Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauB2|2855
Gene name
LocationContig_196:5219..13532
Strand-
Gene length (bp)8313
Transcript length (bp)7743
Coding sequence length (bp)7743
Protein length (aa) 2581

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF12030 DUF3517 Domain of unknown function (DUF3517) 6.1E-91 2092 2507
PF00443 UCH Ubiquitin carboxyl-terminal hydrolase 9.7E-39 1617 1942
PF13423 UCH_1 Ubiquitin carboxyl-terminal hydrolase 6.6E-14 1617 1899

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|Q70CQ2|UBP34_HUMAN Ubiquitin carboxyl-terminal hydrolase 34 OS=Homo sapiens GN=USP34 PE=1 SV=2 1424 2217 1.0E-70
sp|Q6ZQ93|UBP34_MOUSE Ubiquitin carboxyl-terminal hydrolase 34 OS=Mus musculus GN=Usp34 PE=1 SV=3 1601 2217 3.0E-69
sp|B1AY13|UBP24_MOUSE Ubiquitin carboxyl-terminal hydrolase 24 OS=Mus musculus GN=Usp24 PE=1 SV=1 1611 1946 4.0E-51
sp|Q9UPU5|UBP24_HUMAN Ubiquitin carboxyl-terminal hydrolase 24 OS=Homo sapiens GN=USP24 PE=1 SV=3 1611 1946 6.0E-51
sp|P55824|FAF_DROME Probable ubiquitin carboxyl-terminal hydrolase FAF OS=Drosophila melanogaster GN=faf PE=1 SV=2 1581 1944 5.0E-48
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|Q70CQ2|UBP34_HUMAN Ubiquitin carboxyl-terminal hydrolase 34 OS=Homo sapiens GN=USP34 PE=1 SV=2 1424 2217 1.0E-70
sp|Q6ZQ93|UBP34_MOUSE Ubiquitin carboxyl-terminal hydrolase 34 OS=Mus musculus GN=Usp34 PE=1 SV=3 1601 2217 3.0E-69
sp|B1AY13|UBP24_MOUSE Ubiquitin carboxyl-terminal hydrolase 24 OS=Mus musculus GN=Usp24 PE=1 SV=1 1611 1946 4.0E-51
sp|Q9UPU5|UBP24_HUMAN Ubiquitin carboxyl-terminal hydrolase 24 OS=Homo sapiens GN=USP24 PE=1 SV=3 1611 1946 6.0E-51
sp|P55824|FAF_DROME Probable ubiquitin carboxyl-terminal hydrolase FAF OS=Drosophila melanogaster GN=faf PE=1 SV=2 1581 1944 5.0E-48
sp|P70398|USP9X_MOUSE Probable ubiquitin carboxyl-terminal hydrolase FAF-X OS=Mus musculus GN=Usp9x PE=1 SV=2 1611 2194 1.0E-43
sp|Q93008|USP9X_HUMAN Probable ubiquitin carboxyl-terminal hydrolase FAF-X OS=Homo sapiens GN=USP9X PE=1 SV=3 1611 2194 3.0E-43
sp|O00507|USP9Y_HUMAN Probable ubiquitin carboxyl-terminal hydrolase FAF-Y OS=Homo sapiens GN=USP9Y PE=2 SV=2 1611 2194 3.0E-41
sp|Q9UTT1|UBP21_SCHPO Ubiquitin carboxyl-terminal hydrolase 21 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp21 PE=3 SV=2 1611 1985 2.0E-37
sp|Q24574|UBPE_DROME Ubiquitin carboxyl-terminal hydrolase 64E OS=Drosophila melanogaster GN=Ubp64E PE=1 SV=2 1615 1957 8.0E-37
sp|A1A5G2|UBP47_XENTR Ubiquitin carboxyl-terminal hydrolase 47 OS=Xenopus tropicalis GN=usp47 PE=2 SV=1 1615 1949 1.0E-35
sp|Q5U252|UBP47_XENLA Ubiquitin carboxyl-terminal hydrolase 47 OS=Xenopus laevis GN=usp47 PE=2 SV=1 1615 1952 3.0E-35
sp|A3AF13|UBP26_ORYSJ Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. japonica GN=UBP26 PE=3 SV=2 1617 1903 1.0E-32
sp|A2XDG4|UBP26_ORYSI Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. indica GN=UBP26 PE=3 SV=1 1617 1903 1.0E-32
sp|Q93009|UBP7_HUMAN Ubiquitin carboxyl-terminal hydrolase 7 OS=Homo sapiens GN=USP7 PE=1 SV=2 1592 1965 4.0E-32
sp|Q4VSI4|UBP7_RAT Ubiquitin carboxyl-terminal hydrolase 7 OS=Rattus norvegicus GN=Usp7 PE=1 SV=1 1592 1965 5.0E-32
sp|Q86UV5|UBP48_HUMAN Ubiquitin carboxyl-terminal hydrolase 48 OS=Homo sapiens GN=USP48 PE=1 SV=1 1611 2051 7.0E-32
sp|Q8BY87|UBP47_MOUSE Ubiquitin carboxyl-terminal hydrolase 47 OS=Mus musculus GN=Usp47 PE=1 SV=2 1611 1903 8.0E-32
sp|Q9VYQ8|UBP7_DROME Ubiquitin carboxyl-terminal hydrolase 7 OS=Drosophila melanogaster GN=Usp7 PE=1 SV=1 1611 1977 8.0E-32
sp|Q3V0C5|UBP48_MOUSE Ubiquitin carboxyl-terminal hydrolase 48 OS=Mus musculus GN=Usp48 PE=1 SV=2 1611 2051 8.0E-32
sp|Q6A4J8|UBP7_MOUSE Ubiquitin carboxyl-terminal hydrolase 7 OS=Mus musculus GN=Usp7 PE=1 SV=1 1592 1965 1.0E-31
sp|Q96K76|UBP47_HUMAN Ubiquitin carboxyl-terminal hydrolase 47 OS=Homo sapiens GN=USP47 PE=1 SV=3 1611 1903 2.0E-31
sp|E1C1R4|UBP47_CHICK Ubiquitin carboxyl-terminal hydrolase 47 OS=Gallus gallus GN=USP47 PE=3 SV=1 1615 2017 4.0E-31
sp|Q09879|UBP5_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 5 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp5 PE=3 SV=3 1611 1960 7.0E-31
sp|Q6U7I1|UBP7_CHICK Ubiquitin carboxyl-terminal hydrolase 7 OS=Gallus gallus GN=USP7 PE=2 SV=1 1611 1965 9.0E-31
sp|Q84WU2|UBP13_ARATH Ubiquitin carboxyl-terminal hydrolase 13 OS=Arabidopsis thaliana GN=UBP13 PE=1 SV=1 1611 1946 9.0E-31
sp|Q8BWR4|UBP40_MOUSE Ubiquitin carboxyl-terminal hydrolase 40 OS=Mus musculus GN=Usp40 PE=1 SV=2 1609 1907 2.0E-30
sp|Q9SCJ9|UBP26_ARATH Ubiquitin carboxyl-terminal hydrolase 26 OS=Arabidopsis thaliana GN=UBP26 PE=1 SV=3 1617 2078 3.0E-30
sp|Q76LT8|UBP48_RAT Ubiquitin carboxyl-terminal hydrolase 48 OS=Rattus norvegicus GN=Usp48 PE=1 SV=1 1611 2051 9.0E-30
sp|P50101|UBP15_YEAST Ubiquitin carboxyl-terminal hydrolase 15 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP15 PE=1 SV=1 1611 1953 1.0E-29
sp|Q9FPT1|UBP12_ARATH Ubiquitin carboxyl-terminal hydrolase 12 OS=Arabidopsis thaliana GN=UBP12 PE=1 SV=2 1611 1946 2.0E-29
sp|Q9NVE5|UBP40_HUMAN Ubiquitin carboxyl-terminal hydrolase 40 OS=Homo sapiens GN=USP40 PE=1 SV=3 1609 1884 3.0E-29
sp|Q7JKC3|UBP7_CAEEL Ubiquitin carboxyl-terminal hydrolase 7 OS=Caenorhabditis elegans GN=usp-7 PE=3 SV=1 1615 1948 2.0E-28
sp|Q5ZM45|UBP48_CHICK Ubiquitin carboxyl-terminal hydrolase 48 OS=Gallus gallus GN=USP48 PE=2 SV=1 1611 2199 2.0E-28
sp|Q60MK8|UBP7_CAEBR Ubiquitin carboxyl-terminal hydrolase 7 OS=Caenorhabditis briggsae GN=usp-7 PE=3 SV=1 1611 1948 2.0E-27
sp|O74442|UBP16_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 16 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp16 PE=1 SV=1 1618 1903 3.0E-27
sp|Q9FPS2|UBP25_ARATH Ubiquitin carboxyl-terminal hydrolase 25 OS=Arabidopsis thaliana GN=UBP25 PE=2 SV=1 1617 1903 2.0E-24
sp|Q9UMW8|UBP18_HUMAN Ubl carboxyl-terminal hydrolase 18 OS=Homo sapiens GN=USP18 PE=1 SV=1 1591 1944 2.0E-23
sp|A4FUN7|UBP12_DANRE Ubiquitin carboxyl-terminal hydrolase 12A OS=Danio rerio GN=usp12a PE=2 SV=1 1616 1943 2.0E-22
sp|Q5RE63|UBP18_PONAB Ubl carboxyl-terminal hydrolase 18 OS=Pongo abelii GN=USP18 PE=2 SV=1 1591 1944 2.0E-22
sp|C0HB46|UBP12_SALSA Ubiquitin carboxyl-terminal hydrolase 12 OS=Salmo salar GN=usp12 PE=2 SV=1 1616 1943 3.0E-22
sp|Q3LFD5|UBP41_HUMAN Putative ubiquitin carboxyl-terminal hydrolase 41 OS=Homo sapiens GN=USP41 PE=2 SV=2 1615 1918 2.0E-21
sp|Q5RBQ4|UBP46_PONAB Ubiquitin carboxyl-terminal hydrolase 46 OS=Pongo abelii GN=USP46 PE=2 SV=1 1616 1943 5.0E-21
sp|P62069|UBP46_MOUSE Ubiquitin carboxyl-terminal hydrolase 46 OS=Mus musculus GN=Usp46 PE=1 SV=1 1616 1943 5.0E-21
sp|P62068|UBP46_HUMAN Ubiquitin carboxyl-terminal hydrolase 46 OS=Homo sapiens GN=USP46 PE=1 SV=1 1616 1943 5.0E-21
sp|B1AQJ2|UBP36_MOUSE Ubiquitin carboxyl-terminal hydrolase 36 OS=Mus musculus GN=Usp36 PE=1 SV=1 1617 1902 8.0E-21
sp|O57429|UBP2_CHICK Ubiquitin carboxyl-terminal hydrolase 2 OS=Gallus gallus GN=USP2 PE=2 SV=1 1615 1946 8.0E-21
sp|Q9D9M2|UBP12_MOUSE Ubiquitin carboxyl-terminal hydrolase 12 OS=Mus musculus GN=Usp12 PE=2 SV=2 1616 1943 8.0E-21
sp|Q52KZ6|UB12A_XENLA Ubiquitin carboxyl-terminal hydrolase 12-A OS=Xenopus laevis GN=usp12-a PE=2 SV=1 1616 1943 1.0E-20
sp|Q9WTV6|UBP18_MOUSE Ubl carboxyl-terminal hydrolase 18 OS=Mus musculus GN=Usp18 PE=1 SV=2 1605 1947 1.0E-20
sp|Q5M981|UB12B_XENLA Ubiquitin carboxyl-terminal hydrolase 12-B OS=Xenopus laevis GN=usp12-b PE=2 SV=2 1616 1943 1.0E-20
sp|A5D9H7|UBP12_BOVIN Ubiquitin carboxyl-terminal hydrolase 12 OS=Bos taurus GN=USP12 PE=2 SV=1 1616 1943 1.0E-20
sp|O75317|UBP12_HUMAN Ubiquitin carboxyl-terminal hydrolase 12 OS=Homo sapiens GN=USP12 PE=1 SV=2 1616 1943 2.0E-20
sp|P50102|UBP8_YEAST Ubiquitin carboxyl-terminal hydrolase 8 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP8 PE=1 SV=1 1579 1904 3.0E-20
sp|A5WWB0|UBP46_DANRE Ubiquitin carboxyl-terminal hydrolase 46 OS=Danio rerio GN=usp46 PE=3 SV=2 1616 1943 2.0E-19
sp|B2RQC2|UBP42_MOUSE Ubiquitin carboxyl-terminal hydrolase 42 OS=Mus musculus GN=Usp42 PE=1 SV=1 1617 1906 2.0E-19
sp|Q9H9J4|UBP42_HUMAN Ubiquitin carboxyl-terminal hydrolase 42 OS=Homo sapiens GN=USP42 PE=1 SV=3 1617 1906 2.0E-19
sp|D3ZU96|UBP42_RAT Ubiquitin carboxyl-terminal hydrolase 42 OS=Rattus norvegicus GN=Usp42 PE=1 SV=1 1617 1906 2.0E-19
sp|E1B9W9|UBP42_BOVIN Ubiquitin carboxyl-terminal hydrolase 42 OS=Bos taurus GN=USP42 PE=3 SV=1 1617 1906 3.0E-19
sp|Q6QN14|U17L6_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 6 OS=Homo sapiens GN=USP17L6P PE=1 SV=2 1566 1904 4.0E-19
sp|C9JVI0|U17LB_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 11 OS=Homo sapiens GN=USP17L11 PE=3 SV=1 1562 1904 7.0E-19
sp|D6RCP7|U17LJ_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 19 OS=Homo sapiens GN=USP17L19 PE=3 SV=1 1562 1904 7.0E-19
sp|D6R9N7|U17LI_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 18 OS=Homo sapiens GN=USP17L18 PE=3 SV=1 1562 1904 8.0E-19
sp|Q9P275|UBP36_HUMAN Ubiquitin carboxyl-terminal hydrolase 36 OS=Homo sapiens GN=USP36 PE=1 SV=3 1617 1902 2.0E-18
sp|D6RJB6|U17LK_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 20 OS=Homo sapiens GN=USP17L20 PE=3 SV=1 1562 1904 2.0E-18
sp|C9JLJ4|U17LD_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 13 OS=Homo sapiens GN=USP17L13 PE=3 SV=1 1562 1904 2.0E-18
sp|D6RA61|U17LM_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 22 OS=Homo sapiens GN=USP17L22 PE=3 SV=1 1562 1904 2.0E-18
sp|Q0WX57|U17LO_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 24 OS=Homo sapiens GN=USP17L24 PE=1 SV=2 1562 1904 3.0E-18
sp|Q9UPT9|UBP22_HUMAN Ubiquitin carboxyl-terminal hydrolase 22 OS=Homo sapiens GN=USP22 PE=1 SV=2 1606 1903 3.0E-18
sp|Q9FPS4|UBP23_ARATH Ubiquitin carboxyl-terminal hydrolase 23 OS=Arabidopsis thaliana GN=UBP23 PE=2 SV=2 1617 1944 3.0E-18
sp|D6RBQ6|U17LH_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 17 OS=Homo sapiens GN=USP17L17 PE=3 SV=1 1562 1904 3.0E-18
sp|C9JPN9|UL17C_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 12 OS=Homo sapiens GN=USP17L12 PE=3 SV=1 1562 1904 4.0E-18
sp|C9J2P7|U17LF_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 15 OS=Homo sapiens GN=USP17L15 PE=3 SV=1 1562 1904 4.0E-18
sp|D6R901|U17LL_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 21 OS=Homo sapiens GN=USP17L21 PE=3 SV=1 1562 1904 6.0E-18
sp|P0C8Z3|UBP22_BOVIN Ubiquitin carboxyl-terminal hydrolase 22 OS=Bos taurus GN=USP22 PE=2 SV=1 1606 1903 7.0E-18
sp|Q5DU02|UBP22_MOUSE Ubiquitin carboxyl-terminal hydrolase 22 OS=Mus musculus GN=Usp22 PE=2 SV=2 1606 1903 8.0E-18
sp|A6H8I0|UBP22_DANRE Ubiquitin carboxyl-terminal hydrolase 22 OS=Danio rerio GN=usp22 PE=2 SV=1 1615 1903 9.0E-18
sp|A8MUK1|U17L5_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 5 OS=Homo sapiens GN=USP17L5 PE=3 SV=2 1562 1904 9.0E-18
sp|P38187|UBP13_YEAST Ubiquitin carboxyl-terminal hydrolase 13 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP13 PE=1 SV=3 1678 1962 1.0E-17
sp|Q7M764|U17PE_MOUSE Ubiquitin carboxyl-terminal hydrolase 17-like protein E OS=Mus musculus GN=Usp17le PE=3 SV=2 1617 1906 1.0E-17
sp|Q9SB51|UBP16_ARATH Ubiquitin carboxyl-terminal hydrolase 16 OS=Arabidopsis thaliana GN=UBP16 PE=1 SV=1 1618 1946 2.0E-17
sp|Q67XW5|UBP18_ARATH Ubiquitin carboxyl-terminal hydrolase 18 OS=Arabidopsis thaliana GN=UBP18 PE=2 SV=2 1617 1884 3.0E-17
sp|Q6GNI6|UB22A_XENLA Ubiquitin carboxyl-terminal hydrolase 22-A OS=Xenopus laevis GN=usp22-a PE=2 SV=1 1606 1903 4.0E-17
sp|A6NCW0|U17L3_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 3 OS=Homo sapiens GN=USP17L3 PE=3 SV=1 1617 1903 4.0E-17
sp|Q6R6M4|U17L2_HUMAN Ubiquitin carboxyl-terminal hydrolase 17 OS=Homo sapiens GN=USP17L2 PE=1 SV=2 1579 1904 4.0E-17
sp|Q6DCJ1|UB22B_XENLA Ubiquitin carboxyl-terminal hydrolase 22-B OS=Xenopus laevis GN=usp22-b PE=2 SV=2 1606 1903 5.0E-17
sp|Q70EK9|UBP51_HUMAN Ubiquitin carboxyl-terminal hydrolase 51 OS=Homo sapiens GN=USP51 PE=2 SV=1 1615 1903 5.0E-17
sp|C9JJH3|U17LA_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 10 OS=Homo sapiens GN=USP17L10 PE=3 SV=1 1617 1904 5.0E-17
sp|Q7RTZ2|U17L1_HUMAN Ubiquitin carboxyl-terminal hydrolase 17-like protein 1 OS=Homo sapiens GN=USP17L1 PE=3 SV=1 1617 1903 1.0E-16
sp|Q9SJA1|UBP19_ARATH Ubiquitin carboxyl-terminal hydrolase 19 OS=Arabidopsis thaliana GN=UBP19 PE=2 SV=2 1595 1902 2.0E-16
sp|O24454|UBP3_ARATH Ubiquitin carboxyl-terminal hydrolase 3 OS=Arabidopsis thaliana GN=UBP3 PE=1 SV=1 1616 1943 2.0E-16
sp|Q8LAM0|UBP4_ARATH Ubiquitin carboxyl-terminal hydrolase 4 OS=Arabidopsis thaliana GN=UBP4 PE=1 SV=2 1616 1917 2.0E-16
sp|P32571|UBP4_YEAST Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DOA4 PE=1 SV=2 1617 1899 2.0E-16
sp|P0C7I0|U17L8_HUMAN Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 8 OS=Homo sapiens GN=USP17L8 PE=3 SV=1 1617 1904 2.0E-16
sp|B3LGK1|UBP4_YEAS1 Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain RM11-1a) GN=DOA4 PE=3 SV=1 1617 1899 3.0E-16
sp|A6ZY34|UBP4_YEAS7 Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain YJM789) GN=DOA4 PE=3 SV=1 1617 1899 3.0E-16
sp|Q9VVR1|NOT_DROME Ubiquitin carboxyl-terminal hydrolase nonstop OS=Drosophila melanogaster GN=not PE=1 SV=3 1615 1903 4.0E-16
sp|A6NCW7|U17L4_HUMAN Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 4 OS=Homo sapiens GN=USP17L4 PE=3 SV=3 1617 1903 6.0E-16
sp|P34547|UBP46_CAEEL Ubiquitin carboxyl-terminal hydrolase 46 OS=Caenorhabditis elegans GN=usp-46 PE=1 SV=3 1727 1943 6.0E-16
sp|O75604|UBP2_HUMAN Ubiquitin carboxyl-terminal hydrolase 2 OS=Homo sapiens GN=USP2 PE=1 SV=2 1611 1946 1.0E-15
sp|Q9FPS9|UBP15_ARATH Ubiquitin carboxyl-terminal hydrolase 15 OS=Arabidopsis thaliana GN=UBP15 PE=2 SV=2 1618 1945 2.0E-15
sp|O88623|UBP2_MOUSE Ubiquitin carboxyl-terminal hydrolase 2 OS=Mus musculus GN=Usp2 PE=1 SV=2 1611 1946 7.0E-15
sp|Q61068|U17PA_MOUSE Ubiquitin carboxyl-terminal hydrolase 17-like protein A OS=Mus musculus GN=Usp17la PE=1 SV=1 1617 1906 8.0E-15
sp|Q8CEG8|UBP27_MOUSE Ubiquitin carboxyl-terminal hydrolase 27 OS=Mus musculus GN=Usp27 PE=2 SV=2 1615 1903 9.0E-15
sp|Q5U349|UBP2_RAT Ubiquitin carboxyl-terminal hydrolase 2 OS=Rattus norvegicus GN=Usp2 PE=1 SV=1 1611 1946 1.0E-14
sp|A5PN09|UBP20_DANRE Ubiquitin carboxyl-terminal hydrolase 20 OS=Danio rerio GN=usp20 PE=3 SV=1 1766 1981 2.0E-14
sp|Q2KHV7|UBP2_BOVIN Ubiquitin carboxyl-terminal hydrolase 2 OS=Bos taurus GN=USP2 PE=2 SV=1 1611 1899 3.0E-14
sp|Q2KJ72|UBP21_BOVIN Ubiquitin carboxyl-terminal hydrolase 21 OS=Bos taurus GN=USP21 PE=2 SV=1 1615 1913 5.0E-14
sp|A6NNY8|UBP27_HUMAN Ubiquitin carboxyl-terminal hydrolase 27 OS=Homo sapiens GN=USP27X PE=2 SV=3 1615 1903 5.0E-14
sp|Q9Y2K6|UBP20_HUMAN Ubiquitin carboxyl-terminal hydrolase 20 OS=Homo sapiens GN=USP20 PE=1 SV=2 1766 1981 8.0E-14
sp|Q9UK80|UBP21_HUMAN Ubiquitin carboxyl-terminal hydrolase 21 OS=Homo sapiens GN=USP21 PE=1 SV=1 1615 1913 1.0E-13
sp|P39967|UBP9_YEAST Ubiquitin carboxyl-terminal hydrolase 9 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP9 PE=1 SV=1 1678 1953 1.0E-13
sp|Q5R5Z6|UBP20_PONAB Ubiquitin carboxyl-terminal hydrolase 20 OS=Pongo abelii GN=USP20 PE=2 SV=1 1766 1981 1.0E-13
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 1617 1947 1.0E-13
sp|Q96RU2|UBP28_HUMAN Ubiquitin carboxyl-terminal hydrolase 28 OS=Homo sapiens GN=USP28 PE=1 SV=1 1617 1844 1.0E-13
sp|P0C7H9|U17L7_HUMAN Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 7 OS=Homo sapiens GN=USP17L7 PE=3 SV=1 1617 1963 2.0E-13
sp|Q9QZL6|UBP21_MOUSE Ubiquitin carboxyl-terminal hydrolase 21 OS=Mus musculus GN=Usp21 PE=1 SV=1 1615 1913 2.0E-13
sp|Q5ZID5|UBP28_CHICK Ubiquitin carboxyl-terminal hydrolase 28 OS=Gallus gallus GN=USP28 PE=2 SV=1 1617 1844 2.0E-13
sp|A7Z056|UBP20_BOVIN Ubiquitin carboxyl-terminal hydrolase 20 OS=Bos taurus GN=USP20 PE=2 SV=1 1766 1981 3.0E-13
sp|Q8C6M1|UBP20_MOUSE Ubiquitin carboxyl-terminal hydrolase 20 OS=Mus musculus GN=Usp20 PE=1 SV=1 1766 1981 3.0E-13
sp|D3ZJ96|UBP28_RAT Ubiquitin carboxyl-terminal hydrolase 28 OS=Rattus norvegicus GN=Usp28 PE=2 SV=2 1617 1844 4.0E-13
sp|Q9P7V9|UBP9_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 9 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp9 PE=1 SV=1 1700 1945 4.0E-13
sp|B2GUX4|UBP21_RAT Ubiquitin carboxyl-terminal hydrolase 21 OS=Rattus norvegicus GN=Usp21 PE=2 SV=1 1615 1913 4.0E-13
sp|Q5I043|UBP28_MOUSE Ubiquitin carboxyl-terminal hydrolase 28 OS=Mus musculus GN=Usp28 PE=1 SV=1 1617 1844 4.0E-13
sp|Q80U87|UBP8_MOUSE Ubiquitin carboxyl-terminal hydrolase 8 OS=Mus musculus GN=Usp8 PE=1 SV=2 1612 1899 4.0E-13
sp|Q6P8X6|UBP50_MOUSE Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Mus musculus GN=Usp50 PE=2 SV=1 1615 1903 5.0E-13
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 1721 1987 5.0E-13
sp|Q5XGZ2|UP44B_XENLA Ubiquitin carboxyl-terminal hydrolase 44-B OS=Xenopus laevis GN=usp44-b PE=2 SV=1 1659 1899 5.0E-13
sp|Q4R6D3|UBP50_MACFA Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Macaca fascicularis GN=USP50 PE=2 SV=1 1615 1903 5.0E-13
sp|Q7ZUM8|UBP44_DANRE Ubiquitin carboxyl-terminal hydrolase 44 OS=Danio rerio GN=usp44 PE=2 SV=1 1659 1903 7.0E-13
sp|Q6NTR6|UP44A_XENLA Ubiquitin carboxyl-terminal hydrolase 44-A OS=Xenopus laevis GN=usp44-a PE=2 SV=1 1659 1899 9.0E-13
sp|B1WBD7|UBP20_XENLA Ubiquitin carboxyl-terminal hydrolase 20 OS=Xenopus laevis GN=usp20 PE=2 SV=1 1766 1979 1.0E-12
sp|A0JM59|UBP20_XENTR Ubiquitin carboxyl-terminal hydrolase 20 OS=Xenopus tropicalis GN=usp20 PE=2 SV=1 1766 1979 1.0E-12
sp|Q9FIQ1|UBP21_ARATH Ubiquitin carboxyl-terminal hydrolase 21 OS=Arabidopsis thaliana GN=UBP21 PE=2 SV=1 1617 1903 1.0E-12
sp|P40818|UBP8_HUMAN Ubiquitin carboxyl-terminal hydrolase 8 OS=Homo sapiens GN=USP8 PE=1 SV=1 1612 1899 1.0E-12
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 1721 1946 2.0E-12
sp|Q8TEY7|UBP33_HUMAN Ubiquitin carboxyl-terminal hydrolase 33 OS=Homo sapiens GN=USP33 PE=1 SV=2 1766 1946 3.0E-12
sp|Q8R5K2|UBP33_MOUSE Ubiquitin carboxyl-terminal hydrolase 33 OS=Mus musculus GN=Usp33 PE=1 SV=2 1766 1946 3.0E-12
sp|Q5REG5|UBP33_PONAB Ubiquitin carboxyl-terminal hydrolase 33 OS=Pongo abelii GN=USP33 PE=2 SV=1 1766 1946 4.0E-12
sp|B4QIS3|UBP36_DROSI Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila simulans GN=Usp36 PE=3 SV=1 1617 1902 5.0E-12
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 1730 1899 5.0E-12
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 1721 1964 7.0E-12
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 1721 1946 7.0E-12
sp|Q99K46|UBP11_MOUSE Ubiquitin carboxyl-terminal hydrolase 11 OS=Mus musculus GN=Usp11 PE=1 SV=4 1762 1964 7.0E-12
sp|B4IXE0|UBP36_DROGR Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila grimshawi GN=Usp36 PE=3 SV=1 1617 1878 7.0E-12
sp|A5PMR2|UBP33_DANRE Ubiquitin carboxyl-terminal hydrolase 33 OS=Danio rerio GN=usp33 PE=2 SV=1 1766 1946 8.0E-12
sp|Q2UUG8|CREB_ASPOR Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=creB PE=3 SV=2 1721 1946 8.0E-12
sp|B3NC86|UBP36_DROER Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila erecta GN=Usp36 PE=3 SV=1 1617 1902 8.0E-12
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 1721 1964 1.0E-11
sp|Q28CN3|UBP33_XENTR Ubiquitin carboxyl-terminal hydrolase 33 OS=Xenopus tropicalis GN=usp33 PE=2 SV=2 1766 1946 1.0E-11
sp|B3M3M6|UBP36_DROAN Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila ananassae GN=Usp36 PE=3 SV=1 1618 1902 1.0E-11
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 1721 1964 1.0E-11
sp|B4PIW8|UBP36_DROYA Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila yakuba GN=Usp36 PE=3 SV=1 1617 1902 1.0E-11
sp|A6QNM7|UBP33_BOVIN Ubiquitin carboxyl-terminal hydrolase 33 OS=Bos taurus GN=USP33 PE=2 SV=1 1766 1946 2.0E-11
sp|Q0CT11|CREB_ASPTN Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=creB PE=3 SV=2 1721 1953 2.0E-11
sp|B4LG38|UBP36_DROVI Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila virilis GN=Usp36 PE=3 SV=1 1617 1878 2.0E-11
sp|Q2LZB1|UBP36_DROPS Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila pseudoobscura pseudoobscura GN=Usp36 PE=3 SV=2 1617 1878 2.0E-11
sp|Q9LEW0|UBP22_ARATH Ubiquitin carboxyl-terminal hydrolase 22 OS=Arabidopsis thaliana GN=UBP22 PE=2 SV=1 1605 1960 3.0E-11
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 1721 1946 3.0E-11
sp|Q9VRP5|UBP36_DROME Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila melanogaster GN=scny PE=1 SV=3 1617 1902 3.0E-11
sp|Q9FKP5|UBP17_ARATH Ubiquitin carboxyl-terminal hydrolase 17 OS=Arabidopsis thaliana GN=UBP17 PE=2 SV=1 1618 1902 3.0E-11
sp|A8HAL1|UBP16_DANRE Ubiquitin carboxyl-terminal hydrolase 16 OS=Danio rerio GN=usp16 PE=3 SV=1 1761 1946 3.0E-11
sp|B4KXJ5|UBP36_DROMO Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila mojavensis GN=Usp36 PE=3 SV=1 1617 1878 4.0E-11
sp|Q0V9G5|UBP44_XENTR Ubiquitin carboxyl-terminal hydrolase 44 OS=Xenopus tropicalis GN=usp44 PE=2 SV=1 1659 1881 6.0E-11
sp|Q09738|UBP8_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 8 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp8 PE=3 SV=1 1615 1902 8.0E-11
sp|D2HBJ8|UBP44_AILME Ubiquitin carboxyl-terminal hydrolase 44 OS=Ailuropoda melanoleuca GN=USP44 PE=3 SV=1 1659 1903 9.0E-11
sp|Q6P9L4|UBP49_MOUSE Ubiquitin carboxyl-terminal hydrolase 49 OS=Mus musculus GN=Usp49 PE=2 SV=1 1659 1903 2.0E-10
sp|Q9H0E7|UBP44_HUMAN Ubiquitin carboxyl-terminal hydrolase 44 OS=Homo sapiens GN=USP44 PE=1 SV=2 1659 1903 3.0E-10
sp|Q70EL3|UBP50_HUMAN Inactive ubiquitin carboxyl-terminal hydrolase 50 OS=Homo sapiens GN=USP50 PE=2 SV=1 1615 1883 3.0E-10
sp|Q9FPS7|UBP20_ARATH Ubiquitin carboxyl-terminal hydrolase 20 OS=Arabidopsis thaliana GN=UBP20 PE=2 SV=1 1617 1912 3.0E-10
sp|Q70CQ1|UBP49_HUMAN Ubiquitin carboxyl-terminal hydrolase 49 OS=Homo sapiens GN=USP49 PE=1 SV=1 1659 1899 4.0E-10
sp|A7TGY3|UBP4_VANPO Ubiquitin carboxyl-terminal hydrolase 4 OS=Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294) GN=DOA4 PE=3 SV=1 1617 1899 5.0E-10
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 1617 1899 6.0E-10
sp|O60139|UBP4_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp4 PE=1 SV=2 1594 1948 7.0E-10
sp|Q99LG0|UBP16_MOUSE Ubiquitin carboxyl-terminal hydrolase 16 OS=Mus musculus GN=Usp16 PE=1 SV=2 1752 1944 8.0E-10
sp|P57080|UBP25_MOUSE Ubiquitin carboxyl-terminal hydrolase 25 OS=Mus musculus GN=Usp25 PE=1 SV=2 1604 1844 9.0E-10
sp|Q8C2S0|UBP44_MOUSE Ubiquitin carboxyl-terminal hydrolase 44 OS=Mus musculus GN=Usp44 PE=2 SV=3 1659 1903 1.0E-09
sp|Q2KJ09|UBP16_RAT Ubiquitin carboxyl-terminal hydrolase 16 OS=Rattus norvegicus GN=Usp16 PE=1 SV=2 1752 1944 1.0E-09
sp|Q0VA64|UBP16_XENTR Ubiquitin carboxyl-terminal hydrolase 16 OS=Xenopus tropicalis GN=usp16 PE=2 SV=2 1771 1944 2.0E-09
sp|Q9UHP3|UBP25_HUMAN Ubiquitin carboxyl-terminal hydrolase 25 OS=Homo sapiens GN=USP25 PE=1 SV=4 1604 1844 2.0E-09
sp|O94782|UBP1_HUMAN Ubiquitin carboxyl-terminal hydrolase 1 OS=Homo sapiens GN=USP1 PE=1 SV=1 1727 1883 3.0E-09
sp|Q8BJQ2|UBP1_MOUSE Ubiquitin carboxyl-terminal hydrolase 1 OS=Mus musculus GN=Usp1 PE=1 SV=1 1727 1883 3.0E-09
sp|Q569C3|UBP1_RAT Ubiquitin carboxyl-terminal hydrolase 1 OS=Rattus norvegicus GN=Usp1 PE=1 SV=1 1727 1883 4.0E-09
sp|Q29RP1|UBP1_BOVIN Ubiquitin carboxyl-terminal hydrolase 1 OS=Bos taurus GN=USP1 PE=2 SV=1 1727 1883 7.0E-09
sp|Q6PAW2|UBP16_XENLA Ubiquitin carboxyl-terminal hydrolase 16 OS=Xenopus laevis GN=usp16 PE=2 SV=1 1751 1944 8.0E-09
sp|P51784|UBP11_HUMAN Ubiquitin carboxyl-terminal hydrolase 11 OS=Homo sapiens GN=USP11 PE=1 SV=3 1762 1949 8.0E-09
sp|Q9P2H5|UBP35_HUMAN Ubiquitin carboxyl-terminal hydrolase 35 OS=Homo sapiens GN=USP35 PE=1 SV=3 1540 1755 1.0E-08
sp|B4MLR8|UBP36_DROWI Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila willistoni GN=Usp36 PE=3 SV=1 1617 1878 1.0E-08
sp|Q08DA3|UBP16_BOVIN Ubiquitin carboxyl-terminal hydrolase 16 OS=Bos taurus GN=USP16 PE=2 SV=2 1752 1944 3.0E-08
sp|B2GUZ1|UBP4_RAT Ubiquitin carboxyl-terminal hydrolase 4 OS=Rattus norvegicus GN=Usp4 PE=1 SV=1 1728 1944 4.0E-08
sp|Q5UQR3|UBPL1_MIMIV Probable ubiquitin carboxyl-terminal hydrolase R319 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R319 PE=3 SV=1 1744 1951 5.0E-08
sp|P35123|UBP4_MOUSE Ubiquitin carboxyl-terminal hydrolase 4 OS=Mus musculus GN=Usp4 PE=1 SV=3 1728 1944 5.0E-08
sp|Q91W36|UBP3_MOUSE Ubiquitin carboxyl-terminal hydrolase 3 OS=Mus musculus GN=Usp3 PE=2 SV=1 1617 1959 6.0E-08
sp|Q3UJD6|UBP19_MOUSE Ubiquitin carboxyl-terminal hydrolase 19 OS=Mus musculus GN=Usp19 PE=1 SV=1 1739 1947 7.0E-08
sp|Q9P7S5|UBP7_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 7 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp7 PE=1 SV=1 1761 1945 7.0E-08
sp|Q4R6X7|UBP16_MACFA Ubiquitin carboxyl-terminal hydrolase 16 OS=Macaca fascicularis GN=USP16 PE=2 SV=2 1752 1944 7.0E-08
sp|Q9Y5T5|UBP16_HUMAN Ubiquitin carboxyl-terminal hydrolase 16 OS=Homo sapiens GN=USP16 PE=1 SV=1 1752 1944 7.0E-08
sp|O94966|UBP19_HUMAN Ubiquitin carboxyl-terminal hydrolase 19 OS=Homo sapiens GN=USP19 PE=1 SV=2 1739 1947 8.0E-08
sp|Q6J1Y9|UBP19_RAT Ubiquitin carboxyl-terminal hydrolase 19 OS=Rattus norvegicus GN=Usp19 PE=1 SV=1 1739 1947 8.0E-08
sp|Q9ZSB5|UBP10_ARATH Ubiquitin carboxyl-terminal hydrolase 10 OS=Arabidopsis thaliana GN=UBP10 PE=2 SV=2 1766 1961 1.0E-07
sp|Q9Y6I4|UBP3_HUMAN Ubiquitin carboxyl-terminal hydrolase 3 OS=Homo sapiens GN=USP3 PE=1 SV=2 1617 1906 1.0E-07
sp|Q01988|UBP11_CANLF Ubiquitin carboxyl-terminal hydrolase 11 (Fragment) OS=Canis lupus familiaris GN=USP11 PE=2 SV=1 1762 1949 1.0E-07
sp|Q93Y01|UBP9_ARATH Ubiquitin carboxyl-terminal hydrolase 9 OS=Arabidopsis thaliana GN=UBP9 PE=2 SV=1 1766 1961 3.0E-07
sp|P53874|UBP10_YEAST Ubiquitin carboxyl-terminal hydrolase 10 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP10 PE=1 SV=2 1766 1903 5.0E-07
sp|Q9MAQ3|UBP11_ARATH Putative ubiquitin carboxyl-terminal hydrolase 11 OS=Arabidopsis thaliana GN=UBP11 PE=3 SV=2 1739 1947 7.0E-07
sp|Q5RCD3|UBP4_PONAB Ubiquitin carboxyl-terminal hydrolase 4 OS=Pongo abelii GN=USP4 PE=2 SV=1 1755 1944 8.0E-07
sp|Q9C585|UBP8_ARATH Ubiquitin carboxyl-terminal hydrolase 8 OS=Arabidopsis thaliana GN=UBP8 PE=2 SV=2 1766 1944 1.0E-06
sp|Q13107|UBP4_HUMAN Ubiquitin carboxyl-terminal hydrolase 4 OS=Homo sapiens GN=USP4 PE=1 SV=3 1755 1944 2.0E-06
sp|A6QR55|UBP4_BOVIN Ubiquitin carboxyl-terminal hydrolase 4 OS=Bos taurus GN=USP4 PE=2 SV=1 1755 1903 3.0E-06
sp|Q8W4N3|UBP2_ARATH Ubiquitin carboxyl-terminal hydrolase 2 OS=Arabidopsis thaliana GN=UBP2 PE=1 SV=2 1796 1905 3.0E-06
sp|B4HUI5|UBP36_DROSE Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila sechellia GN=Usp36 PE=3 SV=1 1617 1902 4.0E-06
sp|Q8NB14|UBP38_HUMAN Ubiquitin carboxyl-terminal hydrolase 38 OS=Homo sapiens GN=USP38 PE=1 SV=2 1766 1883 4.0E-06
sp|Q6DIJ4|UBP10_XENTR Ubiquitin carboxyl-terminal hydrolase 10 OS=Xenopus tropicalis GN=usp10 PE=2 SV=1 1691 1944 5.0E-06
sp|Q9P2H5|UBP35_HUMAN Ubiquitin carboxyl-terminal hydrolase 35 OS=Homo sapiens GN=USP35 PE=1 SV=3 1759 1899 7.0E-06
sp|Q2NL57|UB10A_XENLA Ubiquitin carboxyl-terminal hydrolase 10-A OS=Xenopus laevis GN=usp10-a PE=2 SV=1 1695 1944 8.0E-06
[Show less]

GO

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

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 33 0.45

Transmembrane Domains

(None)

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|2855
MDSALSSRTAQQEASLSDPPSTRPNPFVDDGDICSRKRRRTSLSASPDVSLHHSVHSVHGPQAPDMHAIKVDGAP
DALETLDQHPTTPGEPSSNSMTISLRRRAHGESPLASLHSTAERLSDVEANSARHAADVLDENVDEALAAASSKR
SSSSTGSPPVELIAVSDDGSDDRQGDTICVENSMDLSASGASTCPNILIADPTTQFPWRNPNESISDTVQRLIQY
LSNTDPVDADILYDLIKWLESYLEFAKNTDPGQVLSSRNSHMHFWLSFPDAMCSLTTKRSEIIKAPVIRNALLAV
YSQYTVLTALFISLDCLACRDARSAFAATGDRRHPEILAPIYLQQLVNALGPLGLSHQGSNDSVAGTNLNHFDLD
LRLVTKFLESPGGSLECLSEFAQELQHVMAQVPRLTDSLAPLSQTLAACVRQSLQQFRAGQQGFSDARRRLELGL
EAWSTISSTLITIIDKHVTCLSSECANISIQALSEVLKCSLQGGHVAAADALADHRNKYPSVAPQDTHEAIAWQW
KFDVLEKLIRSSQMTLRVMAVTTMCNNLVSIWRRHCDGSDEYGSDFFGHLANYLLQTGLIDYILGANCHPEIILE
SANIIGFLVVTRFYVQDHTEQIWRGIISSQDPRVSDALARMIASITNLFDYNGLLQICNRLKQLPLDRFSPSIRH
LLDNVLREMIARSKSEQPTLTFHPYGLCLRLLRESSVFASSSQVADPEMQQFAMQKFRELLGHGPDSEGRRELYL
SCLSDLSAKSPTSLGSLWALSMATRHTLVGQMQILTEQHDLARLIVEEIEHAGNAGRAAGAFPVLFGTCNQPRRD
FVTSLIELQPTAIDGSLGFKLWNLLVGSLSACPDDRRAGWYIILSTSRKTALQNKFLQTCFSDYLPKLAPVYFCE
GMLDFVKEHLHPLLTDRNGLLDFDDETVASRSGIEQLWRIILQAEDEELVKHAISTLAVEVYLESRAITSCALHR
TRQLHLAFVARCLSQMKEAATKLKRSNEGTTREDDESMIIVTTDEENKELQRTMTRSLRLLRFFLERYQSKPRFA
VADLRSFMSEKPQRIDGDSAQLRYQSFNGDKQSDILLLDIGRLNTVSSLLASFRDKTGFDNYRVFYRGRQLLLSE
QDTCKSLQELGIHDGFILVKREESNSSFPSRIKPGSLPLEIEILSHFADFWDYLSMDDCLAEEIYNFVVKLPADG
HILSLFDTDVTSYTDLFLSGQPFKSLYAIHALKEYVESASRAQAVGTDFESNGCYTSRDEAMKRSLRLVVQALSD
PDVLQGSSARLQIRLASSLMQEFVRLIKALYRSVSFAACNTVEAPSPKRLMEVLFDALEYQEQEALPLIASTCSA
ILKIGQLDDHFWKEITTVPSFAQLIQRLVLFDPRREVRLAAVKLIGDAAEFEAQSLQVPPDPAPKRNERTFGLGQ
FLWPIIVELLPETVRLTQQCEEAFALLLKLLLLISNKMLLQIRVDSLAAQTSKLLLEHHSSERITHIEPYDAVVA
GLTSVLHACLQIDSRLPASEVLPDNLVLGLFMRHLFPRKLEQGELCVPQVVLNMETRTKLYDIVFALIRQNHVRC
GQVLDLLNSLVPFYGEDDDPYKYELPYQFDRSKAMRSSCGYVGLRNLSNTCYLNSLLTQLYMNVKFRRFIMTSAC
PDTENPQGLLFETQKIFGFMQESYRRFVDPTSLVSSVKTYEDTVIDIHSQMDVDEFYSLLFDRWEGQLLRPEDKR
RLRSFYGGQLVQQVKSKECEHISERLEPFSAIQCDIKGKSSLEESLQAYVDGEIMEGDNKYKCSSCDRHVDAVKR
ACLKDVPDNVIFHLKRFDFNLRTLQRSKINDHFTFPQKLNMRPYTIEHLSEASTDASEDEFELVGILVHAGTAES
GHYYSYIKERPLSGGKNSWVEFNDDVVSAWDPSLMASSTFGGPETRPLYETNGVAYDKSYSAYMLFYQRASSLRA
EQQAMAAQQIDSPLLVEASMALREHIASENTVLLRRHCLYDPNHVGFVENCFSLAKTLDESEVDGIVSLRPRESQ
ERQRLQAGGHRLRNVAMEMAVSHLDQVVSRACNTPSLVSFSSMLRAAIINCAQCALAFYNYFSRRHKALRALLQR
SPEQHVRCFVGEVLVCAAERIATHFPRLYDSGGDDVESGDNLSDVGGRSVAEGMVDMLNHLWQFFQVHLRSWEEY
FGTVLAFARLGDRETSLLLSNDYLVKVLNIVTADVSTDLPANYARMLANVLRRMSTRPPSYCAILVLMDYLLGQL
EPTLSPQSITDHATDRLRGEAPFLWTSEEIQIVHHSSSDRQPLSFFVEKLVAIDQAWAATSNIVARLVLTGLQMD
LRVFNALRKNMNGEMSAQAMDPFLRVAARYMETTRSTEYANALVRHVCGQARNMQNTEGPVFMMLVNVMLRSEMP
RLDLARSRRECCIKQTPVWGPYMLVFPNSNVRREAECLIEHVLFAADSPKDEASTGHSHEMKDCLDEVAYDLGVR
CLVYLRDMHVKRRVRIERDAALSILSVVGKCVARCDALKDMDDGEDDDLGLLQKEVVEPLRRLMVDEVEDDVSDW
DGSCGSSEPMDASLGIPLQTMSEANDIDLM*
Coding >OphauB2|2855
ATGGATTCAGCCTTGTCCTCGAGAACGGCTCAACAGGAAGCATCCTTGTCTGACCCCCCCTCGACTCGTCCGAAC
CCATTCGTCGATGACGGCGATATTTGCTCTCGCAAGCGGCGCCGCACATCGCTGTCCGCTTCGCCCGACGTCTCC
CTCCATCATAGCGTGCACTCGGTACATGGGCCCCAAGCTCCTGACATGCACGCCATCAAGGTCGACGGTGCCCCT
GACGCCCTAGAGACTTTGGATCAGCATCCCACTACGCCCGGCGAGCCTTCATCAAATAGCATGACCATCAGCTTG
CGAAGGCGTGCCCATGGCGAATCGCCCTTGGCATCCCTTCACTCTACAGCCGAGCGCCTCTCCGACGTCGAGGCC
AACTCCGCGAGGCATGCTGCTGATGTCTTGGATGAGAATGTCGACGAAGCTCTTGCAGCAGCGTCTTCGAAGCGT
TCCTCTTCATCCACTGGAAGCCCCCCCGTCGAGCTCATTGCCGTAAGCGATGACGGCTCGGATGATAGACAAGGC
GATACCATTTGTGTTGAAAACAGCATGGATCTTTCTGCCTCGGGTGCCTCTACTTGTCCCAATATTCTCATTGCC
GACCCGACGACTCAATTCCCATGGAGAAACCCGAATGAAAGTATAAGCGATACAGTTCAACGTTTGATACAATAT
CTCTCAAATACCGACCCCGTTGACGCCGATATTCTCTACGACCTCATCAAATGGCTTGAAAGCTACCTTGAGTTC
GCCAAGAATACAGACCCAGGTCAAGTTTTGTCTTCTAGAAACTCACATATGCACTTCTGGCTGTCATTTCCCGAT
GCAATGTGTTCTCTTACTACAAAGAGGTCTGAAATCATCAAGGCACCAGTCATTCGCAACGCACTCCTGGCAGTC
TACTCTCAGTATACTGTCTTGACGGCTCTATTCATTTCTCTCGATTGCTTAGCCTGTCGCGATGCCCGCTCCGCC
TTCGCTGCGACGGGGGATCGACGCCACCCAGAAATACTTGCTCCCATTTACCTTCAGCAGCTTGTTAATGCCCTT
GGGCCTCTGGGCCTTTCACACCAAGGCTCAAACGATTCAGTTGCTGGTACCAATTTGAATCACTTTGATCTTGAT
CTTCGTTTGGTGACCAAATTTTTGGAGAGCCCTGGAGGCAGCCTCGAATGCCTGTCTGAGTTTGCTCAGGAATTG
CAACATGTCATGGCGCAAGTCCCAAGATTAACAGACAGTCTTGCTCCCTTGAGCCAGACACTGGCTGCCTGTGTG
CGACAGTCGCTTCAACAATTTCGTGCGGGGCAGCAAGGCTTCTCGGATGCGAGACGAAGACTGGAGCTGGGACTC
GAGGCCTGGAGTACCATTTCTAGCACCCTCATCACTATTATCGACAAACACGTTACCTGTTTGAGTAGCGAATGT
GCCAATATTTCTATTCAAGCCTTATCCGAAGTCTTGAAGTGCTCACTTCAGGGCGGACATGTTGCAGCAGCAGAT
GCTCTGGCGGACCATCGCAACAAATATCCGTCTGTGGCTCCTCAAGACACACACGAGGCCATTGCTTGGCAATGG
AAGTTTGATGTGCTGGAAAAACTTATTCGCTCTAGCCAGATGACGCTTCGTGTCATGGCTGTGACAACAATGTGC
AATAATTTGGTCAGCATCTGGAGAAGACATTGCGACGGCAGCGACGAATATGGCAGCGACTTCTTTGGTCACCTG
GCCAACTACTTGTTGCAGACAGGACTCATTGACTACATCCTTGGCGCGAATTGTCACCCAGAGATTATCCTTGAG
AGCGCCAACATTATCGGCTTCCTGGTAGTAACCCGCTTCTACGTCCAGGATCACACTGAACAGATTTGGCGGGGC
ATCATCTCTAGTCAGGATCCTCGAGTGTCGGATGCCTTGGCACGCATGATAGCTAGCATCACCAATCTGTTCGAT
TATAATGGCTTGTTGCAAATTTGCAACAGACTCAAGCAATTGCCTCTGGATCGCTTCTCTCCCTCGATTCGCCAC
CTCTTGGACAACGTTTTGAGAGAAATGATTGCCAGGTCTAAATCGGAGCAGCCAACACTCACATTTCACCCCTAT
GGACTTTGTCTTCGCTTGCTAAGGGAGTCATCCGTCTTTGCCTCCAGCTCTCAAGTCGCAGACCCTGAAATGCAG
CAATTCGCCATGCAGAAATTCAGAGAACTTCTTGGACATGGGCCCGATTCTGAAGGGCGCCGTGAACTTTACCTG
AGCTGCCTGAGCGACCTCTCTGCGAAGTCGCCCACAAGCCTTGGGAGTCTGTGGGCCCTTTCTATGGCTACACGT
CACACTCTGGTTGGCCAAATGCAGATACTTACGGAGCAGCATGATCTTGCAAGACTTATTGTTGAGGAAATTGAG
CACGCTGGCAATGCTGGGCGCGCAGCTGGCGCCTTTCCAGTACTGTTTGGTACCTGCAATCAGCCACGAAGAGAC
TTCGTGACTAGTCTGATTGAGCTCCAGCCGACTGCAATTGATGGGTCTTTGGGGTTCAAGCTGTGGAATCTTCTT
GTTGGTTCGCTATCTGCTTGCCCGGACGACCGAAGAGCGGGATGGTACATCATCTTGAGTACATCAAGAAAGACG
GCATTGCAAAATAAGTTTTTGCAAACCTGCTTTTCAGACTACCTGCCGAAGCTCGCGCCAGTCTACTTTTGTGAA
GGAATGCTTGATTTTGTTAAGGAGCATCTTCATCCCTTGCTCACTGATAGAAACGGGTTACTTGACTTCGACGAT
GAGACTGTTGCCTCGCGCAGCGGTATTGAGCAGCTCTGGAGAATTATACTACAGGCTGAAGATGAGGAACTGGTG
AAGCATGCTATTTCTACACTTGCTGTTGAAGTCTATCTCGAAAGCAGGGCCATTACTTCATGTGCACTTCATCGG
ACGAGACAGCTGCACCTTGCATTTGTGGCACGGTGTTTGAGTCAGATGAAAGAGGCTGCGACCAAACTCAAGCGA
TCAAACGAGGGAACCACACGTGAAGATGACGAGTCCATGATTATCGTCACTACGGATGAGGAAAACAAGGAGTTG
CAACGAACCATGACTCGGTCCCTTCGGCTTCTTAGGTTTTTCCTTGAGCGATATCAGTCAAAGCCCAGGTTTGCG
GTAGCGGATCTGAGGTCTTTCATGTCAGAAAAGCCTCAGAGGATCGATGGCGACTCTGCTCAGCTGAGGTATCAG
TCCTTCAATGGTGACAAACAAAGCGACATATTGCTCTTGGACATTGGCAGGCTAAATACCGTGTCATCTCTGTTG
GCCAGCTTTAGAGACAAGACGGGATTCGACAATTATCGGGTATTTTACCGTGGCCGACAACTGCTTCTGTCAGAA
CAAGATACTTGCAAGTCTTTGCAAGAGCTTGGCATTCACGACGGTTTCATTCTAGTTAAGCGGGAAGAGAGCAAT
TCGTCCTTCCCCTCTAGAATTAAGCCTGGGTCGCTGCCACTTGAGATCGAGATATTGTCTCATTTCGCCGATTTC
TGGGACTATCTCAGTATGGACGACTGTTTGGCCGAAGAGATTTATAACTTTGTTGTGAAATTACCGGCCGATGGC
CACATACTGTCGCTCTTCGACACCGACGTGACTTCGTACACAGACCTCTTCCTTTCAGGACAACCATTTAAGTCA
CTGTACGCCATTCACGCGCTTAAAGAATATGTCGAGAGCGCCTCTAGAGCACAAGCTGTGGGGACTGATTTTGAA
AGCAATGGCTGCTACACTTCGCGTGACGAGGCCATGAAGAGGTCACTGCGTCTAGTTGTTCAAGCTCTTTCTGAC
CCAGATGTCCTACAAGGCAGCAGCGCGAGACTGCAGATACGCCTTGCAAGCTCTCTCATGCAAGAATTTGTGAGG
CTGATCAAAGCTTTGTACCGCTCTGTGTCTTTTGCAGCTTGCAATACTGTTGAGGCACCGTCGCCCAAGCGCCTG
ATGGAAGTCCTTTTCGATGCCCTAGAGTATCAGGAACAAGAGGCGCTGCCGTTGATTGCCAGCACATGCAGTGCC
ATTCTCAAGATCGGGCAGCTGGATGACCATTTTTGGAAGGAAATCACAACGGTGCCAAGTTTTGCTCAGCTGATT
CAGAGACTAGTGCTCTTTGATCCAAGGAGAGAGGTCCGCCTGGCTGCTGTTAAACTGATTGGAGATGCAGCAGAG
TTTGAAGCGCAGTCTCTGCAGGTTCCTCCGGATCCCGCCCCGAAGCGCAACGAGAGGACCTTTGGACTGGGGCAG
TTTCTTTGGCCCATAATAGTCGAACTGCTTCCCGAGACCGTGAGACTAACACAGCAGTGCGAGGAAGCTTTTGCT
TTGCTCCTCAAGCTCCTCTTGCTCATCTCAAACAAGATGCTATTGCAGATTCGGGTTGATTCGCTGGCAGCCCAG
ACAAGCAAGCTTCTGCTGGAGCACCACTCAAGCGAGCGGATTACGCACATTGAGCCGTATGACGCCGTGGTAGCT
GGCCTGACTTCGGTTTTACACGCTTGCTTGCAGATTGACTCTAGACTGCCTGCATCGGAAGTACTCCCCGATAAT
CTGGTACTTGGCCTGTTTATGCGACACCTTTTCCCACGAAAGCTCGAGCAGGGCGAACTGTGCGTTCCACAAGTC
GTTTTGAACATGGAGACTCGAACCAAGCTGTACGATATAGTCTTCGCTTTGATACGCCAGAATCACGTCCGCTGT
GGCCAGGTATTGGACTTACTCAATAGCCTGGTGCCTTTCTACGGTGAAGATGATGATCCATATAAATATGAGCTC
CCCTATCAGTTTGACCGATCAAAAGCGATGCGATCCTCATGTGGCTACGTCGGTCTACGGAACTTGTCGAATACC
TGCTACCTCAACTCGCTCCTCACACAGCTCTATATGAATGTCAAATTCCGCCGTTTCATCATGACGAGTGCTTGC
CCCGACACTGAGAATCCTCAAGGCTTGCTGTTTGAGACGCAGAAAATATTTGGTTTCATGCAGGAAAGCTATCGT
CGATTTGTAGACCCAACAAGTCTTGTATCGTCGGTCAAGACGTACGAAGATACCGTCATCGATATCCACAGTCAG
ATGGATGTAGATGAGTTTTACAGCTTGCTATTTGACAGATGGGAAGGACAGTTGCTGCGTCCAGAGGATAAACGG
CGTCTTCGATCGTTTTACGGAGGACAATTGGTTCAGCAGGTCAAGTCCAAGGAGTGCGAACACATTTCGGAACGC
CTGGAACCATTTTCGGCCATTCAATGCGATATTAAGGGGAAGAGCTCATTGGAGGAAAGCCTACAAGCATATGTT
GACGGCGAGATAATGGAAGGCGACAACAAGTACAAATGCTCTTCATGCGATCGGCATGTTGATGCCGTCAAGAGA
GCATGCCTCAAGGACGTGCCAGACAATGTAATCTTCCACTTGAAGCGCTTCGACTTCAACCTCCGTACCCTTCAG
CGCAGCAAAATCAATGATCACTTCACCTTTCCGCAAAAGTTGAATATGCGACCGTACACCATCGAGCACCTCAGT
GAGGCAAGCACGGATGCATCAGAGGACGAATTCGAGCTGGTTGGAATCCTAGTCCACGCGGGAACGGCAGAGTCG
GGCCACTACTATTCATATATCAAAGAGCGGCCGTTGTCCGGAGGCAAAAACAGCTGGGTGGAATTCAATGACGAT
GTTGTCAGTGCTTGGGACCCGTCCCTGATGGCGAGTTCTACCTTTGGCGGCCCAGAAACCCGCCCGTTGTACGAG
ACGAATGGTGTGGCATACGACAAGAGCTATAGTGCCTACATGCTATTTTACCAGCGGGCCTCGTCGTTGCGGGCC
GAGCAGCAGGCAATGGCTGCACAGCAGATTGATTCGCCTCTGCTTGTTGAGGCATCCATGGCCTTGCGAGAGCAC
ATTGCTAGCGAAAATACGGTTCTGCTCAGGCGGCACTGCCTCTATGACCCTAACCACGTTGGGTTCGTCGAAAAC
TGCTTCAGTCTGGCCAAGACTTTGGACGAAAGCGAGGTGGATGGCATTGTAAGCTTGAGGCCAAGGGAAAGCCAA
GAGAGACAAAGACTGCAAGCAGGTGGTCACAGGCTGAGAAATGTGGCCATGGAGATGGCTGTCTCGCATTTGGAC
CAAGTCGTCTCACGAGCCTGCAACACGCCCTCGTTGGTTTCATTTTCAAGCATGCTACGGGCTGCCATAATCAAC
TGTGCACAGTGCGCGCTGGCGTTTTACAACTATTTCAGTCGGCGCCACAAAGCTCTCCGGGCTTTACTTCAGAGG
AGCCCAGAGCAGCATGTGCGGTGCTTTGTAGGCGAGGTACTTGTTTGTGCCGCTGAAAGGATTGCTACGCATTTC
CCTCGCCTATACGACAGTGGTGGCGATGATGTCGAGTCGGGTGACAACTTGTCCGACGTGGGGGGTAGATCGGTG
GCTGAAGGCATGGTGGACATGCTGAATCACCTTTGGCAGTTTTTTCAAGTTCATCTACGCTCATGGGAAGAATAT
TTCGGCACCGTCTTGGCCTTTGCCCGTCTGGGAGATCGCGAGACGAGCCTCCTCTTGTCCAACGACTACCTTGTC
AAAGTGCTCAACATTGTCACTGCTGACGTGTCTACGGACCTGCCGGCCAACTATGCGCGTATGCTGGCCAATGTG
TTGCGGCGAATGAGCACGCGACCGCCTTCGTATTGCGCCATTTTGGTCCTGATGGATTACCTGCTGGGACAGCTG
GAGCCGACGCTCTCTCCGCAAAGTATAACAGACCATGCTACAGATCGTTTGAGGGGTGAGGCACCGTTTTTGTGG
ACTTCTGAAGAGATTCAGATTGTACACCACTCGTCTTCTGACCGCCAGCCCTTGAGCTTCTTTGTGGAAAAGCTG
GTGGCGATTGATCAGGCTTGGGCTGCCACGAGCAACATTGTGGCTCGCTTGGTCTTGACTGGCCTGCAGATGGAT
CTGAGGGTATTCAATGCACTGCGCAAAAACATGAATGGAGAGATGTCGGCACAAGCCATGGACCCATTTTTGCGA
GTGGCGGCTCGGTACATGGAGACGACAAGGTCGACGGAATACGCAAACGCGCTGGTGCGCCACGTCTGTGGCCAG
GCTCGCAACATGCAGAACACGGAGGGACCTGTGTTTATGATGCTTGTCAATGTCATGCTTCGGTCCGAAATGCCT
CGGCTGGACCTTGCGCGCTCGCGACGAGAGTGTTGCATCAAGCAGACGCCCGTGTGGGGTCCATATATGCTGGTG
TTTCCAAACAGCAATGTGAGGCGCGAAGCCGAGTGTCTGATTGAGCATGTGCTTTTTGCCGCCGACTCGCCCAAA
GATGAGGCAAGCACGGGGCACAGCCACGAGATGAAGGACTGTCTGGACGAGGTTGCATACGATTTGGGAGTGCGA
TGCCTTGTCTACTTGCGGGATATGCACGTCAAGCGAAGAGTCAGGATAGAACGCGACGCTGCTTTGAGCATCCTC
AGCGTGGTGGGCAAGTGCGTGGCTCGCTGTGATGCTCTCAAGGATATGGACGATGGCGAAGATGACGACCTTGGA
CTGTTGCAGAAAGAGGTGGTGGAGCCGCTACGCCGGCTCATGGTGGACGAGGTGGAGGACGATGTGTCTGACTGG
GATGGATCGTGCGGTTCATCAGAGCCCATGGACGCAAGCCTGGGAATACCGCTGCAGACGATGAGCGAGGCCAAT
GACATAGACTTGATGTGA
Transcript >OphauB2|2855
ATGGATTCAGCCTTGTCCTCGAGAACGGCTCAACAGGAAGCATCCTTGTCTGACCCCCCCTCGACTCGTCCGAAC
CCATTCGTCGATGACGGCGATATTTGCTCTCGCAAGCGGCGCCGCACATCGCTGTCCGCTTCGCCCGACGTCTCC
CTCCATCATAGCGTGCACTCGGTACATGGGCCCCAAGCTCCTGACATGCACGCCATCAAGGTCGACGGTGCCCCT
GACGCCCTAGAGACTTTGGATCAGCATCCCACTACGCCCGGCGAGCCTTCATCAAATAGCATGACCATCAGCTTG
CGAAGGCGTGCCCATGGCGAATCGCCCTTGGCATCCCTTCACTCTACAGCCGAGCGCCTCTCCGACGTCGAGGCC
AACTCCGCGAGGCATGCTGCTGATGTCTTGGATGAGAATGTCGACGAAGCTCTTGCAGCAGCGTCTTCGAAGCGT
TCCTCTTCATCCACTGGAAGCCCCCCCGTCGAGCTCATTGCCGTAAGCGATGACGGCTCGGATGATAGACAAGGC
GATACCATTTGTGTTGAAAACAGCATGGATCTTTCTGCCTCGGGTGCCTCTACTTGTCCCAATATTCTCATTGCC
GACCCGACGACTCAATTCCCATGGAGAAACCCGAATGAAAGTATAAGCGATACAGTTCAACGTTTGATACAATAT
CTCTCAAATACCGACCCCGTTGACGCCGATATTCTCTACGACCTCATCAAATGGCTTGAAAGCTACCTTGAGTTC
GCCAAGAATACAGACCCAGGTCAAGTTTTGTCTTCTAGAAACTCACATATGCACTTCTGGCTGTCATTTCCCGAT
GCAATGTGTTCTCTTACTACAAAGAGGTCTGAAATCATCAAGGCACCAGTCATTCGCAACGCACTCCTGGCAGTC
TACTCTCAGTATACTGTCTTGACGGCTCTATTCATTTCTCTCGATTGCTTAGCCTGTCGCGATGCCCGCTCCGCC
TTCGCTGCGACGGGGGATCGACGCCACCCAGAAATACTTGCTCCCATTTACCTTCAGCAGCTTGTTAATGCCCTT
GGGCCTCTGGGCCTTTCACACCAAGGCTCAAACGATTCAGTTGCTGGTACCAATTTGAATCACTTTGATCTTGAT
CTTCGTTTGGTGACCAAATTTTTGGAGAGCCCTGGAGGCAGCCTCGAATGCCTGTCTGAGTTTGCTCAGGAATTG
CAACATGTCATGGCGCAAGTCCCAAGATTAACAGACAGTCTTGCTCCCTTGAGCCAGACACTGGCTGCCTGTGTG
CGACAGTCGCTTCAACAATTTCGTGCGGGGCAGCAAGGCTTCTCGGATGCGAGACGAAGACTGGAGCTGGGACTC
GAGGCCTGGAGTACCATTTCTAGCACCCTCATCACTATTATCGACAAACACGTTACCTGTTTGAGTAGCGAATGT
GCCAATATTTCTATTCAAGCCTTATCCGAAGTCTTGAAGTGCTCACTTCAGGGCGGACATGTTGCAGCAGCAGAT
GCTCTGGCGGACCATCGCAACAAATATCCGTCTGTGGCTCCTCAAGACACACACGAGGCCATTGCTTGGCAATGG
AAGTTTGATGTGCTGGAAAAACTTATTCGCTCTAGCCAGATGACGCTTCGTGTCATGGCTGTGACAACAATGTGC
AATAATTTGGTCAGCATCTGGAGAAGACATTGCGACGGCAGCGACGAATATGGCAGCGACTTCTTTGGTCACCTG
GCCAACTACTTGTTGCAGACAGGACTCATTGACTACATCCTTGGCGCGAATTGTCACCCAGAGATTATCCTTGAG
AGCGCCAACATTATCGGCTTCCTGGTAGTAACCCGCTTCTACGTCCAGGATCACACTGAACAGATTTGGCGGGGC
ATCATCTCTAGTCAGGATCCTCGAGTGTCGGATGCCTTGGCACGCATGATAGCTAGCATCACCAATCTGTTCGAT
TATAATGGCTTGTTGCAAATTTGCAACAGACTCAAGCAATTGCCTCTGGATCGCTTCTCTCCCTCGATTCGCCAC
CTCTTGGACAACGTTTTGAGAGAAATGATTGCCAGGTCTAAATCGGAGCAGCCAACACTCACATTTCACCCCTAT
GGACTTTGTCTTCGCTTGCTAAGGGAGTCATCCGTCTTTGCCTCCAGCTCTCAAGTCGCAGACCCTGAAATGCAG
CAATTCGCCATGCAGAAATTCAGAGAACTTCTTGGACATGGGCCCGATTCTGAAGGGCGCCGTGAACTTTACCTG
AGCTGCCTGAGCGACCTCTCTGCGAAGTCGCCCACAAGCCTTGGGAGTCTGTGGGCCCTTTCTATGGCTACACGT
CACACTCTGGTTGGCCAAATGCAGATACTTACGGAGCAGCATGATCTTGCAAGACTTATTGTTGAGGAAATTGAG
CACGCTGGCAATGCTGGGCGCGCAGCTGGCGCCTTTCCAGTACTGTTTGGTACCTGCAATCAGCCACGAAGAGAC
TTCGTGACTAGTCTGATTGAGCTCCAGCCGACTGCAATTGATGGGTCTTTGGGGTTCAAGCTGTGGAATCTTCTT
GTTGGTTCGCTATCTGCTTGCCCGGACGACCGAAGAGCGGGATGGTACATCATCTTGAGTACATCAAGAAAGACG
GCATTGCAAAATAAGTTTTTGCAAACCTGCTTTTCAGACTACCTGCCGAAGCTCGCGCCAGTCTACTTTTGTGAA
GGAATGCTTGATTTTGTTAAGGAGCATCTTCATCCCTTGCTCACTGATAGAAACGGGTTACTTGACTTCGACGAT
GAGACTGTTGCCTCGCGCAGCGGTATTGAGCAGCTCTGGAGAATTATACTACAGGCTGAAGATGAGGAACTGGTG
AAGCATGCTATTTCTACACTTGCTGTTGAAGTCTATCTCGAAAGCAGGGCCATTACTTCATGTGCACTTCATCGG
ACGAGACAGCTGCACCTTGCATTTGTGGCACGGTGTTTGAGTCAGATGAAAGAGGCTGCGACCAAACTCAAGCGA
TCAAACGAGGGAACCACACGTGAAGATGACGAGTCCATGATTATCGTCACTACGGATGAGGAAAACAAGGAGTTG
CAACGAACCATGACTCGGTCCCTTCGGCTTCTTAGGTTTTTCCTTGAGCGATATCAGTCAAAGCCCAGGTTTGCG
GTAGCGGATCTGAGGTCTTTCATGTCAGAAAAGCCTCAGAGGATCGATGGCGACTCTGCTCAGCTGAGGTATCAG
TCCTTCAATGGTGACAAACAAAGCGACATATTGCTCTTGGACATTGGCAGGCTAAATACCGTGTCATCTCTGTTG
GCCAGCTTTAGAGACAAGACGGGATTCGACAATTATCGGGTATTTTACCGTGGCCGACAACTGCTTCTGTCAGAA
CAAGATACTTGCAAGTCTTTGCAAGAGCTTGGCATTCACGACGGTTTCATTCTAGTTAAGCGGGAAGAGAGCAAT
TCGTCCTTCCCCTCTAGAATTAAGCCTGGGTCGCTGCCACTTGAGATCGAGATATTGTCTCATTTCGCCGATTTC
TGGGACTATCTCAGTATGGACGACTGTTTGGCCGAAGAGATTTATAACTTTGTTGTGAAATTACCGGCCGATGGC
CACATACTGTCGCTCTTCGACACCGACGTGACTTCGTACACAGACCTCTTCCTTTCAGGACAACCATTTAAGTCA
CTGTACGCCATTCACGCGCTTAAAGAATATGTCGAGAGCGCCTCTAGAGCACAAGCTGTGGGGACTGATTTTGAA
AGCAATGGCTGCTACACTTCGCGTGACGAGGCCATGAAGAGGTCACTGCGTCTAGTTGTTCAAGCTCTTTCTGAC
CCAGATGTCCTACAAGGCAGCAGCGCGAGACTGCAGATACGCCTTGCAAGCTCTCTCATGCAAGAATTTGTGAGG
CTGATCAAAGCTTTGTACCGCTCTGTGTCTTTTGCAGCTTGCAATACTGTTGAGGCACCGTCGCCCAAGCGCCTG
ATGGAAGTCCTTTTCGATGCCCTAGAGTATCAGGAACAAGAGGCGCTGCCGTTGATTGCCAGCACATGCAGTGCC
ATTCTCAAGATCGGGCAGCTGGATGACCATTTTTGGAAGGAAATCACAACGGTGCCAAGTTTTGCTCAGCTGATT
CAGAGACTAGTGCTCTTTGATCCAAGGAGAGAGGTCCGCCTGGCTGCTGTTAAACTGATTGGAGATGCAGCAGAG
TTTGAAGCGCAGTCTCTGCAGGTTCCTCCGGATCCCGCCCCGAAGCGCAACGAGAGGACCTTTGGACTGGGGCAG
TTTCTTTGGCCCATAATAGTCGAACTGCTTCCCGAGACCGTGAGACTAACACAGCAGTGCGAGGAAGCTTTTGCT
TTGCTCCTCAAGCTCCTCTTGCTCATCTCAAACAAGATGCTATTGCAGATTCGGGTTGATTCGCTGGCAGCCCAG
ACAAGCAAGCTTCTGCTGGAGCACCACTCAAGCGAGCGGATTACGCACATTGAGCCGTATGACGCCGTGGTAGCT
GGCCTGACTTCGGTTTTACACGCTTGCTTGCAGATTGACTCTAGACTGCCTGCATCGGAAGTACTCCCCGATAAT
CTGGTACTTGGCCTGTTTATGCGACACCTTTTCCCACGAAAGCTCGAGCAGGGCGAACTGTGCGTTCCACAAGTC
GTTTTGAACATGGAGACTCGAACCAAGCTGTACGATATAGTCTTCGCTTTGATACGCCAGAATCACGTCCGCTGT
GGCCAGGTATTGGACTTACTCAATAGCCTGGTGCCTTTCTACGGTGAAGATGATGATCCATATAAATATGAGCTC
CCCTATCAGTTTGACCGATCAAAAGCGATGCGATCCTCATGTGGCTACGTCGGTCTACGGAACTTGTCGAATACC
TGCTACCTCAACTCGCTCCTCACACAGCTCTATATGAATGTCAAATTCCGCCGTTTCATCATGACGAGTGCTTGC
CCCGACACTGAGAATCCTCAAGGCTTGCTGTTTGAGACGCAGAAAATATTTGGTTTCATGCAGGAAAGCTATCGT
CGATTTGTAGACCCAACAAGTCTTGTATCGTCGGTCAAGACGTACGAAGATACCGTCATCGATATCCACAGTCAG
ATGGATGTAGATGAGTTTTACAGCTTGCTATTTGACAGATGGGAAGGACAGTTGCTGCGTCCAGAGGATAAACGG
CGTCTTCGATCGTTTTACGGAGGACAATTGGTTCAGCAGGTCAAGTCCAAGGAGTGCGAACACATTTCGGAACGC
CTGGAACCATTTTCGGCCATTCAATGCGATATTAAGGGGAAGAGCTCATTGGAGGAAAGCCTACAAGCATATGTT
GACGGCGAGATAATGGAAGGCGACAACAAGTACAAATGCTCTTCATGCGATCGGCATGTTGATGCCGTCAAGAGA
GCATGCCTCAAGGACGTGCCAGACAATGTAATCTTCCACTTGAAGCGCTTCGACTTCAACCTCCGTACCCTTCAG
CGCAGCAAAATCAATGATCACTTCACCTTTCCGCAAAAGTTGAATATGCGACCGTACACCATCGAGCACCTCAGT
GAGGCAAGCACGGATGCATCAGAGGACGAATTCGAGCTGGTTGGAATCCTAGTCCACGCGGGAACGGCAGAGTCG
GGCCACTACTATTCATATATCAAAGAGCGGCCGTTGTCCGGAGGCAAAAACAGCTGGGTGGAATTCAATGACGAT
GTTGTCAGTGCTTGGGACCCGTCCCTGATGGCGAGTTCTACCTTTGGCGGCCCAGAAACCCGCCCGTTGTACGAG
ACGAATGGTGTGGCATACGACAAGAGCTATAGTGCCTACATGCTATTTTACCAGCGGGCCTCGTCGTTGCGGGCC
GAGCAGCAGGCAATGGCTGCACAGCAGATTGATTCGCCTCTGCTTGTTGAGGCATCCATGGCCTTGCGAGAGCAC
ATTGCTAGCGAAAATACGGTTCTGCTCAGGCGGCACTGCCTCTATGACCCTAACCACGTTGGGTTCGTCGAAAAC
TGCTTCAGTCTGGCCAAGACTTTGGACGAAAGCGAGGTGGATGGCATTGTAAGCTTGAGGCCAAGGGAAAGCCAA
GAGAGACAAAGACTGCAAGCAGGTGGTCACAGGCTGAGAAATGTGGCCATGGAGATGGCTGTCTCGCATTTGGAC
CAAGTCGTCTCACGAGCCTGCAACACGCCCTCGTTGGTTTCATTTTCAAGCATGCTACGGGCTGCCATAATCAAC
TGTGCACAGTGCGCGCTGGCGTTTTACAACTATTTCAGTCGGCGCCACAAAGCTCTCCGGGCTTTACTTCAGAGG
AGCCCAGAGCAGCATGTGCGGTGCTTTGTAGGCGAGGTACTTGTTTGTGCCGCTGAAAGGATTGCTACGCATTTC
CCTCGCCTATACGACAGTGGTGGCGATGATGTCGAGTCGGGTGACAACTTGTCCGACGTGGGGGGTAGATCGGTG
GCTGAAGGCATGGTGGACATGCTGAATCACCTTTGGCAGTTTTTTCAAGTTCATCTACGCTCATGGGAAGAATAT
TTCGGCACCGTCTTGGCCTTTGCCCGTCTGGGAGATCGCGAGACGAGCCTCCTCTTGTCCAACGACTACCTTGTC
AAAGTGCTCAACATTGTCACTGCTGACGTGTCTACGGACCTGCCGGCCAACTATGCGCGTATGCTGGCCAATGTG
TTGCGGCGAATGAGCACGCGACCGCCTTCGTATTGCGCCATTTTGGTCCTGATGGATTACCTGCTGGGACAGCTG
GAGCCGACGCTCTCTCCGCAAAGTATAACAGACCATGCTACAGATCGTTTGAGGGGTGAGGCACCGTTTTTGTGG
ACTTCTGAAGAGATTCAGATTGTACACCACTCGTCTTCTGACCGCCAGCCCTTGAGCTTCTTTGTGGAAAAGCTG
GTGGCGATTGATCAGGCTTGGGCTGCCACGAGCAACATTGTGGCTCGCTTGGTCTTGACTGGCCTGCAGATGGAT
CTGAGGGTATTCAATGCACTGCGCAAAAACATGAATGGAGAGATGTCGGCACAAGCCATGGACCCATTTTTGCGA
GTGGCGGCTCGGTACATGGAGACGACAAGGTCGACGGAATACGCAAACGCGCTGGTGCGCCACGTCTGTGGCCAG
GCTCGCAACATGCAGAACACGGAGGGACCTGTGTTTATGATGCTTGTCAATGTCATGCTTCGGTCCGAAATGCCT
CGGCTGGACCTTGCGCGCTCGCGACGAGAGTGTTGCATCAAGCAGACGCCCGTGTGGGGTCCATATATGCTGGTG
TTTCCAAACAGCAATGTGAGGCGCGAAGCCGAGTGTCTGATTGAGCATGTGCTTTTTGCCGCCGACTCGCCCAAA
GATGAGGCAAGCACGGGGCACAGCCACGAGATGAAGGACTGTCTGGACGAGGTTGCATACGATTTGGGAGTGCGA
TGCCTTGTCTACTTGCGGGATATGCACGTCAAGCGAAGAGTCAGGATAGAACGCGACGCTGCTTTGAGCATCCTC
AGCGTGGTGGGCAAGTGCGTGGCTCGCTGTGATGCTCTCAAGGATATGGACGATGGCGAAGATGACGACCTTGGA
CTGTTGCAGAAAGAGGTGGTGGAGCCGCTACGCCGGCTCATGGTGGACGAGGTGGAGGACGATGTGTCTGACTGG
GATGGATCGTGCGGTTCATCAGAGCCCATGGACGCAAGCCTGGGAATACCGCTGCAGACGATGAGCGAGGCCAAT
GACATAGACTTGATGTGA
Gene >OphauB2|2855
ATGGATTCAGCCTTGTCCTCGAGAACGGCTCAACAGGAAGCATCCTTGTCTGACCCCCCCTCGACTCGTCCGAAC
CCATTCGTCGATGACGGCGATATTTGCTCTCGCAAGCGGCGCCGCACATCGCTGTCCGCTTCGCCCGACGTCTCC
CTCCATCATAGCGTGCACTCGGTACATGGGCCCCAAGCTCCTGACATGCACGCCATCAAGGTCGACGGTGCCCCT
GACGCCCTAGAGACTTTGGATCAGCATCCCACTACGCCCGGCGAGCCTTCATCAAATAGCATGACCATCAGCTTG
CGAAGGCGTGCCCATGGCGAATCGCCCTTGGCATCCCTTCACTCTACAGCCGAGCGCCTCTCCGACGTCGAGGCC
AACTCCGCGAGGCATGCTGCTGATGTCTTGGATGAGAATGTCGACGAAGCTCTTGCAGCAGCGTCTTCGAAGCGT
TCCTCTTCATCCACTGGAAGCCCCCCCGTCGAGCTCATTGCCGTAAGCGATGACGGCTCGGATGATAGACAAGGC
GATACCATTTGTGTTGAAAACAGCATGGATCTTTCTGCCTCGGGTGCCTCTACTTGTCCCAATATTCTCATTGCC
GACCCGACGACTCAATTCCCATGGAGAAACCCGAATGAAAGTATAAGCGATACAGTTCAACGTTTGATACAATAT
CTCTCAAATAGTAAGCTTTGCTATTGCCTGTCAACGTCTCCACATTGCTGATTGGCTCCAGCCGACCCCGTTGAC
GCCGATATTCTCTACGACCTCATCAAATGGCTTGAAAGCTACCTTGAGTTCGCCAAGAATACAGACCCAGGTCAA
GTTTTGTCTTCTAGAAACTCACATATGCACTTCTGGCTGTCATTTCCCGATGCAATGTGTTCTCTTACTACAAAG
AGGCAAGTTGAAGATTTCTAATTGCCCTTGAATATATTATCCTGACAAGTCCTAGGTCTGAAATCATCAAGGCAC
CAGTCATTCGCAACGCACTCCTGGCAGTCTACTCTCAGTATACTGTCTTGACGGCTCTATTCATTTCTCTCGATT
GCTTAGCCTGTCGCGATGCCCGCTCCGCCTTCGCTGCGACGGGGGATCGACGCCACCCAGAAATACTTGCTCCCA
TTTACCTTCAGCAGCTTGTTAATGCCCTTGGGCCTCTGGGCCTTTCACACCAAGGCTCAAACGATTCAGTTGCTG
GTACCAATTTGAATCACTTTGATCTTGATCTTCGTTTGGTGACCAAATTTTTGGAGAGCCCTGGAGGCAGCCTCG
AATGCCTGTCTGAGTTTGCTCAGGAATTGCAACATGTCATGGCGCAAGTCCCAAGATTAACAGACAGTCTTGCTC
CCTTGAGCCAGACACTGGCTGCCTGTGTGCGACAGTCGCTTCAACAATTTCGTGCGGGGCAGCAAGGCTTCTCGG
ATGCGAGACGAAGACTGGAGCTGGGACTCGAGGCCTGGAGTACCATTTCTAGCACCCTCATCACTATTATCGACA
AACACGTTACCTGTTTGAGTAGCGAATGTGCCAATATTTCTATTCAAGCCTTATCCGAAGTCTTGAAGTGCTCAC
TTCAGGGCGGACATGTTGCAGCAGCAGATGCTCTGGCGGACCATCGCAACAAATATCCGTCTGTGGCTCCTCAAG
ACACACACGAGGCCATTGCTTGGCAATGGAAGTTTGATGTGCTGGAAAAACTTATTCGCTCTAGCCAGATGACGC
TTCGTGTCATGGCTGTGACAACAATGTGCAATAATTTGGTCAGCATCTGGAGAAGACATTGCGACGGCAGCGACG
AATATGGCAGCGACTTCTTTGGTCACCTGGCCAACTACTTGTTGCAGACAGGACTCATTGACTACATCCTTGGCG
CGAATTGTCACCCAGAGATTATCCTTGAGAGCGCCAACATTATCGGCTTCCTGGTAGTAACCCGCTTCTACGTCC
AGGATCACACTGAACAGATTTGGCGGGGCATCATCTCTAGTCAGGATCCTCGAGTGTCGGATGCCTTGGCACGCA
TGATAGCTAGCATCACCAATCTGTTCGATTATAATGGCTTGTTGCAAATTTGCAACAGACTCAAGCAATTGCCTC
TGGATCGCTTCTCTCCCTCGATTCGCCACCTCTTGGACAACGTTTTGAGAGAAATGATTGCCAGGTCTAAATCGG
AGCAGCCAACACTCACATTTCACCCCTATGGACTTTGTCTTCGCTTGCTAAGGGAGTCATCCGTCTTTGCCTCCA
GCTCTCAAGTCGCAGACCCTGAAATGCAGCAATTCGCCATGCAGAAATTCAGAGAACTTCTTGGACATGGGCCCG
ATTCTGAAGGGCGCCGTGAACTTTACCTGAGCTGCCTGAGCGACCTCTCTGCGAAGTCGCCCACAAGCCTTGGGA
GTCTGTGGGCCCTTTCTATGGCTACACGTCACACTCTGGTTGGCCAAATGCAGATACTTACGGAGCAGCATGATC
TTGCAAGACTTATTGTTGAGGAAATTGAGCACGCTGGCAATGCTGGGCGCGCAGCTGGCGCCTTTCCAGTACTGT
TTGGTACCTGCAATCAGCCACGAAGAGACTTCGTGACTAGTCTGATTGAGCTCCAGCCGACTGCAATTGATGGGT
CTTTGGGGTTCAAGCTGTGGAATCTTCTTGTTGGTTCGCTATCTGCTTGCCCGGACGACCGAAGAGCGGGATGGT
ACATCATCTTGAGTACATCAAGAAAGACGGCATTGCAAAATAAGTTTTTGCAAACCTGCTTTTCAGACTACCTGC
CGAAGCTCGCGCCAGTCTACTTTTGTGAAGGAATGCTTGATTTTGTTAAGGAGCATCTTCATCCCTTGCTCACTG
ATAGAAACGGGTTACTTGACTTCGACGATGAGACTGTTGCCTCGCGCAGCGGTATTGAGCAGCTCTGGAGAATTA
TACTACAGGCTGAAGATGAGGAACTGGTGAAGCATGCTATTTCTACACTTGCTGTTGAAGTCTATCTCGAAAGCA
GGGCCATTACTTCATGTGCACTTCATCGGACGAGACAGCTGCACCTTGCATTTGTGGCACGGTGTTTGAGTCAGA
TGAAAGAGGCTGCGACCAAACTCAAGCGATCAAACGAGGGAACCACACGTGAAGATGACGAGTCCATGATTATCG
TCACTACGGATGAGGAAAACAAGGAGTTGCAACGAACCATGACTCGGTCCCTTCGGCTTCTTAGGTTTTTCCTTG
AGCGATATCAGTCAAAGCCCAGGTTTGCGGTAGCGGATCTGAGGTCTTTCATGTCAGAAAAGCCTCAGAGGATCG
ATGGCGACTCTGCTCAGCTGAGGTATCAGTCCTTCAATGGTGACAAACAAAGCGACATATTGCTCTTGGACATTG
GCAGGCTAAATACCGTGTCATCTCTGTTGGCCAGCTTTAGAGACAAGACGGGATTCGACAATTATCGGGTATTTT
ACCGTGGCCGACAACTGCTTCTGTCAGAACAAGATACTTGCAAGTCTTTGCAAGAGCTTGGCATTCACGACGGTT
TCATTCTAGTTAAGCGGGAAGAGAGCAATTCGTCCTTCCCCTCTAGAATTAAGCCTGGGTCGCTGCCACTTGAGA
TCGAGATATTGTCTCATTTCGCCGATTTCTGGGACTATCTCAGTATGGACGACTGTTTGGCCGAAGAGATTTATA
ACTTTGTTGTGAAATTACCGGCCGATGGCCACATACTGTCGCTCTTCGACACCGACGTGACTTCGTACACAGACC
TCTTCCTTTCAGGACAACCATTTAAGTCACTGTACGCCATTCACGCGCTTAAAGAATATGTCGAGAGCGCCTCTA
GAGCACAAGCTGTGGGGACTGATTTTGAAAGCAATGGCTGCTACACTTCGCGTGACGAGGCCATGAAGAGGTCAC
TGCGTCTAGTTGTTCAAGCTCTTTCTGACCCAGATGTCCTACAAGGCAGCAGCGCGAGACTGCAGATACGCCTTG
CAAGCTCTCTCATGCAAGAATTTGTGAGGCTGATCAAAGGTACGCTGCACTACGTTGACGATGTCTCGCATTCAT
TTCTCCCTTGTATGATTAACGGCATGATTGCACAGCTTTGTACCGCTCTGTGTCTTTTGCAGCTTGCAATACTGT
TGAGGCACCGTCGCCCAAGCGCCTGATGGAAGTCCTTTTCGATGCCCTAGAGTATCAGGAACAAGAGGCGCTGCC
GTTGATTGCCAGCACATGCAGTGCCATTCTCAAGATCGGGCAGCTGGATGACCATTTTTGGAAGGAAATCACAAC
GGTGCCAAGTTTTGCTCAGCTGATTCAGAGACTAGTGCTCTTTGATCCAAGGAGAGAGGTCCGCCTGGCTGCTGT
TAAACTGATTGGAGATGCAGCAGAGTTTGAAGCGCAGTCTCTGCAGGTTCCTCCGGATCCCGCCCCGAAGCGCAA
CGAGAGGACCTTTGGACTGGGGCAGTTTCTTTGGCCCATAATAGTCGAACTGCTTCCCGAGACCGTGAGACTAAC
ACAGCAGTGCGAGGAAGCTTTTGCTTTGCTCCTCAAGCTCCTCTTGCTCATCTCAAACAAGATGCTATTGCAGAT
TCGGGTTGATTCGCTGGCAGCCCAGACAAGCAAGCTTCTGCTGGAGCACCACTCAAGCGAGGTAAGCTGCATTTC
GAATTGGGCGCCAGAAAGCATTTCTAACGGGAGCCGCACAGCGGATTACGCACATTGAGCCGTATGACGCCGTGG
TAGCTGGCCTGACTTCGGTTTTACACGCTTGCTTGCAGATTGACTCTAGACTGCCTGCATCGGAAGTACTCCCCG
AGTAAGGCAATTGAATCGCTTGTATCTGCTCGTAATGGGCTAACCTTGCTAGTAATCTGGTACTTGGCCTGTTTA
TGCGACACCTTTTCCCACGAAAGCTCGAGCAGGGCGAACTGTGCGTTCCACAAGTCGTTTTGAACATGGAGACTC
GAACCAAGCTGTACGATATAGTCTTCGCTTTGATACGCCAGAATCACGTCCGCTGTGGCCAGGTATTGGACTTAC
TCAATAGCCTGGTGCCTTTCTACGGTGAAGATGGTATGGATGCCAGTCAAGTTGAAACTGCATCTTGCTCACCAT
TGTTCTAGATGATCCATATAAATATGAGCTCCCCTATCAGTTTGACCGATCAAAAGCGATGCGATCCTCATGTGG
CTACGTCGGTCTACGGAACTTGTCGAATACCTGCTACCTCAACTCGCTCCTCACACAGCTCTATATGAATGTCAA
ATTCCGCCGTTTCATCATGACGAGTGCTTGCCCCGACACTGAGAATCCTCAAGGCTTGCTGTTTGAGACGCAGAA
AATATTTGGTTTCATGCAGGAAAGCTATCGTCGATTTGTAGACCCAACAAGTCTTGTATCGTCGGTCAAGACGTA
CGAAGATACCGTCATCGATATCCACAGTCAGATGGATGTAGATGAGTTTTACAGCTTGCTATTTGACAGATGGGA
AGGACAGTTGCTGCGTCCAGAGGATAAACGGCGTCTTCGATCGTTTTACGGAGGACAATTGGTTCAGCAGGTCAA
GTCCAAGGAGTGCGAACACATTTCGGAACGCCTGGAACCATTTTCGGCCATTCAATGCGATATTAAGGGGAAGAG
CTCATTGGAGGAAAGCCTACAAGCATATGTTGACGGCGAGATAATGGAAGGCGGTATGGCTAGCCAAGCGCTGCA
TATCTTGGAGCATTGGCTGACAATGGGATTTAGACAACAAGTACAAATGCTCTTCATGCGATCGGCATGTTGATG
CCGTCAAGAGGTACGAGGCTCTGAAGGCTGCTCGGCATGAGCTTCGCATTATCTCTAACCCTTTTCACAGAGCAT
GCCTCAAGGACGTGCCAGACAATGTAATCTTCCACTTGAAGCGCTTCGACTTCAACCTCCGTACCCTTCAGCGCA
GCAAAATCAATGATCACTTCACCTTTCCGCAAAAGTTGAATATGCGACCGTACACCATCGAGCACCTCAGTGAGG
CAAGCACGGATGCATCAGAGGACGAATTCGAGCTGGTTGGAATCCTAGTCCACGCGGGAACGGCAGAGTCGGGCC
ACTACTATTCATATATCAAAGAGCGGCCGTTGTCCGGAGGCAAAAACAGCTGGGTGGAATTCAATGACGATGTTG
TCAGTGCTTGGGACCCGTCCCTGATGGCGAGTTCTACCTTTGGCGGCCCAGAAACCCGCCCGTTGTACGAGACGA
ATGGTGTGGCATACGACAAGAGCTATAGTGCCTACATGCTATTTTACCAGCGGGCCTCGTCGTTGCGGGCCGAGC
AGCAGGCAATGGCTGCACAGCAGATTGATTCGCCTCTGCTTGTTGAGGCATCCATGGCCTTGCGAGAGCACATTG
CTAGCGAAAATACGGTTCTGCTCAGGCGGCACTGCCTCTATGACCCTAACCACGTTGGGTTCGTCGAAAACTGCT
TCAGTCTGGCCAAGACTTTGGACGAAAGCGAGGTGGATGGCATTGTAAGCTTGAGGCCAAGGGAAAGCCAAGAGA
GACAAAGACTGCAAGCAGGTGGTCACAGGCTGAGAAATGTGGCCATGGAGATGGCTGTCTCGCATTTGGACCAAG
TCGTCTCACGAGCCTGCAACACGCCCTCGTTGGTTTCATTTTCAAGCATGCTACGGGCTGCCATAATCAACTGTG
CACAGTGCGCGCTGGCGTTTTACAACTATTTCAGTCGGCGCCACAAAGCTCTCCGGGCTTTACTTCAGAGGAGCC
CAGAGCAGCATGTGCGGTGCTTTGTAGGCGAGGTACTTGTTTGTGCCGCTGAAAGGATTGCTACGCATTTCCCTC
GCCTATACGACAGTGGTGGCGATGATGTCGAGTCGGGTGACAACTTGTCCGACGTGGGGGGTAGATCGGTGGCTG
AAGGCATGGTGGACATGCTGAATCACCTTTGGCAGTTTTTTCAAGTTCATCTACGCTCATGGGAAGAATATTTCG
GCACCGTCTTGGCCTTTGCCCGTCTGGGAGATCGCGAGACGAGCCTCCTCTTGTCCAACGACTACCTTGTCAAAG
TGCTCAACATTGTCACTGCTGACGTGTCTACGGACCTGCCGGCCAACTATGCGCGTATGCTGGCCAATGTGTTGC
GGCGAATGAGCACGCGACCGCCTTCGTATTGCGCCATTTTGGTCCTGATGGATTACCTGCTGGGACAGCTGGAGC
CGACGCTCTCTCCGCAAAGTATAACAGACCATGCTACAGATCGTTTGAGGGGTGAGGCACCGTTTTTGTGGACTT
CTGAAGAGATTCAGATTGTACACCACTCGTCTTCTGACCGCCAGCCCTTGAGCTTCTTTGTGGAAAAGCTGGTGG
CGATTGATCAGGCTTGGGCTGCCACGAGCAACATTGTGGCTCGCTTGGTCTTGACTGGCCTGCAGATGGATCTGA
GGGTATTCAATGCACTGCGCAAAAACATGAATGGAGAGATGTCGGCACAAGCCATGGACCCATTTTTGCGAGTGG
CGGCTCGGTACATGGAGACGACAAGGTCGACGGAATACGCAAACGCGCTGGTGCGCCACGTCTGTGGCCAGGCTC
GCAACATGCAGAACACGGAGGGACCTGTGTTTATGATGCTTGTCAATGTCATGCTTCGGTCCGAAATGCCTCGGC
TGGACCTTGCGCGCTCGCGACGAGAGTGTTGCATCAAGCAGACGCCCGTGTGGGGTCCATATATGCTGGTGTTTC
CAAACAGCAATGTGAGGCGCGAAGCCGAGTGTCTGATTGAGCATGTGCTTTTTGCCGCCGACTCGCCCAAAGATG
AGGCAAGCACGGGGCACAGCCACGAGATGAAGGACTGTCTGGACGAGGTTGCATACGATTTGGGAGTGCGATGCC
TTGTCTACTTGCGGGATATGCACGTCAAGCGAAGAGTCAGGATAGAACGCGACGCTGCTTTGAGCATCCTCAGCG
TGGTGGGCAAGTGCGTGGCTCGCTGTGATGCTCTCAAGGATATGGACGATGGCGAAGATGACGACCTTGGACTGT
TGCAGAAAGGTGAGTAAAAGGGGGGCAGAGTGGCGGGCAGTTGCAGAGGCGGCTACTAACGCCCGAGACAGAGGT
GGTGGAGCCGCTACGCCGGCTCATGGTGGACGAGGTGGAGGACGATGTGTCTGGTAAGAGGATGCAAAAGACGGC
ACAGGCCGGCAATGAGGACGCGGACTAACCGACTGACTAGACTGGGATGGATCGTGCGGTTCATCAGAGCCCATG
GACGCAAGCCTGGGAATACCGCTGCAGACGATGAGCGAGGCCAATGACATAGACTTGATGTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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