© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|2841 |
| Gene name | |
| Location | scaffold_228:15476..17401 |
| Strand | + |
| Gene length (bp) | 1925 |
| Transcript length (bp) | 1755 |
| Coding sequence length (bp) | 1752 |
| Protein length (aa) | 584 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00481 | PP2C | Protein phosphatase 2C | 7.3E-43 | 185 | 447 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q12511|PDP1_YEAST | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC5 PE=1 SV=1 | 128 | 579 | 9.0E-106 |
| sp|O14189|PP2C5_SCHPO | Protein phosphatase 2C homolog C10F6.17c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC10F6.17c PE=3 SV=4 | 137 | 558 | 3.0E-96 |
| sp|P35816|PDP1_BOVIN | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Bos taurus GN=PDP1 PE=1 SV=1 | 123 | 560 | 3.0E-50 |
| sp|Q5RA52|PDP1_PONAB | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Pongo abelii GN=PDP1 PE=2 SV=1 | 123 | 560 | 4.0E-50 |
| sp|Q9P0J1|PDP1_HUMAN | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Homo sapiens GN=PDP1 PE=1 SV=3 | 123 | 560 | 4.0E-50 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q12511|PDP1_YEAST | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC5 PE=1 SV=1 | 128 | 579 | 9.0E-106 |
| sp|O14189|PP2C5_SCHPO | Protein phosphatase 2C homolog C10F6.17c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC10F6.17c PE=3 SV=4 | 137 | 558 | 3.0E-96 |
| sp|P35816|PDP1_BOVIN | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Bos taurus GN=PDP1 PE=1 SV=1 | 123 | 560 | 3.0E-50 |
| sp|Q5RA52|PDP1_PONAB | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Pongo abelii GN=PDP1 PE=2 SV=1 | 123 | 560 | 4.0E-50 |
| sp|Q9P0J1|PDP1_HUMAN | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Homo sapiens GN=PDP1 PE=1 SV=3 | 123 | 560 | 4.0E-50 |
| sp|Q3UV70|PDP1_MOUSE | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Mus musculus GN=Pdp1 PE=1 SV=1 | 123 | 560 | 5.0E-50 |
| sp|O88483|PDP1_RAT | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial OS=Rattus norvegicus GN=Pdp1 PE=1 SV=1 | 123 | 560 | 8.0E-49 |
| sp|O88484|PDP2_RAT | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 2, mitochondrial OS=Rattus norvegicus GN=Pdp2 PE=2 SV=1 | 118 | 560 | 5.0E-45 |
| sp|Q9P2J9|PDP2_HUMAN | [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 2, mitochondrial OS=Homo sapiens GN=PDP2 PE=2 SV=2 | 131 | 560 | 1.0E-43 |
| sp|Q9LUS8|P2C40_ARATH | Probable protein phosphatase 2C 40 OS=Arabidopsis thaliana GN=At3g16560 PE=2 SV=1 | 182 | 444 | 2.0E-19 |
| sp|Q501F9|P2C67_ARATH | Probable protein phosphatase 2C 67 OS=Arabidopsis thaliana GN=At5g02760 PE=2 SV=1 | 195 | 437 | 7.0E-18 |
| sp|Q7XVF9|P2C39_ORYSJ | Probable protein phosphatase 2C 39 OS=Oryza sativa subsp. japonica GN=Os04g0403701 PE=2 SV=2 | 182 | 441 | 3.0E-17 |
| sp|Q7Y138|P2C36_ORYSJ | Probable protein phosphatase 2C 36 OS=Oryza sativa subsp. japonica GN=Os03g0832400 PE=2 SV=1 | 197 | 437 | 8.0E-17 |
| sp|Q9LHJ9|P2C38_ARATH | Probable protein phosphatase 2C 38 OS=Arabidopsis thaliana GN=At3g12620 PE=2 SV=1 | 195 | 437 | 1.0E-16 |
| sp|Q9XGZ9|P2C72_ARATH | Probable protein phosphatase 2C 72 OS=Arabidopsis thaliana GN=At5g26010 PE=2 SV=2 | 189 | 437 | 2.0E-16 |
| sp|P35813|PPM1A_HUMAN | Protein phosphatase 1A OS=Homo sapiens GN=PPM1A PE=1 SV=1 | 136 | 443 | 3.0E-16 |
| sp|P20650|PPM1A_RAT | Protein phosphatase 1A OS=Rattus norvegicus GN=Ppm1a PE=1 SV=1 | 136 | 443 | 4.0E-16 |
| sp|P35814|PPM1A_RABIT | Protein phosphatase 1A OS=Oryctolagus cuniculus GN=PPM1A PE=2 SV=1 | 136 | 443 | 5.0E-16 |
| sp|O62830|PPM1B_BOVIN | Protein phosphatase 1B OS=Bos taurus GN=PPM1B PE=2 SV=2 | 189 | 443 | 5.0E-16 |
| sp|O62829|PPM1A_BOVIN | Protein phosphatase 1A OS=Bos taurus GN=PPM1A PE=2 SV=1 | 136 | 443 | 6.0E-16 |
| sp|P49443|PPM1A_MOUSE | Protein phosphatase 1A OS=Mus musculus GN=Ppm1a PE=1 SV=1 | 136 | 443 | 6.0E-16 |
| sp|Q7XUC5|P2C43_ORYSJ | Probable protein phosphatase 2C 43 OS=Oryza sativa subsp. japonica GN=Os04g0584300 PE=3 SV=2 | 195 | 437 | 6.0E-16 |
| sp|P35815|PPM1B_RAT | Protein phosphatase 1B OS=Rattus norvegicus GN=Ppm1b PE=2 SV=1 | 189 | 443 | 6.0E-16 |
| sp|Q0D673|P2C62_ORYSJ | Probable protein phosphatase 2C 62 OS=Oryza sativa subsp. japonica GN=Os07g0507000 PE=2 SV=1 | 158 | 460 | 1.0E-15 |
| sp|Q7XHN8|P2C61_ORYSJ | Probable protein phosphatase 2C 61 OS=Oryza sativa subsp. japonica GN=Os07g0114000 PE=2 SV=1 | 197 | 439 | 1.0E-15 |
| sp|Q5Z8P0|P2C60_ORYSJ | Probable protein phosphatase 2C 60 OS=Oryza sativa subsp. japonica GN=Os06g0717800 PE=2 SV=1 | 195 | 437 | 1.0E-15 |
| sp|Q10S32|P2C28_ORYSJ | Probable protein phosphatase 2C 28 OS=Oryza sativa subsp. japonica GN=Os03g0137200 PE=2 SV=1 | 195 | 437 | 1.0E-15 |
| sp|Q5PNS9|P2C64_ARATH | Probable protein phosphatase 2C 64 OS=Arabidopsis thaliana GN=At4g38520 PE=2 SV=1 | 195 | 437 | 2.0E-15 |
| sp|Q94CL8|P2C48_ARATH | Probable protein phosphatase 2C 48 OS=Arabidopsis thaliana GN=PP2C6 PE=2 SV=1 | 195 | 460 | 3.0E-15 |
| sp|Q9LQN6|P2C04_ARATH | Probable protein phosphatase 2C 4 OS=Arabidopsis thaliana GN=PLL5 PE=2 SV=1 | 185 | 444 | 4.0E-15 |
| sp|O82637|P2C61_ARATH | Probable protein phosphatase 2C 61 OS=Arabidopsis thaliana GN=At4g32950 PE=3 SV=1 | 189 | 462 | 6.0E-15 |
| sp|Q2QN36|P2C78_ORYSJ | Probable protein phosphatase 2C 78 OS=Oryza sativa subsp. japonica GN=Os12g0580900 PE=2 SV=1 | 158 | 437 | 7.0E-15 |
| sp|P36993|PPM1B_MOUSE | Protein phosphatase 1B OS=Mus musculus GN=Ppm1b PE=1 SV=1 | 189 | 443 | 9.0E-15 |
| sp|Q9SD12|P2C46_ARATH | Probable protein phosphatase 2C 46 OS=Arabidopsis thaliana GN=At3g51370 PE=2 SV=1 | 195 | 437 | 9.0E-15 |
| sp|Q9XEE8|P2C30_ARATH | Probable protein phosphatase 2C 30 OS=Arabidopsis thaliana GN=PP2C5 PE=2 SV=1 | 168 | 437 | 1.0E-14 |
| sp|Q6ZHC8|P2C25_ORYSJ | Probable protein phosphatase 2C 25 OS=Oryza sativa subsp. japonica GN=Os02g0685600 PE=2 SV=1 | 195 | 437 | 1.0E-14 |
| sp|Q9ZV25|P2C23_ARATH | Probable protein phosphatase 2C 23 OS=Arabidopsis thaliana GN=PLL4 PE=2 SV=1 | 185 | 444 | 2.0E-14 |
| sp|Q9FXE4|P2C14_ARATH | Probable protein phosphatase 2C 14 OS=Arabidopsis thaliana GN=At1g67820 PE=2 SV=2 | 189 | 448 | 2.0E-14 |
| sp|Q9FKX4|P2C79_ARATH | Probable protein phosphatase 2C 79 OS=Arabidopsis thaliana GN=At5g66080 PE=2 SV=1 | 195 | 437 | 2.0E-14 |
| sp|Q9LNW3|P2C03_ARATH | Protein phosphatase 2C 3 OS=Arabidopsis thaliana GN=AIP1 PE=1 SV=1 | 180 | 455 | 2.0E-14 |
| sp|O75688|PPM1B_HUMAN | Protein phosphatase 1B OS=Homo sapiens GN=PPM1B PE=1 SV=1 | 189 | 443 | 3.0E-14 |
| sp|Q94H98|P2C34_ORYSJ | Probable protein phosphatase 2C 34 OS=Oryza sativa subsp. japonica GN=BIPP2C2 PE=2 SV=1 | 197 | 437 | 3.0E-14 |
| sp|Q5MFV5|P2C34_ORYSI | Probable protein phosphatase 2C 34 OS=Oryza sativa subsp. indica GN=BIPP2C2 PE=2 SV=2 | 197 | 437 | 3.0E-14 |
| sp|Q8H063|P2C29_ORYSJ | Probable protein phosphatase 2C 29 OS=Oryza sativa subsp. japonica GN=Os03g0207400 PE=2 SV=1 | 158 | 437 | 4.0E-14 |
| sp|Q84JD5|P2C68_ARATH | Probable protein phosphatase 2C 68 OS=Arabidopsis thaliana GN=At5g06750 PE=2 SV=1 | 158 | 439 | 6.0E-14 |
| sp|Q0V7V2|P2C42_ARATH | Probable protein phosphatase 2C 42 OS=Arabidopsis thaliana GN=At3g17090 PE=2 SV=1 | 195 | 437 | 7.0E-14 |
| sp|A3AZ89|P2C46_ORYSJ | Putative protein phosphatase 2C 46 OS=Oryza sativa subsp. japonica GN=Os05g0111800 PE=3 SV=2 | 185 | 437 | 1.0E-13 |
| sp|Q9SR24|P2C36_ARATH | Probable protein phosphatase 2C 36 OS=Arabidopsis thaliana GN=PLL3 PE=2 SV=1 | 279 | 453 | 1.0E-12 |
| sp|Q8RWN7|P2C32_ARATH | Protein phosphatase 2C 32 OS=Arabidopsis thaliana GN=POL PE=1 SV=2 | 317 | 454 | 2.0E-12 |
| sp|O81760|P2C63_ARATH | Probable protein phosphatase 2C 63 OS=Arabidopsis thaliana GN=At4g33920 PE=2 SV=1 | 172 | 460 | 2.0E-12 |
| sp|Q5N9N2|P2C09_ORYSJ | Probable protein phosphatase 2C 9 OS=Oryza sativa subsp. japonica GN=Os01g0846300 PE=2 SV=1 | 193 | 453 | 3.0E-12 |
| sp|Q9FIF5|P2C78_ARATH | Probable protein phosphatase 2C 78 OS=Arabidopsis thaliana GN=At5g59220 PE=2 SV=1 | 180 | 452 | 3.0E-12 |
| sp|Q9LZ86|P2C66_ARATH | Probable protein phosphatase 2C 66 OS=Arabidopsis thaliana GN=PLL2 PE=2 SV=1 | 279 | 453 | 3.0E-12 |
| sp|Q9H0C8|ILKAP_HUMAN | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Homo sapiens GN=ILKAP PE=1 SV=1 | 195 | 461 | 5.0E-12 |
| sp|Q5JJY4|P2C04_ORYSJ | Protein kinase and PP2C-like domain-containing protein OS=Oryza sativa subsp. japonica GN=Os01g0541900 PE=2 SV=1 | 191 | 437 | 6.0E-12 |
| sp|Q84T94|P2C35_ORYSJ | Protein phosphatase 2C 35 OS=Oryza sativa subsp. japonica GN=XB15 PE=1 SV=1 | 256 | 443 | 7.0E-12 |
| sp|Q7XCJ7|P2C72_ORYSJ | Probable protein phosphatase 2C 72 OS=Oryza sativa subsp. japonica GN=Os10g0544900 PE=2 SV=1 | 197 | 437 | 7.0E-12 |
| sp|Q65XK7|P2C51_ORYSJ | Probable protein phosphatase 2C 51 OS=Oryza sativa subsp. japonica GN=Os05g0572700 PE=2 SV=1 | 195 | 450 | 8.0E-12 |
| sp|Q5SN75|P2C08_ORYSJ | Probable protein phosphatase 2C 8 OS=Oryza sativa subsp. japonica GN=Os01g0656200 PE=2 SV=1 | 195 | 452 | 1.0E-11 |
| sp|Q6ZGY0|P2C26_ORYSJ | Probable protein phosphatase 2C 26 OS=Oryza sativa subsp. japonica GN=Os02g0690500 PE=2 SV=1 | 279 | 442 | 1.0E-11 |
| sp|Q9Z1Z6|ILKAP_RAT | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Rattus norvegicus GN=Ilkap PE=2 SV=1 | 195 | 461 | 2.0E-11 |
| sp|Q8R0F6|ILKAP_MOUSE | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Mus musculus GN=Ilkap PE=1 SV=1 | 195 | 442 | 2.0E-11 |
| sp|Q7XU84|P2C42_ORYSJ | Probable protein phosphatase 2C 42 OS=Oryza sativa subsp. japonica GN=Os04g0500900 PE=3 SV=4 | 188 | 437 | 2.0E-11 |
| sp|Q7XQU7|P2C41_ORYSJ | Probable protein phosphatase 2C 41 OS=Oryza sativa subsp. japonica GN=Os04g0452000 PE=2 SV=2 | 158 | 453 | 2.0E-11 |
| sp|Q10NB9|P2C31_ORYSJ | Probable protein phosphatase 2C 31 OS=Oryza sativa subsp. japonica GN=Os03g0275100 PE=2 SV=1 | 280 | 444 | 3.0E-11 |
| sp|Q65XG6|P2C49_ORYSJ | Probable protein phosphatase 2C 49 OS=Oryza sativa subsp. japonica GN=Os05g0457200 PE=3 SV=1 | 195 | 450 | 6.0E-11 |
| sp|Q9ZW21|P2C24_ARATH | Probable protein phosphatase 2C 24 OS=Arabidopsis thaliana GN=At2g29380 PE=2 SV=1 | 195 | 436 | 7.0E-11 |
| sp|Q67UP9|P2C58_ORYSJ | Probable protein phosphatase 2C 58 OS=Oryza sativa subsp. japonica GN=Os06g0651600 PE=2 SV=1 | 188 | 449 | 9.0E-11 |
| sp|Q0IIF0|ILKAP_BOVIN | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Bos taurus GN=ILKAP PE=2 SV=1 | 195 | 444 | 9.0E-11 |
| sp|A3A8W2|P2C21_ORYSJ | Probable protein phosphatase 2C 21 OS=Oryza sativa subsp. japonica GN=Os02g0606900 PE=2 SV=2 | 195 | 441 | 1.0E-10 |
| sp|Q7XW27|P2C38_ORYSJ | Probable protein phosphatase 2C 38 OS=Oryza sativa subsp. japonica GN=Os04g0321800 PE=2 SV=2 | 192 | 462 | 2.0E-10 |
| sp|Q0J2L7|P2C68_ORYSJ | Probable protein phosphatase 2C 68 OS=Oryza sativa subsp. japonica GN=Os09g0325700 PE=2 SV=2 | 195 | 431 | 2.0E-10 |
| sp|O82302|P2C29_ARATH | Protein phosphatase 2C 29 OS=Arabidopsis thaliana GN=PLL1 PE=1 SV=2 | 317 | 436 | 2.0E-10 |
| sp|Q6ETK3|P2C11_ORYSJ | Probable protein phosphatase 2C 11 OS=Oryza sativa subsp. japonica GN=Os02g0180000 PE=2 SV=1 | 195 | 449 | 2.0E-10 |
| sp|Q2R637|P2C75_ORYSJ | Probable protein phosphatase 2C 75 OS=Oryza sativa subsp. japonica GN=Os11g0417400 PE=2 SV=1 | 188 | 458 | 2.0E-10 |
| sp|Q6AUQ4|P2C47_ORYSJ | Probable protein phosphatase 2C 47 OS=Oryza sativa subsp. japonica GN=Os05g0134200 PE=2 SV=1 | 195 | 448 | 3.0E-10 |
| sp|P93006|P2C27_ARATH | Probable protein phosphatase 2C 27 OS=Arabidopsis thaliana GN=At2g33700 PE=2 SV=1 | 195 | 476 | 5.0E-10 |
| sp|P49598|P2C37_ARATH | Protein phosphatase 2C 37 OS=Arabidopsis thaliana GN=PP2CA PE=1 SV=1 | 187 | 436 | 5.0E-10 |
| sp|Q9FG61|P2C74_ARATH | Probable protein phosphatase 2C 74 OS=Arabidopsis thaliana GN=At5g36250 PE=1 SV=1 | 192 | 439 | 5.0E-10 |
| sp|Q9SZ53|P2C60_ARATH | Probable protein phosphatase 2C 60 OS=Arabidopsis thaliana GN=At4g31860 PE=2 SV=1 | 195 | 444 | 6.0E-10 |
| sp|Q9LRZ4|P2C41_ARATH | Probable protein phosphatase 2C 41 OS=Arabidopsis thaliana GN=At3g16800 PE=2 SV=1 | 192 | 437 | 9.0E-10 |
| sp|P49444|PP2C1_PARTE | Protein phosphatase 2C 1 OS=Paramecium tetraurelia GN=GSPATT00029903001 PE=1 SV=2 | 188 | 441 | 1.0E-09 |
| sp|Q0WRB2|P2C73_ARATH | Probable protein phosphatase 2C 73 OS=Arabidopsis thaliana GN=PPC6-7 PE=2 SV=1 | 192 | 460 | 1.0E-09 |
| sp|Q2QWE3|P2C77_ORYSJ | Probable protein phosphatase 2C 77 OS=Oryza sativa subsp. japonica GN=Os12g0198200 PE=3 SV=1 | 188 | 432 | 2.0E-09 |
| sp|Q6EN45|P2C13_ORYSJ | Probable protein phosphatase 2C 13 OS=Oryza sativa subsp. japonica GN=Os02g0255100 PE=2 SV=1 | 180 | 436 | 2.0E-09 |
| sp|P38089|PP2C4_YEAST | Protein phosphatase 2C homolog 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC4 PE=1 SV=1 | 196 | 437 | 2.0E-09 |
| sp|Q8RX37|P2C02_ARATH | Probable protein phosphatase 2C 2 OS=Arabidopsis thaliana GN=At1g07160 PE=2 SV=1 | 143 | 436 | 3.0E-09 |
| sp|Q10MX1|P2C32_ORYSJ | Probable protein phosphatase 2C 32 OS=Oryza sativa subsp. japonica GN=Os03g0292100 PE=2 SV=1 | 195 | 436 | 3.0E-09 |
| sp|P40371|PP2C1_SCHPO | Protein phosphatase 2C homolog 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc1 PE=2 SV=1 | 189 | 446 | 4.0E-09 |
| sp|Q8VZN9|P2C11_ARATH | Probable protein phosphatase 2C 11 OS=Arabidopsis thaliana GN=At1g43900 PE=2 SV=1 | 180 | 437 | 4.0E-09 |
| sp|O81716|P2C21_ARATH | Probable protein phosphatase 2C 21 OS=Arabidopsis thaliana GN=PPC4-2 PE=1 SV=1 | 281 | 444 | 6.0E-09 |
| sp|Q9S9Z7|P2C10_ARATH | Probable protein phosphatase 2C 10 OS=Arabidopsis thaliana GN=At1g34750 PE=2 SV=1 | 150 | 436 | 8.0E-09 |
| sp|O80871|P2C25_ARATH | Probable protein phosphatase 2C 25 OS=Arabidopsis thaliana GN=At2g30020 PE=1 SV=1 | 189 | 436 | 8.0E-09 |
| sp|Q84JI0|P2C30_ORYSJ | Probable protein phosphatase 2C 30 OS=Oryza sativa subsp. japonica GN=Os03g0268600 PE=2 SV=1 | 195 | 437 | 1.0E-08 |
| sp|Q9LNF4|P2C13_ARATH | Probable protein phosphatase 2C 13 OS=Arabidopsis thaliana GN=At1g48040 PE=2 SV=2 | 165 | 448 | 1.0E-08 |
| sp|P34221|PP2C3_YEAST | Protein phosphatase 2C homolog 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC3 PE=1 SV=4 | 195 | 437 | 1.0E-08 |
| sp|Q8RXV3|P2C59_ARATH | Probable protein phosphatase 2C 59 OS=Arabidopsis thaliana GN=WIN2 PE=1 SV=1 | 195 | 437 | 1.0E-08 |
| sp|Q9LMT1|P2C08_ARATH | Probable protein phosphatase 2C 8 OS=Arabidopsis thaliana GN=At1g18030 PE=2 SV=2 | 189 | 442 | 1.0E-08 |
| sp|Q6Z8B9|P2C12_ORYSJ | Probable protein phosphatase 2C 12 OS=Oryza sativa subsp. japonica GN=Os02g0224100 PE=2 SV=1 | 276 | 462 | 2.0E-08 |
| sp|Q9FYN7|P2C02_ORYSJ | Probable protein phosphatase 2C 2 OS=Oryza sativa subsp. japonica GN=Os01g0295700 PE=2 SV=1 | 195 | 448 | 2.0E-08 |
| sp|Q53Q11|P2C74_ORYSJ | Probable protein phosphatase 2C 74 OS=Oryza sativa subsp. japonica GN=Os11g0242200 PE=3 SV=1 | 188 | 437 | 2.0E-08 |
| sp|Q653S3|P2C70_ORYSJ | Probable protein phosphatase 2C 70 OS=Oryza sativa subsp. japonica GN=Os09g0558000 PE=2 SV=2 | 195 | 454 | 2.0E-08 |
| sp|Q3EAF9|P2C49_ARATH | Probable protein phosphatase 2C 49 OS=Arabidopsis thaliana GN=At3g62260 PE=2 SV=1 | 195 | 437 | 3.0E-08 |
| sp|P49596|PP2C2_CAEEL | Probable protein phosphatase 2C T23F11.1 OS=Caenorhabditis elegans GN=ppm-2 PE=3 SV=2 | 169 | 454 | 3.0E-08 |
| sp|Q6L4R7|P2C53_ORYSJ | Probable protein phosphatase 2C 53 OS=Oryza sativa subsp. japonica GN=Os05g0592800 PE=2 SV=1 | 195 | 434 | 3.0E-08 |
| sp|A0BQL0|PP2C3_PARTE | Probable protein phosphatase 2C 3 OS=Paramecium tetraurelia GN=GSPATT00031056001 PE=3 SV=1 | 188 | 437 | 4.0E-08 |
| sp|O04719|P2C77_ARATH | Protein phosphatase 2C 77 OS=Arabidopsis thaliana GN=ABI2 PE=1 SV=1 | 195 | 441 | 5.0E-08 |
| sp|Q8LAY8|P2C69_ARATH | Probable protein phosphatase 2C 69 OS=Arabidopsis thaliana GN=At5g10740 PE=2 SV=1 | 195 | 437 | 6.0E-08 |
| sp|Q4PSE8|P2C71_ARATH | Probable protein phosphatase 2C 71 OS=Arabidopsis thaliana GN=At5g24940 PE=2 SV=1 | 195 | 439 | 8.0E-08 |
| sp|P49595|PP2C1_CAEEL | Probable protein phosphatase 2C F42G9.1 OS=Caenorhabditis elegans GN=F42G9.1 PE=3 SV=2 | 281 | 437 | 1.0E-07 |
| sp|Q6L482|P2C48_ORYSJ | Probable protein phosphatase 2C 48 OS=Oryza sativa subsp. japonica GN=Os05g0358500 PE=2 SV=1 | 194 | 460 | 1.0E-07 |
| sp|Q8BGL1|PPM1N_MOUSE | Probable protein phosphatase 1N OS=Mus musculus GN=Ppm1n PE=2 SV=1 | 169 | 437 | 1.0E-07 |
| sp|O64583|P2C28_ARATH | Probable protein phosphatase 2C 28 OS=Arabidopsis thaliana GN=At2g34740 PE=2 SV=2 | 195 | 433 | 1.0E-07 |
| sp|Q7XJ53|P2C35_ARATH | Probable protein phosphatase 2C 35 OS=Arabidopsis thaliana GN=At3g06270 PE=2 SV=1 | 185 | 458 | 2.0E-07 |
| sp|Q0JLP9|P2C06_ORYSJ | Probable protein phosphatase 2C 6 OS=Oryza sativa subsp. japonica GN=Os01g0583100 PE=1 SV=1 | 195 | 434 | 2.0E-07 |
| sp|Q61074|PPM1G_MOUSE | Protein phosphatase 1G OS=Mus musculus GN=Ppm1g PE=1 SV=3 | 281 | 441 | 2.0E-07 |
| sp|F1LNI5|PPM1G_RAT | Protein phosphatase 1G OS=Rattus norvegicus GN=Ppm1g PE=1 SV=2 | 281 | 441 | 2.0E-07 |
| sp|Q4R4V2|PPM1G_MACFA | Protein phosphatase 1G OS=Macaca fascicularis GN=PPM1G PE=2 SV=1 | 281 | 441 | 3.0E-07 |
| sp|O15355|PPM1G_HUMAN | Protein phosphatase 1G OS=Homo sapiens GN=PPM1G PE=1 SV=1 | 281 | 441 | 3.0E-07 |
| sp|Q6L5C4|P2C52_ORYSJ | Probable protein phosphatase 2C 52 OS=Oryza sativa subsp. japonica GN=Os05g0587100 PE=2 SV=1 | 195 | 477 | 3.0E-07 |
| sp|Q9CAJ0|P2C16_ARATH | Protein phosphatase 2C 16 OS=Arabidopsis thaliana GN=HAB1 PE=1 SV=1 | 195 | 447 | 3.0E-07 |
| sp|Q652Z7|P2C55_ORYSJ | Probable protein phosphatase 2C 55 OS=Oryza sativa subsp. japonica GN=Os06g0526700 PE=2 SV=2 | 195 | 454 | 4.0E-07 |
| sp|P79126|PPM1G_BOVIN | Protein phosphatase 1G OS=Bos taurus GN=PPM1G PE=2 SV=2 | 281 | 441 | 4.0E-07 |
| sp|P39966|PP2C2_YEAST | Protein phosphatase 2C homolog 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC2 PE=1 SV=1 | 195 | 437 | 4.0E-07 |
| sp|Q7K4Q5|Y0417_DROME | Probable protein phosphatase CG10417 OS=Drosophila melanogaster GN=CG10417 PE=1 SV=1 | 281 | 437 | 7.0E-07 |
| sp|Q69QZ0|P2C27_ORYSJ | Probable protein phosphatase 2C 27 OS=Oryza sativa subsp. japonica GN=Os02g0799000 PE=2 SV=1 | 195 | 434 | 8.0E-07 |
| sp|Q5JKN1|P2C05_ORYSJ | Probable protein phosphatase 2C 5 OS=Oryza sativa subsp. japonica GN=Os01g0552300 PE=2 SV=1 | 195 | 437 | 9.0E-07 |
| sp|Q5Z6F5|P2C59_ORYSJ | Probable protein phosphatase 2C 59 OS=Oryza sativa subsp. japonica GN=Os06g0698300 PE=2 SV=1 | 195 | 479 | 1.0E-06 |
| sp|Q94AT1|P2C76_ARATH | Probable protein phosphatase 2C 76 OS=Arabidopsis thaliana GN=At5g53140 PE=2 SV=1 | 180 | 451 | 2.0E-06 |
| sp|Q67UX7|P2C10_ORYSJ | Probable protein phosphatase 2C 10 OS=Oryza sativa subsp. japonica GN=Os02g0149800 PE=2 SV=1 | 195 | 467 | 2.0E-06 |
| sp|Q940A2|P2C31_ARATH | Protein kinase and PP2C-like domain-containing protein OS=Arabidopsis thaliana GN=At2g40860/At2g40870 PE=2 SV=1 | 195 | 437 | 2.0E-06 |
| sp|Q9FLI3|P2C75_ARATH | Probable protein phosphatase 2C 75 OS=Arabidopsis thaliana GN=AHG1 PE=2 SV=1 | 195 | 430 | 3.0E-06 |
| sp|Q8N819|PPM1N_HUMAN | Probable protein phosphatase 1N OS=Homo sapiens GN=PPM1N PE=2 SV=2 | 169 | 493 | 5.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0004722 | protein serine/threonine phosphatase activity | Yes |
| GO:0004721 | phosphoprotein phosphatase activity | No |
| GO:0016791 | phosphatase activity | No |
| GO:0016787 | hydrolase activity | No |
| GO:0140096 | catalytic activity, acting on a protein | No |
| GO:0003824 | catalytic activity | No |
| GO:0042578 | phosphoric ester hydrolase activity | No |
| GO:0003674 | molecular_function | No |
| GO:0016788 | hydrolase activity, acting on ester bonds | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 28 | 0.5 |
| 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|2841 MHRAALRALRTTSTYIGAVRHAARFSSTPYRVQLLLPPDAAQVPLRSSMHLRRLPTLIVSGIVIGYGAWYSLKAT AGGPRSLTSTQGSAPPQPTRTVLVIGDDELRQGTVVGEGPIEKPTTDEGRRIVEMLTPEQATLKLRRQEKSFSVN RGEGVTRYDIVQLPSNDPIEDDHAEQIIQFPARPSEQDGTRDWMFWGVFDGHSGWTTSATLRRSLISYVARELNN TYMASKPSAPTAEDLDLAIKTGFNRLDHDIVHKSVEKVFKAKSKPVAAGLLQPALSGSCALLSFYDSRTKLLRVA CTGDSRAVLGRRSESGKWTASALSDDQTGSNPREAERMRSEHPGEDNVVRNGRVLGGLEPTRAFGDAVYKWSREV AGKLRESFFGRSPSPLLKTPPYVTAEPVVTTTRIEPDKGDFLVLATDGLWEMLTNDEVVGLVGQWIETQAAPQAP TSQFQNAWSKIFGSPDKPLPVEQQRQKPQHSNGAHGADGQKTPIRVLQWGISPDAKDRFTTRDNNVATHLVRNAL GGKNEELVRALLTLPAPFSRRYRDDLTVQVIFFGNGAKTGEVTLNLDATTEPDPPKAEL |
| Coding | >Ophio5|2841 ATGCACCGCGCCGCCCTCCGGGCCCTCCGAACGACGTCGACGTACATCGGCGCCGTGCGGCACGCGGCCCGCTTC TCGTCGACGCCTTACCGGGTCCAGCTGCTGCTGCCGCCAGACGCGGCCCAAGTGCCTCTCCGGTCATCCATGCAT CTCCGCAGGCTGCCGACCCTCATCGTCTCGGGCATCGTCATCGGCTACGGCGCCTGGTACTCGTTGAAGGCCACA GCAGGTGGTCCGCGAAGCCTCACCTCGACGCAGGGCTCTGCCCCGCCGCAGCCCACGCGTACTGTACTCGTCATA GGCGATGACGAGCTAAGACAGGGCACCGTCGTCGGAGAGGGGCCAATCGAGAAGCCTACGACGGACGAAGGACGG AGGATCGTCGAGATGTTGACGCCCGAGCAGGCTACCCTCAAGCTCCGCCGGCAGGAGAAGTCCTTTTCTGTCAAC AGGGGCGAGGGCGTTACTCGCTACGATATAGTTCAGCTGCCGAGCAACGATCCGATCGAGGATGATCACGCCGAG CAGATAATTCAGTTCCCGGCCCGACCAAGCGAGCAGGACGGGACTCGAGACTGGATGTTTTGGGGCGTCTTTGAC GGCCATTCCGGCTGGACCACGTCGGCCACCCTACGCAGAAGCCTCATCAGCTACGTCGCCAGGGAGCTCAACAAC ACCTACATGGCCTCCAAGCCCAGCGCGCCGACCGCCGAAGACCTCGACCTGGCCATCAAAACAGGCTTCAACCGG CTCGACCACGACATCGTCCACAAAAGCGTCGAGAAAGTCTTCAAAGCAAAGTCTAAGCCCGTCGCCGCCGGCCTG CTCCAGCCCGCCCTTTCCGGCTCGTGTGCCCTCCTTTCCTTCTACGACAGCAGGACCAAGCTCCTGCGTGTGGCC TGCACCGGTGATTCGCGCGCCGTGCTGGGCCGTCGCTCCGAGTCCGGCAAATGGACGGCTTCGGCACTGTCGGAC GACCAGACGGGCAGCAACCCGCGCGAGGCGGAGCGCATGCGCAGCGAGCACCCGGGGGAGGATAACGTCGTGCGC AACGGCCGCGTCCTCGGAGGCCTGGAGCCGACGCGTGCGTTTGGTGACGCCGTGTACAAGTGGAGCAGGGAGGTG GCCGGCAAGCTGCGAGAGAGCTTCTTCGGCCGCAGTCCGTCGCCTCTGCTCAAGACGCCGCCGTACGTGACGGCC GAGCCTGTCGTGACGACGACGCGCATCGAACCCGACAAGGGCGACTTCCTCGTCCTCGCCACTGACGGGCTCTGG GAGATGCTCACCAACGACGAGGTCGTCGGCCTGGTCGGTCAGTGGATCGAGACGCAGGCCGCTCCGCAGGCGCCC ACGTCGCAGTTCCAGAACGCATGGTCCAAGATCTTCGGCTCCCCTGACAAGCCGCTCCCCGTAGAGCAGCAGCGG CAGAAGCCGCAGCATAGCAACGGCGCCCATGGGGCAGACGGGCAGAAGACGCCCATCCGCGTGCTGCAGTGGGGG ATCAGCCCGGACGCCAAGGATCGCTTCACCACCCGGGACAACAACGTGGCTACCCATCTCGTCCGCAACGCCCTC GGCGGCAAAAATGAAGAGCTGGTTCGCGCCCTGCTCACCCTCCCGGCGCCCTTTTCGCGGAGATACCGTGACGAC CTCACCGTCCAAGTCATCTTTTTCGGCAACGGCGCCAAGACGGGCGAGGTGACTCTCAACCTCGACGCCACGACC GAGCCGGACCCGCCCAAGGCCGAGCTC |
| Transcript | >Ophio5|2841 ATGCACCGCGCCGCCCTCCGGGCCCTCCGAACGACGTCGACGTACATCGGCGCCGTGCGGCACGCGGCCCGCTTC TCGTCGACGCCTTACCGGGTCCAGCTGCTGCTGCCGCCAGACGCGGCCCAAGTGCCTCTCCGGTCATCCATGCAT CTCCGCAGGCTGCCGACCCTCATCGTCTCGGGCATCGTCATCGGCTACGGCGCCTGGTACTCGTTGAAGGCCACA GCAGGTGGTCCGCGAAGCCTCACCTCGACGCAGGGCTCTGCCCCGCCGCAGCCCACGCGTACTGTACTCGTCATA GGCGATGACGAGCTAAGACAGGGCACCGTCGTCGGAGAGGGGCCAATCGAGAAGCCTACGACGGACGAAGGACGG AGGATCGTCGAGATGTTGACGCCCGAGCAGGCTACCCTCAAGCTCCGCCGGCAGGAGAAGTCCTTTTCTGTCAAC AGGGGCGAGGGCGTTACTCGCTACGATATAGTTCAGCTGCCGAGCAACGATCCGATCGAGGATGATCACGCCGAG CAGATAATTCAGTTCCCGGCCCGACCAAGCGAGCAGGACGGGACTCGAGACTGGATGTTTTGGGGCGTCTTTGAC GGCCATTCCGGCTGGACCACGTCGGCCACCCTACGCAGAAGCCTCATCAGCTACGTCGCCAGGGAGCTCAACAAC ACCTACATGGCCTCCAAGCCCAGCGCGCCGACCGCCGAAGACCTCGACCTGGCCATCAAAACAGGCTTCAACCGG CTCGACCACGACATCGTCCACAAAAGCGTCGAGAAAGTCTTCAAAGCAAAGTCTAAGCCCGTCGCCGCCGGCCTG CTCCAGCCCGCCCTTTCCGGCTCGTGTGCCCTCCTTTCCTTCTACGACAGCAGGACCAAGCTCCTGCGTGTGGCC TGCACCGGTGATTCGCGCGCCGTGCTGGGCCGTCGCTCCGAGTCCGGCAAATGGACGGCTTCGGCACTGTCGGAC GACCAGACGGGCAGCAACCCGCGCGAGGCGGAGCGCATGCGCAGCGAGCACCCGGGGGAGGATAACGTCGTGCGC AACGGCCGCGTCCTCGGAGGCCTGGAGCCGACGCGTGCGTTTGGTGACGCCGTGTACAAGTGGAGCAGGGAGGTG GCCGGCAAGCTGCGAGAGAGCTTCTTCGGCCGCAGTCCGTCGCCTCTGCTCAAGACGCCGCCGTACGTGACGGCC GAGCCTGTCGTGACGACGACGCGCATCGAACCCGACAAGGGCGACTTCCTCGTCCTCGCCACTGACGGGCTCTGG GAGATGCTCACCAACGACGAGGTCGTCGGCCTGGTCGGTCAGTGGATCGAGACGCAGGCCGCTCCGCAGGCGCCC ACGTCGCAGTTCCAGAACGCATGGTCCAAGATCTTCGGCTCCCCTGACAAGCCGCTCCCCGTAGAGCAGCAGCGG CAGAAGCCGCAGCATAGCAACGGCGCCCATGGGGCAGACGGGCAGAAGACGCCCATCCGCGTGCTGCAGTGGGGG ATCAGCCCGGACGCCAAGGATCGCTTCACCACCCGGGACAACAACGTGGCTACCCATCTCGTCCGCAACGCCCTC GGCGGCAAAAATGAAGAGCTGGTTCGCGCCCTGCTCACCCTCCCGGCGCCCTTTTCGCGGAGATACCGTGACGAC CTCACCGTCCAAGTCATCTTTTTCGGCAACGGCGCCAAGACGGGCGAGGTGACTCTCAACCTCGACGCCACGACC GAGCCGGACCCGCCCAAGGCCGAGCTCTAG |
| Gene | >Ophio5|2841 ATGCACCGCGCCGCCCTCCGGGCCCTCCGAACGACGTCGACGTACATCGGCGCCGTGCGGCACGCGGCCCGCTTC TCGTCGACGCCTTACCGGGTCCAGCTGCTGCTGCCGCCAGACGCGGCCCAAGTGCCTCTCCGGTCATCCATGCAT CTCCGCAGGCTGCCGACCCTCATCGTCTCGGGCATCGTCATCGGCTACGGCGCCTGGTACTCGTTGAAGGCCACA GCAGGTGGTCCGCGAAGCCTCACCTCGACGCAGGGCTCTGCCCCGCCGCAGCCCACGCGTACTGTACTCGTCATA GGCGATGACGAGCTAAGACAGGGCACCGTCGTCGGAGAGGGGCCAATCGAGAAGCCTACGACGGACGAAGGACGG AGGATCGTCGAGATGTTGACGCCCGAGCAGGCTACCCTCAAGCTCCGCCGGCAGGAGAAGTCCTTTTCTGTCAAC AGGGGCGAGGGCGTTACTCGCTACGATATAGTTCAGCTGCCGAGCAACGATCCGATCGAGGATGATCACGCCGAG CAGATAATTCAGTTCCCGGCCCGACCAAGCGAGCAGGACGGGACTCGAGACTGGATGTTTTGGGGCGTCTTTGAC GGCCATTCGTAAGTTTACCTCCCCTAGGGCGACATCTGCGGCGCTGACCATGTCTTCCTTATCCAGCGGCTGGAC CACGTCGGCCACCCTACGCAGAAGCCTCATCAGCTACGTCGCCAGGGAGCTCAACAACACCTACATGGCCTCCAA GCCCAGCGCGCCGACCGCCGAAGACCTCGACCTGGCCATCAAAACAGGCTTCAACCGGCTCGACCACGACATCGT CCACAAAAGCGTCGAGAAAGTCTTCAAAGCAAAGTCTAAGCCCGTCGCCGCCGGCCTGCTCCAGCCCGCCCTTTC CGGCTCGTGTGCCCTCCTTTCCTTCTACGACAGCAGGACCAAGCTCCTGCGTGTGGCCTGCACCGGTGATTCGCG CGCCGTGCTGGGCCGTCGCTCCGAGTCCGGCAAATGGACGGCTTCGGCACTGTCGGACGACCAGACGGGCAGCAA CCCGCGCGAGGCGGAGCGCATGCGCAGCGAGCACCCGGGGGAGGATAACGTCGTGCGCAACGGCCGCGTCCTCGG AGGCCTGGAGCCGACGCGTGCGTTTGGTGACGCCGTGTACAAGTGGAGCAGGGAGGTGGCCGGCAAGCTGCGAGA GAGCTTCTTCGGCCGCAGTCCGTCGCCTCTGCTCAAGACGCCGCCGTACGTGACGGCCGAGCCTGTCGTGACGAC GACGCGCATCGAACCCGACAAGGGCGACTTCCTCGTCCTCGCCACTGACGGGCTCTGGGAGATGCTCACCAACGA CGAGGTCGTCGGCCTGGTCGGTCAGTGGATCGAGACGCAGGCCGCTCCGCAGGCGCCCACGTCGCAGTTCCAGAA CGCATGGTCCAAGATCTTCGGCTCCCCTGACAAGCCGCTCCCCGTAGAGCAGCAGCGGCAGAAGCCGCAGCATAG CAACGGCGCCCATGGGGCAGACGGGCAGAAGACGCCCATCCGCGTGCTGCAGTGGGGGATCAGCCCGGACGCCAA GGATCGCTTCACCACCCGGGACAACAACGTGGCTACCCATCTCGTCCGCAACGCCCTCGGCGGCAAAAATGAAGA GCTGGTTCGCGCCCTGCTCACCCTCCCGGCGCCCTTTTCGCGGAGATACCGGTGAGCCCACCTGCCCTCCCCCTC CCCTTTTTTTCCCCTTCTCTTCGGGTAGCGGACAGTCAGGCCCGTTTGGGTCAAAGCAGTACTAAAAATCTCTCT TCTCCGATGATAGTGACGACCTCACCGTCCAAGTCATCTTTTTCGGCAACGGCGCCAAGACGGGCGAGGTGACTC TCAACCTCGACGCCACGACCGAGCCGGACCCGCCCAAGGCCGAGCTCTAG |