapiens GN=USP46 PE=1 SV=1 414 775 1.0E-19
sp|Q2KHV7|UBP2_BOVIN Ubiquitin carboxyl-terminal hydrolase 2 OS=Bos taurus GN=USP2 PE=2 SV=1 414 762 2.0E-18
sp|Q70EK9|UBP51_HUMAN Ubiquitin carboxyl-terminal hydrolase 51 OS=Homo sapiens GN=USP51 PE=2 SV=1 406 773 9.0E-18
sp|A5WWB0|UBP46_DANRE Ubiquitin carboxyl-terminal hydrolase 46 OS=Danio rerio GN=usp46 PE=3 SV=2 414 775 9.0E-18
sp|B4HUI5|UBP36_DROSE Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila sechellia GN=Usp36 PE=3 SV=1 414 774 2.0E-17
sp|Q9FPS4|UBP23_ARATH Ubiquitin carboxyl-terminal hydrolase 23 OS=Arabidopsis thaliana GN=UBP23 PE=2 SV=2 414 773 3.0E-17
sp|P50102|UBP8_YEAST Ubiquitin carboxyl-terminal hydrolase 8 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP8 PE=1 SV=1 363 775 4.0E-17
sp|O74442|UBP16_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 16 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp16 PE=1 SV=1 414 762 1.0E-16
sp|Q8CEG8|UBP27_MOUSE Ubiquitin carboxyl-terminal hydrolase 27 OS=Mus musculus GN=Usp27 PE=2 SV=2 385 775 2.0E-16
sp|O75604|UBP2_HUMAN Ubiquitin carboxyl-terminal hydrolase 2 OS=Homo sapiens GN=USP2 PE=1 SV=2 414 763 3.0E-16
sp|O60139|UBP4_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp4 PE=1 SV=2 411 791 4.0E-16
sp|Q9FIQ1|UBP21_ARATH Ubiquitin carboxyl-terminal hydrolase 21 OS=Arabidopsis thaliana GN=UBP21 PE=2 SV=1 414 773 5.0E-16
sp|Q5U349|UBP2_RAT Ubiquitin carboxyl-terminal hydrolase 2 OS=Rattus norvegicus GN=Usp2 PE=1 SV=1 414 763 6.0E-16
sp|Q7M764|U17PE_MOUSE Ubiquitin carboxyl-terminal hydrolase 17-like protein E OS=Mus musculus GN=Usp17le PE=3 SV=2 369 768 7.0E-16
sp|Q6QN14|U17L6_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 6 OS=Homo sapiens GN=USP17L6P PE=1 SV=2 414 762 7.0E-16
sp|P34547|UBP46_CAEEL Ubiquitin carboxyl-terminal hydrolase 46 OS=Caenorhabditis elegans GN=usp-46 PE=1 SV=3 414 775 8.0E-16
sp|Q9SB51|UBP16_ARATH Ubiquitin carboxyl-terminal hydrolase 16 OS=Arabidopsis thaliana GN=UBP16 PE=1 SV=1 410 765 9.0E-16
sp|Q80U87|UBP8_MOUSE Ubiquitin carboxyl-terminal hydrolase 8 OS=Mus musculus GN=Usp8 PE=1 SV=2 414 762 9.0E-16
sp|P0C7I0|U17L8_HUMAN Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 8 OS=Homo sapiens GN=USP17L8 PE=3 SV=1 414 762 1.0E-15
sp|A6NNY8|UBP27_HUMAN Ubiquitin carboxyl-terminal hydrolase 27 OS=Homo sapiens GN=USP27X PE=2 SV=3 375 775 1.0E-15
sp|P40818|UBP8_HUMAN Ubiquitin carboxyl-terminal hydrolase 8 OS=Homo sapiens GN=USP8 PE=1 SV=1 414 762 1.0E-15
sp|C9JVI0|U17LB_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 11 OS=Homo sapiens GN=USP17L11 PE=3 SV=1 414 762 1.0E-15
sp|D6R9N7|U17LI_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 18 OS=Homo sapiens GN=USP17L18 PE=3 SV=1 414 762 2.0E-15
sp|D6RCP7|U17LJ_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 19 OS=Homo sapiens GN=USP17L19 PE=3 SV=1 414 762 2.0E-15
sp|D6RA61|U17LM_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 22 OS=Homo sapiens GN=USP17L22 PE=3 SV=1 414 762 2.0E-15
sp|D6RBQ6|U17LH_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 17 OS=Homo sapiens GN=USP17L17 PE=3 SV=1 414 762 2.0E-15
sp|Q6R6M4|U17L2_HUMAN Ubiquitin carboxyl-terminal hydrolase 17 OS=Homo sapiens GN=USP17L2 PE=1 SV=2 414 762 2.0E-15
sp|D6RJB6|U17LK_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 20 OS=Homo sapiens GN=USP17L20 PE=3 SV=1 414 762 3.0E-15
sp|Q0WX57|U17LO_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 24 OS=Homo sapiens GN=USP17L24 PE=1 SV=2 414 762 4.0E-15
sp|A8MUK1|U17L5_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 5 OS=Homo sapiens GN=USP17L5 PE=3 SV=2 414 762 4.0E-15
sp|C9J2P7|U17LF_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 15 OS=Homo sapiens GN=USP17L15 PE=3 SV=1 414 762 4.0E-15
sp|C9JPN9|UL17C_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 12 OS=Homo sapiens GN=USP17L12 PE=3 SV=1 414 762 6.0E-15
sp|C9JLJ4|U17LD_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 13 OS=Homo sapiens GN=USP17L13 PE=3 SV=1 414 762 6.0E-15
sp|Q61068|U17PA_MOUSE Ubiquitin carboxyl-terminal hydrolase 17-like protein A OS=Mus musculus GN=Usp17la PE=1 SV=1 393 768 7.0E-15
sp|D6R901|U17LL_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 21 OS=Homo sapiens GN=USP17L21 PE=3 SV=1 414 762 7.0E-15
sp|C9JJH3|U17LA_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 10 OS=Homo sapiens GN=USP17L10 PE=3 SV=1 414 762 8.0E-15
sp|Q9UPT9|UBP22_HUMAN Ubiquitin carboxyl-terminal hydrolase 22 OS=Homo sapiens GN=USP22 PE=1 SV=2 413 775 3.0E-14
sp|Q6GNI6|UB22A_XENLA Ubiquitin carboxyl-terminal hydrolase 22-A OS=Xenopus laevis GN=usp22-a PE=2 SV=1 413 775 4.0E-14
sp|Q6DCJ1|UB22B_XENLA Ubiquitin carboxyl-terminal hydrolase 22-B OS=Xenopus laevis GN=usp22-b PE=2 SV=2 413 775 4.0E-14
sp|A6NCW0|U17L3_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 3 OS=Homo sapiens GN=USP17L3 PE=3 SV=1 414 762 4.0E-14
sp|A6H8I0|UBP22_DANRE Ubiquitin carboxyl-terminal hydrolase 22 OS=Danio rerio GN=usp22 PE=2 SV=1 413 775 5.0E-14
sp|Q5DU02|UBP22_MOUSE Ubiquitin carboxyl-terminal hydrolase 22 OS=Mus musculus GN=Usp22 PE=2 SV=2 413 775 6.0E-14
sp|P39967|UBP9_YEAST Ubiquitin carboxyl-terminal hydrolase 9 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP9 PE=1 SV=1 500 775 7.0E-14
sp|P0C8Z3|UBP22_BOVIN Ubiquitin carboxyl-terminal hydrolase 22 OS=Bos taurus GN=USP22 PE=2 SV=1 413 775 9.0E-14
sp|Q91W36|UBP3_MOUSE Ubiquitin carboxyl-terminal hydrolase 3 OS=Mus musculus GN=Usp3 PE=2 SV=1 414 776 1.0E-13
sp|Q9Y6I4|UBP3_HUMAN Ubiquitin carboxyl-terminal hydrolase 3 OS=Homo sapiens GN=USP3 PE=1 SV=2 414 776 1.0E-13
sp|Q9HFS7|UBP4_KLULA Ubiquitin carboxyl-terminal hydrolase 4 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=DOA4 PE=3 SV=1 325 772 1.0E-13
sp|A6NCW7|U17L4_HUMAN Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 4 OS=Homo sapiens GN=USP17L4 PE=3 SV=3 414 762 1.0E-13
sp|P39944|UBP5_YEAST Ubiquitin carboxyl-terminal hydrolase 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP5 PE=1 SV=1 414 766 2.0E-13
sp|P38187|UBP13_YEAST Ubiquitin carboxyl-terminal hydrolase 13 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP13 PE=1 SV=3 520 779 2.0E-13
sp|Q7RTZ2|U17L1_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 1 OS=Homo sapiens GN=USP17L1 PE=3 SV=1 414 762 2.0E-13
sp|Q8LAM0|UBP4_ARATH Ubiquitin carboxyl-terminal hydrolase 4 OS=Arabidopsis thaliana GN=UBP4 PE=1 SV=2 414 762 3.0E-13
sp|Q2UUG8|CREB_ASPOR Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=creB PE=3 SV=2 398 768 7.0E-13
sp|B8NSV5|CREB_ASPFN Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=creB PE=3 SV=1 398 768 8.0E-13
sp|Q754R5|UBP4_ASHGO Ubiquitin carboxyl-terminal hydrolase 4 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=DOA4 PE=3 SV=2 414 770 8.0E-13
sp|O24454|UBP3_ARATH Ubiquitin carboxyl-terminal hydrolase 3 OS=Arabidopsis thaliana GN=UBP3 PE=1 SV=1 414 762 9.0E-13
sp|Q9SJA1|UBP19_ARATH Ubiquitin carboxyl-terminal hydrolase 19 OS=Arabidopsis thaliana GN=UBP19 PE=2 SV=2 409 773 1.0E-12
sp|Q84WU2|UBP13_ARATH Ubiquitin carboxyl-terminal hydrolase 13 OS=Arabidopsis thaliana GN=UBP13 PE=1 SV=1 414 782 3.0E-12
sp|Q9VYQ8|UBP7_DROME Ubiquitin carboxyl-terminal hydrolase 7 OS=Drosophila melanogaster GN=Usp7 PE=1 SV=1 597 782 3.0E-12
sp|Q9VVR1|NOT_DROME Ubiquitin carboxyl-terminal hydrolase nonstop OS=Drosophila melanogaster GN=not PE=1 SV=3 389 765 5.0E-12
sp|Q7ZUM8|UBP44_DANRE Ubiquitin carboxyl-terminal hydrolase 44 OS=Danio rerio GN=usp44 PE=2 SV=1 517 776 9.0E-12
sp|Q9H0E7|UBP44_HUMAN Ubiquitin carboxyl-terminal hydrolase 44 OS=Homo sapiens GN=USP44 PE=1 SV=2 414 776 5.0E-11
sp|Q09879|UBP5_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 5 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp5 PE=3 SV=3 573 775 7.0E-11
sp|Q9FPT1|UBP12_ARATH Ubiquitin carboxyl-terminal hydrolase 12 OS=Arabidopsis thaliana GN=UBP12 PE=1 SV=2 414 782 1.0E-10
sp|Q6FQF0|UBP4_CANGA Ubiquitin carboxyl-terminal hydrolase 4 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=DOA4 PE=3 SV=1 414 772 1.0E-10
sp|Q09738|UBP8_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 8 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp8 PE=3 SV=1 583 773 2.0E-10
sp|A1CW53|CREB_NEOFI Probable ubiquitin carboxyl-terminal hydrolase creB OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=creB PE=3 SV=2 515 768 2.0E-10
sp|P70398|USP9X_MOUSE Probable ubiquitin carboxyl-terminal hydrolase FAF-X OS=Mus musculus GN=Usp9x PE=1 SV=2 618 784 2.0E-10
sp|Q93008|USP9X_HUMAN Probable ubiquitin carboxyl-terminal hydrolase FAF-X OS=Homo sapiens GN=USP9X PE=1 SV=3 618 784 3.0E-10
sp|D2HBJ8|UBP44_AILME Ubiquitin carboxyl-terminal hydrolase 44 OS=Ailuropoda melanoleuca GN=USP44 PE=3 SV=1 496 776 3.0E-10
sp|B0Y4P5|CREB_ASPFC Probable ubiquitin carboxyl-terminal hydrolase creB OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=creB PE=3 SV=1 515 765 4.0E-10
sp|Q4WQI1|CREB_ASPFU Probable ubiquitin carboxyl-terminal hydrolase creB OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=creB PE=3 SV=3 515 765 4.0E-10
sp|Q9P7V9|UBP9_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 9 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp9 PE=1 SV=1 492 762 5.0E-10
sp|Q96V54|CREB_EMENI Ubiquitin carboxyl-terminal hydrolase creB OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=creB PE=1 SV=1 499 765 8.0E-10
sp|Q6NTR6|UP44A_XENLA Ubiquitin carboxyl-terminal hydrolase 44-A OS=Xenopus laevis GN=usp44-a PE=2 SV=1 501 776 1.0E-09
sp|Q0CT11|CREB_ASPTN Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=creB PE=3 SV=2 515 765 1.0E-09
sp|A1CIL1|CREB_ASPCL Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=creB PE=3 SV=2 515 765 1.0E-09
sp|O00507|USP9Y_HUMAN Probable ubiquitin carboxyl-terminal hydrolase FAF-Y OS=Homo sapiens GN=USP9Y PE=2 SV=2 618 784 3.0E-09
sp|Q70CQ1|UBP49_HUMAN Ubiquitin carboxyl-terminal hydrolase 49 OS=Homo sapiens GN=USP49 PE=1 SV=1 517 775 3.0E-09
sp|Q6P9L4|UBP49_MOUSE Ubiquitin carboxyl-terminal hydrolase 49 OS=Mus musculus GN=Usp49 PE=2 SV=1 517 775 3.0E-09
sp|Q5XGZ2|UP44B_XENLA Ubiquitin carboxyl-terminal hydrolase 44-B OS=Xenopus laevis GN=usp44-b PE=2 SV=1 520 798 3.0E-09
sp|P50101|UBP15_YEAST Ubiquitin carboxyl-terminal hydrolase 15 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP15 PE=1 SV=1 573 775 7.0E-09
sp|P53874|UBP10_YEAST Ubiquitin carboxyl-terminal hydrolase 10 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP10 PE=1 SV=2 658 773 7.0E-09
sp|Q9UTT1|UBP21_SCHPO Ubiquitin carboxyl-terminal hydrolase 21 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp21 PE=3 SV=2 584 798 1.0E-08
sp|Q8C2S0|UBP44_MOUSE Ubiquitin carboxyl-terminal hydrolase 44 OS=Mus musculus GN=Usp44 PE=2 SV=3 496 773 1.0E-08
sp|A3AF13|UBP26_ORYSJ Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. japonica GN=UBP26 PE=3 SV=2 412 805 3.0E-08
sp|Q6U7I1|UBP7_CHICK Ubiquitin carboxyl-terminal hydrolase 7 OS=Gallus gallus GN=USP7 PE=2 SV=1 583 782 4.0E-08
sp|A2XDG4|UBP26_ORYSI Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. indica GN=UBP26 PE=3 SV=1 412 762 4.0E-08
sp|Q6A4J8|UBP7_MOUSE Ubiquitin carboxyl-terminal hydrolase 7 OS=Mus musculus GN=Usp7 PE=1 SV=1 583 782 5.0E-08
sp|Q93009|UBP7_HUMAN Ubiquitin carboxyl-terminal hydrolase 7 OS=Homo sapiens GN=USP7 PE=1 SV=2 583 782 6.0E-08
sp|Q4VSI4|UBP7_RAT Ubiquitin carboxyl-terminal hydrolase 7 OS=Rattus norvegicus GN=Usp7 PE=1 SV=1 583 782 7.0E-08
sp|A2Q9N1|CREB_ASPNC Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=creB PE=3 SV=2 589 765 2.0E-07
sp|P55824|FAF_DROME Probable ubiquitin carboxyl-terminal hydrolase FAF OS=Drosophila melanogaster GN=faf PE=1 SV=2 627 779 2.0E-07
sp|Q9UPU5|UBP24_HUMAN Ubiquitin carboxyl-terminal hydrolase 24 OS=Homo sapiens GN=USP24 PE=1 SV=3 623 772 3.0E-07
sp|Q3V0C5|UBP48_MOUSE Ubiquitin carboxyl-terminal hydrolase 48 OS=Mus musculus GN=Usp48 PE=1 SV=2 612 783 4.0E-07
sp|Q86UV5|UBP48_HUMAN Ubiquitin carboxyl-terminal hydrolase 48 OS=Homo sapiens GN=USP48 PE=1 SV=1 414 782 6.0E-07
sp|Q5ZM45|UBP48_CHICK Ubiquitin carboxyl-terminal hydrolase 48 OS=Gallus gallus GN=USP48 PE=2 SV=1 612 782 7.0E-07
sp|B1AY13|UBP24_MOUSE Ubiquitin carboxyl-terminal hydrolase 24 OS=Mus musculus GN=Usp24 PE=1 SV=1 623 772 8.0E-07
sp|Q76LT8|UBP48_RAT Ubiquitin carboxyl-terminal hydrolase 48 OS=Rattus norvegicus GN=Usp48 PE=1 SV=1 612 784 1.0E-06
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GO

GO Term Description Terminal node
GO:0004843 cysteine-type deubiquitinase activity Yes
GO:0016579 protein deubiquitination Yes
GO:0140096 catalytic activity, acting on a protein No
GO:0043170 macromolecule metabolic process No
GO:0008150 biological_process No
GO:1901564 organonitrogen compound metabolic process No
GO:0044238 primary metabolic process No
GO:0006508 proteolysis No
GO:0101005 deubiquitinase activity No
GO:0043412 macromolecule modification No
GO:0008152 metabolic process No
GO:0003674 molecular_function No
GO:0008233 peptidase activity No
GO:0071704 organic substance metabolic process No
GO:0070646 protein modification by small protein removal No
GO:0016787 hydrolase activity No
GO:0070647 protein modification by small protein conjugation or removal No
GO:0019538 protein metabolic process No
GO:0036211 protein modification process No
GO:0006807 nitrogen compound metabolic process No
GO:0019783 ubiquitin-like protein peptidase activity No
GO:0003824 catalytic activity No
GO:0008234 cysteine-type peptidase activity No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 14 0.45

Transmembrane Domains

(None)

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|318
MSAGPGGGPGGGPGGGPRRRQPQYVPAYHHHPPQHQQMVYPGYLPYGPQAYYGLPPQFQNGGMPSPAYMTYQGYG
RSPPSMPQYVPMVGVSVPPAYSARPSQHSPSLSTSYQPPPAPASIPPQTPSSSHSSQILHPPTPPTPQTADHGST
GPPPSLQLESSMEQRESFRPPLPWYSCPESDFPTKTPRSKRRRKPLTADGVTVSLPLEQHGSFTENDAPSTKDAI
APSSISSKTSHNDPPASVSSGPSAPQVHPARPSAVSSAAGGDAAAATVDRPAAPVLPVLPAVPRHMSKSSSAGDT
KKQAADASKSSPSNGAASAAAGAHASADTAGSPPAPKLAPTSWANLFSKTSVKEPSNTAEPNGSNPANGSVLPGA
TAPTSGPAFSKSNTNLLAEAIRAYRVGGTDSVSFLEPRGLINTGNMCYMNSVLQVLIFCTPFFDFLDQVSKKAAY
SFKSDTPLIDAIIMFVREYKVLASAPTANALRRKLKSDDLEKYGEPFTPEFVYEAIRQLPRFASMRRGHQQDAEE
FLGFLLQSLDDECTKVLSNLPSSDSDTASVDMTASQSSAMNSPGDWLEVGRKQRAAITRSSGSNSSTPVAKIFGG
LLRSEFRVPGLKDSITTEPYQPLQLDIGSPDVRNVVDALRGLTRPERLQGDFNSPRGKDVTATKQVFIESLPPVL
ILHLKRFQFDAEGHGTIKVWKKIGYPLELEIPREAVSRQKRHSMGDGAMPKYRLISVVYHHGKNASGGHYTVDVR
RQDGLEWIRMDDTVLRRVRSEDVAEGGSEEELKDGRKDGGSGASSNRFGVINDEDAGGEGWKQVTASTSGSKRWS
SVVDGNGSTEERQQQQLKESIKDNKVAYLLFYQRM
Coding >Ophio5|318
ATGAGCGCAGGCCCTGGTGGAGGCCCCGGCGGAGGCCCCGGCGGAGGTCCGCGGCGGAGGCAGCCTCAGTACGTT
CCGGCGTACCACCATCATCCTCCCCAGCACCAGCAGATGGTCTATCCCGGATACCTCCCTTATGGGCCTCAAGCC
TACTACGGCTTGCCGCCTCAGTTCCAAAATGGCGGCATGCCCTCTCCGGCCTACATGACCTATCAGGGCTATGGC
CGGTCGCCGCCCTCGATGCCTCAATACGTCCCCATGGTGGGCGTCAGCGTGCCTCCGGCCTATTCTGCTCGGCCC
TCGCAGCATTCGCCTAGCCTGTCTACCTCCTATCAGCCTCCGCCGGCACCAGCTTCTATTCCGCCTCAGACTCCT
TCGTCGTCGCACTCGTCACAGATACTCCATCCTCCCACTCCGCCCACGCCGCAGACGGCAGACCACGGCAGCACA
GGCCCTCCTCCATCTCTGCAGCTCGAGAGCTCCATGGAGCAGCGTGAATCCTTCCGCCCGCCGCTTCCTTGGTAC
TCGTGCCCCGAATCCGATTTTCCTACCAAAACGCCTCGATCGAAGCGGCGGAGAAAACCGTTGACGGCGGATGGC
GTCACTGTCTCCCTACCGCTTGAACAGCATGGATCCTTTACAGAAAACGATGCGCCCAGCACCAAGGACGCAATA
GCACCGTCTAGCATCTCGTCTAAGACGTCGCACAACGATCCTCCGGCTAGTGTCAGTTCGGGTCCATCTGCGCCA
CAAGTTCACCCAGCTCGTCCATCGGCAGTCTCTAGTGCGGCGGGCGGCGATGCGGCTGCCGCGACAGTGGACCGA
CCCGCTGCTCCAGTTCTTCCTGTTCTCCCGGCCGTACCGAGGCACATGTCCAAGTCATCCAGCGCCGGTGACACA
AAGAAGCAGGCTGCCGATGCCAGCAAAAGCTCCCCTTCCAACGGTGCCGCCTCTGCCGCTGCTGGTGCTCATGCT
AGCGCCGACACCGCCGGCAGCCCCCCCGCGCCTAAGCTGGCTCCCACCAGCTGGGCGAACCTCTTCTCCAAAACC
TCCGTCAAAGAACCTTCCAATACGGCTGAGCCCAACGGATCCAATCCTGCCAATGGCTCCGTGTTACCGGGTGCT
ACCGCGCCGACTTCTGGTCCGGCCTTTTCCAAGTCCAACACAAACTTGCTCGCCGAGGCAATTCGAGCATACCGT
GTAGGAGGCACTGATAGCGTTTCTTTTCTTGAGCCACGAGGCCTCATTAATACTGGCAATATGTGCTATATGAAT
TCGGTTCTTCAGGTCCTCATCTTCTGCACACCCTTTTTTGATTTCTTGGACCAGGTCAGCAAGAAGGCAGCTTAC
AGTTTCAAGAGCGATACTCCTCTCATTGACGCCATCATCATGTTCGTGCGCGAGTACAAAGTGCTTGCCTCGGCG
CCGACGGCCAACGCACTGCGCCGCAAGCTCAAGAGCGACGATCTCGAAAAGTACGGCGAACCTTTTACGCCCGAA
TTTGTCTATGAAGCCATAAGACAGCTCCCGCGGTTTGCAAGCATGAGGCGTGGTCACCAGCAAGACGCCGAAGAG
TTTCTGGGCTTCCTGCTTCAGTCGCTTGATGACGAATGCACCAAGGTCCTGAGCAATCTGCCCTCTAGCGACTCG
GACACGGCTTCAGTTGATATGACAGCCAGCCAGAGCTCGGCAATGAATTCACCGGGCGACTGGCTCGAGGTCGGT
CGCAAGCAGCGCGCAGCCATCACACGCTCGTCCGGCTCCAACTCGTCGACACCCGTCGCCAAGATCTTTGGGGGG
CTGCTTCGCTCCGAGTTTCGCGTGCCTGGTCTCAAGGACTCCATCACGACCGAGCCCTACCAGCCGCTCCAACTC
GACATTGGGTCCCCGGATGTGCGCAACGTGGTCGACGCCTTACGCGGGCTTACCCGGCCGGAACGTCTCCAGGGA
GACTTCAACTCTCCTCGCGGCAAGGACGTGACGGCTACGAAGCAAGTGTTTATCGAGTCACTGCCCCCGGTGCTC
ATTCTGCACCTGAAGCGCTTCCAGTTCGACGCCGAGGGCCATGGCACCATCAAGGTTTGGAAAAAGATTGGCTAC
CCTTTGGAGTTGGAGATTCCGCGCGAGGCCGTCTCGAGGCAGAAACGCCACAGCATGGGCGACGGCGCCATGCCC
AAGTACAGGCTCATCAGCGTCGTCTATCACCACGGCAAAAACGCCAGCGGCGGCCACTACACCGTCGATGTCCGC
CGGCAGGATGGCCTGGAGTGGATTCGCATGGACGACACCGTCCTTCGTCGTGTGCGCAGCGAAGACGTGGCCGAG
GGCGGCTCCGAAGAAGAGTTGAAGGATGGTCGAAAGGACGGCGGCTCCGGCGCATCGTCCAACCGATTTGGCGTT
ATCAACGACGAAGACGCCGGCGGCGAGGGGTGGAAGCAGGTCACAGCTTCGACTAGCGGCAGCAAGCGATGGAGC
AGCGTCGTCGACGGCAATGGAAGCACAGAGGAAAGACAGCAGCAGCAGTTGAAGGAGAGCATCAAGGACAACAAG
GTCGCTTATCTGTTGTTTTACCAGCGCATG
Transcript >Ophio5|318
ATGAGCGCAGGCCCTGGTGGAGGCCCCGGCGGAGGCCCCGGCGGAGGTCCGCGGCGGAGGCAGCCTCAGTACGTT
CCGGCGTACCACCATCATCCTCCCCAGCACCAGCAGATGGTCTATCCCGGATACCTCCCTTATGGGCCTCAAGCC
TACTACGGCTTGCCGCCTCAGTTCCAAAATGGCGGCATGCCCTCTCCGGCCTACATGACCTATCAGGGCTATGGC
CGGTCGCCGCCCTCGATGCCTCAATACGTCCCCATGGTGGGCGTCAGCGTGCCTCCGGCCTATTCTGCTCGGCCC
TCGCAGCATTCGCCTAGCCTGTCTACCTCCTATCAGCCTCCGCCGGCACCAGCTTCTATTCCGCCTCAGACTCCT
TCGTCGTCGCACTCGTCACAGATACTCCATCCTCCCACTCCGCCCACGCCGCAGACGGCAGACCACGGCAGCACA
GGCCCTCCTCCATCTCTGCAGCTCGAGAGCTCCATGGAGCAGCGTGAATCCTTCCGCCCGCCGCTTCCTTGGTAC
TCGTGCCCCGAATCCGATTTTCCTACCAAAACGCCTCGATCGAAGCGGCGGAGAAAACCGTTGACGGCGGATGGC
GTCACTGTCTCCCTACCGCTTGAACAGCATGGATCCTTTACAGAAAACGATGCGCCCAGCACCAAGGACGCAATA
GCACCGTCTAGCATCTCGTCTAAGACGTCGCACAACGATCCTCCGGCTAGTGTCAGTTCGGGTCCATCTGCGCCA
CAAGTTCACCCAGCTCGTCCATCGGCAGTCTCTAGTGCGGCGGGCGGCGATGCGGCTGCCGCGACAGTGGACCGA
CCCGCTGCTCCAGTTCTTCCTGTTCTCCCGGCCGTACCGAGGCACATGTCCAAGTCATCCAGCGCCGGTGACACA
AAGAAGCAGGCTGCCGATGCCAGCAAAAGCTCCCCTTCCAACGGTGCCGCCTCTGCCGCTGCTGGTGCTCATGCT
AGCGCCGACACCGCCGGCAGCCCCCCCGCGCCTAAGCTGGCTCCCACCAGCTGGGCGAACCTCTTCTCCAAAACC
TCCGTCAAAGAACCTTCCAATACGGCTGAGCCCAACGGATCCAATCCTGCCAATGGCTCCGTGTTACCGGGTGCT
ACCGCGCCGACTTCTGGTCCGGCCTTTTCCAAGTCCAACACAAACTTGCTCGCCGAGGCAATTCGAGCATACCGT
GTAGGAGGCACTGATAGCGTTTCTTTTCTTGAGCCACGAGGCCTCATTAATACTGGCAATATGTGCTATATGAAT
TCGGTTCTTCAGGTCCTCATCTTCTGCACACCCTTTTTTGATTTCTTGGACCAGGTCAGCAAGAAGGCAGCTTAC
AGTTTCAAGAGCGATACTCCTCTCATTGACGCCATCATCATGTTCGTGCGCGAGTACAAAGTGCTTGCCTCGGCG
CCGACGGCCAACGCACTGCGCCGCAAGCTCAAGAGCGACGATCTCGAAAAGTACGGCGAACCTTTTACGCCCGAA
TTTGTCTATGAAGCCATAAGACAGCTCCCGCGGTTTGCAAGCATGAGGCGTGGTCACCAGCAAGACGCCGAAGAG
TTTCTGGGCTTCCTGCTTCAGTCGCTTGATGACGAATGCACCAAGGTCCTGAGCAATCTGCCCTCTAGCGACTCG
GACACGGCTTCAGTTGATATGACAGCCAGCCAGAGCTCGGCAATGAATTCACCGGGCGACTGGCTCGAGGTCGGT
CGCAAGCAGCGCGCAGCCATCACACGCTCGTCCGGCTCCAACTCGTCGACACCCGTCGCCAAGATCTTTGGGGGG
CTGCTTCGCTCCGAGTTTCGCGTGCCTGGTCTCAAGGACTCCATCACGACCGAGCCCTACCAGCCGCTCCAACTC
GACATTGGGTCCCCGGATGTGCGCAACGTGGTCGACGCCTTACGCGGGCTTACCCGGCCGGAACGTCTCCAGGGA
GACTTCAACTCTCCTCGCGGCAAGGACGTGACGGCTACGAAGCAAGTGTTTATCGAGTCACTGCCCCCGGTGCTC
ATTCTGCACCTGAAGCGCTTCCAGTTCGACGCCGAGGGCCATGGCACCATCAAGGTTTGGAAAAAGATTGGCTAC
CCTTTGGAGTTGGAGATTCCGCGCGAGGCCGTCTCGAGGCAGAAACGCCACAGCATGGGCGACGGCGCCATGCCC
AAGTACAGGCTCATCAGCGTCGTCTATCACCACGGCAAAAACGCCAGCGGCGGCCACTACACCGTCGATGTCCGC
CGGCAGGATGGCCTGGAGTGGATTCGCATGGACGACACCGTCCTTCGTCGTGTGCGCAGCGAAGACGTGGCCGAG
GGCGGCTCCGAAGAAGAGTTGAAGGATGGTCGAAAGGACGGCGGCTCCGGCGCATCGTCCAACCGATTTGGCGTT
ATCAACGACGAAGACGCCGGCGGCGAGGGGTGGAAGCAGGTCACAGCTTCGACTAGCGGCAGCAAGCGATGGAGC
AGCGTCGTCGACGGCAATGGAAGCACAGAGGAAAGACAGCAGCAGCAGTTGAAGGAGAGCATCAAGGACAACAAG
GTCGCTTATCTGTTGTTTTACCAGCGCATGTAA
Gene >Ophio5|318
ATGAGCGCAGGCCCTGGTGGAGGCCCCGGCGGAGGCCCCGGCGGAGGTCCGCGGCGGAGGCAGCCTCAGTACGTT
CCGGCGTACCACCATCATCCTCCCCAGCACCAGCAGATGGTCTATCCCGGATACCTCCCTTATGGGCCTCAAGCC
TACTACGGCTTGCCGCCTCAGTTCCAAAATGGCGGCATGCCCTCTCCGGCCTACATGACCTATCAGGGCTATGGC
CGGTCGCCGCCCTCGATGCCTCAATACGTCCCCATGGTGGGCGTCAGCGTGCCTCCGGCCTATTCTGCTCGGCCC
TCGCAGCATTCGCCTAGCCTGTCTACCTCCTATCAGCCTCCGCCGGCACCAGCTTCTATTCCGCCTCAGACTCCT
TCGTCGTCGCACTCGTCACAGATACTCCATCCTCCCACTCCGCCCACGCCGCAGACGGCAGACCACGGCAGCACA
GGCCCTCCTCCATCTCTGCAGCTCGAGAGCTCCATGGAGCAGCGTGAATCCTTCCGCCCGCCGGTGAGTTGGCGC
ATCTACTTGATTTTCCTTTCATCGCTGACCTGTCTGATATAGCTTCCTTGGTACTCGTGCCCCGAATCCGATTTT
CCTACCAAAACGCCTCGATCGAAGCGGCGGAGAAAACCGTTGACGGCGGATGGCGTCACTGTCTCCCTACCGCTT
GAACAGCATGGATCCTTTACAGAAAACGATGCGCCCAGCACCAAGGACGCAATAGCACCGTCTAGCATCTCGTCT
AAGACGTCGCACAACGATCCTCCGGCTAGTGTCAGTTCGGGTCCATCTGCGCCACAAGTTCACCCAGCTCGTCCA
TCGGCAGTCTCTAGTGCGGCGGGCGGCGATGCGGCTGCCGCGACAGTGGACCGACCCGCTGCTCCAGTTCTTCCT
GTTCTCCCGGCCGTACCGAGGCACATGTCCAAGTCATCCAGCGCCGGTGACACAAAGAAGCAGGCTGCCGATGCC
AGCAAAAGCTCCCCTTCCAACGGTGCCGCCTCTGCCGCTGCTGGTGCTCATGCTAGCGCCGACACCGCCGGCAGC
CCCCCCGCGCCTAAGCTGGCTCCCACCAGCTGGGCGAACCTCTTCTCCAAAACCTCCGTCAAAGAACCTTCCAAT
ACGGCTGAGCCCAACGGATCCAATCCTGCCAATGGCTCCGTGTTACCGGGTGCTACCGCGCCGACTTCTGGTCCG
GCCTTTTCCAAGTCCAACACAAACTTGCTCGCCGAGGCAATTCGAGCATACCGTGTAGGAGGCACTGATAGCGTT
TCTTTTCTTGAGCCACGAGGCCTCATTAATACTGGCAATATGTGCTATATGAATTCGGTATGGCCACTGATGGGG
CTTCTGGCGCTCTTATTGAACCAGTTTGCTGACGTCTTTGTTTCTTTGCCCGGCCTTCAGGTTCTTCAGGTCCTC
ATCTTCTGCACACCCTTTTTTGATTTCTTGGACCAGGTCAGCAAGAAGGCAGCTTACAGTTTCAAGAGCGATACT
CCTCTCATTGACGCCATGTACGTTTCCCAGTCTGCTCATGGCGTGGCGGCCTGTCGTTGACGAGAACGCAGCATC
ATGTTCGTGCGCGAGTACAAAGTGCTTGCCTCGGCGCCGACGGCCAACGCACTGCGCCGCAAGCTCAAGAGCGAC
GATCTCGAAAAGTACGGCGAACCTTTTACGCCCGAATTTGTCTATGAAGCCATAAGACAGCTCCCGCGGTTTGCA
AGCATGAGGGTAGGTCTTGCTACGGCAGAGGCGGCCAGAAGCCATACTGAAATGTCCTCACCAGCGTGGTCACCA
GCAAGACGCCGAAGAGTTTCTGGGCTTCCTGCTTCAGTCGCTTGATGACGAATGCACCAAGGTCCTGAGCAATCT
GCCCTCTAGCGACTCGGACACGGCTTCAGTTGATATGACAGCCAGCCAGAGCTCGGCAATGAATTCACCGGGCGA
CTGGCTCGAGGTCGGTCGCAAGCAGCGCGCAGCCATCACACGCTCGTCCGGCTCCAACTCGTCGACACCCGTCGC
CAAGATCTTTGGGGGGCTGCTTCGCTCCGAGTTTCGCGTGCCTGGTCTCAAGGACTCCATCACGACCGAGCCCTA
CCAGCCGCTCCAACTCGACATTGGGTCCCCGGATGTGCGCAACGTGGTCGACGCCTTACGCGGGCTTACCCGGCC
GGAACGTCTCCAGGGAGACTTCAACTCTCCTCGCGGCAAGGACGTGACGGCTACGAAGCAAGTGTTTATCGAGTC
ACTGCCCCCGGTGCTCATTCTGCACCTGAAGCGCTTCCAGTTCGACGCCGAGGGCCATGGCACCATCAAGGTTTG
GAAAAAGATTGGCTACCCTTTGGAGTTGGAGATTCCGCGCGAGGCCGTCTCGAGGCAGAAACGCCACAGCATGGG
CGACGGCGCCATGCCCAAGTACAGGCTCATCAGCGTCGTCTATCACCACGGCAAAAACGCCAGCGGCGGCCACTA
CACCGTCGATGTCCGCCGGCAGGATGGCCTGGAGTGGATTCGCATGGACGACACCGTCCTTCGTCGTGTGCGCAG
CGAAGACGTGGCCGAGGGCGGCTCCGAAGAAGAGTTGAAGGATGGTCGAAAGGACGGCGGCTCCGGCGCATCGTC
CAACCGATTTGGCGTTATCAACGACGAAGACGCCGGCGGCGAGGGGTGGAAGCAGGTCACAGCTTCGACTAGCGG
CAGCAAGCGATGGAGCAGCGTCGTCGACGGCAATGGAAGCACAGAGGAAAGACAGCAGCAGCAGTTGAAGGAGAG
CATCAAGGACAACAAGGTCGCTTATCTGTTGTTTTACCAGCGCATGTAA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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