© 2022 - Robin Ohm - Utrecht University - The Netherlands
Built with Python Django and Wagtail
| Protein ID | Hirsu2|5511 |
| Gene name | |
| Location | Contig_276:20290..24174 |
| Strand | + |
| Gene length (bp) | 3884 |
| Transcript length (bp) | 3414 |
| Coding sequence length (bp) | 3414 |
| Protein length (aa) | 1138 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF12030 | DUF3517 | Domain of unknown function (DUF3517) | 1.3E-98 | 732 | 1068 |
| PF00443 | UCH | Ubiquitin carboxyl-terminal hydrolase | 9.6E-39 | 160 | 486 |
| PF13423 | UCH_1 | Ubiquitin carboxyl-terminal hydrolase | 1.2E-18 | 160 | 443 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q6ZQ93|UBP34_MOUSE | Ubiquitin carboxyl-terminal hydrolase 34 OS=Mus musculus GN=Usp34 PE=1 SV=3 | 144 | 752 | 2.0E-60 |
| sp|Q70CQ2|UBP34_HUMAN | Ubiquitin carboxyl-terminal hydrolase 34 OS=Homo sapiens GN=USP34 PE=1 SV=2 | 144 | 488 | 8.0E-60 |
| sp|B1AY13|UBP24_MOUSE | Ubiquitin carboxyl-terminal hydrolase 24 OS=Mus musculus GN=Usp24 PE=1 SV=1 | 154 | 490 | 1.0E-49 |
| sp|Q9UPU5|UBP24_HUMAN | Ubiquitin carboxyl-terminal hydrolase 24 OS=Homo sapiens GN=USP24 PE=1 SV=3 | 154 | 490 | 2.0E-49 |
| sp|P55824|FAF_DROME | Probable ubiquitin carboxyl-terminal hydrolase FAF OS=Drosophila melanogaster GN=faf PE=1 SV=2 | 123 | 534 | 4.0E-49 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q6ZQ93|UBP34_MOUSE | Ubiquitin carboxyl-terminal hydrolase 34 OS=Mus musculus GN=Usp34 PE=1 SV=3 | 144 | 752 | 2.0E-60 |
| sp|Q70CQ2|UBP34_HUMAN | Ubiquitin carboxyl-terminal hydrolase 34 OS=Homo sapiens GN=USP34 PE=1 SV=2 | 144 | 488 | 8.0E-60 |
| sp|B1AY13|UBP24_MOUSE | Ubiquitin carboxyl-terminal hydrolase 24 OS=Mus musculus GN=Usp24 PE=1 SV=1 | 154 | 490 | 1.0E-49 |
| sp|Q9UPU5|UBP24_HUMAN | Ubiquitin carboxyl-terminal hydrolase 24 OS=Homo sapiens GN=USP24 PE=1 SV=3 | 154 | 490 | 2.0E-49 |
| sp|P55824|FAF_DROME | Probable ubiquitin carboxyl-terminal hydrolase FAF OS=Drosophila melanogaster GN=faf PE=1 SV=2 | 123 | 534 | 4.0E-49 |
| sp|Q93008|USP9X_HUMAN | Probable ubiquitin carboxyl-terminal hydrolase FAF-X OS=Homo sapiens GN=USP9X PE=1 SV=3 | 154 | 525 | 7.0E-44 |
| sp|P70398|USP9X_MOUSE | Probable ubiquitin carboxyl-terminal hydrolase FAF-X OS=Mus musculus GN=Usp9x PE=1 SV=2 | 154 | 525 | 1.0E-43 |
| sp|O00507|USP9Y_HUMAN | Probable ubiquitin carboxyl-terminal hydrolase FAF-Y OS=Homo sapiens GN=USP9Y PE=2 SV=2 | 154 | 497 | 1.0E-42 |
| sp|Q9UTT1|UBP21_SCHPO | Ubiquitin carboxyl-terminal hydrolase 21 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp21 PE=3 SV=2 | 154 | 492 | 3.0E-39 |
| sp|Q24574|UBPE_DROME | Ubiquitin carboxyl-terminal hydrolase 64E OS=Drosophila melanogaster GN=Ubp64E PE=1 SV=2 | 151 | 531 | 7.0E-39 |
| sp|Q9VYQ8|UBP7_DROME | Ubiquitin carboxyl-terminal hydrolase 7 OS=Drosophila melanogaster GN=Usp7 PE=1 SV=1 | 158 | 512 | 3.0E-34 |
| sp|P50101|UBP15_YEAST | Ubiquitin carboxyl-terminal hydrolase 15 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP15 PE=1 SV=1 | 154 | 512 | 5.0E-34 |
| sp|Q3V0C5|UBP48_MOUSE | Ubiquitin carboxyl-terminal hydrolase 48 OS=Mus musculus GN=Usp48 PE=1 SV=2 | 154 | 525 | 8.0E-33 |
| sp|A1A5G2|UBP47_XENTR | Ubiquitin carboxyl-terminal hydrolase 47 OS=Xenopus tropicalis GN=usp47 PE=2 SV=1 | 158 | 487 | 1.0E-32 |
| sp|Q5U252|UBP47_XENLA | Ubiquitin carboxyl-terminal hydrolase 47 OS=Xenopus laevis GN=usp47 PE=2 SV=1 | 158 | 487 | 1.0E-32 |
| sp|Q86UV5|UBP48_HUMAN | Ubiquitin carboxyl-terminal hydrolase 48 OS=Homo sapiens GN=USP48 PE=1 SV=1 | 154 | 444 | 2.0E-32 |
| sp|Q84WU2|UBP13_ARATH | Ubiquitin carboxyl-terminal hydrolase 13 OS=Arabidopsis thaliana GN=UBP13 PE=1 SV=1 | 154 | 512 | 3.0E-32 |
| sp|Q09879|UBP5_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 5 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp5 PE=3 SV=3 | 158 | 518 | 3.0E-32 |
| sp|Q76LT8|UBP48_RAT | Ubiquitin carboxyl-terminal hydrolase 48 OS=Rattus norvegicus GN=Usp48 PE=1 SV=1 | 154 | 444 | 4.0E-32 |
| sp|Q6U7I1|UBP7_CHICK | Ubiquitin carboxyl-terminal hydrolase 7 OS=Gallus gallus GN=USP7 PE=2 SV=1 | 158 | 492 | 5.0E-32 |
| sp|Q4VSI4|UBP7_RAT | Ubiquitin carboxyl-terminal hydrolase 7 OS=Rattus norvegicus GN=Usp7 PE=1 SV=1 | 158 | 492 | 6.0E-32 |
| sp|Q93009|UBP7_HUMAN | Ubiquitin carboxyl-terminal hydrolase 7 OS=Homo sapiens GN=USP7 PE=1 SV=2 | 158 | 492 | 7.0E-32 |
| sp|Q5ZM45|UBP48_CHICK | Ubiquitin carboxyl-terminal hydrolase 48 OS=Gallus gallus GN=USP48 PE=2 SV=1 | 154 | 525 | 1.0E-31 |
| sp|Q6A4J8|UBP7_MOUSE | Ubiquitin carboxyl-terminal hydrolase 7 OS=Mus musculus GN=Usp7 PE=1 SV=1 | 158 | 492 | 2.0E-31 |
| sp|Q9FPT1|UBP12_ARATH | Ubiquitin carboxyl-terminal hydrolase 12 OS=Arabidopsis thaliana GN=UBP12 PE=1 SV=2 | 154 | 512 | 2.0E-31 |
| sp|Q7JKC3|UBP7_CAEEL | Ubiquitin carboxyl-terminal hydrolase 7 OS=Caenorhabditis elegans GN=usp-7 PE=3 SV=1 | 158 | 492 | 1.0E-30 |
| sp|A3AF13|UBP26_ORYSJ | Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. japonica GN=UBP26 PE=3 SV=2 | 160 | 447 | 3.0E-30 |
| sp|Q60MK8|UBP7_CAEBR | Ubiquitin carboxyl-terminal hydrolase 7 OS=Caenorhabditis briggsae GN=usp-7 PE=3 SV=1 | 158 | 492 | 4.0E-30 |
| sp|A2XDG4|UBP26_ORYSI | Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. indica GN=UBP26 PE=3 SV=1 | 160 | 447 | 4.0E-30 |
| sp|Q8BY87|UBP47_MOUSE | Ubiquitin carboxyl-terminal hydrolase 47 OS=Mus musculus GN=Usp47 PE=1 SV=2 | 154 | 447 | 7.0E-30 |
| sp|Q96K76|UBP47_HUMAN | Ubiquitin carboxyl-terminal hydrolase 47 OS=Homo sapiens GN=USP47 PE=1 SV=3 | 154 | 447 | 3.0E-29 |
| sp|Q9SCJ9|UBP26_ARATH | Ubiquitin carboxyl-terminal hydrolase 26 OS=Arabidopsis thaliana GN=UBP26 PE=1 SV=3 | 147 | 528 | 3.0E-29 |
| sp|E1C1R4|UBP47_CHICK | Ubiquitin carboxyl-terminal hydrolase 47 OS=Gallus gallus GN=USP47 PE=3 SV=1 | 158 | 447 | 6.0E-29 |
| sp|Q9NVE5|UBP40_HUMAN | Ubiquitin carboxyl-terminal hydrolase 40 OS=Homo sapiens GN=USP40 PE=1 SV=3 | 149 | 428 | 2.0E-28 |
| sp|Q8BWR4|UBP40_MOUSE | Ubiquitin carboxyl-terminal hydrolase 40 OS=Mus musculus GN=Usp40 PE=1 SV=2 | 161 | 428 | 9.0E-28 |
| sp|O74442|UBP16_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 16 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp16 PE=1 SV=1 | 161 | 447 | 1.0E-27 |
| sp|A4FUN7|UBP12_DANRE | Ubiquitin carboxyl-terminal hydrolase 12A OS=Danio rerio GN=usp12a PE=2 SV=1 | 159 | 487 | 1.0E-24 |
| sp|C0HB46|UBP12_SALSA | Ubiquitin carboxyl-terminal hydrolase 12 OS=Salmo salar GN=usp12 PE=2 SV=1 | 159 | 487 | 4.0E-24 |
| sp|O57429|UBP2_CHICK | Ubiquitin carboxyl-terminal hydrolase 2 OS=Gallus gallus GN=USP2 PE=2 SV=1 | 158 | 490 | 1.0E-23 |
| sp|B1AQJ2|UBP36_MOUSE | Ubiquitin carboxyl-terminal hydrolase 36 OS=Mus musculus GN=Usp36 PE=1 SV=1 | 160 | 519 | 9.0E-23 |
| sp|A5D9H7|UBP12_BOVIN | Ubiquitin carboxyl-terminal hydrolase 12 OS=Bos taurus GN=USP12 PE=2 SV=1 | 159 | 487 | 1.0E-22 |
| sp|Q52KZ6|UB12A_XENLA | Ubiquitin carboxyl-terminal hydrolase 12-A OS=Xenopus laevis GN=usp12-a PE=2 SV=1 | 159 | 487 | 1.0E-22 |
| sp|Q5M981|UB12B_XENLA | Ubiquitin carboxyl-terminal hydrolase 12-B OS=Xenopus laevis GN=usp12-b PE=2 SV=2 | 159 | 487 | 2.0E-22 |
| sp|Q9D9M2|UBP12_MOUSE | Ubiquitin carboxyl-terminal hydrolase 12 OS=Mus musculus GN=Usp12 PE=2 SV=2 | 159 | 487 | 2.0E-22 |
| sp|O75317|UBP12_HUMAN | Ubiquitin carboxyl-terminal hydrolase 12 OS=Homo sapiens GN=USP12 PE=1 SV=2 | 159 | 487 | 2.0E-22 |
| sp|Q9FPS2|UBP25_ARATH | Ubiquitin carboxyl-terminal hydrolase 25 OS=Arabidopsis thaliana GN=UBP25 PE=2 SV=1 | 160 | 510 | 4.0E-22 |
| sp|Q5RBQ4|UBP46_PONAB | Ubiquitin carboxyl-terminal hydrolase 46 OS=Pongo abelii GN=USP46 PE=2 SV=1 | 159 | 487 | 4.0E-22 |
| sp|P62069|UBP46_MOUSE | Ubiquitin carboxyl-terminal hydrolase 46 OS=Mus musculus GN=Usp46 PE=1 SV=1 | 159 | 487 | 4.0E-22 |
| sp|P62068|UBP46_HUMAN | Ubiquitin carboxyl-terminal hydrolase 46 OS=Homo sapiens GN=USP46 PE=1 SV=1 | 159 | 487 | 4.0E-22 |
| sp|Q9P275|UBP36_HUMAN | Ubiquitin carboxyl-terminal hydrolase 36 OS=Homo sapiens GN=USP36 PE=1 SV=3 | 160 | 519 | 5.0E-22 |
| sp|A5WWB0|UBP46_DANRE | Ubiquitin carboxyl-terminal hydrolase 46 OS=Danio rerio GN=usp46 PE=3 SV=2 | 159 | 487 | 2.0E-21 |
| sp|Q9UMW8|UBP18_HUMAN | Ubl carboxyl-terminal hydrolase 18 OS=Homo sapiens GN=USP18 PE=1 SV=1 | 148 | 488 | 2.0E-21 |
| sp|Q67XW5|UBP18_ARATH | Ubiquitin carboxyl-terminal hydrolase 18 OS=Arabidopsis thaliana GN=UBP18 PE=2 SV=2 | 155 | 428 | 2.0E-21 |
| sp|E1B9W9|UBP42_BOVIN | Ubiquitin carboxyl-terminal hydrolase 42 OS=Bos taurus GN=USP42 PE=3 SV=1 | 160 | 538 | 9.0E-21 |
| sp|Q9H9J4|UBP42_HUMAN | Ubiquitin carboxyl-terminal hydrolase 42 OS=Homo sapiens GN=USP42 PE=1 SV=3 | 160 | 538 | 1.0E-20 |
| sp|B2RQC2|UBP42_MOUSE | Ubiquitin carboxyl-terminal hydrolase 42 OS=Mus musculus GN=Usp42 PE=1 SV=1 | 160 | 526 | 2.0E-20 |
| sp|Q5RE63|UBP18_PONAB | Ubl carboxyl-terminal hydrolase 18 OS=Pongo abelii GN=USP18 PE=2 SV=1 | 148 | 488 | 3.0E-20 |
| sp|Q9SJA1|UBP19_ARATH | Ubiquitin carboxyl-terminal hydrolase 19 OS=Arabidopsis thaliana GN=UBP19 PE=2 SV=2 | 145 | 428 | 5.0E-20 |
| sp|D3ZU96|UBP42_RAT | Ubiquitin carboxyl-terminal hydrolase 42 OS=Rattus norvegicus GN=Usp42 PE=1 SV=1 | 160 | 498 | 7.0E-20 |
| sp|O75604|UBP2_HUMAN | Ubiquitin carboxyl-terminal hydrolase 2 OS=Homo sapiens GN=USP2 PE=1 SV=2 | 154 | 490 | 1.0E-19 |
| sp|Q3LFD5|UBP41_HUMAN | Putative ubiquitin carboxyl-terminal hydrolase 41 OS=Homo sapiens GN=USP41 PE=2 SV=2 | 158 | 463 | 3.0E-19 |
| sp|Q5U349|UBP2_RAT | Ubiquitin carboxyl-terminal hydrolase 2 OS=Rattus norvegicus GN=Usp2 PE=1 SV=1 | 154 | 490 | 3.0E-19 |
| sp|O88623|UBP2_MOUSE | Ubiquitin carboxyl-terminal hydrolase 2 OS=Mus musculus GN=Usp2 PE=1 SV=2 | 154 | 490 | 3.0E-19 |
| sp|Q6QN14|U17L6_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 6 OS=Homo sapiens GN=USP17L6P PE=1 SV=2 | 160 | 499 | 4.0E-19 |
| sp|Q9WTV6|UBP18_MOUSE | Ubl carboxyl-terminal hydrolase 18 OS=Mus musculus GN=Usp18 PE=1 SV=2 | 148 | 480 | 7.0E-19 |
| sp|Q9SB51|UBP16_ARATH | Ubiquitin carboxyl-terminal hydrolase 16 OS=Arabidopsis thaliana GN=UBP16 PE=1 SV=1 | 122 | 490 | 8.0E-19 |
| sp|Q7M764|U17PE_MOUSE | Ubiquitin carboxyl-terminal hydrolase 17-like protein E OS=Mus musculus GN=Usp17le PE=3 SV=2 | 149 | 450 | 9.0E-19 |
| sp|C9JVI0|U17LB_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 11 OS=Homo sapiens GN=USP17L11 PE=3 SV=1 | 160 | 499 | 1.0E-18 |
| sp|D6R9N7|U17LI_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 18 OS=Homo sapiens GN=USP17L18 PE=3 SV=1 | 160 | 499 | 1.0E-18 |
| sp|D6RJB6|U17LK_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 20 OS=Homo sapiens GN=USP17L20 PE=3 SV=1 | 160 | 499 | 1.0E-18 |
| sp|D6RCP7|U17LJ_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 19 OS=Homo sapiens GN=USP17L19 PE=3 SV=1 | 160 | 499 | 1.0E-18 |
| sp|Q0WX57|U17LO_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 24 OS=Homo sapiens GN=USP17L24 PE=1 SV=2 | 160 | 499 | 1.0E-18 |
| sp|D6RA61|U17LM_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 22 OS=Homo sapiens GN=USP17L22 PE=3 SV=1 | 160 | 499 | 1.0E-18 |
| sp|D6R901|U17LL_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 21 OS=Homo sapiens GN=USP17L21 PE=3 SV=1 | 160 | 499 | 2.0E-18 |
| sp|D6RBQ6|U17LH_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 17 OS=Homo sapiens GN=USP17L17 PE=3 SV=1 | 160 | 499 | 2.0E-18 |
| sp|C9JPN9|UL17C_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 12 OS=Homo sapiens GN=USP17L12 PE=3 SV=1 | 160 | 499 | 3.0E-18 |
| sp|A8MUK1|U17L5_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 5 OS=Homo sapiens GN=USP17L5 PE=3 SV=2 | 160 | 499 | 4.0E-18 |
| sp|C9JLJ4|U17LD_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 13 OS=Homo sapiens GN=USP17L13 PE=3 SV=1 | 160 | 499 | 4.0E-18 |
| sp|C9J2P7|U17LF_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 15 OS=Homo sapiens GN=USP17L15 PE=3 SV=1 | 160 | 499 | 5.0E-18 |
| sp|Q9FPS4|UBP23_ARATH | Ubiquitin carboxyl-terminal hydrolase 23 OS=Arabidopsis thaliana GN=UBP23 PE=2 SV=2 | 160 | 488 | 7.0E-18 |
| sp|C9JJH3|U17LA_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 10 OS=Homo sapiens GN=USP17L10 PE=3 SV=1 | 160 | 499 | 2.0E-17 |
| sp|Q2KHV7|UBP2_BOVIN | Ubiquitin carboxyl-terminal hydrolase 2 OS=Bos taurus GN=USP2 PE=2 SV=1 | 154 | 443 | 4.0E-17 |
| sp|A6NCW0|U17L3_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 3 OS=Homo sapiens GN=USP17L3 PE=3 SV=1 | 160 | 499 | 5.0E-17 |
| sp|P34547|UBP46_CAEEL | Ubiquitin carboxyl-terminal hydrolase 46 OS=Caenorhabditis elegans GN=usp-46 PE=1 SV=3 | 259 | 487 | 6.0E-17 |
| sp|Q7RTZ2|U17L1_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17-like protein 1 OS=Homo sapiens GN=USP17L1 PE=3 SV=1 | 160 | 499 | 8.0E-17 |
| sp|Q6R6M4|U17L2_HUMAN | Ubiquitin carboxyl-terminal hydrolase 17 OS=Homo sapiens GN=USP17L2 PE=1 SV=2 | 160 | 499 | 8.0E-17 |
| sp|Q9UPT9|UBP22_HUMAN | Ubiquitin carboxyl-terminal hydrolase 22 OS=Homo sapiens GN=USP22 PE=1 SV=2 | 149 | 447 | 1.0E-16 |
| sp|Q70EK9|UBP51_HUMAN | Ubiquitin carboxyl-terminal hydrolase 51 OS=Homo sapiens GN=USP51 PE=2 SV=1 | 158 | 447 | 1.0E-16 |
| sp|Q61068|U17PA_MOUSE | Ubiquitin carboxyl-terminal hydrolase 17-like protein A OS=Mus musculus GN=Usp17la PE=1 SV=1 | 142 | 493 | 1.0E-16 |
| sp|P0C8Z3|UBP22_BOVIN | Ubiquitin carboxyl-terminal hydrolase 22 OS=Bos taurus GN=USP22 PE=2 SV=1 | 149 | 447 | 2.0E-16 |
| sp|Q5DU02|UBP22_MOUSE | Ubiquitin carboxyl-terminal hydrolase 22 OS=Mus musculus GN=Usp22 PE=2 SV=2 | 149 | 447 | 2.0E-16 |
| sp|A6H8I0|UBP22_DANRE | Ubiquitin carboxyl-terminal hydrolase 22 OS=Danio rerio GN=usp22 PE=2 SV=1 | 158 | 447 | 3.0E-16 |
| sp|P38187|UBP13_YEAST | Ubiquitin carboxyl-terminal hydrolase 13 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP13 PE=1 SV=3 | 221 | 503 | 3.0E-16 |
| sp|Q6GNI6|UB22A_XENLA | Ubiquitin carboxyl-terminal hydrolase 22-A OS=Xenopus laevis GN=usp22-a PE=2 SV=1 | 158 | 447 | 3.0E-16 |
| sp|Q6DCJ1|UB22B_XENLA | Ubiquitin carboxyl-terminal hydrolase 22-B OS=Xenopus laevis GN=usp22-b PE=2 SV=2 | 158 | 447 | 3.0E-16 |
| sp|P0C7I0|U17L8_HUMAN | Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 8 OS=Homo sapiens GN=USP17L8 PE=3 SV=1 | 160 | 499 | 3.0E-16 |
| sp|Q9FIQ1|UBP21_ARATH | Ubiquitin carboxyl-terminal hydrolase 21 OS=Arabidopsis thaliana GN=UBP21 PE=2 SV=1 | 160 | 447 | 3.0E-16 |
| sp|Q9FPS9|UBP15_ARATH | Ubiquitin carboxyl-terminal hydrolase 15 OS=Arabidopsis thaliana GN=UBP15 PE=2 SV=2 | 161 | 489 | 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 | 160 | 499 | 6.0E-16 |
| sp|P32571|UBP4_YEAST | Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DOA4 PE=1 SV=2 | 160 | 448 | 1.0E-15 |
| sp|B3LGK1|UBP4_YEAS1 | Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain RM11-1a) GN=DOA4 PE=3 SV=1 | 160 | 448 | 1.0E-15 |
| sp|Q8CEG8|UBP27_MOUSE | Ubiquitin carboxyl-terminal hydrolase 27 OS=Mus musculus GN=Usp27 PE=2 SV=2 | 158 | 447 | 2.0E-15 |
| sp|A6ZY34|UBP4_YEAS7 | Ubiquitin carboxyl-terminal hydrolase 4 OS=Saccharomyces cerevisiae (strain YJM789) GN=DOA4 PE=3 SV=1 | 160 | 448 | 2.0E-15 |
| sp|Q2KJ72|UBP21_BOVIN | Ubiquitin carboxyl-terminal hydrolase 21 OS=Bos taurus GN=USP21 PE=2 SV=1 | 158 | 457 | 2.0E-15 |
| sp|Q9FKP5|UBP17_ARATH | Ubiquitin carboxyl-terminal hydrolase 17 OS=Arabidopsis thaliana GN=UBP17 PE=2 SV=1 | 161 | 472 | 4.0E-15 |
| sp|Q8TEY7|UBP33_HUMAN | Ubiquitin carboxyl-terminal hydrolase 33 OS=Homo sapiens GN=USP33 PE=1 SV=2 | 309 | 520 | 4.0E-15 |
| sp|Q6P8X6|UBP50_MOUSE | Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Mus musculus GN=Usp50 PE=2 SV=1 | 158 | 447 | 5.0E-15 |
| sp|Q9UK80|UBP21_HUMAN | Ubiquitin carboxyl-terminal hydrolase 21 OS=Homo sapiens GN=USP21 PE=1 SV=1 | 158 | 457 | 5.0E-15 |
| sp|Q5ZID5|UBP28_CHICK | Ubiquitin carboxyl-terminal hydrolase 28 OS=Gallus gallus GN=USP28 PE=2 SV=1 | 160 | 387 | 5.0E-15 |
| sp|Q9VVR1|NOT_DROME | Ubiquitin carboxyl-terminal hydrolase nonstop OS=Drosophila melanogaster GN=not PE=1 SV=3 | 158 | 447 | 6.0E-15 |
| sp|Q8R5K2|UBP33_MOUSE | Ubiquitin carboxyl-terminal hydrolase 33 OS=Mus musculus GN=Usp33 PE=1 SV=2 | 309 | 520 | 7.0E-15 |
| sp|Q9QZL6|UBP21_MOUSE | Ubiquitin carboxyl-terminal hydrolase 21 OS=Mus musculus GN=Usp21 PE=1 SV=1 | 158 | 457 | 7.0E-15 |
| sp|Q5REG5|UBP33_PONAB | Ubiquitin carboxyl-terminal hydrolase 33 OS=Pongo abelii GN=USP33 PE=2 SV=1 | 309 | 520 | 7.0E-15 |
| sp|A5PN09|UBP20_DANRE | Ubiquitin carboxyl-terminal hydrolase 20 OS=Danio rerio GN=usp20 PE=3 SV=1 | 309 | 523 | 1.0E-14 |
| sp|P50102|UBP8_YEAST | Ubiquitin carboxyl-terminal hydrolase 8 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP8 PE=1 SV=1 | 158 | 447 | 1.0E-14 |
| sp|Q9Y2K6|UBP20_HUMAN | Ubiquitin carboxyl-terminal hydrolase 20 OS=Homo sapiens GN=USP20 PE=1 SV=2 | 309 | 523 | 1.0E-14 |
| sp|B3NC86|UBP36_DROER | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila erecta GN=Usp36 PE=3 SV=1 | 160 | 448 | 2.0E-14 |
| sp|B2GUX4|UBP21_RAT | Ubiquitin carboxyl-terminal hydrolase 21 OS=Rattus norvegicus GN=Usp21 PE=2 SV=1 | 158 | 457 | 2.0E-14 |
| sp|Q28CN3|UBP33_XENTR | Ubiquitin carboxyl-terminal hydrolase 33 OS=Xenopus tropicalis GN=usp33 PE=2 SV=2 | 309 | 520 | 2.0E-14 |
| sp|B4QIS3|UBP36_DROSI | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila simulans GN=Usp36 PE=3 SV=1 | 160 | 448 | 2.0E-14 |
| sp|Q96RU2|UBP28_HUMAN | Ubiquitin carboxyl-terminal hydrolase 28 OS=Homo sapiens GN=USP28 PE=1 SV=1 | 160 | 387 | 2.0E-14 |
| sp|A6QNM7|UBP33_BOVIN | Ubiquitin carboxyl-terminal hydrolase 33 OS=Bos taurus GN=USP33 PE=2 SV=1 | 309 | 520 | 3.0E-14 |
| sp|A8HAL1|UBP16_DANRE | Ubiquitin carboxyl-terminal hydrolase 16 OS=Danio rerio GN=usp16 PE=3 SV=1 | 304 | 490 | 3.0E-14 |
| sp|A6NNY8|UBP27_HUMAN | Ubiquitin carboxyl-terminal hydrolase 27 OS=Homo sapiens GN=USP27X PE=2 SV=3 | 158 | 447 | 3.0E-14 |
| sp|Q9P7V9|UBP9_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 9 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp9 PE=1 SV=1 | 243 | 521 | 3.0E-14 |
| sp|Q5R5Z6|UBP20_PONAB | Ubiquitin carboxyl-terminal hydrolase 20 OS=Pongo abelii GN=USP20 PE=2 SV=1 | 309 | 447 | 3.0E-14 |
| sp|Q8C6M1|UBP20_MOUSE | Ubiquitin carboxyl-terminal hydrolase 20 OS=Mus musculus GN=Usp20 PE=1 SV=1 | 309 | 523 | 4.0E-14 |
| sp|B4IXE0|UBP36_DROGR | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila grimshawi GN=Usp36 PE=3 SV=1 | 160 | 448 | 4.0E-14 |
| sp|P0C7H9|U17L7_HUMAN | Inactive ubiquitin carboxyl-terminal hydrolase 17-like protein 7 OS=Homo sapiens GN=USP17L7 PE=3 SV=1 | 160 | 499 | 5.0E-14 |
| sp|B1WBD7|UBP20_XENLA | Ubiquitin carboxyl-terminal hydrolase 20 OS=Xenopus laevis GN=usp20 PE=2 SV=1 | 309 | 497 | 7.0E-14 |
| sp|A7Z056|UBP20_BOVIN | Ubiquitin carboxyl-terminal hydrolase 20 OS=Bos taurus GN=USP20 PE=2 SV=1 | 309 | 490 | 8.0E-14 |
| sp|A0JM59|UBP20_XENTR | Ubiquitin carboxyl-terminal hydrolase 20 OS=Xenopus tropicalis GN=usp20 PE=2 SV=1 | 309 | 497 | 8.0E-14 |
| sp|Q9VRP5|UBP36_DROME | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila melanogaster GN=scny PE=1 SV=3 | 160 | 448 | 9.0E-14 |
| sp|Q99K46|UBP11_MOUSE | Ubiquitin carboxyl-terminal hydrolase 11 OS=Mus musculus GN=Usp11 PE=1 SV=4 | 305 | 513 | 1.0E-13 |
| sp|B3M3M6|UBP36_DROAN | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila ananassae GN=Usp36 PE=3 SV=1 | 161 | 448 | 1.0E-13 |
| sp|B4PIW8|UBP36_DROYA | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila yakuba GN=Usp36 PE=3 SV=1 | 160 | 448 | 2.0E-13 |
| sp|Q9FPS7|UBP20_ARATH | Ubiquitin carboxyl-terminal hydrolase 20 OS=Arabidopsis thaliana GN=UBP20 PE=2 SV=1 | 160 | 491 | 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 | 160 | 491 | 2.0E-13 |
| sp|Q8LAM0|UBP4_ARATH | Ubiquitin carboxyl-terminal hydrolase 4 OS=Arabidopsis thaliana GN=UBP4 PE=1 SV=2 | 159 | 491 | 3.0E-13 |
| sp|B4LG38|UBP36_DROVI | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila virilis GN=Usp36 PE=3 SV=1 | 160 | 448 | 3.0E-13 |
| sp|B4KXJ5|UBP36_DROMO | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila mojavensis GN=Usp36 PE=3 SV=1 | 160 | 448 | 5.0E-13 |
| sp|Q4R6D3|UBP50_MACFA | Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Macaca fascicularis GN=USP50 PE=2 SV=1 | 156 | 447 | 7.0E-13 |
| sp|Q5I043|UBP28_MOUSE | Ubiquitin carboxyl-terminal hydrolase 28 OS=Mus musculus GN=Usp28 PE=1 SV=1 | 160 | 387 | 1.0E-12 |
| sp|Q2LZB1|UBP36_DROPS | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila pseudoobscura pseudoobscura GN=Usp36 PE=3 SV=2 | 160 | 448 | 2.0E-12 |
| sp|O24454|UBP3_ARATH | Ubiquitin carboxyl-terminal hydrolase 3 OS=Arabidopsis thaliana GN=UBP3 PE=1 SV=1 | 159 | 487 | 2.0E-12 |
| sp|P40818|UBP8_HUMAN | Ubiquitin carboxyl-terminal hydrolase 8 OS=Homo sapiens GN=USP8 PE=1 SV=1 | 160 | 443 | 2.0E-12 |
| sp|D3ZJ96|UBP28_RAT | Ubiquitin carboxyl-terminal hydrolase 28 OS=Rattus norvegicus GN=Usp28 PE=2 SV=2 | 160 | 387 | 2.0E-12 |
| sp|Q80U87|UBP8_MOUSE | Ubiquitin carboxyl-terminal hydrolase 8 OS=Mus musculus GN=Usp8 PE=1 SV=2 | 160 | 443 | 3.0E-12 |
| sp|P39967|UBP9_YEAST | Ubiquitin carboxyl-terminal hydrolase 9 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP9 PE=1 SV=1 | 221 | 498 | 3.0E-12 |
| sp|A5PMR2|UBP33_DANRE | Ubiquitin carboxyl-terminal hydrolase 33 OS=Danio rerio GN=usp33 PE=2 SV=1 | 309 | 490 | 3.0E-12 |
| sp|B4MLR8|UBP36_DROWI | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila willistoni GN=Usp36 PE=3 SV=1 | 160 | 448 | 7.0E-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 | 264 | 500 | 7.0E-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 | 257 | 428 | 9.0E-12 |
| 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 | 264 | 505 | 2.0E-11 |
| 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 | 264 | 505 | 2.0E-11 |
| 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 | 264 | 499 | 2.0E-11 |
| sp|Q2UUG8|CREB_ASPOR | Probable ubiquitin carboxyl-terminal hydrolase creB OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=creB PE=3 SV=2 | 264 | 499 | 2.0E-11 |
| 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 | 264 | 505 | 2.0E-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 | 264 | 505 | 3.0E-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 | 264 | 506 | 4.0E-11 |
| 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 | 264 | 515 | 4.0E-11 |
| 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 | 160 | 448 | 4.0E-11 |
| sp|P51784|UBP11_HUMAN | Ubiquitin carboxyl-terminal hydrolase 11 OS=Homo sapiens GN=USP11 PE=1 SV=3 | 310 | 488 | 5.0E-11 |
| sp|Q2KJ09|UBP16_RAT | Ubiquitin carboxyl-terminal hydrolase 16 OS=Rattus norvegicus GN=Usp16 PE=1 SV=2 | 295 | 488 | 6.0E-11 |
| sp|Q99LG0|UBP16_MOUSE | Ubiquitin carboxyl-terminal hydrolase 16 OS=Mus musculus GN=Usp16 PE=1 SV=2 | 295 | 488 | 7.0E-11 |
| sp|P57080|UBP25_MOUSE | Ubiquitin carboxyl-terminal hydrolase 25 OS=Mus musculus GN=Usp25 PE=1 SV=2 | 134 | 387 | 8.0E-11 |
| sp|Q91W36|UBP3_MOUSE | Ubiquitin carboxyl-terminal hydrolase 3 OS=Mus musculus GN=Usp3 PE=2 SV=1 | 160 | 450 | 1.0E-10 |
| sp|Q5XGZ2|UP44B_XENLA | Ubiquitin carboxyl-terminal hydrolase 44-B OS=Xenopus laevis GN=usp44-b PE=2 SV=1 | 243 | 444 | 1.0E-10 |
| sp|Q7ZUM8|UBP44_DANRE | Ubiquitin carboxyl-terminal hydrolase 44 OS=Danio rerio GN=usp44 PE=2 SV=1 | 158 | 447 | 2.0E-10 |
| sp|Q6NTR6|UP44A_XENLA | Ubiquitin carboxyl-terminal hydrolase 44-A OS=Xenopus laevis GN=usp44-a PE=2 SV=1 | 243 | 444 | 2.0E-10 |
| sp|Q9Y6I4|UBP3_HUMAN | Ubiquitin carboxyl-terminal hydrolase 3 OS=Homo sapiens GN=USP3 PE=1 SV=2 | 160 | 450 | 3.0E-10 |
| sp|O60139|UBP4_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp4 PE=1 SV=2 | 160 | 493 | 3.0E-10 |
| sp|Q9UHP3|UBP25_HUMAN | Ubiquitin carboxyl-terminal hydrolase 25 OS=Homo sapiens GN=USP25 PE=1 SV=4 | 134 | 387 | 4.0E-10 |
| sp|Q01988|UBP11_CANLF | Ubiquitin carboxyl-terminal hydrolase 11 (Fragment) OS=Canis lupus familiaris GN=USP11 PE=2 SV=1 | 305 | 488 | 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 | 160 | 489 | 5.0E-10 |
| sp|Q3UJD6|UBP19_MOUSE | Ubiquitin carboxyl-terminal hydrolase 19 OS=Mus musculus GN=Usp19 PE=1 SV=1 | 282 | 491 | 1.0E-09 |
| sp|Q08DA3|UBP16_BOVIN | Ubiquitin carboxyl-terminal hydrolase 16 OS=Bos taurus GN=USP16 PE=2 SV=2 | 340 | 488 | 1.0E-09 |
| sp|Q6J1Y9|UBP19_RAT | Ubiquitin carboxyl-terminal hydrolase 19 OS=Rattus norvegicus GN=Usp19 PE=1 SV=1 | 282 | 491 | 1.0E-09 |
| sp|Q09738|UBP8_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 8 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp8 PE=3 SV=1 | 158 | 446 | 1.0E-09 |
| sp|O94966|UBP19_HUMAN | Ubiquitin carboxyl-terminal hydrolase 19 OS=Homo sapiens GN=USP19 PE=1 SV=2 | 282 | 488 | 2.0E-09 |
| sp|Q70EL2|UBP45_HUMAN | Ubiquitin carboxyl-terminal hydrolase 45 OS=Homo sapiens GN=USP45 PE=1 SV=3 | 309 | 488 | 3.0E-09 |
| sp|Q4R6X7|UBP16_MACFA | Ubiquitin carboxyl-terminal hydrolase 16 OS=Macaca fascicularis GN=USP16 PE=2 SV=2 | 295 | 488 | 3.0E-09 |
| sp|Q9Y5T5|UBP16_HUMAN | Ubiquitin carboxyl-terminal hydrolase 16 OS=Homo sapiens GN=USP16 PE=1 SV=1 | 295 | 488 | 4.0E-09 |
| sp|Q9LEW0|UBP22_ARATH | Ubiquitin carboxyl-terminal hydrolase 22 OS=Arabidopsis thaliana GN=UBP22 PE=2 SV=1 | 148 | 446 | 4.0E-09 |
| sp|B2GUZ1|UBP4_RAT | Ubiquitin carboxyl-terminal hydrolase 4 OS=Rattus norvegicus GN=Usp4 PE=1 SV=1 | 258 | 488 | 1.0E-08 |
| sp|D2HBJ8|UBP44_AILME | Ubiquitin carboxyl-terminal hydrolase 44 OS=Ailuropoda melanoleuca GN=USP44 PE=3 SV=1 | 243 | 447 | 1.0E-08 |
| sp|Q9H0E7|UBP44_HUMAN | Ubiquitin carboxyl-terminal hydrolase 44 OS=Homo sapiens GN=USP44 PE=1 SV=2 | 243 | 447 | 1.0E-08 |
| sp|B4HUI5|UBP36_DROSE | Ubiquitin carboxyl-terminal hydrolase 36 OS=Drosophila sechellia GN=Usp36 PE=3 SV=1 | 160 | 448 | 1.0E-08 |
| sp|Q8K387|UBP45_MOUSE | Ubiquitin carboxyl-terminal hydrolase 45 OS=Mus musculus GN=Usp45 PE=1 SV=1 | 309 | 488 | 1.0E-08 |
| sp|Q0V9G5|UBP44_XENTR | Ubiquitin carboxyl-terminal hydrolase 44 OS=Xenopus tropicalis GN=usp44 PE=2 SV=1 | 243 | 426 | 2.0E-08 |
| sp|P35123|UBP4_MOUSE | Ubiquitin carboxyl-terminal hydrolase 4 OS=Mus musculus GN=Usp4 PE=1 SV=3 | 258 | 488 | 2.0E-08 |
| sp|Q9P2H5|UBP35_HUMAN | Ubiquitin carboxyl-terminal hydrolase 35 OS=Homo sapiens GN=USP35 PE=1 SV=3 | 154 | 298 | 2.0E-08 |
| sp|Q8W4N3|UBP2_ARATH | Ubiquitin carboxyl-terminal hydrolase 2 OS=Arabidopsis thaliana GN=UBP2 PE=1 SV=2 | 338 | 446 | 4.0E-08 |
| sp|Q70EL3|UBP50_HUMAN | Inactive ubiquitin carboxyl-terminal hydrolase 50 OS=Homo sapiens GN=USP50 PE=2 SV=1 | 277 | 433 | 4.0E-08 |
| sp|Q8C2S0|UBP44_MOUSE | Ubiquitin carboxyl-terminal hydrolase 44 OS=Mus musculus GN=Usp44 PE=2 SV=3 | 194 | 447 | 6.0E-08 |
| sp|P39538|UBP12_YEAST | Ubiquitin carboxyl-terminal hydrolase 12 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP12 PE=1 SV=1 | 309 | 459 | 9.0E-08 |
| sp|Q0VA64|UBP16_XENTR | Ubiquitin carboxyl-terminal hydrolase 16 OS=Xenopus tropicalis GN=usp16 PE=2 SV=2 | 290 | 488 | 1.0E-07 |
| sp|Q6P9L4|UBP49_MOUSE | Ubiquitin carboxyl-terminal hydrolase 49 OS=Mus musculus GN=Usp49 PE=2 SV=1 | 204 | 444 | 2.0E-07 |
| sp|Q6PAW2|UBP16_XENLA | Ubiquitin carboxyl-terminal hydrolase 16 OS=Xenopus laevis GN=usp16 PE=2 SV=1 | 294 | 429 | 2.0E-07 |
| sp|Q70CQ1|UBP49_HUMAN | Ubiquitin carboxyl-terminal hydrolase 49 OS=Homo sapiens GN=USP49 PE=1 SV=1 | 204 | 444 | 2.0E-07 |
| sp|O22207|UBP5_ARATH | Ubiquitin carboxyl-terminal hydrolase 5 OS=Arabidopsis thaliana GN=UBP5 PE=1 SV=2 | 293 | 490 | 3.0E-07 |
| sp|Q9ZSB5|UBP10_ARATH | Ubiquitin carboxyl-terminal hydrolase 10 OS=Arabidopsis thaliana GN=UBP10 PE=2 SV=2 | 309 | 508 | 4.0E-07 |
| sp|Q9P7S5|UBP7_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 7 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp7 PE=1 SV=1 | 304 | 489 | 5.0E-07 |
| sp|Q569C3|UBP1_RAT | Ubiquitin carboxyl-terminal hydrolase 1 OS=Rattus norvegicus GN=Usp1 PE=1 SV=1 | 270 | 427 | 1.0E-06 |
| sp|Q8BJQ2|UBP1_MOUSE | Ubiquitin carboxyl-terminal hydrolase 1 OS=Mus musculus GN=Usp1 PE=1 SV=1 | 270 | 427 | 1.0E-06 |
| sp|O94782|UBP1_HUMAN | Ubiquitin carboxyl-terminal hydrolase 1 OS=Homo sapiens GN=USP1 PE=1 SV=1 | 270 | 427 | 1.0E-06 |
| sp|Q93Y01|UBP9_ARATH | Ubiquitin carboxyl-terminal hydrolase 9 OS=Arabidopsis thaliana GN=UBP9 PE=2 SV=1 | 309 | 489 | 1.0E-06 |
| sp|Q9MAQ3|UBP11_ARATH | Putative ubiquitin carboxyl-terminal hydrolase 11 OS=Arabidopsis thaliana GN=UBP11 PE=3 SV=2 | 282 | 491 | 1.0E-06 |
| sp|P53874|UBP10_YEAST | Ubiquitin carboxyl-terminal hydrolase 10 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP10 PE=1 SV=2 | 309 | 447 | 2.0E-06 |
| sp|Q29RP1|UBP1_BOVIN | Ubiquitin carboxyl-terminal hydrolase 1 OS=Bos taurus GN=USP1 PE=2 SV=1 | 270 | 427 | 2.0E-06 |
| sp|Q8NB14|UBP38_HUMAN | Ubiquitin carboxyl-terminal hydrolase 38 OS=Homo sapiens GN=USP38 PE=1 SV=2 | 314 | 427 | 6.0E-06 |
| sp|Q5UQR3|UBPL1_MIMIV | Probable ubiquitin carboxyl-terminal hydrolase R319 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R319 PE=3 SV=1 | 287 | 495 | 6.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016579 | protein deubiquitination | Yes |
| GO:0036459 | thiol-dependent ubiquitinyl hydrolase activity | Yes |
| GO:0006508 | proteolysis | No |
| GO:0006464 | cellular protein modification process | No |
| GO:0070647 | protein modification by small protein conjugation or removal | No |
| GO:0003674 | molecular_function | No |
| GO:0036211 | protein modification process | No |
| GO:0070646 | protein modification by small protein removal | No |
| GO:0044260 | cellular macromolecule metabolic process | No |
| GO:0008150 | biological_process | No |
| GO:0008152 | metabolic process | No |
| GO:0044267 | cellular protein metabolic process | No |
| GO:0101005 | ubiquitinyl hydrolase activity | No |
| GO:0044238 | primary metabolic process | No |
| GO:0006807 | nitrogen compound metabolic process | No |
| GO:0071704 | organic substance metabolic process | No |
| GO:0070011 | peptidase activity, acting on L-amino acid peptides | No |
| GO:0043170 | macromolecule metabolic process | No |
| GO:0044237 | cellular metabolic process | No |
| GO:0043412 | macromolecule modification | No |
| GO:0140096 | catalytic activity, acting on a protein | No |
| GO:0019783 | ubiquitin-like protein-specific protease activity | No |
| GO:0008233 | peptidase activity | No |
| GO:0019538 | protein metabolic process | No |
| GO:0008234 | cysteine-type peptidase activity | No |
| GO:0016787 | hydrolase activity | No |
| GO:0003824 | catalytic activity | No |
| GO:1901564 | organonitrogen compound metabolic process | No |
| GO:0009987 | cellular process | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 11 | 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 | >Hirsu2|5511 MASTLSGQLQLDRLTAQATKLLLEHTSTEDVSQPEPYDPISSGLSSILHLCLQIDSSLSTSEVLPEDTARSLLWR HLFPRRLNQGADTVPRVILNTDTRGRLYEVIFRLVGHDRRQFGQILHLLNGLVPFYCEDSDDPYLYDLPFQFDRS KAMRSPCGYVGLRNLSNTCYLNSLLTQLYMNTEFRRFIMAAPCRGPTGPQQLLFHTQKVFGFMQESYRRYVDPTS LVSSIKTYEDTIIDIHNQMDVDEFYSLLFDRWEGQLLRPEDKRTLRSFYGGQLVQQVKSKECEHISERLEPFSAI QCDIKGKGTLEESLQAYVDGEIMEGDNRYKCSTCDHHVVAVKRACLKDVPDNVMFHLKRFDFNLRTLQRSKINDH FSFPRTIDLRPYTIEHLSEAGSDVAEEDVFELVGILVHSGTAESGHYYSYIKERPSAADNDSWIEFNDDVVTPWD PSLMAGSTFGGPDSRPVYETNGIIYDKSYSAYMLFYQRASTLKAEKESMMAKQLSTPLRVEMPVLLKEHIVNENT VILRRHCLFDPGHAIFVQNCFGRARYIDTTAMESEKMARDAEGAAARVPPPNHDLQNLAMEMMLSHLDQVIARTK DTQFFGTFSNAIRAAVTQCPRCALALYDYFDARHASYRALLQRNPEQHVRAFAGEILIRAAEKMADKLPRLYERG GPTTGEAEAIDGEDGMERDRAAEADGVAEHSAMEGIMLMLNHLWQFFQIHLRSWDEYFSTVLAFAKLGHREVGLL LAEDYLIKLLRIVAADTALDLPPNYARMLNNVLRRINTRPPSYSAILSLIDYLLSQLVPVLGPEFIVEQPTERLG LRAPFAWTSEEVHAVHHHPDRHMSSFLVEKLVSIDQAWIPTNDIVARLVSTGALMDLRILNTLRKNIHGDLSTQP MDSFLRVASRYVECSQSAEHVQTLVRHVGAQARSLQNTEGAAFLSFFRSALRSEKPKEELARSRRENSVATIPMW APYLLVYPDANTRRDAEQLIEDEVFRFSSLHEAAEGDEEETDERERFDQVVMELGRKCLVYLREMHVNRRNRIER DAAWSILRIIGRCGPCFEGGRDGGGNEDVEFAALQGEIMDPLRRLMVDEVEEDASDWDESCASSDPMDANAGIPV QTMNELNDADLI* |
| Coding | >Hirsu2|5511 ATGGCGAGCACGCTTTCCGGGCAACTGCAGCTTGACCGGCTGACGGCACAGGCGACCAAGCTTCTGCTGGAACAT ACTTCGACAGAGGATGTGAGTCAACCCGAGCCTTACGATCCCATTTCCAGTGGCCTGTCCTCGATCTTGCACCTG TGCCTACAGATCGACTCCTCGCTATCGACCTCAGAGGTGCTACCTGAAGACACGGCCCGGAGCTTGCTCTGGCGG CATCTCTTTCCGCGCAGGCTTAACCAAGGAGCCGACACTGTGCCCCGTGTGATATTGAACACGGATACCCGAGGG AGGCTCTACGAAGTCATATTTCGCCTCGTCGGACACGACCGTCGCCAGTTTGGCCAGATTCTGCACCTGCTCAAC GGTCTCGTGCCGTTCTACTGCGAGGACTCCGACGACCCGTATCTATACGACCTACCCTTTCAGTTCGACCGCTCA AAGGCCATGCGGTCTCCCTGTGGCTACGTCGGCCTGCGCAATCTCTCCAACACCTGCTACCTGAACTCCCTTCTC ACGCAGCTCTACATGAACACGGAGTTCCGCCGCTTCATCATGGCGGCTCCATGTCGGGGGCCCACGGGTCCTCAG CAGTTACTGTTCCATACCCAAAAGGTGTTTGGGTTCATGCAGGAGAGCTACCGCCGATACGTGGATCCGACAAGC CTCGTCAGCTCCATCAAGACGTACGAGGACACTATCATCGACATCCACAATCAGATGGACGTGGACGAGTTCTAC AGCCTATTGTTCGACCGGTGGGAGGGGCAGCTACTTCGGCCTGAGGACAAGCGAACACTTCGCTCGTTTTACGGC GGACAACTCGTACAGCAGGTGAAGTCGAAGGAATGCGAGCACATCTCCGAACGACTTGAGCCATTTTCCGCGATA CAGTGCGATATCAAGGGAAAAGGCACGTTGGAGGAGAGCCTGCAGGCATATGTCGATGGAGAGATCATGGAAGGC GATAATCGATACAAGTGTTCCACATGCGACCACCACGTCGTTGCCGTGAAAAGGGCGTGCTTGAAGGACGTGCCG GACAACGTCATGTTTCACTTGAAGCGCTTTGATTTCAACTTGCGCACCCTGCAGAGGAGCAAGATCAACGACCAC TTTTCCTTTCCTCGGACAATCGACCTGCGGCCCTACACCATCGAGCACCTGAGCGAAGCGGGCTCGGACGTTGCG GAGGAGGACGTGTTCGAGCTTGTCGGTATCCTCGTGCACTCTGGAACCGCAGAGTCAGGCCACTACTATTCCTAC ATCAAAGAGCGCCCGTCGGCGGCGGACAACGACAGCTGGATCGAGTTCAACGACGACGTCGTCACCCCGTGGGAC CCATCTCTCATGGCCGGATCGACCTTTGGGGGACCCGACAGTCGGCCGGTATACGAAACCAACGGTATCATCTAC GACAAGAGCTACAGCGCCTACATGCTTTTCTACCAACGCGCGTCGACGCTCAAGGCCGAGAAGGAATCCATGATG GCGAAGCAGCTCTCGACGCCACTACGCGTCGAAATGCCCGTGCTGTTGAAGGAGCACATCGTCAACGAGAATACC GTCATCCTACGACGACACTGCCTCTTTGATCCGGGACACGCAATCTTTGTGCAGAACTGTTTTGGCCGGGCGAGG TACATCGACACCACGGCGATGGAGAGCGAAAAGATGGCCAGGGATGCCGAAGGCGCCGCCGCCCGGGTGCCGCCC CCGAATCACGACCTTCAAAACCTGGCGATGGAGATGATGCTCTCCCATCTGGACCAAGTCATCGCAAGGACCAAG GACACACAGTTCTTTGGAACCTTCTCGAACGCGATCAGAGCTGCGGTGACCCAGTGCCCCAGGTGCGCCCTGGCG CTCTACGACTACTTCGACGCGCGTCACGCGTCATATCGAGCCCTCCTTCAGCGGAATCCAGAGCAGCACGTTCGG GCGTTCGCCGGCGAGATCCTGATACGGGCGGCGGAGAAGATGGCCGACAAGCTCCCGCGCCTGTACGAGCGCGGG GGCCCGACCACGGGTGAGGCGGAGGCAATCGACGGGGAAGACGGCATGGAGCGCGACCGCGCCGCGGAGGCGGAC GGCGTCGCAGAGCATTCGGCGATGGAGGGCATCATGCTGATGCTGAACCATCTGTGGCAGTTCTTCCAGATCCAC CTCCGGTCGTGGGACGAATATTTCAGCACGGTGCTGGCGTTCGCCAAGCTGGGCCACCGCGAGGTCGGCCTTCTC CTGGCGGAAGACTACCTGATCAAGCTGCTGCGGATCGTGGCGGCCGACACGGCCTTGGACCTCCCGCCCAACTAT GCGCGCATGCTCAACAACGTCCTGCGGCGGATCAACACGCGGCCGCCGTCGTATTCTGCGATACTGTCCCTGATC GACTACCTCCTCTCACAGCTTGTGCCGGTGCTGGGTCCGGAGTTCATAGTGGAACAGCCGACGGAGCGGCTCGGG CTCAGGGCGCCGTTCGCGTGGACGTCAGAGGAGGTGCACGCGGTGCACCACCACCCCGACCGGCACATGAGCAGT TTCTTGGTGGAGAAGCTCGTGTCGATCGACCAGGCTTGGATCCCGACCAACGACATTGTGGCCCGGCTGGTCTCG ACGGGAGCGCTGATGGACCTCAGGATCCTCAACACGCTGCGCAAGAACATACACGGCGACCTGTCGACGCAGCCC ATGGACTCCTTCCTCAGGGTCGCGTCCCGGTACGTGGAGTGTAGCCAGTCGGCGGAGCACGTGCAGACGCTGGTG CGGCACGTGGGCGCGCAGGCTCGGAGCCTGCAGAACACGGAGGGAGCAGCCTTTCTCAGCTTCTTCCGCTCGGCA TTGCGTTCGGAGAAGCCGAAGGAAGAGCTGGCACGGTCGCGGCGAGAGAACAGCGTTGCGACGATACCGATGTGG GCGCCGTACCTGCTGGTGTACCCGGACGCCAACACGAGGCGCGACGCCGAACAGCTGATTGAGGACGAGGTCTTC CGCTTCTCCTCGCTCCACGAGGCCGCGGAGGGGGACGAGGAGGAGACGGACGAGCGAGAGCGGTTCGACCAGGTG GTTATGGAGCTGGGACGCAAGTGCCTGGTCTATCTGCGCGAGATGCACGTCAACCGGCGGAACAGGATCGAACGC GACGCGGCGTGGAGCATCCTGCGAATCATCGGCCGGTGCGGGCCGTGTTTCGAGGGCGGCCGAGACGGCGGCGGG AACGAAGACGTTGAGTTTGCGGCGCTGCAGGGAGAAATCATGGATCCGCTCCGCCGGCTGATGGTGGACGAGGTT GAGGAAGACGCATCCGACTGGGACGAATCGTGTGCGTCTTCGGACCCGATGGACGCCAACGCGGGCATACCGGTG CAGACGATGAACGAGCTGAACGACGCAGACTTGATCTGA |
| Transcript | >Hirsu2|5511 ATGGCGAGCACGCTTTCCGGGCAACTGCAGCTTGACCGGCTGACGGCACAGGCGACCAAGCTTCTGCTGGAACAT ACTTCGACAGAGGATGTGAGTCAACCCGAGCCTTACGATCCCATTTCCAGTGGCCTGTCCTCGATCTTGCACCTG TGCCTACAGATCGACTCCTCGCTATCGACCTCAGAGGTGCTACCTGAAGACACGGCCCGGAGCTTGCTCTGGCGG CATCTCTTTCCGCGCAGGCTTAACCAAGGAGCCGACACTGTGCCCCGTGTGATATTGAACACGGATACCCGAGGG AGGCTCTACGAAGTCATATTTCGCCTCGTCGGACACGACCGTCGCCAGTTTGGCCAGATTCTGCACCTGCTCAAC GGTCTCGTGCCGTTCTACTGCGAGGACTCCGACGACCCGTATCTATACGACCTACCCTTTCAGTTCGACCGCTCA AAGGCCATGCGGTCTCCCTGTGGCTACGTCGGCCTGCGCAATCTCTCCAACACCTGCTACCTGAACTCCCTTCTC ACGCAGCTCTACATGAACACGGAGTTCCGCCGCTTCATCATGGCGGCTCCATGTCGGGGGCCCACGGGTCCTCAG CAGTTACTGTTCCATACCCAAAAGGTGTTTGGGTTCATGCAGGAGAGCTACCGCCGATACGTGGATCCGACAAGC CTCGTCAGCTCCATCAAGACGTACGAGGACACTATCATCGACATCCACAATCAGATGGACGTGGACGAGTTCTAC AGCCTATTGTTCGACCGGTGGGAGGGGCAGCTACTTCGGCCTGAGGACAAGCGAACACTTCGCTCGTTTTACGGC GGACAACTCGTACAGCAGGTGAAGTCGAAGGAATGCGAGCACATCTCCGAACGACTTGAGCCATTTTCCGCGATA CAGTGCGATATCAAGGGAAAAGGCACGTTGGAGGAGAGCCTGCAGGCATATGTCGATGGAGAGATCATGGAAGGC GATAATCGATACAAGTGTTCCACATGCGACCACCACGTCGTTGCCGTGAAAAGGGCGTGCTTGAAGGACGTGCCG GACAACGTCATGTTTCACTTGAAGCGCTTTGATTTCAACTTGCGCACCCTGCAGAGGAGCAAGATCAACGACCAC TTTTCCTTTCCTCGGACAATCGACCTGCGGCCCTACACCATCGAGCACCTGAGCGAAGCGGGCTCGGACGTTGCG GAGGAGGACGTGTTCGAGCTTGTCGGTATCCTCGTGCACTCTGGAACCGCAGAGTCAGGCCACTACTATTCCTAC ATCAAAGAGCGCCCGTCGGCGGCGGACAACGACAGCTGGATCGAGTTCAACGACGACGTCGTCACCCCGTGGGAC CCATCTCTCATGGCCGGATCGACCTTTGGGGGACCCGACAGTCGGCCGGTATACGAAACCAACGGTATCATCTAC GACAAGAGCTACAGCGCCTACATGCTTTTCTACCAACGCGCGTCGACGCTCAAGGCCGAGAAGGAATCCATGATG GCGAAGCAGCTCTCGACGCCACTACGCGTCGAAATGCCCGTGCTGTTGAAGGAGCACATCGTCAACGAGAATACC GTCATCCTACGACGACACTGCCTCTTTGATCCGGGACACGCAATCTTTGTGCAGAACTGTTTTGGCCGGGCGAGG TACATCGACACCACGGCGATGGAGAGCGAAAAGATGGCCAGGGATGCCGAAGGCGCCGCCGCCCGGGTGCCGCCC CCGAATCACGACCTTCAAAACCTGGCGATGGAGATGATGCTCTCCCATCTGGACCAAGTCATCGCAAGGACCAAG GACACACAGTTCTTTGGAACCTTCTCGAACGCGATCAGAGCTGCGGTGACCCAGTGCCCCAGGTGCGCCCTGGCG CTCTACGACTACTTCGACGCGCGTCACGCGTCATATCGAGCCCTCCTTCAGCGGAATCCAGAGCAGCACGTTCGG GCGTTCGCCGGCGAGATCCTGATACGGGCGGCGGAGAAGATGGCCGACAAGCTCCCGCGCCTGTACGAGCGCGGG GGCCCGACCACGGGTGAGGCGGAGGCAATCGACGGGGAAGACGGCATGGAGCGCGACCGCGCCGCGGAGGCGGAC GGCGTCGCAGAGCATTCGGCGATGGAGGGCATCATGCTGATGCTGAACCATCTGTGGCAGTTCTTCCAGATCCAC CTCCGGTCGTGGGACGAATATTTCAGCACGGTGCTGGCGTTCGCCAAGCTGGGCCACCGCGAGGTCGGCCTTCTC CTGGCGGAAGACTACCTGATCAAGCTGCTGCGGATCGTGGCGGCCGACACGGCCTTGGACCTCCCGCCCAACTAT GCGCGCATGCTCAACAACGTCCTGCGGCGGATCAACACGCGGCCGCCGTCGTATTCTGCGATACTGTCCCTGATC GACTACCTCCTCTCACAGCTTGTGCCGGTGCTGGGTCCGGAGTTCATAGTGGAACAGCCGACGGAGCGGCTCGGG CTCAGGGCGCCGTTCGCGTGGACGTCAGAGGAGGTGCACGCGGTGCACCACCACCCCGACCGGCACATGAGCAGT TTCTTGGTGGAGAAGCTCGTGTCGATCGACCAGGCTTGGATCCCGACCAACGACATTGTGGCCCGGCTGGTCTCG ACGGGAGCGCTGATGGACCTCAGGATCCTCAACACGCTGCGCAAGAACATACACGGCGACCTGTCGACGCAGCCC ATGGACTCCTTCCTCAGGGTCGCGTCCCGGTACGTGGAGTGTAGCCAGTCGGCGGAGCACGTGCAGACGCTGGTG CGGCACGTGGGCGCGCAGGCTCGGAGCCTGCAGAACACGGAGGGAGCAGCCTTTCTCAGCTTCTTCCGCTCGGCA TTGCGTTCGGAGAAGCCGAAGGAAGAGCTGGCACGGTCGCGGCGAGAGAACAGCGTTGCGACGATACCGATGTGG GCGCCGTACCTGCTGGTGTACCCGGACGCCAACACGAGGCGCGACGCCGAACAGCTGATTGAGGACGAGGTCTTC CGCTTCTCCTCGCTCCACGAGGCCGCGGAGGGGGACGAGGAGGAGACGGACGAGCGAGAGCGGTTCGACCAGGTG GTTATGGAGCTGGGACGCAAGTGCCTGGTCTATCTGCGCGAGATGCACGTCAACCGGCGGAACAGGATCGAACGC GACGCGGCGTGGAGCATCCTGCGAATCATCGGCCGGTGCGGGCCGTGTTTCGAGGGCGGCCGAGACGGCGGCGGG AACGAAGACGTTGAGTTTGCGGCGCTGCAGGGAGAAATCATGGATCCGCTCCGCCGGCTGATGGTGGACGAGGTT GAGGAAGACGCATCCGACTGGGACGAATCGTGTGCGTCTTCGGACCCGATGGACGCCAACGCGGGCATACCGGTG CAGACGATGAACGAGCTGAACGACGCAGACTTGATCTGA |
| Gene | >Hirsu2|5511 ATGGCGAGCACGCTTTCCGGGCAACTGCAGCTTGACCGGCTGACGGCACAGGCGACCAAGCTTCTGCTGGAACAT ACTTCGACAGAGGTCAGTTTCATCTGTCTTCCCAGGGGTCGAGTAACACAGAAATGTGCTGATAGTTGGCTTTCC CAGGATGTGAGTCAACCCGAGCCTTACGATCCCATTTCCAGTGGCCTGTCCTCGATCTTGCACCTGTGCCTACAG ATCGACTCCTCGCTATCGACCTCAGAGGTGCTACCTGAGTAAGTCACATCGACGCCGTAACTCCACTTGCGGATT GCCATTAACAGTTGAATGTTTGCAGAGACACGGCCCGGAGCTTGCTCTGGCGGCATCTCTTTCCGCGCAGGCTTA ACCAAGGAGCCGACACTGTGCCCCGTGTGATATTGAACACGGATACCCGAGGGAGGCTCTACGAAGTCATATTTC GCCTCGTCGGACACGACCGTCGCCAGTTTGGCCAGATTCTGCACCTGCTCAACGGTCTCGTGCCGTTCTACTGCG AGGACTCCGGTAGGCTCAAATCAGCTCCGAATTCTCTCCGTGTTGCTCATGGTCTCGCGCAAGACGACCCGTATC TATACGACCTACCCTTTCAGTTCGACCGCTCAAAGGCCATGCGGTCTCCCTGTGGCTACGTCGGCCTGCGCAATC TCTCCAACACCTGCTACCTGAACTCCCTTCTCACGCAGCTCTACATGAACACGGAGTTCCGCCGCTTCATCATGG CGGCTCCATGTCGGGGGCCCACGGGTCCTCAGCAGTTACTGTTCCATACCCAAAAGGTGTTTGGGTTCATGCAGG AGAGCTACCGCCGATACGTGGATCCGACAAGCCTCGTCAGCTCCATCAAGACGTACGAGGACACTATCATCGACA TCCACAATCAGATGGACGTGGACGAGTTCTACAGCCTATTGTTCGACCGGTGGGAGGGGCAGCTACTTCGGCCTG AGGACAAGCGAACACTTCGCTCGTTTTACGGCGGACAACTCGTACAGCAGGTGAAGTCGAAGGAATGCGAGCACA TCTCCGAACGACTTGAGCCATTTTCCGCGATACAGTGCGATATCAAGGGAAAAGGCACGTTGGAGGAGAGCCTGC AGGCATATGTCGATGGAGAGATCATGGAAGGCGGTAAGCTGTCATCTGCCCCCTCTTCCTTCATCCTCCACCGTC CTCCCGAGTTGCGTGGCGCCGCTGATACCCGGCCCAGATAATCGATACAAGTGTTCCACATGCGACCACCACGTC GTTGCCGTGAAAAGGTAGGTCGCTTCGGCTTATTGGCGAGGGATGAGGGTGAGCAGCCAGCTGACATGGTACAGG GCGTGCTTGAAGGACGTGCCGGACAACGTCATGTTTCACTTGAAGCGCTTTGATTTCAACTTGCGCACCCTGCAG AGGAGCAAGATCAACGACCACTTTTCCTTTCCTCGGACAATCGACCTGCGGCCCTACACCATCGAGCACCTGAGC GAAGCGGGCTCGGACGTTGCGGAGGAGGACGTGTTCGAGCTTGTCGGTATCCTCGTGCACTCTGGAACCGCAGAG TCAGGCCACTACTATTCCTACATCAAAGAGCGCCCGTCGGCGGCGGACAACGACAGCTGGATCGAGTTCAACGAC GACGTCGTCACCCCGTGGGACCCATCTCTCATGGCCGGATCGACCTTTGGGGGACCCGACAGTCGGCCGGTATAC GAAACCAACGGTATCATCTACGACAAGAGCTACAGCGCCTACATGCTTTTCTACCAACGCGCGTCGACGCTCAAG GCCGAGAAGGAATCCATGATGGCGAAGCAGCTCTCGACGCCACTACGCGTCGAAATGCCCGTGCTGTTGAAGGAG CACATCGTCAACGAGAATACCGTCATCCTACGACGACACTGCCTCTTTGATCCGGGACACGCAATCTTTGTGCAG AACTGTTTTGGCCGGGCGAGGTACATCGACACCACGGCGATGGAGAGCGAAAAGATGGCCAGGGATGCCGAAGGC GCCGCCGCCCGGGTGCCGCCCCCGAATCACGACCTTCAAAACCTGGCGATGGAGATGATGCTCTCCCATCTGGAC CAAGTCATCGCAAGGACCAAGGACACACAGTTCTTTGGAACCTTCTCGAACGCGATCAGAGCTGCGGTGACCCAG TGCCCCAGGTGCGCCCTGGCGCTCTACGACTACTTCGACGCGCGTCACGCGTCATATCGAGCCCTCCTTCAGCGG AATCCAGAGCAGCACGTTCGGGCGTTCGCCGGCGAGATCCTGATACGGGCGGCGGAGAAGATGGCCGACAAGCTC CCGCGCCTGTACGAGCGCGGGGGCCCGACCACGGGTGAGGCGGAGGCAATCGACGGGGAAGACGGCATGGAGCGC GACCGCGCCGCGGAGGCGGACGGCGTCGCAGAGCATTCGGCGATGGAGGGCATCATGCTGATGCTGAACCATCTG TGGCAGTTCTTCCAGATCCACCTCCGGTCGTGGGACGAATATTTCAGCACGGTGCTGGCGTTCGCCAAGCTGGGC CACCGCGAGGTCGGCCTTCTCCTGGCGGAAGACTACCTGATCAAGCTGCTGCGGATCGTGGCGGCCGACACGGCC TTGGACCTCCCGCCCAACTATGCGCGCATGCTCAACAACGTCCTGCGGCGGATCAACACGCGGCCGCCGTCGTAT TCTGCGATACTGTCCCTGATCGACTACCTCCTCTCACAGCTTGTGCCGGTGCTGGGTCCGGAGTTCATAGTGGAA CAGCCGACGGAGCGGCTCGGGCTCAGGGCGCCGTTCGCGTGGACGTCAGAGGAGGTGCACGCGGTGCACCACCAC CCCGACCGGCACATGAGCAGTTTCTTGGTGGAGAAGCTCGTGTCGATCGACCAGGCTTGGATCCCGACCAACGAC ATTGTGGCCCGGCTGGTCTCGACGGGAGCGCTGATGGACCTCAGGATCCTCAACACGCTGCGCAAGAACATACAC GGCGACCTGTCGACGCAGCCCATGGACTCCTTCCTCAGGGTCGCGTCCCGGTACGTGGAGTGTAGCCAGTCGGCG GAGCACGTGCAGACGCTGGTGCGGCACGTGGGCGCGCAGGCTCGGAGCCTGCAGAACACGGAGGGAGCAGCCTTT CTCAGCTTCTTCCGCTCGGCATTGCGTTCGGAGAAGCCGAAGGAAGAGCTGGCACGGTCGCGGCGAGAGAACAGC GTTGCGACGATACCGATGTGGGCGCCGTACCTGCTGGTGTACCCGGACGCCAACACGAGGCGCGACGCCGAACAG CTGATTGAGGACGAGGTCTTCCGCTTCTCCTCGCTCCACGAGGCCGCGGAGGGGGACGAGGAGGAGACGGACGAG CGAGAGCGGTTCGACCAGGTGGTTATGGAGCTGGGACGCAAGTGCCTGGTCTATCTGCGCGAGATGCACGTCAAC CGGCGGAACAGGATCGAACGCGACGCGGCGTGGAGCATCCTGCGAATCATCGGCCGGTGCGGGCCGTGTTTCGAG GGCGGCCGAGACGGCGGCGGGAACGAAGACGTTGAGTTTGCGGCGCTGCAGGGAGGTGAGTACTGAAGAGGGCTC GGGTCGGAGGTGAGGCGACGGTCGCTGACTTTGCGAGACAGAAATCATGGATCCGCTCCGCCGGCTGATGGTGGA CGAGGTTGAGGAAGACGCATCCGGTAAGCGCGGGATACCCTTGAGGCTGAAGTAGGCCGAGTCGAAAAGTAGTAA CACTGGCTGGCCCTGGGGGAGGGCCGGCGCGTGCAGACTGGGACGAATCGTGTGCGTCTTCGGACCCGATGGACG CCAACGCGGGCATACCGGTGCAGACGATGAACGAGCTGAACGACGCAGACTTGATCTGA |