© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|1902 |
| Gene name | |
| Location | scaffold_173:6624..9769 |
| Strand | - |
| Gene length (bp) | 3145 |
| Transcript length (bp) | 3081 |
| Coding sequence length (bp) | 3078 |
| Protein length (aa) | 1026 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00443 | UCH | Ubiquitin carboxyl-terminal hydrolase | 1.9E-37 | 656 | 994 |
| PF13423 | UCH_1 | Ubiquitin carboxyl-terminal hydrolase | 3.7E-09 | 755 | 990 |
| PF00581 | Rhodanese | Rhodanese-like domain | 2.1E-05 | 355 | 485 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q80U87|UBP8_MOUSE | Ubiquitin carboxyl-terminal hydrolase 8 OS=Mus musculus GN=Usp8 PE=1 SV=2 | 635 | 987 | 5.0E-36 |
| sp|P40818|UBP8_HUMAN | Ubiquitin carboxyl-terminal hydrolase 8 OS=Homo sapiens GN=USP8 PE=1 SV=1 | 635 | 987 | 6.0E-36 |
| sp|P39944|UBP5_YEAST | Ubiquitin carboxyl-terminal hydrolase 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP5 PE=1 SV=1 | 368 | 988 | 1.0E-27 |
| sp|Q9UK80|UBP21_HUMAN | Ubiquitin carboxyl-terminal hydrolase 21 OS=Homo sapiens GN=USP21 PE=1 SV=1 | 750 | 993 | 8.0E-18 |
| sp|Q6P8X6|UBP50_MOUSE | Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Mus musculus GN=Usp50 PE=2 SV=1 | 656 | 1016 | 1.0E-17 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q80U87|UBP8_MOUSE | Ubiquitin carboxyl-terminal hydrolase 8 OS=Mus musculus GN=Usp8 PE=1 SV=2 | 635 | 987 | 5.0E-36 |
| sp|P40818|UBP8_HUMAN | Ubiquitin carboxyl-terminal hydrolase 8 OS=Homo sapiens GN=USP8 PE=1 SV=1 | 635 | 987 | 6.0E-36 |
| sp|P39944|UBP5_YEAST | Ubiquitin carboxyl-terminal hydrolase 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP5 PE=1 SV=1 | 368 | 988 | 1.0E-27 |
| sp|Q9UK80|UBP21_HUMAN | Ubiquitin carboxyl-terminal hydrolase 21 OS=Homo sapiens GN=USP21 PE=1 SV=1 | 750 | 993 | 8.0E-18 |
| sp|Q6P8X6|UBP50_MOUSE | Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Mus musculus GN=Usp50 PE=2 SV=1 | 656 | 1016 | 1.0E-17 |
| sp|D3ZU96|UBP42_RAT | Ubiquitin carboxyl-terminal hydrolase 42 OS=Rattus norvegicus GN=Usp42 PE=1 SV=1 | 657 | 997 | 2.0E-17 |
| sp|B2RQC2|UBP42_MOUSE | Ubiquitin carboxyl-terminal hydrolase 42 OS=Mus musculus GN=Usp42 PE=1 SV=1 | 657 | 995 | 2.0E-17 |
| sp|P32571|UBP4_YEAST | Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DOA4 PE=1 SV=2 | 656 | 1023 | 3.0E-17 |
| sp|Q7M764|U17PE_MOUSE | Ubiquitin carboxyl-terminal hydrolase 17-like protein E OS=Mus musculus GN=Usp17le PE=3 SV=2 | 656 | 997 | 4.0E-17 |
| sp|Q9H9J4|UBP42_HUMAN | Ubiquitin carboxyl-terminal hydrolase 42 OS=Homo sapiens GN=USP42 PE=1 SV=3 | 657 | 997 | 4.0E-17 |
| sp|A6ZY34|UBP4_YEAS7 | Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain YJM789) GN=DOA4 PE=3 SV=1 | 656 | 1023 | 4.0E-17 |
| sp|O57429|UBP2_CHICK | Ubiquitin carboxyl-terminal hydrolase 2 OS=Gallus gallus GN=USP2 PE=2 SV=1 | 648 | 1000 | 4.0E-17 |
| sp|Q2KJ72|UBP21_BOVIN | Ubiquitin carboxyl-terminal hydrolase 21 OS=Bos taurus GN=USP21 PE=2 SV=1 | 750 | 993 | 5.0E-17 |
| sp|B3LGK1|UBP4_YEAS1 | Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain RM11-1a) GN=DOA4 PE=3 SV=1 | 656 | 1023 | 6.0E-17 |
| sp|E1B9W9|UBP42_BOVIN | Ubiquitin carboxyl-terminal hydrolase 42 OS=Bos taurus GN=USP42 PE=3 SV=1 | 657 | 997 | 1.0E-16 |
| sp|Q9QZL6|UBP21_MOUSE | Ubiquitin carboxyl-terminal hydrolase 21 OS=Mus musculus GN=Usp21 PE=1 SV=1 | 750 | 993 | 1.0E-16 |
| sp|O75604|UBP2_HUMAN | Ubiquitin carboxyl-terminal hydrolase 2 OS=Homo sapiens GN=USP2 PE=1 SV=2 | 541 | 991 | 1.0E-16 |
| sp|Q9FIQ1|UBP21_ARATH | Ubiquitin carboxyl-terminal hydrolase 21 OS=Arabidopsis thaliana GN=UBP21 PE=2 SV=1 | 748 | 993 | 1.0E-16 |
| sp|Q5U349|UBP2_RAT | Ubiquitin carboxyl-terminal hydrolase 2 OS=Rattus norvegicus GN=Usp2 PE=1 SV=1 | 657 | 991 | 2.0E-16 |
| sp|O88623|UBP2_MOUSE | Ubiquitin carboxyl-terminal hydrolase 2 OS=Mus musculus GN=Usp2 PE=1 SV=2 | 657 | 991 | 2.0E-16 |
| 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 | 657 | 982 | 2.0E-16 |
| sp|B1AQJ2|UBP36_MOUSE | Ubiquitin carboxyl-terminal hydrolase 36 OS=Mus musculus GN=Usp36 PE=1 SV=1 | 651 | 995 | 3.0E-16 |
| sp|B2GUX4|UBP21_RAT | Ubiquitin carboxyl-terminal hydrolase 21 OS=Rattus norvegicus GN=Usp21 PE=2 SV=1 | 750 | 993 | 3.0E-16 |
| sp|B4KXJ5|UBP36_DROMO | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila mojavensis GN=Usp36 PE=3 SV=1 | 657 | 997 | 8.0E-16 |
| sp|B3NC86|UBP36_DROER | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila erecta GN=Usp36 PE=3 SV=1 | 656 | 997 | 8.0E-16 |
| sp|Q9P275|UBP36_HUMAN | Ubiquitin carboxyl-terminal hydrolase 36 OS=Homo sapiens GN=USP36 PE=1 SV=3 | 651 | 995 | 1.0E-15 |
| sp|A7TGY3|UBP4_VANPO | Ubiquitin carboxyl-terminal hydrolase 4 OS=Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294) GN=DOA4 PE=3 SV=1 | 637 | 988 | 1.0E-15 |
| sp|Q2KHV7|UBP2_BOVIN | Ubiquitin carboxyl-terminal hydrolase 2 OS=Bos taurus GN=USP2 PE=2 SV=1 | 597 | 987 | 2.0E-15 |
| sp|Q9FPS2|UBP25_ARATH | Ubiquitin carboxyl-terminal hydrolase 25 OS=Arabidopsis thaliana GN=UBP25 PE=2 SV=1 | 657 | 991 | 3.0E-15 |
| sp|B4PIW8|UBP36_DROYA | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila yakuba GN=Usp36 PE=3 SV=1 | 656 | 997 | 4.0E-15 |
| sp|Q8CEG8|UBP27_MOUSE | Ubiquitin carboxyl-terminal hydrolase 27 OS=Mus musculus GN=Usp27 PE=2 SV=2 | 657 | 1024 | 4.0E-15 |
| sp|Q9VRP5|UBP36_DROME | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila melanogaster GN=scny PE=1 SV=3 | 656 | 997 | 6.0E-15 |
| sp|B4LG38|UBP36_DROVI | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila virilis GN=Usp36 PE=3 SV=1 | 657 | 997 | 6.0E-15 |
| sp|A6NNY8|UBP27_HUMAN | Ubiquitin carboxyl-terminal hydrolase 27 OS=Homo sapiens GN=USP27X PE=2 SV=3 | 657 | 1024 | 8.0E-15 |
| sp|B4QIS3|UBP36_DROSI | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila simulans GN=Usp36 PE=3 SV=1 | 656 | 995 | 1.0E-14 |
| sp|B4IXE0|UBP36_DROGR | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila grimshawi GN=Usp36 PE=3 SV=1 | 656 | 969 | 1.0E-14 |
| sp|Q61068|U17PA_MOUSE | Ubiquitin carboxyl-terminal hydrolase 17-like protein A OS=Mus musculus GN=Usp17la PE=1 SV=1 | 656 | 997 | 4.0E-14 |
| sp|D6RBQ6|U17LH_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 17 OS=Homo sapiens GN=USP17L17 PE=3 SV=1 | 657 | 997 | 5.0E-14 |
| sp|B3M3M6|UBP36_DROAN | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila ananassae GN=Usp36 PE=3 SV=1 | 656 | 1012 | 5.0E-14 |
| sp|O60139|UBP4_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp4 PE=1 SV=2 | 657 | 1023 | 5.0E-14 |
| sp|D6R9N7|U17LI_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 18 OS=Homo sapiens GN=USP17L18 PE=3 SV=1 | 657 | 997 | 6.0E-14 |
| sp|C9JVI0|U17LB_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 11 OS=Homo sapiens GN=USP17L11 PE=3 SV=1 | 657 | 997 | 6.0E-14 |
| sp|D6RCP7|U17LJ_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 19 OS=Homo sapiens GN=USP17L19 PE=3 SV=1 | 657 | 997 | 6.0E-14 |
| sp|D6RA61|U17LM_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 22 OS=Homo sapiens GN=USP17L22 PE=3 SV=1 | 657 | 997 | 7.0E-14 |
| sp|Q2LZB1|UBP36_DROPS | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila pseudoobscura pseudoobscura GN=Usp36 PE=3 SV=2 | 656 | 997 | 9.0E-14 |
| sp|D6RJB6|U17LK_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 20 OS=Homo sapiens GN=USP17L20 PE=3 SV=1 | 657 | 997 | 1.0E-13 |
| sp|Q9FPS4|UBP23_ARATH | Ubiquitin carboxyl-terminal hydrolase 23 OS=Arabidopsis thaliana GN=UBP23 PE=2 SV=2 | 653 | 1023 | 1.0E-13 |
| sp|Q0WX57|U17LO_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 24 OS=Homo sapiens GN=USP17L24 PE=1 SV=2 | 657 | 997 | 1.0E-13 |
| sp|C9JLJ4|U17LD_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 13 OS=Homo sapiens GN=USP17L13 PE=3 SV=1 | 657 | 997 | 1.0E-13 |
| sp|Q6R6M4|U17L2_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17 OS=Homo sapiens GN=USP17L2 PE=1 SV=2 | 657 | 997 | 1.0E-13 |
| sp|Q6QN14|U17L6_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 6 OS=Homo sapiens GN=USP17L6P PE=1 SV=2 | 657 | 997 | 2.0E-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 | 656 | 971 | 2.0E-13 |
| sp|Q4R6D3|UBP50_MACFA | Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Macaca fascicularis GN=USP50 PE=2 SV=1 | 636 | 1016 | 2.0E-13 |
| sp|Q9VVR1|NOT_DROME | Ubiquitin carboxyl-terminal hydrolase nonstop OS=Drosophila melanogaster GN=not PE=1 SV=3 | 657 | 1023 | 2.0E-13 |
| sp|C9JPN9|UL17C_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 12 OS=Homo sapiens GN=USP17L12 PE=3 SV=1 | 657 | 997 | 2.0E-13 |
| sp|D6R901|U17LL_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 21 OS=Homo sapiens GN=USP17L21 PE=3 SV=1 | 657 | 997 | 3.0E-13 |
| sp|B4MLR8|UBP36_DROWI | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila willistoni GN=Usp36 PE=3 SV=1 | 657 | 997 | 3.0E-13 |
| sp|Q7ZUM8|UBP44_DANRE | Ubiquitin carboxyl-terminal hydrolase 44 OS=Danio rerio GN=usp44 PE=2 SV=1 | 750 | 991 | 3.0E-13 |
| sp|Q6P9L4|UBP49_MOUSE | Ubiquitin carboxyl-terminal hydrolase 49 OS=Mus musculus GN=Usp49 PE=2 SV=1 | 750 | 1024 | 4.0E-13 |
| sp|A6H8I0|UBP22_DANRE | Ubiquitin carboxyl-terminal hydrolase 22 OS=Danio rerio GN=usp22 PE=2 SV=1 | 657 | 1024 | 4.0E-13 |
| sp|A8MUK1|U17L5_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 5 OS=Homo sapiens GN=USP17L5 PE=3 SV=2 | 657 | 997 | 4.0E-13 |
| sp|Q3KR59|UBP10_RAT | Ubiquitin carboxyl-terminal hydrolase 10 OS=Rattus norvegicus GN=Usp10 PE=1 SV=1 | 657 | 1025 | 6.0E-13 |
| sp|D2HBJ8|UBP44_AILME | Ubiquitin carboxyl-terminal hydrolase 44 OS=Ailuropoda melanoleuca GN=USP44 PE=3 SV=1 | 750 | 991 | 6.0E-13 |
| sp|Q70CQ1|UBP49_HUMAN | Ubiquitin carboxyl-terminal hydrolase 49 OS=Homo sapiens GN=USP49 PE=1 SV=1 | 750 | 991 | 1.0E-12 |
| sp|Q70EK9|UBP51_HUMAN | Ubiquitin carboxyl-terminal hydrolase 51 OS=Homo sapiens GN=USP51 PE=2 SV=1 | 657 | 1024 | 1.0E-12 |
| sp|P0C7I0|U17L8_HUMAN | Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 8 OS=Homo sapiens GN=USP17L8 PE=3 SV=1 | 657 | 997 | 2.0E-12 |
| sp|Q9R085|UBP15_RAT | Ubiquitin carboxyl-terminal hydrolase 15 OS=Rattus norvegicus GN=Usp15 PE=1 SV=1 | 657 | 856 | 2.0E-12 |
| sp|Q8R5H1|UBP15_MOUSE | Ubiquitin carboxyl-terminal hydrolase 15 OS=Mus musculus GN=Usp15 PE=1 SV=1 | 657 | 856 | 2.0E-12 |
| sp|Q9Y4E8|UBP15_HUMAN | Ubiquitin carboxyl-terminal hydrolase 15 OS=Homo sapiens GN=USP15 PE=1 SV=3 | 657 | 855 | 2.0E-12 |
| sp|Q5DU02|UBP22_MOUSE | Ubiquitin carboxyl-terminal hydrolase 22 OS=Mus musculus GN=Usp22 PE=2 SV=2 | 657 | 1024 | 5.0E-12 |
| sp|C9J2P7|U17LF_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 15 OS=Homo sapiens GN=USP17L15 PE=3 SV=1 | 657 | 997 | 5.0E-12 |
| sp|Q9UPT9|UBP22_HUMAN | Ubiquitin carboxyl-terminal hydrolase 22 OS=Homo sapiens GN=USP22 PE=1 SV=2 | 657 | 1024 | 6.0E-12 |
| sp|Q9C585|UBP8_ARATH | Ubiquitin carboxyl-terminal hydrolase 8 OS=Arabidopsis thaliana GN=UBP8 PE=2 SV=2 | 656 | 858 | 6.0E-12 |
| sp|Q9SJA1|UBP19_ARATH | Ubiquitin carboxyl-terminal hydrolase 19 OS=Arabidopsis thaliana GN=UBP19 PE=2 SV=2 | 656 | 995 | 6.0E-12 |
| sp|A6NCW0|U17L3_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 3 OS=Homo sapiens GN=USP17L3 PE=3 SV=1 | 657 | 997 | 7.0E-12 |
| sp|C9JJH3|U17LA_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 10 OS=Homo sapiens GN=USP17L10 PE=3 SV=1 | 657 | 997 | 8.0E-12 |
| sp|Q99K46|UBP11_MOUSE | Ubiquitin carboxyl-terminal hydrolase 11 OS=Mus musculus GN=Usp11 PE=1 SV=4 | 657 | 856 | 8.0E-12 |
| sp|Q2HJE4|UBP15_BOVIN | Ubiquitin carboxyl-terminal hydrolase 15 OS=Bos taurus GN=USP15 PE=2 SV=1 | 657 | 855 | 8.0E-12 |
| sp|Q86UV5|UBP48_HUMAN | Ubiquitin carboxyl-terminal hydrolase 48 OS=Homo sapiens GN=USP48 PE=1 SV=1 | 654 | 993 | 1.0E-11 |
| sp|Q6GNI6|UB22A_XENLA | Ubiquitin carboxyl-terminal hydrolase 22-A OS=Xenopus laevis GN=usp22-a PE=2 SV=1 | 657 | 1024 | 1.0E-11 |
| sp|B2GUZ1|UBP4_RAT | Ubiquitin carboxyl-terminal hydrolase 4 OS=Rattus norvegicus GN=Usp4 PE=1 SV=1 | 657 | 856 | 1.0E-11 |
| sp|P0C8Z3|UBP22_BOVIN | Ubiquitin carboxyl-terminal hydrolase 22 OS=Bos taurus GN=USP22 PE=2 SV=1 | 657 | 1024 | 1.0E-11 |
| sp|P55824|FAF_DROME | Probable ubiquitin carboxyl-terminal hydrolase FAF OS=Drosophila melanogaster GN=faf PE=1 SV=2 | 827 | 995 | 1.0E-11 |
| 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 | 335 | 501 | 2.0E-11 |
| sp|F6Z5C0|UBP15_XENTR | Ubiquitin carboxyl-terminal hydrolase 15 OS=Xenopus tropicalis GN=usp15 PE=2 SV=2 | 657 | 856 | 2.0E-11 |
| sp|Q6DCJ1|UB22B_XENLA | Ubiquitin carboxyl-terminal hydrolase 22-B OS=Xenopus laevis GN=usp22-b PE=2 SV=2 | 657 | 1024 | 3.0E-11 |
| sp|Q9H0E7|UBP44_HUMAN | Ubiquitin carboxyl-terminal hydrolase 44 OS=Homo sapiens GN=USP44 PE=1 SV=2 | 750 | 991 | 3.0E-11 |
| sp|Q5XGZ2|UP44B_XENLA | Ubiquitin carboxyl-terminal hydrolase 44-B OS=Xenopus laevis GN=usp44-b PE=2 SV=1 | 672 | 995 | 4.0E-11 |
| sp|Q9FPS3|UBP24_ARATH | Ubiquitin carboxyl-terminal hydrolase 24 OS=Arabidopsis thaliana GN=UBP24 PE=1 SV=1 | 652 | 993 | 4.0E-11 |
| sp|Q09738|UBP8_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 8 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp8 PE=3 SV=1 | 657 | 1024 | 4.0E-11 |
| sp|Q6NTR6|UP44A_XENLA | Ubiquitin carboxyl-terminal hydrolase 44-A OS=Xenopus laevis GN=usp44-a PE=2 SV=1 | 750 | 995 | 5.0E-11 |
| sp|Q7RTZ2|U17L1_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 1 OS=Homo sapiens GN=USP17L1 PE=3 SV=1 | 657 | 997 | 5.0E-11 |
| sp|Q9FPS9|UBP15_ARATH | Ubiquitin carboxyl-terminal hydrolase 15 OS=Arabidopsis thaliana GN=UBP15 PE=2 SV=2 | 657 | 993 | 5.0E-11 |
| sp|Q8C2S0|UBP44_MOUSE | Ubiquitin carboxyl-terminal hydrolase 44 OS=Mus musculus GN=Usp44 PE=2 SV=3 | 750 | 991 | 6.0E-11 |
| sp|Q0V9G5|UBP44_XENTR | Ubiquitin carboxyl-terminal hydrolase 44 OS=Xenopus tropicalis GN=usp44 PE=2 SV=1 | 750 | 971 | 6.0E-11 |
| sp|P35125|UBP6_HUMAN | Ubiquitin carboxyl-terminal hydrolase 6 OS=Homo sapiens GN=USP6 PE=1 SV=2 | 653 | 845 | 6.0E-11 |
| sp|P35123|UBP4_MOUSE | Ubiquitin carboxyl-terminal hydrolase 4 OS=Mus musculus GN=Usp4 PE=1 SV=3 | 657 | 856 | 6.0E-11 |
| sp|A6NCW7|U17L4_HUMAN | Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 4 OS=Homo sapiens GN=USP17L4 PE=3 SV=3 | 657 | 997 | 7.0E-11 |
| sp|Q3V0C5|UBP48_MOUSE | Ubiquitin carboxyl-terminal hydrolase 48 OS=Mus musculus GN=Usp48 PE=1 SV=2 | 654 | 993 | 7.0E-11 |
| sp|O74442|UBP16_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 16 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp16 PE=1 SV=1 | 597 | 995 | 8.0E-11 |
| sp|Q9D9M2|UBP12_MOUSE | Ubiquitin carboxyl-terminal hydrolase 12 OS=Mus musculus GN=Usp12 PE=2 SV=2 | 651 | 1025 | 9.0E-11 |
| sp|P51784|UBP11_HUMAN | Ubiquitin carboxyl-terminal hydrolase 11 OS=Homo sapiens GN=USP11 PE=1 SV=3 | 657 | 856 | 1.0E-10 |
| sp|A5D9H7|UBP12_BOVIN | Ubiquitin carboxyl-terminal hydrolase 12 OS=Bos taurus GN=USP12 PE=2 SV=1 | 651 | 1025 | 2.0E-10 |
| sp|Q70EL3|UBP50_HUMAN | Inactive ubiquitin carboxyl-terminal hydrolase 50 OS=Homo sapiens GN=USP50 PE=2 SV=1 | 755 | 977 | 2.0E-10 |
| sp|Q5RCD3|UBP4_PONAB | Ubiquitin carboxyl-terminal hydrolase 4 OS=Pongo abelii GN=USP4 PE=2 SV=1 | 657 | 856 | 3.0E-10 |
| sp|Q76LT8|UBP48_RAT | Ubiquitin carboxyl-terminal hydrolase 48 OS=Rattus norvegicus GN=Usp48 PE=1 SV=1 | 654 | 993 | 3.0E-10 |
| sp|P39967|UBP9_YEAST | Ubiquitin carboxyl-terminal hydrolase 9 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP9 PE=1 SV=1 | 750 | 994 | 4.0E-10 |
| sp|Q9SB51|UBP16_ARATH | Ubiquitin carboxyl-terminal hydrolase 16 OS=Arabidopsis thaliana GN=UBP16 PE=1 SV=1 | 657 | 1023 | 4.0E-10 |
| sp|Q6J1Y9|UBP19_RAT | Ubiquitin carboxyl-terminal hydrolase 19 OS=Rattus norvegicus GN=Usp19 PE=1 SV=1 | 655 | 845 | 4.0E-10 |
| sp|Q3UJD6|UBP19_MOUSE | Ubiquitin carboxyl-terminal hydrolase 19 OS=Mus musculus GN=Usp19 PE=1 SV=1 | 655 | 845 | 5.0E-10 |
| sp|B1AY13|UBP24_MOUSE | Ubiquitin carboxyl-terminal hydrolase 24 OS=Mus musculus GN=Usp24 PE=1 SV=1 | 655 | 996 | 5.0E-10 |
| sp|O94966|UBP19_HUMAN | Ubiquitin carboxyl-terminal hydrolase 19 OS=Homo sapiens GN=USP19 PE=1 SV=2 | 655 | 845 | 6.0E-10 |
| sp|Q91W36|UBP3_MOUSE | Ubiquitin carboxyl-terminal hydrolase 3 OS=Mus musculus GN=Usp3 PE=2 SV=1 | 656 | 991 | 6.0E-10 |
| sp|Q9Y6I4|UBP3_HUMAN | Ubiquitin carboxyl-terminal hydrolase 3 OS=Homo sapiens GN=USP3 PE=1 SV=2 | 656 | 991 | 6.0E-10 |
| sp|A6QR55|UBP4_BOVIN | Ubiquitin carboxyl-terminal hydrolase 4 OS=Bos taurus GN=USP4 PE=2 SV=1 | 657 | 856 | 7.0E-10 |
| sp|Q8NFA0|UBP32_HUMAN | Ubiquitin carboxyl-terminal hydrolase 32 OS=Homo sapiens GN=USP32 PE=1 SV=1 | 653 | 845 | 8.0E-10 |
| sp|Q52KZ6|UB12A_XENLA | Ubiquitin carboxyl-terminal hydrolase 12-A OS=Xenopus laevis GN=usp12-a PE=2 SV=1 | 655 | 1025 | 8.0E-10 |
| sp|Q13107|UBP4_HUMAN | Ubiquitin carboxyl-terminal hydrolase 4 OS=Homo sapiens GN=USP4 PE=1 SV=3 | 657 | 856 | 1.0E-09 |
| sp|P0C7H9|U17L7_HUMAN | Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 7 OS=Homo sapiens GN=USP17L7 PE=3 SV=1 | 750 | 997 | 1.0E-09 |
| sp|Q67XW5|UBP18_ARATH | Ubiquitin carboxyl-terminal hydrolase 18 OS=Arabidopsis thaliana GN=UBP18 PE=2 SV=2 | 656 | 995 | 1.0E-09 |
| sp|Q9UPU5|UBP24_HUMAN | Ubiquitin carboxyl-terminal hydrolase 24 OS=Homo sapiens GN=USP24 PE=1 SV=3 | 655 | 996 | 1.0E-09 |
| sp|Q9C585|UBP8_ARATH | Ubiquitin carboxyl-terminal hydrolase 8 OS=Arabidopsis thaliana GN=UBP8 PE=2 SV=2 | 849 | 993 | 2.0E-09 |
| sp|Q5M981|UB12B_XENLA | Ubiquitin carboxyl-terminal hydrolase 12-B OS=Xenopus laevis GN=usp12-b PE=2 SV=2 | 655 | 1025 | 2.0E-09 |
| sp|O22207|UBP5_ARATH | Ubiquitin carboxyl-terminal hydrolase 5 OS=Arabidopsis thaliana GN=UBP5 PE=1 SV=2 | 749 | 855 | 3.0E-09 |
| sp|O22207|UBP5_ARATH | Ubiquitin carboxyl-terminal hydrolase 5 OS=Arabidopsis thaliana GN=UBP5 PE=1 SV=2 | 853 | 1024 | 3.0E-09 |
| sp|P38187|UBP13_YEAST | Ubiquitin carboxyl-terminal hydrolase 13 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP13 PE=1 SV=3 | 750 | 994 | 3.0E-09 |
| sp|O24454|UBP3_ARATH | Ubiquitin carboxyl-terminal hydrolase 3 OS=Arabidopsis thaliana GN=UBP3 PE=1 SV=1 | 655 | 1021 | 3.0E-09 |
| sp|O75317|UBP12_HUMAN | Ubiquitin carboxyl-terminal hydrolase 12 OS=Homo sapiens GN=USP12 PE=1 SV=2 | 655 | 1025 | 4.0E-09 |
| sp|Q9LEW0|UBP22_ARATH | Ubiquitin carboxyl-terminal hydrolase 22 OS=Arabidopsis thaliana GN=UBP22 PE=2 SV=1 | 657 | 993 | 6.0E-09 |
| sp|Q70CQ2|UBP34_HUMAN | Ubiquitin carboxyl-terminal hydrolase 34 OS=Homo sapiens GN=USP34 PE=1 SV=2 | 655 | 990 | 7.0E-09 |
| sp|Q8BUM9|UBP43_MOUSE | Ubiquitin carboxyl-terminal hydrolase 43 OS=Mus musculus GN=Usp43 PE=1 SV=2 | 854 | 994 | 7.0E-09 |
| sp|Q70EL4|UBP43_HUMAN | Ubiquitin carboxyl-terminal hydrolase 43 OS=Homo sapiens GN=USP43 PE=1 SV=2 | 854 | 994 | 7.0E-09 |
| sp|P50102|UBP8_YEAST | Ubiquitin carboxyl-terminal hydrolase 8 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP8 PE=1 SV=1 | 656 | 1021 | 8.0E-09 |
| sp|Q9MAQ3|UBP11_ARATH | Putative ubiquitin carboxyl-terminal hydrolase 11 OS=Arabidopsis thaliana GN=UBP11 PE=3 SV=2 | 657 | 855 | 1.0E-08 |
| sp|P39538|UBP12_YEAST | Ubiquitin carboxyl-terminal hydrolase 12 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP12 PE=1 SV=1 | 656 | 855 | 1.0E-08 |
| sp|Q70CQ4|UBP31_HUMAN | Ubiquitin carboxyl-terminal hydrolase 31 OS=Homo sapiens GN=USP31 PE=2 SV=2 | 854 | 1026 | 1.0E-08 |
| sp|Q93008|USP9X_HUMAN | Probable ubiquitin carboxyl-terminal hydrolase FAF-X OS=Homo sapiens GN=USP9X PE=1 SV=3 | 827 | 1026 | 1.0E-08 |
| sp|A7TGY3|UBP4_VANPO | Ubiquitin carboxyl-terminal hydrolase 4 OS=Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294) GN=DOA4 PE=3 SV=1 | 346 | 465 | 2.0E-08 |
| sp|P70398|USP9X_MOUSE | Probable ubiquitin carboxyl-terminal hydrolase FAF-X OS=Mus musculus GN=Usp9x PE=1 SV=2 | 827 | 1026 | 2.0E-08 |
| sp|Q5ZM45|UBP48_CHICK | Ubiquitin carboxyl-terminal hydrolase 48 OS=Gallus gallus GN=USP48 PE=2 SV=1 | 754 | 993 | 2.0E-08 |
| 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 | 755 | 993 | 2.0E-08 |
| sp|Q2UUG8|CREB_ASPOR | Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=creB PE=3 SV=2 | 755 | 993 | 2.0E-08 |
| sp|Q9USM5|UBP1_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp1 PE=3 SV=1 | 657 | 845 | 2.0E-08 |
| sp|A4FUN7|UBP12_DANRE | Ubiquitin carboxyl-terminal hydrolase 12A OS=Danio rerio GN=usp12a PE=2 SV=1 | 643 | 993 | 3.0E-08 |
| sp|Q0CT11|CREB_ASPTN | Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=creB PE=3 SV=2 | 756 | 993 | 3.0E-08 |
| 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 | 351 | 440 | 4.0E-08 |
| 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 | 755 | 1024 | 4.0E-08 |
| 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 | 750 | 993 | 4.0E-08 |
| sp|A5PMR2|UBP33_DANRE | Ubiquitin carboxyl-terminal hydrolase 33 OS=Danio rerio GN=usp33 PE=2 SV=1 | 810 | 993 | 5.0E-08 |
| sp|A3AF13|UBP26_ORYSJ | Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. japonica GN=UBP26 PE=3 SV=2 | 652 | 993 | 7.0E-08 |
| sp|A2XDG4|UBP26_ORYSI | Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. indica GN=UBP26 PE=3 SV=1 | 652 | 993 | 7.0E-08 |
| sp|Q28CN3|UBP33_XENTR | Ubiquitin carboxyl-terminal hydrolase 33 OS=Xenopus tropicalis GN=usp33 PE=2 SV=2 | 837 | 993 | 7.0E-08 |
| 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 | 756 | 1024 | 8.0E-08 |
| sp|Q9FPS7|UBP20_ARATH | Ubiquitin carboxyl-terminal hydrolase 20 OS=Arabidopsis thaliana GN=UBP20 PE=2 SV=1 | 750 | 993 | 9.0E-08 |
| 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 | 756 | 1024 | 9.0E-08 |
| sp|Q84WU2|UBP13_ARATH | Ubiquitin carboxyl-terminal hydrolase 13 OS=Arabidopsis thaliana GN=UBP13 PE=1 SV=1 | 655 | 992 | 1.0E-07 |
| sp|A4QNN3|UBP30_XENTR | Ubiquitin carboxyl-terminal hydrolase 30 OS=Xenopus tropicalis GN=usp30 PE=2 SV=1 | 657 | 1023 | 1.0E-07 |
| sp|Q5UQR3|UBPL1_MIMIV | Probable ubiquitin carboxyl-terminal hydrolase R319 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R319 PE=3 SV=1 | 750 | 1010 | 1.0E-07 |
| sp|B4HUI5|UBP36_DROSE | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila sechellia GN=Usp36 PE=3 SV=1 | 656 | 995 | 1.0E-07 |
| sp|Q9Y2K6|UBP20_HUMAN | Ubiquitin carboxyl-terminal hydrolase 20 OS=Homo sapiens GN=USP20 PE=1 SV=2 | 842 | 993 | 1.0E-07 |
| sp|Q8R5K2|UBP33_MOUSE | Ubiquitin carboxyl-terminal hydrolase 33 OS=Mus musculus GN=Usp33 PE=1 SV=2 | 810 | 993 | 2.0E-07 |
| sp|Q5R5Z6|UBP20_PONAB | Ubiquitin carboxyl-terminal hydrolase 20 OS=Pongo abelii GN=USP20 PE=2 SV=1 | 842 | 993 | 2.0E-07 |
| sp|P53874|UBP10_YEAST | Ubiquitin carboxyl-terminal hydrolase 10 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP10 PE=1 SV=2 | 871 | 993 | 2.0E-07 |
| sp|Q9FPT1|UBP12_ARATH | Ubiquitin carboxyl-terminal hydrolase 12 OS=Arabidopsis thaliana GN=UBP12 PE=1 SV=2 | 655 | 992 | 2.0E-07 |
| sp|A5PN09|UBP20_DANRE | Ubiquitin carboxyl-terminal hydrolase 20 OS=Danio rerio GN=usp20 PE=3 SV=1 | 853 | 993 | 2.0E-07 |
| sp|F1SRY5|UBP37_PIG | Ubiquitin carboxyl-terminal hydrolase 37 OS=Sus scrofa GN=USP37 PE=3 SV=1 | 634 | 905 | 2.0E-07 |
| sp|Q9MAQ3|UBP11_ARATH | Putative ubiquitin carboxyl-terminal hydrolase 11 OS=Arabidopsis thaliana GN=UBP11 PE=3 SV=2 | 853 | 993 | 3.0E-07 |
| 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 | 350 | 484 | 4.0E-07 |
| sp|Q9ZSB5|UBP10_ARATH | Ubiquitin carboxyl-terminal hydrolase 10 OS=Arabidopsis thaliana GN=UBP10 PE=2 SV=2 | 853 | 993 | 4.0E-07 |
| sp|Q93Y01|UBP9_ARATH | Ubiquitin carboxyl-terminal hydrolase 9 OS=Arabidopsis thaliana GN=UBP9 PE=2 SV=1 | 634 | 855 | 4.0E-07 |
| sp|Q5RBQ4|UBP46_PONAB | Ubiquitin carboxyl-terminal hydrolase 46 OS=Pongo abelii GN=USP46 PE=2 SV=1 | 655 | 993 | 4.0E-07 |
| sp|P62069|UBP46_MOUSE | Ubiquitin carboxyl-terminal hydrolase 46 OS=Mus musculus GN=Usp46 PE=1 SV=1 | 655 | 993 | 4.0E-07 |
| sp|P62068|UBP46_HUMAN | Ubiquitin carboxyl-terminal hydrolase 46 OS=Homo sapiens GN=USP46 PE=1 SV=1 | 655 | 993 | 4.0E-07 |
| sp|A6QNM7|UBP33_BOVIN | Ubiquitin carboxyl-terminal hydrolase 33 OS=Bos taurus GN=USP33 PE=2 SV=1 | 842 | 993 | 4.0E-07 |
| sp|Q93Y01|UBP9_ARATH | Ubiquitin carboxyl-terminal hydrolase 9 OS=Arabidopsis thaliana GN=UBP9 PE=2 SV=1 | 853 | 993 | 5.0E-07 |
| sp|Q9P7V9|UBP9_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 9 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp9 PE=1 SV=1 | 750 | 993 | 5.0E-07 |
| sp|Q5REG5|UBP33_PONAB | Ubiquitin carboxyl-terminal hydrolase 33 OS=Pongo abelii GN=USP33 PE=2 SV=1 | 842 | 993 | 5.0E-07 |
| sp|Q9WTV6|UBP18_MOUSE | Ubl carboxyl-terminal hydrolase 18 OS=Mus musculus GN=Usp18 PE=1 SV=2 | 854 | 993 | 5.0E-07 |
| sp|Q8TEY7|UBP33_HUMAN | Ubiquitin carboxyl-terminal hydrolase 33 OS=Homo sapiens GN=USP33 PE=1 SV=2 | 842 | 993 | 8.0E-07 |
| sp|Q3UN04|UBP30_MOUSE | Ubiquitin carboxyl-terminal hydrolase 30 OS=Mus musculus GN=Usp30 PE=1 SV=1 | 657 | 946 | 3.0E-06 |
| sp|Q70CQ3|UBP30_HUMAN | Ubiquitin carboxyl-terminal hydrolase 30 OS=Homo sapiens GN=USP30 PE=1 SV=1 | 657 | 930 | 3.0E-06 |
| 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 signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 36 | 0.45 |
| Type of sequence | Sequence |
|---|---|
| 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|1902 MAADATHGLSPAYDSISPRSTPSSPAPIPHIDDLVAIPTDVGPNQSIKRLLEMAQTALRQSEISRDFNRPAIALQ EYIRASVIAIQIITNHKDYPGLRTDHTDSARVHNALLRRIKQQSDDYESIKRDIIEDNKRSGVQPTVRRSLCPNK VQGLGLASKQADLVNGHALPPVNGSPGKVKPVVHPKPHALAGNLLPGRGRAASSNGATLDLAARFANLRGPQSSP GQDPRIKTYPIPTQRPAGPRQMPQDQQLNLDTDAATSSALPKVPDAIYSPARGSVSGDLARLPTSTSRGLFSRTG SSTSVPAATPQGSELAPAVVSPRMPSPRIPPRIPSPRVPEGADEPLPLPAGDGITPEQLVEVMRGNWSILLIDIR SREAFNEGHIMSSSIICIEPSILLRDNISSEEISESLVLSPSPEQALFEKRDSCDLVVFYDEDSHQVIQSPKNAD EQVILSLHRALIHLNYGRDLKRPPRLLIGGLAAWADLVGPLALQSGASSMFKGPHARYKRNGIVQRRGSKYIVTS LQPADVKAWENTLEKDARQTATRPSFPRTGEEFLRFSPVSTQQQSMSSPPMASEQGQEHGLVHKFGSLHQLPAPP ARPCAAVKRLSHSGLSQGDDGHEAYGETGAVVPPRLPARSKKAMEQLAGGVVKTYTGLNNPRNWCYANSTLQSLL ASPGFGRELADSGWMSRYIVPRKAEETIDQPQLMIRIISHLFQWMSTGNFETLKAQTLMEYSRNLCKSSDPQSQF GGPEQQDAQEFMSFVMEQMHDETNSRRDRAGKVEQPKAARGRPLVEAAIEYWRNHTQLNQSIIDRYWRGVELSAV ECMGCHTRTHTFSPFGWVPVTVGPGRDMTLYEALNHYVAENRLDDFACDHCQGKRVAMQSMSFARMPPLLCISFR RFNYDGRDFSKSNAAISWDFNDVDLSPYFLGADADSGGGDSAFTAPFRYECYAVIVHSGRQLNTGHYFAYVRDAS SHDPYAWYCCNDSHVSKVRIGSGDAADVQKDVFRSDPDRVPYLVFFHRKDA |
| Coding | >Ophio5|1902 ATGGCTGCCGACGCCACTCATGGCCTCTCCCCGGCCTACGATAGCATCAGCCCGCGCTCTACGCCGTCCTCACCA GCGCCTATACCGCACATCGACGACCTCGTCGCCATCCCGACCGACGTGGGCCCCAACCAGTCCATTAAGCGACTG CTTGAAATGGCTCAGACCGCCTTGCGACAGTCTGAAATCAGTCGCGACTTCAACCGGCCCGCCATCGCCCTCCAG GAGTACATCAGGGCCTCCGTCATCGCCATCCAGATCATTACCAACCACAAAGACTATCCCGGACTGAGGACAGAT CATACCGACTCCGCCCGCGTACACAACGCCCTGCTCAGGCGCATCAAGCAGCAGAGTGACGACTACGAGAGCATC AAGCGCGACATCATCGAGGACAATAAGAGATCCGGCGTCCAACCGACCGTGAGACGGTCCTTGTGTCCGAACAAG GTTCAGGGCCTCGGCCTGGCATCCAAGCAAGCCGACTTGGTCAACGGTCACGCCTTGCCCCCCGTCAACGGCTCT CCGGGCAAGGTTAAGCCCGTCGTCCACCCGAAGCCTCACGCTCTCGCCGGCAATCTCCTGCCTGGCCGAGGGCGC GCCGCGTCGTCGAATGGCGCCACGCTCGACCTGGCCGCTCGCTTCGCCAACCTTCGCGGCCCCCAGTCCTCTCCA GGCCAAGATCCACGCATCAAGACGTATCCCATACCGACACAAAGGCCTGCCGGGCCCAGACAGATGCCACAGGAC CAGCAGCTGAACCTCGATACCGACGCCGCCACCTCGTCAGCCCTCCCCAAGGTGCCCGACGCCATCTACAGCCCC GCGCGGGGGAGCGTGTCCGGCGATCTGGCAAGGCTTCCGACCAGCACGTCTCGCGGCCTGTTCAGCCGCACCGGC TCGTCGACCTCGGTTCCCGCGGCGACGCCACAGGGCAGCGAACTCGCACCGGCTGTTGTGAGCCCCAGGATGCCC AGCCCCAGGATACCCCCAAGGATACCCAGCCCCAGAGTCCCTGAAGGAGCAGACGAGCCGCTCCCTCTACCGGCG GGAGACGGCATCACCCCCGAGCAGCTCGTCGAGGTCATGAGAGGCAACTGGTCCATTCTTCTCATCGACATCCGA TCCCGCGAGGCATTTAACGAGGGCCACATCATGTCGTCATCCATCATATGTATCGAACCGAGTATCCTGCTGCGA GACAACATCTCTTCGGAGGAAATATCGGAGAGCCTGGTGCTCTCGCCCAGCCCAGAGCAGGCACTCTTCGAGAAG CGTGACTCTTGCGACCTGGTCGTCTTCTACGACGAAGACTCACATCAAGTCATTCAATCTCCCAAGAACGCCGAC GAGCAGGTCATCCTGTCGCTGCACCGGGCTCTGATCCACCTCAACTACGGCCGAGACCTCAAGCGGCCCCCGAGG CTACTGATTGGGGGTCTGGCCGCTTGGGCCGATCTCGTGGGACCCCTTGCACTACAGTCTGGGGCCTCGTCGATG TTCAAGGGTCCCCATGCAAGATACAAGCGGAATGGAATTGTCCAGCGAAGGGGATCCAAGTACATCGTGACGTCT TTGCAGCCGGCCGACGTCAAGGCATGGGAGAATACGCTCGAAAAAGACGCGCGCCAGACGGCCACCCGGCCGAGC TTCCCTCGGACGGGCGAAGAGTTCTTGCGGTTCTCCCCAGTATCGACGCAGCAGCAGTCCATGTCGTCTCCCCCG ATGGCGAGCGAGCAGGGGCAGGAACATGGTCTGGTGCACAAGTTTGGCTCTCTCCACCAGCTCCCCGCCCCTCCG GCACGGCCATGCGCCGCGGTGAAGCGACTCAGCCATAGCGGCCTTTCTCAGGGAGACGACGGCCACGAGGCTTAC GGCGAGACGGGTGCCGTCGTACCGCCCCGACTGCCGGCGCGGTCTAAGAAAGCCATGGAGCAGCTGGCGGGAGGC GTCGTCAAGACTTACACCGGGCTCAACAACCCTCGCAACTGGTGTTACGCCAACAGCACGCTGCAGTCGCTACTG GCCTCTCCGGGCTTTGGACGAGAGCTGGCCGACTCGGGATGGATGAGCAGATACATTGTGCCGCGGAAGGCGGAG GAAACAATCGACCAGCCGCAACTCATGATCCGCATCATATCCCACCTGTTCCAATGGATGAGCACAGGCAATTTT GAGACGCTCAAGGCCCAGACTCTGATGGAATACTCGCGGAACCTCTGCAAGTCCAGCGATCCGCAGTCGCAGTTT GGCGGGCCGGAACAGCAGGACGCACAGGAATTCATGTCGTTTGTCATGGAGCAGATGCACGACGAGACCAACTCG CGGCGGGACCGGGCGGGAAAGGTCGAGCAGCCCAAGGCGGCTAGGGGACGGCCGCTGGTGGAGGCGGCCATTGAG TACTGGCGCAACCACACGCAGCTGAACCAGTCCATCATCGATCGATACTGGCGCGGAGTCGAGCTCTCGGCTGTC GAGTGCATGGGATGCCACACGCGGACTCACACCTTCTCGCCCTTTGGCTGGGTGCCGGTGACGGTCGGCCCCGGA CGCGACATGACGCTCTACGAGGCGCTCAACCACTACGTTGCCGAGAACCGGCTCGACGACTTCGCCTGCGACCAC TGCCAGGGCAAGCGGGTGGCGATGCAGTCCATGTCGTTTGCCCGGATGCCTCCGCTGCTCTGCATCAGCTTCCGA CGCTTCAACTACGACGGCCGCGATTTCTCCAAGTCCAACGCGGCCATCTCGTGGGACTTTAACGACGTCGACCTC TCGCCCTACTTCCTCGGCGCGGACGCGGACTCGGGCGGCGGCGACAGCGCCTTCACCGCCCCCTTCCGCTACGAA TGCTACGCCGTCATCGTCCACAGCGGTCGTCAGCTCAACACGGGCCATTACTTCGCCTACGTCCGAGACGCCAGC TCCCACGACCCCTACGCCTGGTACTGCTGCAACGACAGCCACGTGTCAAAGGTGCGCATCGGTAGCGGCGACGCG GCCGACGTGCAGAAGGATGTCTTTCGTTCGGATCCCGATCGCGTCCCGTACCTGGTCTTTTTCCACCGCAAGGAC GCG |
| Transcript | >Ophio5|1902 ATGGCTGCCGACGCCACTCATGGCCTCTCCCCGGCCTACGATAGCATCAGCCCGCGCTCTACGCCGTCCTCACCA GCGCCTATACCGCACATCGACGACCTCGTCGCCATCCCGACCGACGTGGGCCCCAACCAGTCCATTAAGCGACTG CTTGAAATGGCTCAGACCGCCTTGCGACAGTCTGAAATCAGTCGCGACTTCAACCGGCCCGCCATCGCCCTCCAG GAGTACATCAGGGCCTCCGTCATCGCCATCCAGATCATTACCAACCACAAAGACTATCCCGGACTGAGGACAGAT CATACCGACTCCGCCCGCGTACACAACGCCCTGCTCAGGCGCATCAAGCAGCAGAGTGACGACTACGAGAGCATC AAGCGCGACATCATCGAGGACAATAAGAGATCCGGCGTCCAACCGACCGTGAGACGGTCCTTGTGTCCGAACAAG GTTCAGGGCCTCGGCCTGGCATCCAAGCAAGCCGACTTGGTCAACGGTCACGCCTTGCCCCCCGTCAACGGCTCT CCGGGCAAGGTTAAGCCCGTCGTCCACCCGAAGCCTCACGCTCTCGCCGGCAATCTCCTGCCTGGCCGAGGGCGC GCCGCGTCGTCGAATGGCGCCACGCTCGACCTGGCCGCTCGCTTCGCCAACCTTCGCGGCCCCCAGTCCTCTCCA GGCCAAGATCCACGCATCAAGACGTATCCCATACCGACACAAAGGCCTGCCGGGCCCAGACAGATGCCACAGGAC CAGCAGCTGAACCTCGATACCGACGCCGCCACCTCGTCAGCCCTCCCCAAGGTGCCCGACGCCATCTACAGCCCC GCGCGGGGGAGCGTGTCCGGCGATCTGGCAAGGCTTCCGACCAGCACGTCTCGCGGCCTGTTCAGCCGCACCGGC TCGTCGACCTCGGTTCCCGCGGCGACGCCACAGGGCAGCGAACTCGCACCGGCTGTTGTGAGCCCCAGGATGCCC AGCCCCAGGATACCCCCAAGGATACCCAGCCCCAGAGTCCCTGAAGGAGCAGACGAGCCGCTCCCTCTACCGGCG GGAGACGGCATCACCCCCGAGCAGCTCGTCGAGGTCATGAGAGGCAACTGGTCCATTCTTCTCATCGACATCCGA TCCCGCGAGGCATTTAACGAGGGCCACATCATGTCGTCATCCATCATATGTATCGAACCGAGTATCCTGCTGCGA GACAACATCTCTTCGGAGGAAATATCGGAGAGCCTGGTGCTCTCGCCCAGCCCAGAGCAGGCACTCTTCGAGAAG CGTGACTCTTGCGACCTGGTCGTCTTCTACGACGAAGACTCACATCAAGTCATTCAATCTCCCAAGAACGCCGAC GAGCAGGTCATCCTGTCGCTGCACCGGGCTCTGATCCACCTCAACTACGGCCGAGACCTCAAGCGGCCCCCGAGG CTACTGATTGGGGGTCTGGCCGCTTGGGCCGATCTCGTGGGACCCCTTGCACTACAGTCTGGGGCCTCGTCGATG TTCAAGGGTCCCCATGCAAGATACAAGCGGAATGGAATTGTCCAGCGAAGGGGATCCAAGTACATCGTGACGTCT TTGCAGCCGGCCGACGTCAAGGCATGGGAGAATACGCTCGAAAAAGACGCGCGCCAGACGGCCACCCGGCCGAGC TTCCCTCGGACGGGCGAAGAGTTCTTGCGGTTCTCCCCAGTATCGACGCAGCAGCAGTCCATGTCGTCTCCCCCG ATGGCGAGCGAGCAGGGGCAGGAACATGGTCTGGTGCACAAGTTTGGCTCTCTCCACCAGCTCCCCGCCCCTCCG GCACGGCCATGCGCCGCGGTGAAGCGACTCAGCCATAGCGGCCTTTCTCAGGGAGACGACGGCCACGAGGCTTAC GGCGAGACGGGTGCCGTCGTACCGCCCCGACTGCCGGCGCGGTCTAAGAAAGCCATGGAGCAGCTGGCGGGAGGC GTCGTCAAGACTTACACCGGGCTCAACAACCCTCGCAACTGGTGTTACGCCAACAGCACGCTGCAGTCGCTACTG GCCTCTCCGGGCTTTGGACGAGAGCTGGCCGACTCGGGATGGATGAGCAGATACATTGTGCCGCGGAAGGCGGAG GAAACAATCGACCAGCCGCAACTCATGATCCGCATCATATCCCACCTGTTCCAATGGATGAGCACAGGCAATTTT GAGACGCTCAAGGCCCAGACTCTGATGGAATACTCGCGGAACCTCTGCAAGTCCAGCGATCCGCAGTCGCAGTTT GGCGGGCCGGAACAGCAGGACGCACAGGAATTCATGTCGTTTGTCATGGAGCAGATGCACGACGAGACCAACTCG CGGCGGGACCGGGCGGGAAAGGTCGAGCAGCCCAAGGCGGCTAGGGGACGGCCGCTGGTGGAGGCGGCCATTGAG TACTGGCGCAACCACACGCAGCTGAACCAGTCCATCATCGATCGATACTGGCGCGGAGTCGAGCTCTCGGCTGTC GAGTGCATGGGATGCCACACGCGGACTCACACCTTCTCGCCCTTTGGCTGGGTGCCGGTGACGGTCGGCCCCGGA CGCGACATGACGCTCTACGAGGCGCTCAACCACTACGTTGCCGAGAACCGGCTCGACGACTTCGCCTGCGACCAC TGCCAGGGCAAGCGGGTGGCGATGCAGTCCATGTCGTTTGCCCGGATGCCTCCGCTGCTCTGCATCAGCTTCCGA CGCTTCAACTACGACGGCCGCGATTTCTCCAAGTCCAACGCGGCCATCTCGTGGGACTTTAACGACGTCGACCTC TCGCCCTACTTCCTCGGCGCGGACGCGGACTCGGGCGGCGGCGACAGCGCCTTCACCGCCCCCTTCCGCTACGAA TGCTACGCCGTCATCGTCCACAGCGGTCGTCAGCTCAACACGGGCCATTACTTCGCCTACGTCCGAGACGCCAGC TCCCACGACCCCTACGCCTGGTACTGCTGCAACGACAGCCACGTGTCAAAGGTGCGCATCGGTAGCGGCGACGCG GCCGACGTGCAGAAGGATGTCTTTCGTTCGGATCCCGATCGCGTCCCGTACCTGGTCTTTTTCCACCGCAAGGAC GCGTGA |
| Gene | >Ophio5|1902 ATGGCTGCCGACGCCACTCATGGCCTCTCCCCGGCCTACGATAGCATCAGCCCGCGCTCTACGCCGTCCTCACCA GCGCCTATACCGCACATCGACGACCTCGTCGCCATCCCGACCGACGTGGGCCCCAACCAGTCCATTAAGCGACTG CTTGAAATGGCTCAGACCGCCTTGCGACAGTCTGAAATCAGTCGCGACTTCAACCGGCCCGCCATCGCCCTCCAG GAGTACATCAGGGCCTCCGTCATCGCCATCCAGATCATTACCAACCACAAAGACTATCCCGGACTGAGGACAGAT CATACCGACTCCGCCCGCGTACACAACGCCCTGCTCAGGCGCATCAAGCAGCAGAGTGACGACTACGAGAGCATC AAGCGCGACATCATCGAGGACAATAAGAGATCCGGCGTCCAACCGACCGTGAGACGGTCCTTGTGTCCGAACAAG GTTCAGGGCCTCGGCCTGGCATCCAAGCAAGCCGACTTGGTCAACGGTCACGCCTTGCCCCCCGTCAACGGCTCT CCGGGCAAGGTTAAGCCCGTCGTCCACCCGAAGCCTCACGCTCTCGCCGGCAATCTCCTGCCTGGCCGAGGGCGC GCCGCGTCGTCGAATGGCGCCACGCTCGACCTGGCCGCTCGCTTCGCCAACCTTCGCGGCCCCCAGTCCTCTCCA GGCCAAGATCCACGCATCAAGACGTATCCCATACCGACACAAAGGCCTGCCGGGCCCAGACAGATGCCACAGGAC CAGCAGCTGAACCTCGATACCGACGCCGCCACCTCGTCAGCCCTCCCCAAGGTGCCCGACGCCATCTACAGCCCC GCGCGGGGGAGCGTGTCCGGCGATCTGGCAAGGCTTCCGACCAGCACGTCTCGCGGCCTGTTCAGCCGCACCGGC TCGTCGACCTCGGTTCCCGCGGCGACGCCACAGGGCAGCGAACTCGCACCGGCTGTTGTGAGCCCCAGGATGCCC AGCCCCAGGATACCCCCAAGGATACCCAGCCCCAGAGTCCCTGAAGGAGCAGACGAGCCGCTCCCTCTACCGGCG GGAGACGGCATCACCCCCGAGCAGCTCGTCGAGGTCATGAGAGGCAACTGGTCCATTCTTCTCATCGACATCCGA TCCCGCGAGGCATTTAACGAGGGCCACATCATGTCGTCATCCATCATATGTATCGAACCGAGTATCCTGCTGCGA GACAACATCTCTTCGGAGGAAATATCGGAGAGCCTGGTGCTCTCGCCCAGCCCAGAGCAGGCACTCTTCGAGAAG CGTGACTCTTGCGACCTGGTCGTCTTCTACGACGAAGACTCACATCAAGTCATTCAATCTCCCAAGAACGCCGAC GAGCAGGTCATCCTGTCGCTGCACCGGGCTCTGATCCACCTCAACTACGGCCGAGACCTCAAGCGGCCCCCGAGG CTACTGATTGGGGGTCTGGCCGCTTGGGCCGATCTCGTGGGACCCCTTGCACTACAGTCTGGGGCCTCGTCGATG TTCAAGGGTCCCCATGCAAGATACAAGCGGAATGGAATTGTCCAGCGAAGGGGATCCAAGTACATCGTGACGTCT TTGCAGCCGGCCGACGTCAAGGCATGGGAGAATACGCTCGAAAAAGACGCGCGCCAGACGGCCACCCGGCCGAGC TTCCCTCGGACGGGCGAAGAGTTCTTGCGGTTCTCCCCAGTATCGACGCAGCAGCAGTCCATGTCGTCTCCCCCG ATGGCGAGCGAGCAGGGGCAGGAACATGGTCTGGTGCACAAGTTTGGCTCTCTCCACCAGCTCCCCGCCCCTCCG GCACGGCCATGCGCCGCGGTGAAGCGACTCAGCCATAGCGGCCTTTCTCAGGGAGACGACGGCCACGAGGCTTAC GGCGAGACGGGTGCCGTCGTACCGCCCCGACTGCCGGCGCGGTCTAAGAAAGCCATGGAGCAGCTGGCGGGAGGC GTCGTCAAGACTTACACCGGGCTCAACAACCCTCGCAACTGGTGTTACGCCAACAGCACGCTGCAGTCGCTACTG GCCTCTCCGGGCTTTGGACGAGAGCTGGCCGACTCGGGATGGATGAGCAGATACATTGTGCCGCGGAAGGCGGAG GAAACAATCGACCAGCCGCAACTCATGATCCGCATCATATCCCACCTGTTCCAATGGATGAGCACAGGCAATTTT GAGACGCTCAAGGCCCAGACTCTGATGGTAAGAAGGAATCCCGTCATAGGGAGGAACCGGCGAGACTGACGTGGA CGGCTGGCGGTGGCAGGAATACTCGCGGAACCTCTGCAAGTCCAGCGATCCGCAGTCGCAGTTTGGCGGGCCGGA ACAGCAGGACGCACAGGAATTCATGTCGTTTGTCATGGAGCAGATGCACGACGAGACCAACTCGCGGCGGGACCG GGCGGGAAAGGTCGAGCAGCCCAAGGCGGCTAGGGGACGGCCGCTGGTGGAGGCGGCCATTGAGTACTGGCGCAA CCACACGCAGCTGAACCAGTCCATCATCGATCGATACTGGCGCGGAGTCGAGCTCTCGGCTGTCGAGTGCATGGG ATGCCACACGCGGACTCACACCTTCTCGCCCTTTGGCTGGGTGCCGGTGACGGTCGGCCCCGGACGCGACATGAC GCTCTACGAGGCGCTCAACCACTACGTTGCCGAGAACCGGCTCGACGACTTCGCCTGCGACCACTGCCAGGGCAA GCGGGTGGCGATGCAGTCCATGTCGTTTGCCCGGATGCCTCCGCTGCTCTGCATCAGCTTCCGACGCTTCAACTA CGACGGCCGCGATTTCTCCAAGTCCAACGCGGCCATCTCGTGGGACTTTAACGACGTCGACCTCTCGCCCTACTT CCTCGGCGCGGACGCGGACTCGGGCGGCGGCGACAGCGCCTTCACCGCCCCCTTCCGCTACGAATGCTACGCCGT CATCGTCCACAGCGGTCGTCAGCTCAACACGGGCCATTACTTCGCCTACGTCCGAGACGCCAGCTCCCACGACCC CTACGCCTGGTACTGCTGCAACGACAGCCACGTGTCAAAGGTGCGCATCGGTAGCGGCGACGCGGCCGACGTGCA GAAGGATGTCTTTCGTTCGGATCCCGATCGCGTCCCGTACCTGGTCTTTTTCCACCGCAAGGACGCGTGA |