© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | AgabiH97|045990 |
| Gene name | |
| Location | scaffold_2:1845568..1846886 |
| Strand | + |
| Gene length (bp) | 1318 |
| Transcript length (bp) | 1164 |
| Coding sequence length (bp) | 1164 |
| Protein length (aa) | 388 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00481 | PP2C | Protein phosphatase 2C | 1.0E-10 | 37 | 141 |
| PF00481 | PP2C | Protein phosphatase 2C | 5.1E-53 | 196 | 373 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P40371|PP2C1_SCHPO | Protein phosphatase 2C homolog 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc1 PE=2 SV=1 | 238 | 382 | 2.0E-51 |
| sp|P35182|PP2C1_YEAST | Protein phosphatase 2C homolog 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC1 PE=1 SV=1 | 239 | 378 | 2.0E-47 |
| sp|Q9SZ53|P2C60_ARATH | Probable protein phosphatase 2C 60 OS=Arabidopsis thaliana GN=At4g31860 PE=2 SV=1 | 31 | 383 | 4.0E-38 |
| sp|Q653S3|P2C70_ORYSJ | Probable protein phosphatase 2C 70 OS=Oryza sativa subsp. japonica GN=Os09g0558000 PE=2 SV=2 | 38 | 387 | 6.0E-38 |
| sp|O81716|P2C21_ARATH | Probable protein phosphatase 2C 21 OS=Arabidopsis thaliana GN=PPC4-2 PE=1 SV=1 | 37 | 383 | 5.0E-37 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P40371|PP2C1_SCHPO | Protein phosphatase 2C homolog 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc1 PE=2 SV=1 | 238 | 382 | 2.0E-51 |
| sp|P35182|PP2C1_YEAST | Protein phosphatase 2C homolog 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC1 PE=1 SV=1 | 239 | 378 | 2.0E-47 |
| sp|Q9SZ53|P2C60_ARATH | Probable protein phosphatase 2C 60 OS=Arabidopsis thaliana GN=At4g31860 PE=2 SV=1 | 31 | 383 | 4.0E-38 |
| sp|Q653S3|P2C70_ORYSJ | Probable protein phosphatase 2C 70 OS=Oryza sativa subsp. japonica GN=Os09g0558000 PE=2 SV=2 | 38 | 387 | 6.0E-38 |
| sp|O81716|P2C21_ARATH | Probable protein phosphatase 2C 21 OS=Arabidopsis thaliana GN=PPC4-2 PE=1 SV=1 | 37 | 383 | 5.0E-37 |
| sp|Q67UX7|P2C10_ORYSJ | Probable protein phosphatase 2C 10 OS=Oryza sativa subsp. japonica GN=Os02g0149800 PE=2 SV=1 | 228 | 380 | 2.0E-36 |
| sp|Q7XR06|P2C45_ORYSJ | Probable protein phosphatase 2C 45 OS=Oryza sativa subsp. japonica GN=Os04g0659500 PE=2 SV=2 | 228 | 380 | 4.0E-36 |
| sp|Q6ETK3|P2C11_ORYSJ | Probable protein phosphatase 2C 11 OS=Oryza sativa subsp. japonica GN=Os02g0180000 PE=2 SV=1 | 35 | 384 | 1.0E-35 |
| sp|Q5Z6F5|P2C59_ORYSJ | Probable protein phosphatase 2C 59 OS=Oryza sativa subsp. japonica GN=Os06g0698300 PE=2 SV=1 | 211 | 380 | 4.0E-34 |
| sp|Q8RXV3|P2C59_ARATH | Probable protein phosphatase 2C 59 OS=Arabidopsis thaliana GN=WIN2 PE=1 SV=1 | 228 | 380 | 4.0E-34 |
| sp|Q6L5C4|P2C52_ORYSJ | Probable protein phosphatase 2C 52 OS=Oryza sativa subsp. japonica GN=Os05g0587100 PE=2 SV=1 | 242 | 381 | 2.0E-33 |
| sp|Q4PSE8|P2C71_ARATH | Probable protein phosphatase 2C 71 OS=Arabidopsis thaliana GN=At5g24940 PE=2 SV=1 | 228 | 380 | 3.0E-33 |
| sp|Q8LAY8|P2C69_ARATH | Probable protein phosphatase 2C 69 OS=Arabidopsis thaliana GN=At5g10740 PE=2 SV=1 | 242 | 380 | 8.0E-33 |
| sp|Q9LNF4|P2C13_ARATH | Probable protein phosphatase 2C 13 OS=Arabidopsis thaliana GN=At1g48040 PE=2 SV=2 | 209 | 385 | 2.0E-32 |
| sp|Q0JL75|P2C07_ORYSJ | Probable protein phosphatase 2C 7 OS=Oryza sativa subsp. japonica GN=Os01g0618200 PE=2 SV=2 | 242 | 380 | 2.0E-32 |
| sp|Q9FYN7|P2C02_ORYSJ | Probable protein phosphatase 2C 2 OS=Oryza sativa subsp. japonica GN=Os01g0295700 PE=2 SV=1 | 224 | 380 | 3.0E-32 |
| sp|Q6AUQ4|P2C47_ORYSJ | Probable protein phosphatase 2C 47 OS=Oryza sativa subsp. japonica GN=Os05g0134200 PE=2 SV=1 | 224 | 380 | 3.0E-31 |
| sp|Q652Z7|P2C55_ORYSJ | Probable protein phosphatase 2C 55 OS=Oryza sativa subsp. japonica GN=Os06g0526700 PE=2 SV=2 | 216 | 380 | 4.0E-31 |
| sp|Q9LUU7|P2C43_ARATH | Probable protein phosphatase 2C 43 OS=Arabidopsis thaliana GN=At3g17250 PE=2 SV=1 | 216 | 380 | 1.0E-30 |
| sp|Q0JAA0|P2C44_ORYSJ | Probable protein phosphatase 2C 44 OS=Oryza sativa subsp. japonica GN=Os04g0609600 PE=2 SV=1 | 196 | 381 | 1.0E-30 |
| sp|Q94AT1|P2C76_ARATH | Probable protein phosphatase 2C 76 OS=Arabidopsis thaliana GN=At5g53140 PE=2 SV=1 | 242 | 381 | 3.0E-30 |
| sp|Q8VZN9|P2C11_ARATH | Probable protein phosphatase 2C 11 OS=Arabidopsis thaliana GN=At1g43900 PE=2 SV=1 | 242 | 381 | 3.0E-30 |
| sp|Q3EAF9|P2C49_ARATH | Probable protein phosphatase 2C 49 OS=Arabidopsis thaliana GN=At3g62260 PE=2 SV=1 | 216 | 380 | 4.0E-30 |
| sp|P93006|P2C27_ARATH | Probable protein phosphatase 2C 27 OS=Arabidopsis thaliana GN=At2g33700 PE=2 SV=1 | 199 | 380 | 5.0E-29 |
| sp|Q0DBU3|P2C56_ORYSJ | Probable protein phosphatase 2C 56 OS=Oryza sativa subsp. japonica GN=Os06g0526800 PE=3 SV=2 | 230 | 380 | 9.0E-29 |
| sp|Q9SLA1|P2C22_ARATH | Probable protein phosphatase 2C 22 OS=Arabidopsis thaliana GN=At2g25620 PE=2 SV=1 | 230 | 386 | 3.0E-28 |
| sp|Q10MX1|P2C32_ORYSJ | Probable protein phosphatase 2C 32 OS=Oryza sativa subsp. japonica GN=Os03g0292100 PE=2 SV=1 | 223 | 382 | 7.0E-28 |
| sp|Q6EN45|P2C13_ORYSJ | Probable protein phosphatase 2C 13 OS=Oryza sativa subsp. japonica GN=Os02g0255100 PE=2 SV=1 | 242 | 380 | 7.0E-28 |
| sp|Q9LDA7|P2C39_ARATH | Probable protein phosphatase 2C 39 OS=Arabidopsis thaliana GN=At3g15260 PE=2 SV=1 | 228 | 381 | 9.0E-28 |
| sp|Q69VD9|P2C57_ORYSJ | Probable protein phosphatase 2C 57 OS=Oryza sativa subsp. japonica GN=Os06g0597200 PE=2 SV=1 | 206 | 380 | 9.0E-28 |
| sp|Q67UP9|P2C58_ORYSJ | Probable protein phosphatase 2C 58 OS=Oryza sativa subsp. japonica GN=Os06g0651600 PE=2 SV=1 | 242 | 384 | 1.0E-27 |
| sp|Q9SD02|P2C47_ARATH | Probable protein phosphatase 2C 47 OS=Arabidopsis thaliana GN=At3g51470 PE=1 SV=1 | 230 | 380 | 1.0E-27 |
| sp|A0DSB3|PP2C6_PARTE | Probable protein phosphatase 2C 6 OS=Paramecium tetraurelia GN=GSPATT00019634001 PE=3 SV=1 | 221 | 381 | 3.0E-27 |
| sp|Q09172|PP2C2_SCHPO | Protein phosphatase 2C homolog 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc2 PE=3 SV=1 | 193 | 380 | 3.0E-27 |
| sp|P49596|PP2C2_CAEEL | Probable protein phosphatase 2C T23F11.1 OS=Caenorhabditis elegans GN=ppm-2 PE=3 SV=2 | 165 | 378 | 4.0E-26 |
| sp|Q9SIU8|P2C20_ARATH | Probable protein phosphatase 2C 20 OS=Arabidopsis thaliana GN=PPC3-1.2 PE=1 SV=3 | 190 | 380 | 5.0E-26 |
| sp|Q9LNW3|P2C03_ARATH | Protein phosphatase 2C 3 OS=Arabidopsis thaliana GN=AIP1 PE=1 SV=1 | 228 | 382 | 8.0E-26 |
| sp|Q0D673|P2C62_ORYSJ | Probable protein phosphatase 2C 62 OS=Oryza sativa subsp. japonica GN=Os07g0507000 PE=2 SV=1 | 242 | 380 | 1.0E-25 |
| sp|Q0J2L7|P2C68_ORYSJ | Probable protein phosphatase 2C 68 OS=Oryza sativa subsp. japonica GN=Os09g0325700 PE=2 SV=2 | 228 | 382 | 1.0E-25 |
| sp|Q5SMK6|P2C54_ORYSJ | Probable protein phosphatase 2C 54 OS=Oryza sativa subsp. japonica GN=Os06g0179700 PE=2 SV=1 | 222 | 380 | 1.0E-25 |
| sp|Q8L7I4|P2C17_ARATH | Probable protein phosphatase 2C 17 OS=Arabidopsis thaliana GN=At1g78200 PE=2 SV=1 | 224 | 381 | 2.0E-25 |
| sp|Q69QZ0|P2C27_ORYSJ | Probable protein phosphatase 2C 27 OS=Oryza sativa subsp. japonica GN=Os02g0799000 PE=2 SV=1 | 230 | 382 | 2.0E-25 |
| sp|A0CUB5|PP2C5_PARTE | Probable protein phosphatase 2C 5 OS=Paramecium tetraurelia GN=GSPATT00010582001 PE=3 SV=1 | 223 | 381 | 3.0E-25 |
| sp|Q7K4Q5|Y0417_DROME | Probable protein phosphatase CG10417 OS=Drosophila melanogaster GN=CG10417 PE=1 SV=1 | 231 | 385 | 3.0E-25 |
| sp|Q5SN75|P2C08_ORYSJ | Probable protein phosphatase 2C 8 OS=Oryza sativa subsp. japonica GN=Os01g0656200 PE=2 SV=1 | 228 | 382 | 5.0E-25 |
| sp|Q93YW5|P2C58_ARATH | Probable protein phosphatase 2C 58 OS=Arabidopsis thaliana GN=At4g28400 PE=2 SV=1 | 190 | 380 | 5.0E-25 |
| sp|Q9ZW21|P2C24_ARATH | Probable protein phosphatase 2C 24 OS=Arabidopsis thaliana GN=At2g29380 PE=2 SV=1 | 180 | 382 | 7.0E-25 |
| sp|Q09173|PP2C3_SCHPO | Protein phosphatase 2C homolog 3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc3 PE=3 SV=1 | 242 | 382 | 9.0E-25 |
| sp|Q9FIF5|P2C78_ARATH | Probable protein phosphatase 2C 78 OS=Arabidopsis thaliana GN=At5g59220 PE=2 SV=1 | 228 | 348 | 1.0E-24 |
| sp|Q7XU84|P2C42_ORYSJ | Probable protein phosphatase 2C 42 OS=Oryza sativa subsp. japonica GN=Os04g0500900 PE=3 SV=4 | 226 | 386 | 2.0E-24 |
| sp|Q9XEE8|P2C30_ARATH | Probable protein phosphatase 2C 30 OS=Arabidopsis thaliana GN=PP2C5 PE=2 SV=1 | 223 | 381 | 3.0E-24 |
| sp|P49598|P2C37_ARATH | Protein phosphatase 2C 37 OS=Arabidopsis thaliana GN=PP2CA PE=1 SV=1 | 188 | 348 | 3.0E-24 |
| sp|A5PJZ2|PPM1L_BOVIN | Protein phosphatase 1L OS=Bos taurus GN=PPM1L PE=2 SV=1 | 227 | 381 | 5.0E-24 |
| sp|O15743|SPNA_DICDI | Protein spalten OS=Dictyostelium discoideum GN=spnA PE=1 SV=1 | 230 | 378 | 6.0E-24 |
| sp|O62829|PPM1A_BOVIN | Protein phosphatase 1A OS=Bos taurus GN=PPM1A PE=2 SV=1 | 230 | 380 | 7.0E-24 |
| sp|Q940A2|P2C31_ARATH | Protein kinase and PP2C-like domain-containing protein OS=Arabidopsis thaliana GN=At2g40860/At2g40870 PE=2 SV=1 | 232 | 384 | 7.0E-24 |
| sp|P49595|PP2C1_CAEEL | Probable protein phosphatase 2C F42G9.1 OS=Caenorhabditis elegans GN=F42G9.1 PE=3 SV=2 | 230 | 380 | 8.0E-24 |
| sp|Q7XQU7|P2C41_ORYSJ | Probable protein phosphatase 2C 41 OS=Oryza sativa subsp. japonica GN=Os04g0452000 PE=2 SV=2 | 221 | 381 | 1.0E-23 |
| sp|Q65XG6|P2C49_ORYSJ | Probable protein phosphatase 2C 49 OS=Oryza sativa subsp. japonica GN=Os05g0457200 PE=3 SV=1 | 208 | 348 | 1.0E-23 |
| sp|Q5SGD2|PPM1L_HUMAN | Protein phosphatase 1L OS=Homo sapiens GN=PPM1L PE=1 SV=1 | 227 | 381 | 1.0E-23 |
| sp|Q8BHN0|PPM1L_MOUSE | Protein phosphatase 1L OS=Mus musculus GN=Ppm1l PE=1 SV=1 | 227 | 381 | 2.0E-23 |
| sp|Q9LME4|P2C09_ARATH | Probable protein phosphatase 2C 9 OS=Arabidopsis thaliana GN=At1g22280 PE=1 SV=1 | 228 | 381 | 2.0E-23 |
| sp|P20650|PPM1A_RAT | Protein phosphatase 1A OS=Rattus norvegicus GN=Ppm1a PE=1 SV=1 | 230 | 380 | 2.0E-23 |
| sp|P35813|PPM1A_HUMAN | Protein phosphatase 1A OS=Homo sapiens GN=PPM1A PE=1 SV=1 | 230 | 380 | 2.0E-23 |
| sp|P35814|PPM1A_RABIT | Protein phosphatase 1A OS=Oryctolagus cuniculus GN=PPM1A PE=2 SV=1 | 230 | 380 | 2.0E-23 |
| sp|O80871|P2C25_ARATH | Probable protein phosphatase 2C 25 OS=Arabidopsis thaliana GN=At2g30020 PE=1 SV=1 | 227 | 382 | 2.0E-23 |
| sp|P49443|PPM1A_MOUSE | Protein phosphatase 1A OS=Mus musculus GN=Ppm1a PE=1 SV=1 | 230 | 380 | 2.0E-23 |
| sp|Q8N3J5|PPM1K_HUMAN | Protein phosphatase 1K, mitochondrial OS=Homo sapiens GN=PPM1K PE=1 SV=1 | 191 | 380 | 2.0E-23 |
| sp|Q9S9Z7|P2C10_ARATH | Probable protein phosphatase 2C 10 OS=Arabidopsis thaliana GN=At1g34750 PE=2 SV=1 | 228 | 381 | 2.0E-23 |
| sp|Q8BXN7|PPM1K_MOUSE | Protein phosphatase 1K, mitochondrial OS=Mus musculus GN=Ppm1k PE=1 SV=1 | 199 | 380 | 3.0E-23 |
| sp|Q5JJY4|P2C04_ORYSJ | Protein kinase and PP2C-like domain-containing protein OS=Oryza sativa subsp. japonica GN=Os01g0541900 PE=2 SV=1 | 232 | 384 | 3.0E-23 |
| sp|Q6L5H6|P2C50_ORYSJ | Probable protein phosphatase 2C 50 OS=Oryza sativa subsp. japonica GN=Os05g0537400 PE=3 SV=1 | 203 | 381 | 3.0E-23 |
| sp|Q6ING9|PPM1K_XENLA | Protein phosphatase 1K, mitochondrial OS=Xenopus laevis GN=ppm1k PE=2 SV=1 | 222 | 380 | 4.0E-23 |
| sp|Q2PC20|PPM1K_BOVIN | Protein phosphatase 1K, mitochondrial OS=Bos taurus GN=PPM1K PE=2 SV=1 | 222 | 380 | 4.0E-23 |
| sp|Q9FXE4|P2C14_ARATH | Probable protein phosphatase 2C 14 OS=Arabidopsis thaliana GN=At1g67820 PE=2 SV=2 | 242 | 347 | 1.0E-22 |
| sp|Q65XK7|P2C51_ORYSJ | Probable protein phosphatase 2C 51 OS=Oryza sativa subsp. japonica GN=Os05g0572700 PE=2 SV=1 | 230 | 382 | 2.0E-22 |
| sp|Q5N9N2|P2C09_ORYSJ | Probable protein phosphatase 2C 9 OS=Oryza sativa subsp. japonica GN=Os01g0846300 PE=2 SV=1 | 228 | 382 | 3.0E-22 |
| sp|Q9LNP9|P2C07_ARATH | Protein phosphatase 2C 7 OS=Arabidopsis thaliana GN=HAB2 PE=1 SV=2 | 224 | 381 | 4.0E-22 |
| sp|P36993|PPM1B_MOUSE | Protein phosphatase 1B OS=Mus musculus GN=Ppm1b PE=1 SV=1 | 230 | 380 | 4.0E-22 |
| sp|P49444|PP2C1_PARTE | Protein phosphatase 2C 1 OS=Paramecium tetraurelia GN=GSPATT00029903001 PE=1 SV=2 | 146 | 382 | 5.0E-22 |
| sp|Q4R4V2|PPM1G_MACFA | Protein phosphatase 1G OS=Macaca fascicularis GN=PPM1G PE=2 SV=1 | 230 | 381 | 6.0E-22 |
| sp|F1LNI5|PPM1G_RAT | Protein phosphatase 1G OS=Rattus norvegicus GN=Ppm1g PE=1 SV=2 | 230 | 381 | 6.0E-22 |
| sp|O15355|PPM1G_HUMAN | Protein phosphatase 1G OS=Homo sapiens GN=PPM1G PE=1 SV=1 | 230 | 381 | 6.0E-22 |
| sp|Q61074|PPM1G_MOUSE | Protein phosphatase 1G OS=Mus musculus GN=Ppm1g PE=1 SV=3 | 230 | 381 | 7.0E-22 |
| sp|Q0JLP9|P2C06_ORYSJ | Probable protein phosphatase 2C 6 OS=Oryza sativa subsp. japonica GN=Os01g0583100 PE=1 SV=1 | 242 | 381 | 7.0E-22 |
| sp|A0BQL0|PP2C3_PARTE | Probable protein phosphatase 2C 3 OS=Paramecium tetraurelia GN=GSPATT00031056001 PE=3 SV=1 | 146 | 382 | 8.0E-22 |
| sp|P79126|PPM1G_BOVIN | Protein phosphatase 1G OS=Bos taurus GN=PPM1G PE=2 SV=2 | 230 | 381 | 9.0E-22 |
| sp|Q53Q11|P2C74_ORYSJ | Probable protein phosphatase 2C 74 OS=Oryza sativa subsp. japonica GN=Os11g0242200 PE=3 SV=1 | 242 | 382 | 1.0E-21 |
| sp|O04719|P2C77_ARATH | Protein phosphatase 2C 77 OS=Arabidopsis thaliana GN=ABI2 PE=1 SV=1 | 200 | 381 | 1.0E-21 |
| sp|Q6L4R7|P2C53_ORYSJ | Probable protein phosphatase 2C 53 OS=Oryza sativa subsp. japonica GN=Os05g0592800 PE=2 SV=1 | 228 | 381 | 1.0E-21 |
| sp|Q9FLI3|P2C75_ARATH | Probable protein phosphatase 2C 75 OS=Arabidopsis thaliana GN=AHG1 PE=2 SV=1 | 219 | 381 | 1.0E-21 |
| sp|P35815|PPM1B_RAT | Protein phosphatase 1B OS=Rattus norvegicus GN=Ppm1b PE=2 SV=1 | 230 | 380 | 1.0E-21 |
| sp|P49597|P2C56_ARATH | Protein phosphatase 2C 56 OS=Arabidopsis thaliana GN=ABI1 PE=1 SV=2 | 242 | 381 | 1.0E-21 |
| sp|Q9H0C8|ILKAP_HUMAN | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Homo sapiens GN=ILKAP PE=1 SV=1 | 216 | 380 | 2.0E-21 |
| sp|A0BLX0|PP2C2_PARTE | Probable protein phosphatase 2C 2 OS=Paramecium tetraurelia GN=GSPATT00030171001 PE=3 SV=1 | 146 | 382 | 2.0E-21 |
| sp|Q8R0F6|ILKAP_MOUSE | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Mus musculus GN=Ilkap PE=1 SV=1 | 216 | 380 | 2.0E-21 |
| sp|Q9Z1Z6|ILKAP_RAT | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Rattus norvegicus GN=Ilkap PE=2 SV=1 | 216 | 380 | 2.0E-21 |
| sp|O62830|PPM1B_BOVIN | Protein phosphatase 1B OS=Bos taurus GN=PPM1B PE=2 SV=2 | 230 | 380 | 3.0E-21 |
| sp|A0DTY1|PP2C4_PARTE | Probable protein phosphatase 2C 4 OS=Paramecium tetraurelia GN=GSPATT00020181001 PE=3 SV=1 | 223 | 381 | 3.0E-21 |
| sp|A3A8W2|P2C21_ORYSJ | Probable protein phosphatase 2C 21 OS=Oryza sativa subsp. japonica GN=Os02g0606900 PE=2 SV=2 | 225 | 381 | 3.0E-21 |
| sp|O75688|PPM1B_HUMAN | Protein phosphatase 1B OS=Homo sapiens GN=PPM1B PE=1 SV=1 | 230 | 380 | 3.0E-21 |
| sp|Q84JI0|P2C30_ORYSJ | Probable protein phosphatase 2C 30 OS=Oryza sativa subsp. japonica GN=Os03g0268600 PE=2 SV=1 | 210 | 348 | 3.0E-21 |
| sp|Q9CAJ0|P2C16_ARATH | Protein phosphatase 2C 16 OS=Arabidopsis thaliana GN=HAB1 PE=1 SV=1 | 224 | 381 | 5.0E-21 |
| sp|Q54T01|Y2105_DICDI | Probable protein phosphatase DDB_G0282105 OS=Dictyostelium discoideum GN=DDB_G0282105 PE=3 SV=1 | 240 | 380 | 5.0E-21 |
| sp|Q0IIF0|ILKAP_BOVIN | Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Bos taurus GN=ILKAP PE=2 SV=1 | 216 | 380 | 8.0E-21 |
| sp|Q5UPZ7|YR307_MIMIV | PP2C-like domain-containing protein R307 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R307 PE=1 SV=1 | 237 | 382 | 9.0E-21 |
| sp|P35182|PP2C1_YEAST | Protein phosphatase 2C homolog 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC1 PE=1 SV=1 | 34 | 224 | 1.0E-20 |
| sp|Q8RX37|P2C02_ARATH | Probable protein phosphatase 2C 2 OS=Arabidopsis thaliana GN=At1g07160 PE=2 SV=1 | 227 | 380 | 1.0E-20 |
| sp|P39966|PP2C2_YEAST | Protein phosphatase 2C homolog 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC2 PE=1 SV=1 | 238 | 378 | 2.0E-20 |
| sp|O64583|P2C28_ARATH | Probable protein phosphatase 2C 28 OS=Arabidopsis thaliana GN=At2g34740 PE=2 SV=2 | 228 | 384 | 5.0E-20 |
| sp|Q80Z30|PPM1E_RAT | Protein phosphatase 1E OS=Rattus norvegicus GN=Ppm1e PE=1 SV=1 | 230 | 381 | 2.0E-19 |
| sp|Q8WY54|PPM1E_HUMAN | Protein phosphatase 1E OS=Homo sapiens GN=PPM1E PE=1 SV=2 | 230 | 381 | 2.0E-19 |
| sp|Q80TL0|PPM1E_MOUSE | Protein phosphatase 1E OS=Mus musculus GN=Ppm1e PE=1 SV=2 | 241 | 381 | 2.0E-19 |
| sp|P49606|CYAA_USTMA | Adenylate cyclase OS=Ustilago maydis (strain 521 / FGSC 9021) GN=UAC1 PE=3 SV=1 | 242 | 378 | 7.0E-19 |
| sp|Q9WTR8|PHLP1_RAT | PH domain leucine-rich repeat protein phosphatase 1 OS=Rattus norvegicus GN=Phlpp1 PE=1 SV=1 | 242 | 380 | 9.0E-19 |
| sp|P34221|PP2C3_YEAST | Protein phosphatase 2C homolog 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC3 PE=1 SV=4 | 228 | 347 | 1.0E-18 |
| sp|O60346|PHLP1_HUMAN | PH domain leucine-rich repeat-containing protein phosphatase 1 OS=Homo sapiens GN=PHLPP1 PE=1 SV=3 | 242 | 380 | 1.0E-18 |
| sp|Q9WVR7|PPM1F_RAT | Protein phosphatase 1F OS=Rattus norvegicus GN=Ppm1f PE=2 SV=1 | 165 | 384 | 2.0E-18 |
| sp|Q9LMT1|P2C08_ARATH | Probable protein phosphatase 2C 8 OS=Arabidopsis thaliana GN=At1g18030 PE=2 SV=2 | 242 | 382 | 4.0E-18 |
| sp|Q8CHE4|PHLP1_MOUSE | PH domain leucine-rich repeat-containing protein phosphatase 1 OS=Mus musculus GN=Phlpp1 PE=1 SV=2 | 242 | 380 | 5.0E-18 |
| sp|P49593|PPM1F_HUMAN | Protein phosphatase 1F OS=Homo sapiens GN=PPM1F PE=1 SV=3 | 230 | 383 | 5.0E-18 |
| sp|Q8CGA0|PPM1F_MOUSE | Protein phosphatase 1F OS=Mus musculus GN=Ppm1f PE=1 SV=1 | 230 | 384 | 6.0E-18 |
| sp|Q6K5I0|P2C20_ORYSJ | Probable protein phosphatase 2C 20 OS=Oryza sativa subsp. japonica GN=Os02g0600000 PE=3 SV=2 | 39 | 381 | 4.0E-17 |
| sp|P49599|P2C57_ARATH | Protein phosphatase 2C 57 OS=Arabidopsis thaliana GN=PPH1 PE=1 SV=2 | 241 | 377 | 7.0E-17 |
| sp|P38089|PP2C4_YEAST | Protein phosphatase 2C homolog 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC4 PE=1 SV=1 | 203 | 378 | 8.0E-17 |
| sp|Q0J2R1|P2C67_ORYSJ | Probable protein phosphatase 2C 67 OS=Oryza sativa subsp. japonica GN=Os09g0314400 PE=2 SV=1 | 216 | 381 | 1.0E-16 |
| sp|Q6ZVD8|PHLP2_HUMAN | PH domain leucine-rich repeat-containing protein phosphatase 2 OS=Homo sapiens GN=PHLPP2 PE=1 SV=3 | 242 | 380 | 2.0E-16 |
| sp|P40371|PP2C1_SCHPO | Protein phosphatase 2C homolog 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc1 PE=2 SV=1 | 28 | 143 | 3.0E-16 |
| sp|Q8BXA7|PHLP2_MOUSE | PH domain leucine-rich repeat-containing protein phosphatase 2 OS=Mus musculus GN=Phlpp2 PE=1 SV=3 | 242 | 380 | 5.0E-16 |
| sp|Q8N819|PPM1N_HUMAN | Probable protein phosphatase 1N OS=Homo sapiens GN=PPM1N PE=2 SV=2 | 223 | 387 | 1.0E-15 |
| sp|P23466|CYAA_LACKL | Adenylate cyclase OS=Lachancea kluyveri GN=CYR1 PE=3 SV=1 | 242 | 384 | 1.0E-15 |
| sp|P49594|FEM2_CAEEL | Ca(2+)/calmodulin-dependent protein kinase phosphatase OS=Caenorhabditis elegans GN=fem-2 PE=1 SV=2 | 239 | 383 | 2.0E-15 |
| sp|A8MPX8|PP2D1_HUMAN | Protein phosphatase 2C-like domain-containing protein 1 OS=Homo sapiens GN=PP2D1 PE=2 SV=2 | 37 | 346 | 3.0E-15 |
| sp|Q01631|CYAA_NEUCR | Adenylate cyclase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=cr-1 PE=1 SV=2 | 242 | 378 | 5.0E-15 |
| sp|Q8BGL1|PPM1N_MOUSE | Probable protein phosphatase 1N OS=Mus musculus GN=Ppm1n PE=2 SV=1 | 228 | 380 | 7.0E-15 |
| sp|Q54WS9|Y9461_DICDI | Probable protein phosphatase DDB_G0279461 OS=Dictyostelium discoideum GN=DDB_G0279461 PE=3 SV=2 | 239 | 381 | 9.0E-15 |
| sp|Q7XP01|P2C37_ORYSJ | Probable protein phosphatase 2C 37 OS=Oryza sativa subsp. japonica GN=Os04g0167900 PE=3 SV=2 | 230 | 359 | 1.0E-14 |
| sp|Q0WRB2|P2C73_ARATH | Probable protein phosphatase 2C 73 OS=Arabidopsis thaliana GN=PPC6-7 PE=2 SV=1 | 230 | 378 | 1.0E-14 |
| sp|P08678|CYAA_YEAST | Adenylate cyclase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CYR1 PE=1 SV=2 | 242 | 385 | 2.0E-14 |
| sp|Q9M9W9|P2C34_ARATH | Probable protein phosphatase 2C 34 OS=Arabidopsis thaliana GN=At3g05640 PE=2 SV=1 | 230 | 365 | 2.0E-14 |
| sp|Q9LRZ4|P2C41_ARATH | Probable protein phosphatase 2C 41 OS=Arabidopsis thaliana GN=At3g16800 PE=2 SV=1 | 242 | 381 | 3.0E-14 |
| sp|Q5JKN1|P2C05_ORYSJ | Probable protein phosphatase 2C 5 OS=Oryza sativa subsp. japonica GN=Os01g0552300 PE=2 SV=1 | 241 | 377 | 3.0E-14 |
| sp|Q6Z8B9|P2C12_ORYSJ | Probable protein phosphatase 2C 12 OS=Oryza sativa subsp. japonica GN=Os02g0224100 PE=2 SV=1 | 230 | 365 | 1.0E-13 |
| sp|Q9SUF4|P2C53_ARATH | Putative protein phosphatase 2C 53 OS=Arabidopsis thaliana GN=At4g08260 PE=5 SV=1 | 227 | 384 | 8.0E-13 |
| sp|Q2QWE3|P2C77_ORYSJ | Probable protein phosphatase 2C 77 OS=Oryza sativa subsp. japonica GN=Os12g0198200 PE=3 SV=1 | 242 | 383 | 8.0E-13 |
| sp|Q9M9C6|P2C15_ARATH | Probable protein phosphatase 2C 15 OS=Arabidopsis thaliana GN=At1g68410 PE=2 SV=1 | 245 | 383 | 9.0E-13 |
| sp|Q2QN36|P2C78_ORYSJ | Probable protein phosphatase 2C 78 OS=Oryza sativa subsp. japonica GN=Os12g0580900 PE=2 SV=1 | 214 | 364 | 9.0E-13 |
| sp|Q6YTI2|P2C15_ORYSJ | Probable protein phosphatase 2C 15 OS=Oryza sativa subsp. japonica GN=Os02g0567200 PE=2 SV=1 | 245 | 378 | 1.0E-12 |
| sp|P46014|P2C70_ARATH | Protein phosphatase 2C 70 OS=Arabidopsis thaliana GN=KAPP PE=1 SV=2 | 244 | 380 | 2.0E-12 |
| sp|Q7XTC7|P2C40_ORYSJ | Probable protein phosphatase 2C 40 OS=Oryza sativa subsp. japonica GN=Os04g0449400 PE=3 SV=3 | 241 | 387 | 3.0E-12 |
| sp|P36982|PP2C_LEICH | Protein phosphatase 2C OS=Leishmania chagasi PE=2 SV=1 | 242 | 381 | 4.0E-12 |
| sp|Q5R522|PPM1K_PONAB | Protein phosphatase 1K, mitochondrial OS=Pongo abelii GN=PPM1K PE=2 SV=1 | 191 | 315 | 1.0E-11 |
| sp|Q6K1U4|P2C16_ORYSJ | Probable protein phosphatase 2C 16 OS=Oryza sativa subsp. japonica GN=Os02g0598400 PE=2 SV=1 | 39 | 381 | 1.0E-11 |
| sp|Q501F9|P2C67_ARATH | Probable protein phosphatase 2C 67 OS=Arabidopsis thaliana GN=At5g02760 PE=2 SV=1 | 241 | 349 | 1.0E-11 |
| sp|Q8BVT6|PP2D1_MOUSE | Protein phosphatase 2C-like domain-containing protein 1 OS=Mus musculus GN=Pp2d1 PE=2 SV=1 | 235 | 347 | 2.0E-11 |
| sp|Q6L482|P2C48_ORYSJ | Probable protein phosphatase 2C 48 OS=Oryza sativa subsp. japonica GN=Os05g0358500 PE=2 SV=1 | 241 | 383 | 2.0E-11 |
| sp|Q3EAZ3|P2C45_ARATH | Putative protein phosphatase 2C-like protein 45 OS=Arabidopsis thaliana GN=At3g27140 PE=5 SV=1 | 223 | 385 | 3.0E-11 |
| sp|Q9SD12|P2C46_ARATH | Probable protein phosphatase 2C 46 OS=Arabidopsis thaliana GN=At3g51370 PE=2 SV=1 | 241 | 378 | 3.0E-11 |
| sp|O80492|P2C05_ARATH | Probable protein phosphatase 2C 5 OS=Arabidopsis thaliana GN=At1g09160 PE=2 SV=1 | 242 | 378 | 1.0E-10 |
| sp|Q01513|CYAA_PODAS | Adenylate cyclase OS=Podospora anserina PE=3 SV=1 | 242 | 378 | 1.0E-10 |
| sp|Q6NKS1|P2C65_ARATH | Probable protein phosphatase 2C 65 OS=Arabidopsis thaliana GN=At5g01700 PE=2 SV=1 | 230 | 378 | 1.0E-10 |
| sp|Q8H4S6|P2C64_ORYSJ | Probable protein phosphatase 2C 64 OS=Oryza sativa subsp. japonica GN=Os07g0566200 PE=2 SV=2 | 242 | 370 | 2.0E-10 |
| sp|Q0JMD4|P2C03_ORYSJ | Probable protein phosphatase 2C 3 OS=Oryza sativa subsp. japonica GN=Os01g0513100 PE=2 SV=2 | 245 | 383 | 2.0E-10 |
| sp|P14605|CYAA_SCHPO | Adenylate cyclase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=cyr1 PE=1 SV=1 | 243 | 380 | 2.0E-10 |
| sp|Q94CL8|P2C48_ARATH | Probable protein phosphatase 2C 48 OS=Arabidopsis thaliana GN=PP2C6 PE=2 SV=1 | 241 | 378 | 3.0E-10 |
| sp|Q9FX08|P2C12_ARATH | Probable protein phosphatase 2C 12 OS=Arabidopsis thaliana GN=At1g47380 PE=2 SV=1 | 241 | 378 | 4.0E-10 |
| sp|Q9LHJ9|P2C38_ARATH | Probable protein phosphatase 2C 38 OS=Arabidopsis thaliana GN=At3g12620 PE=2 SV=1 | 241 | 378 | 5.0E-10 |
| sp|Q9SL76|P2C19_ARATH | Protein phosphatase 2C and cyclic nucleotide-binding/kinase domain-containing protein OS=Arabidopsis thaliana GN=At2g20050/At2g20040 PE=2 SV=2 | 230 | 378 | 8.0E-10 |
| sp|Q7XCJ7|P2C72_ORYSJ | Probable protein phosphatase 2C 72 OS=Oryza sativa subsp. japonica GN=Os10g0544900 PE=2 SV=1 | 242 | 380 | 1.0E-09 |
| sp|Q6K1U0|P2C17_ORYSJ | Probable protein phosphatase 2C 17 OS=Oryza sativa subsp. japonica GN=Os02g0599150 PE=2 SV=1 | 39 | 381 | 1.0E-09 |
| sp|Q2RBJ6|P2C73_ORYSJ | Probable protein phosphatase 2C 73 OS=Oryza sativa subsp. japonica GN=Os11g0109000 PE=2 SV=1 | 242 | 365 | 1.0E-09 |
| sp|Q9SLA1|P2C22_ARATH | Probable protein phosphatase 2C 22 OS=Arabidopsis thaliana GN=At2g25620 PE=2 SV=1 | 33 | 140 | 2.0E-09 |
| sp|Q9M8R7|P2C33_ARATH | Probable protein phosphatase 2C 33 OS=Arabidopsis thaliana GN=PPC6-1 PE=1 SV=1 | 230 | 365 | 3.0E-09 |
| sp|Q8GY60|P2C52_ARATH | Probable protein phosphatase 2C 52 OS=Arabidopsis thaliana GN=At4g03415 PE=2 SV=1 | 226 | 347 | 3.0E-09 |
| sp|Q6ZKL8|P2C66_ORYSJ | Probable protein phosphatase 2C 66 OS=Oryza sativa subsp. japonica GN=Os08g0500300 PE=2 SV=1 | 242 | 347 | 3.0E-09 |
| sp|Q2R637|P2C75_ORYSJ | Probable protein phosphatase 2C 75 OS=Oryza sativa subsp. japonica GN=Os11g0417400 PE=2 SV=1 | 230 | 383 | 4.0E-09 |
| sp|Q10MN6|P2C33_ORYSJ | Probable protein phosphatase 2C 33 OS=Oryza sativa subsp. japonica GN=Os03g0301700 PE=2 SV=1 | 206 | 378 | 5.0E-09 |
| sp|Q9LR65|P2C01_ARATH | Probable protein phosphatase 2C 1 OS=Arabidopsis thaliana GN=PPC6-6 PE=1 SV=1 | 242 | 347 | 5.0E-09 |
| sp|Q9FKX4|P2C79_ARATH | Probable protein phosphatase 2C 79 OS=Arabidopsis thaliana GN=At5g66080 PE=2 SV=1 | 242 | 365 | 7.0E-09 |
| sp|Q7Y138|P2C36_ORYSJ | Probable protein phosphatase 2C 36 OS=Oryza sativa subsp. japonica GN=Os03g0832400 PE=2 SV=1 | 217 | 378 | 7.0E-09 |
| sp|Q9M1V8|P2C50_ARATH | Putative protein phosphatase 2C 50 OS=Arabidopsis thaliana GN=At3g63320 PE=3 SV=1 | 66 | 381 | 7.0E-09 |
| sp|Q6ZHC8|P2C25_ORYSJ | Probable protein phosphatase 2C 25 OS=Oryza sativa subsp. japonica GN=Os02g0685600 PE=2 SV=1 | 236 | 361 | 1.0E-08 |
| sp|O14156|PP2C4_SCHPO | Protein phosphatase 2C homolog 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc4 PE=1 SV=2 | 241 | 380 | 1.0E-08 |
| sp|Q7XUC5|P2C43_ORYSJ | Probable protein phosphatase 2C 43 OS=Oryza sativa subsp. japonica GN=Os04g0584300 PE=3 SV=2 | 216 | 365 | 2.0E-08 |
| sp|Q8RXZ4|P2C18_ARATH | Probable protein phosphatase 2C 18 OS=Arabidopsis thaliana GN=At1g79630 PE=2 SV=1 | 242 | 365 | 2.0E-08 |
| sp|Q5PNS9|P2C64_ARATH | Probable protein phosphatase 2C 64 OS=Arabidopsis thaliana GN=At4g38520 PE=2 SV=1 | 242 | 380 | 4.0E-08 |
| sp|Q9FG61|P2C74_ARATH | Probable protein phosphatase 2C 74 OS=Arabidopsis thaliana GN=At5g36250 PE=1 SV=1 | 230 | 365 | 5.0E-08 |
| sp|O82637|P2C61_ARATH | Probable protein phosphatase 2C 61 OS=Arabidopsis thaliana GN=At4g32950 PE=3 SV=1 | 230 | 357 | 5.0E-08 |
| sp|Q09173|PP2C3_SCHPO | Protein phosphatase 2C homolog 3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc3 PE=3 SV=1 | 38 | 142 | 6.0E-08 |
| sp|Q9XGZ9|P2C72_ARATH | Probable protein phosphatase 2C 72 OS=Arabidopsis thaliana GN=At5g26010 PE=2 SV=2 | 242 | 381 | 7.0E-08 |
| sp|Q5Z8P0|P2C60_ORYSJ | Probable protein phosphatase 2C 60 OS=Oryza sativa subsp. japonica GN=Os06g0717800 PE=2 SV=1 | 241 | 378 | 7.0E-08 |
| sp|Q9LW60|P2C44_ARATH | Putative protein phosphatase 2C-like protein 44 OS=Arabidopsis thaliana GN=At3g23360 PE=5 SV=1 | 242 | 380 | 8.0E-08 |
| sp|Q93YS2|P2C51_ARATH | Probable protein phosphatase 2C 51 OS=Arabidopsis thaliana GN=At3g63340 PE=2 SV=2 | 260 | 381 | 8.0E-08 |
| sp|A3CCP9|P2C76_ORYSJ | Putative protein phosphatase 2C 76 OS=Oryza sativa subsp. japonica GN=Os11g0586001 PE=3 SV=2 | 263 | 378 | 8.0E-08 |
| sp|Q7XW27|P2C38_ORYSJ | Probable protein phosphatase 2C 38 OS=Oryza sativa subsp. japonica GN=Os04g0321800 PE=2 SV=2 | 242 | 386 | 9.0E-08 |
| sp|O62829|PPM1A_BOVIN | Protein phosphatase 1A OS=Bos taurus GN=PPM1A PE=2 SV=1 | 38 | 140 | 1.0E-07 |
| sp|P20650|PPM1A_RAT | Protein phosphatase 1A OS=Rattus norvegicus GN=Ppm1a PE=1 SV=1 | 38 | 140 | 1.0E-07 |
| sp|P35813|PPM1A_HUMAN | Protein phosphatase 1A OS=Homo sapiens GN=PPM1A PE=1 SV=1 | 38 | 140 | 1.0E-07 |
| sp|P49443|PPM1A_MOUSE | Protein phosphatase 1A OS=Mus musculus GN=Ppm1a PE=1 SV=1 | 38 | 140 | 1.0E-07 |
| sp|Q0V7V2|P2C42_ARATH | Probable protein phosphatase 2C 42 OS=Arabidopsis thaliana GN=At3g17090 PE=2 SV=1 | 230 | 365 | 1.0E-07 |
| sp|Q8H063|P2C29_ORYSJ | Probable protein phosphatase 2C 29 OS=Oryza sativa subsp. japonica GN=Os03g0207400 PE=2 SV=1 | 199 | 378 | 1.0E-07 |
| sp|Q9SA22|P2C06_ARATH | Probable protein phosphatase 2C 6 OS=Arabidopsis thaliana GN=At1g16220 PE=2 SV=1 | 230 | 347 | 1.0E-07 |
| sp|P35814|PPM1A_RABIT | Protein phosphatase 1A OS=Oryctolagus cuniculus GN=PPM1A PE=2 SV=1 | 38 | 140 | 2.0E-07 |
| sp|Q10S32|P2C28_ORYSJ | Probable protein phosphatase 2C 28 OS=Oryza sativa subsp. japonica GN=Os03g0137200 PE=2 SV=1 | 242 | 378 | 2.0E-07 |
| sp|Q9LUS8|P2C40_ARATH | Probable protein phosphatase 2C 40 OS=Arabidopsis thaliana GN=At3g16560 PE=2 SV=1 | 242 | 347 | 2.0E-07 |
| sp|Q8BGL1|PPM1N_MOUSE | Probable protein phosphatase 1N OS=Mus musculus GN=Ppm1n PE=2 SV=1 | 25 | 140 | 5.0E-07 |
| sp|Q7XU84|P2C42_ORYSJ | Probable protein phosphatase 2C 42 OS=Oryza sativa subsp. japonica GN=Os04g0500900 PE=3 SV=4 | 29 | 93 | 8.0E-07 |
| sp|Q6K6N7|P2C14_ORYSJ | Probable protein phosphatase 2C 14 OS=Oryza sativa subsp. japonica GN=Os02g0471500 PE=2 SV=1 | 230 | 361 | 8.0E-07 |
| sp|P47354|PPH_MYCGE | Putative protein phosphatase OS=Mycoplasma genitalium (strain ATCC 33530 / G-37 / NCTC 10195) GN=MG108 PE=3 SV=1 | 233 | 382 | 1.0E-06 |
| sp|O81760|P2C63_ARATH | Probable protein phosphatase 2C 63 OS=Arabidopsis thaliana GN=At4g33920 PE=2 SV=1 | 199 | 382 | 1.0E-06 |
| sp|Q67J17|P2C69_ORYSJ | Probable protein phosphatase 2C 69 OS=Oryza sativa subsp. japonica GN=Os09g0459600 PE=2 SV=1 | 220 | 383 | 1.0E-06 |
| sp|Q5N9N2|P2C09_ORYSJ | Probable protein phosphatase 2C 9 OS=Oryza sativa subsp. japonica GN=Os01g0846300 PE=2 SV=1 | 38 | 140 | 2.0E-06 |
| sp|Q67UP9|P2C58_ORYSJ | Probable protein phosphatase 2C 58 OS=Oryza sativa subsp. japonica GN=Os06g0651600 PE=2 SV=1 | 35 | 92 | 3.0E-06 |
| sp|A0DTY1|PP2C4_PARTE | Probable protein phosphatase 2C 4 OS=Paramecium tetraurelia GN=GSPATT00020181001 PE=3 SV=1 | 37 | 140 | 5.0E-06 |
| sp|A3AZ89|P2C46_ORYSJ | Putative protein phosphatase 2C 46 OS=Oryza sativa subsp. japonica GN=Os05g0111800 PE=3 SV=2 | 255 | 347 | 5.0E-06 |
| sp|A3A8Q4|P2C18_ORYSJ | Probable protein phosphatase 2C 18 OS=Oryza sativa subsp. japonica GN=Os02g0599200 PE=2 SV=2 | 242 | 381 | 6.0E-06 |
| sp|P39966|PP2C2_YEAST | Protein phosphatase 2C homolog 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC2 PE=1 SV=1 | 36 | 140 | 9.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0004722 | protein serine/threonine phosphatase activity | Yes |
| GO:0140096 | catalytic activity, acting on a protein | No |
| GO:0003674 | molecular_function | No |
| GO:0016791 | phosphatase activity | No |
| GO:0016787 | hydrolase activity | No |
| GO:0003824 | catalytic activity | No |
| GO:0016788 | hydrolase activity, acting on ester bonds | No |
| GO:0004721 | phosphoprotein phosphatase activity | No |
| GO:0042578 | phosphoric ester hydrolase activity | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 11 | 0.45 |
Expression values
| Label | Description | Expression (RPKM) | Confidence interval (low) | Confidence interval (high) |
|---|---|---|---|---|
| Casing | Casing mycelium | 93.56 | 56.24 | 130.87 |
| Initials | Initials knots | 84.61 | 50.84 | 118.38 |
| Pileal_Stipeal_center | Stage I stipe center | 151.22 | 90.01 | 212.42 |
| Pileal_Stipeal_shell | Stage I stipe shell | 86.27 | 51.49 | 121.06 |
| DIF_stipe_center | Stage II stipe center | 123.60 | 73.87 | 173.34 |
| DIF_stipe_shell | Stage II stipe shell | 182.27 | 106.88 | 257.66 |
| DIF_stipe_skin | Stage II stipe skin | 143.84 | 85.57 | 202.12 |
| DIF_cap_skin | Stage II cap skin | 86.96 | 51.77 | 122.16 |
| DIF_cap_tissue | Stage II cap tissue | 82.96 | 49.86 | 116.05 |
| DIF_gill_tissue | Stage II gill tissue | 86.99 | 52.35 | 121.62 |
| YFB_stipe_center | Young fruiting body stipe center | 110.21 | 66.22 | 154.21 |
| YFB_stipe_shell | Young fruiting body stipe shell | 137.24 | 81.27 | 193.20 |
| YFB_stipe_skin | Young fruiting body stipe skin | 121.34 | 72.26 | 170.42 |
| YFB_cap_skin | Young fruiting body cap skin | 109.53 | 65.72 | 153.34 |
| YFB_cap_tissue | Young fruiting body cap tissue | 98.41 | 58.07 | 138.74 |
| YFB_gill_tissue | Young fruiting body gill tissue | 115.06 | 69.12 | 160.99 |
| YFB_veil | Young fruiting body veil | 105.09 | 61.54 | 148.65 |
Differential expression
| Label1 | Label2 | Q-value | Significant difference |
|---|---|---|---|
| Casing | DIF_gill_tissue | 0.879326 | no |
| Casing | YFB_stipe_center | 0.669737 | no |
| Casing | YFB_stipe_shell | 0.189511 | no |
| Casing | YFB_stipe_skin | 0.437374 | no |
| Casing | YFB_cap_skin | 0.686379 | no |
| Casing | YFB_cap_tissue | 0.920385 | no |
| Casing | YFB_gill_tissue | 0.556302 | no |
| Casing | YFB_veil | 0.793288 | no |
| Casing | Initials | 0.824014 | no |
| Casing | Pileal_Stipeal_center | 0.079829 | no |
| Casing | Pileal_Stipeal_shell | 0.864586 | no |
| Casing | DIF_stipe_center | 0.392751 | no |
| Casing | DIF_stipe_shell | 0.009773 | yes |
| Casing | DIF_stipe_skin | 0.129247 | no |
| Casing | DIF_cap_skin | 0.878362 | no |
| Casing | DIF_cap_tissue | 0.778273 | no |
| DIF_gill_tissue | YFB_stipe_center | 0.484325 | no |
| DIF_gill_tissue | YFB_stipe_shell | 0.099759 | no |
| DIF_gill_tissue | YFB_stipe_skin | 0.271845 | no |
| DIF_gill_tissue | YFB_cap_skin | 0.501293 | no |
| DIF_gill_tissue | YFB_cap_tissue | 0.775797 | no |
| DIF_gill_tissue | YFB_gill_tissue | 0.379747 | no |
| DIF_gill_tissue | YFB_veil | 0.619845 | no |
| YFB_stipe_center | YFB_stipe_shell | 0.540630 | no |
| YFB_stipe_center | YFB_stipe_skin | 0.834248 | no |
| YFB_stipe_center | YFB_cap_skin | 0.990581 | no |
| YFB_stipe_center | YFB_cap_tissue | 0.795974 | no |
| YFB_stipe_center | YFB_gill_tissue | 0.934722 | no |
| YFB_stipe_center | YFB_veil | 0.927567 | no |
| YFB_stipe_shell | YFB_stipe_skin | 0.782013 | no |
| YFB_stipe_shell | YFB_cap_skin | 0.522288 | no |
| YFB_stipe_shell | YFB_cap_tissue | 0.279565 | no |
| YFB_stipe_shell | YFB_gill_tissue | 0.645740 | no |
| YFB_stipe_shell | YFB_veil | 0.440936 | no |
| YFB_stipe_skin | YFB_cap_skin | 0.823069 | no |
| YFB_stipe_skin | YFB_cap_tissue | 0.566542 | no |
| YFB_stipe_skin | YFB_gill_tissue | 0.919861 | no |
| YFB_stipe_skin | YFB_veil | 0.737140 | no |
| YFB_cap_skin | YFB_cap_tissue | 0.814128 | no |
| YFB_cap_skin | YFB_gill_tissue | 0.925263 | no |
| YFB_cap_skin | YFB_veil | 0.938755 | no |
| YFB_cap_tissue | YFB_gill_tissue | 0.693610 | no |
| YFB_cap_tissue | YFB_veil | 0.896775 | no |
| YFB_gill_tissue | YFB_veil | 0.852842 | no |
| Initials | DIF_gill_tissue | 0.957899 | no |
| Initials | YFB_stipe_center | 0.421150 | no |
| Initials | YFB_stipe_shell | 0.080179 | no |
| Initials | YFB_stipe_skin | 0.224247 | no |
| Initials | YFB_cap_skin | 0.433898 | no |
| Initials | YFB_cap_tissue | 0.710717 | no |
| Initials | YFB_gill_tissue | 0.321351 | no |
| Initials | YFB_veil | 0.553322 | no |
| Initials | Pileal_Stipeal_center | 0.025711 | yes |
| Initials | Pileal_Stipeal_shell | 0.970934 | no |
| Initials | DIF_stipe_center | 0.194969 | no |
| Initials | DIF_stipe_shell | 0.001140 | yes |
| Initials | DIF_stipe_skin | 0.047798 | yes |
| Initials | DIF_cap_skin | 0.959371 | no |
| Initials | DIF_cap_tissue | 0.970464 | no |
| Pileal_Stipeal_center | DIF_gill_tissue | 0.036228 | yes |
| Pileal_Stipeal_center | YFB_stipe_center | 0.306536 | no |
| Pileal_Stipeal_center | YFB_stipe_shell | 0.838189 | no |
| Pileal_Stipeal_center | YFB_stipe_skin | 0.540745 | no |
| Pileal_Stipeal_center | YFB_cap_skin | 0.295235 | no |
| Pileal_Stipeal_center | YFB_cap_tissue | 0.127349 | no |
| Pileal_Stipeal_center | YFB_gill_tissue | 0.401082 | no |
| Pileal_Stipeal_center | YFB_veil | 0.235806 | no |
| Pileal_Stipeal_center | Pileal_Stipeal_shell | 0.036911 | yes |
| Pileal_Stipeal_center | DIF_stipe_center | 0.585032 | no |
| Pileal_Stipeal_center | DIF_stipe_shell | 0.627575 | no |
| Pileal_Stipeal_center | DIF_stipe_skin | 0.924674 | no |
| Pileal_Stipeal_center | DIF_cap_skin | 0.035993 | yes |
| Pileal_Stipeal_center | DIF_cap_tissue | 0.021846 | yes |
| Pileal_Stipeal_shell | DIF_gill_tissue | 0.986192 | no |
| Pileal_Stipeal_shell | YFB_stipe_center | 0.472441 | no |
| Pileal_Stipeal_shell | YFB_stipe_shell | 0.096942 | no |
| Pileal_Stipeal_shell | YFB_stipe_skin | 0.268563 | no |
| Pileal_Stipeal_shell | YFB_cap_skin | 0.489964 | no |
| Pileal_Stipeal_shell | YFB_cap_tissue | 0.756560 | no |
| Pileal_Stipeal_shell | YFB_gill_tissue | 0.373094 | no |
| Pileal_Stipeal_shell | YFB_veil | 0.604397 | no |
| Pileal_Stipeal_shell | DIF_stipe_center | 0.234962 | no |
| Pileal_Stipeal_shell | DIF_stipe_shell | 0.002084 | yes |
| Pileal_Stipeal_shell | DIF_stipe_skin | 0.057945 | no |
| Pileal_Stipeal_shell | DIF_cap_skin | 0.987573 | no |
| Pileal_Stipeal_shell | DIF_cap_tissue | 0.939991 | no |
| DIF_stipe_center | DIF_gill_tissue | 0.241254 | no |
| DIF_stipe_center | YFB_stipe_center | 0.794075 | no |
| DIF_stipe_center | YFB_stipe_shell | 0.822629 | no |
| DIF_stipe_center | YFB_stipe_skin | 0.972803 | no |
| DIF_stipe_center | YFB_cap_skin | 0.779964 | no |
| DIF_stipe_center | YFB_cap_tissue | 0.517621 | no |
| DIF_stipe_center | YFB_gill_tissue | 0.884509 | no |
| DIF_stipe_center | YFB_veil | 0.690567 | no |
| DIF_stipe_center | DIF_stipe_shell | 0.188408 | no |
| DIF_stipe_center | DIF_stipe_skin | 0.712426 | no |
| DIF_stipe_center | DIF_cap_skin | 0.248983 | no |
| DIF_stipe_center | DIF_cap_tissue | 0.160253 | no |
| DIF_stipe_shell | DIF_gill_tissue | 0.003365 | yes |
| DIF_stipe_shell | YFB_stipe_center | 0.064141 | no |
| DIF_stipe_shell | YFB_stipe_shell | 0.395202 | no |
| DIF_stipe_shell | YFB_stipe_skin | 0.160388 | no |
| DIF_stipe_shell | YFB_cap_skin | 0.057747 | no |
| DIF_stipe_shell | YFB_cap_tissue | 0.019715 | yes |
| DIF_stipe_shell | YFB_gill_tissue | 0.097608 | no |
| DIF_stipe_shell | YFB_veil | 0.042260 | yes |
| DIF_stipe_shell | DIF_stipe_skin | 0.508639 | no |
| DIF_stipe_shell | DIF_cap_skin | 0.002525 | yes |
| DIF_stipe_shell | DIF_cap_tissue | 0.001625 | yes |
| DIF_stipe_skin | DIF_gill_tissue | 0.058926 | no |
| DIF_stipe_skin | YFB_stipe_center | 0.418001 | no |
| DIF_stipe_skin | YFB_stipe_shell | 0.932286 | no |
| DIF_stipe_skin | YFB_stipe_skin | 0.668023 | no |
| DIF_stipe_skin | YFB_cap_skin | 0.401643 | no |
| DIF_stipe_skin | YFB_cap_tissue | 0.193131 | no |
| DIF_stipe_skin | YFB_gill_tissue | 0.523438 | no |
| DIF_stipe_skin | YFB_veil | 0.330910 | no |
| DIF_stipe_skin | DIF_cap_skin | 0.060697 | no |
| DIF_stipe_skin | DIF_cap_tissue | 0.038495 | yes |
| DIF_cap_skin | DIF_gill_tissue | 0.999400 | no |
| DIF_cap_skin | YFB_stipe_center | 0.487984 | no |
| DIF_cap_skin | YFB_stipe_shell | 0.104587 | no |
| DIF_cap_skin | YFB_stipe_skin | 0.280761 | no |
| DIF_cap_skin | YFB_cap_skin | 0.504869 | no |
| DIF_cap_skin | YFB_cap_tissue | 0.776943 | no |
| DIF_cap_skin | YFB_gill_tissue | 0.387601 | no |
| DIF_cap_skin | YFB_veil | 0.624459 | no |
| DIF_cap_skin | DIF_cap_tissue | 0.927927 | no |
| DIF_cap_tissue | DIF_gill_tissue | 0.925381 | no |
| DIF_cap_tissue | YFB_stipe_center | 0.372326 | no |
| DIF_cap_tissue | YFB_stipe_shell | 0.066767 | no |
| DIF_cap_tissue | YFB_stipe_skin | 0.193627 | no |
| DIF_cap_tissue | YFB_cap_skin | 0.385213 | no |
| DIF_cap_tissue | YFB_cap_tissue | 0.656034 | no |
| DIF_cap_tissue | YFB_gill_tissue | 0.281825 | no |
| DIF_cap_tissue | YFB_veil | 0.502622 | no |
| 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 | >AgabiH97|045990 MAFTDSPNARSKSITSADLETYGILNRVSNNHPTFSLGVSEDKGSRRTMEDAHSFVVDFDSVRGQGFYAIFDGHA GKHAAEWCGQHFHEYLLDALHHNPDKPIPDILNSTFHNVDGSLSRMCEESDGKIHSGCTAVTAFLRIEDDEGHQS FIKDAAMHSPDSDDDGTGSNKASSGDSLSVNGDPKDGKELKSKSHQSRIKGAFRHFSNKPSASSTLASPSTAKVS SEGVTVAVPPLTTRRVLYCANAGDARGVLCRKGKAVRLTYDHKGSDRQEAKRITDAGGFVLSGRVNGVLAVTRSL GDSSMKEFVVGAPYTTETELCNDDEFLILACDGLWDVINDQPAVDLVRDMQDAQAASAKLLKHALSHHTTDNVTV IVIRFKQPVRNS* |
| Coding | >AgabiH97|045990 ATGGCCTTTACTGACTCCCCAAATGCGCGCTCAAAATCAATAACCTCGGCCGACCTCGAAACATATGGTATCCTC AACCGCGTCTCCAACAACCACCCCACATTCTCCTTAGGGGTATCGGAGGACAAAGGAAGCAGGCGTACCATGGAA GATGCACATTCATTCGTAGTCGACTTTGATTCCGTTCGCGGCCAAGGCTTCTATGCCATATTCGATGGCCACGCC GGCAAACACGCCGCCGAATGGTGCGGCCAGCACTTTCATGAGTATCTTTTGGATGCCCTTCATCACAACCCAGAC AAACCGATTCCCGACATCCTCAACAGCACCTTCCACAACGTCGACGGTAGCTTGTCGCGTATGTGTGAGGAGTCA GATGGGAAGATCCACTCTGGTTGCACCGCAGTGACGGCGTTCCTCCGGATTGAGGATGATGAGGGTCATCAATCT TTTATTAAAGACGCCGCGATGCATTCGCCTGATTCTGATGACGATGGCACCGGCAGCAATAAAGCAAGTAGTGGC GATAGCCTTTCGGTCAATGGTGATCCCAAAGACGGCAAGGAATTAAAGTCAAAATCTCATCAGAGTCGGATTAAA GGTGCCTTCAGACACTTCTCTAATAAGCCTTCTGCTTCTTCGACTCTTGCTTCACCATCTACGGCCAAAGTCTCT TCAGAAGGCGTCACAGTCGCAGTTCCTCCTCTAACGACCAGACGCGTTCTATATTGTGCAAATGCCGGTGATGCT CGGGGCGTGCTCTGCCGGAAAGGAAAAGCAGTGCGTTTAACATATGACCATAAGGGTTCCGACAGACAAGAAGCC AAGCGAATAACAGATGCTGGTGGGTTCGTTTTAAGTGGACGCGTTAATGGAGTATTAGCCGTAACGAGAAGTTTG GGTGATTCGTCAATGAAAGAATTTGTTGTCGGTGCACCATATACTACTGAGACGGAGCTATGCAACGACGATGAA TTTTTGATTCTGGCTTGCGACGGACTCTGGGACGTCATTAATGACCAGCCGGCCGTTGACCTTGTCCGTGATATG CAAGACGCTCAAGCAGCCAGTGCCAAGCTCCTGAAGCACGCCCTTTCTCACCACACCACCGACAACGTCACGGTT ATCGTCATTCGTTTTAAACAGCCCGTGCGAAATTCATGA |
| Transcript | >AgabiH97|045990 ATGGCCTTTACTGACTCCCCAAATGCGCGCTCAAAATCAATAACCTCGGCCGACCTCGAAACATATGGTATCCTC AACCGCGTCTCCAACAACCACCCCACATTCTCCTTAGGGGTATCGGAGGACAAAGGAAGCAGGCGTACCATGGAA GATGCACATTCATTCGTAGTCGACTTTGATTCCGTTCGCGGCCAAGGCTTCTATGCCATATTCGATGGCCACGCC GGCAAACACGCCGCCGAATGGTGCGGCCAGCACTTTCATGAGTATCTTTTGGATGCCCTTCATCACAACCCAGAC AAACCGATTCCCGACATCCTCAACAGCACCTTCCACAACGTCGACGGTAGCTTGTCGCGTATGTGTGAGGAGTCA GATGGGAAGATCCACTCTGGTTGCACCGCAGTGACGGCGTTCCTCCGGATTGAGGATGATGAGGGTCATCAATCT TTTATTAAAGACGCCGCGATGCATTCGCCTGATTCTGATGACGATGGCACCGGCAGCAATAAAGCAAGTAGTGGC GATAGCCTTTCGGTCAATGGTGATCCCAAAGACGGCAAGGAATTAAAGTCAAAATCTCATCAGAGTCGGATTAAA GGTGCCTTCAGACACTTCTCTAATAAGCCTTCTGCTTCTTCGACTCTTGCTTCACCATCTACGGCCAAAGTCTCT TCAGAAGGCGTCACAGTCGCAGTTCCTCCTCTAACGACCAGACGCGTTCTATATTGTGCAAATGCCGGTGATGCT CGGGGCGTGCTCTGCCGGAAAGGAAAAGCAGTGCGTTTAACATATGACCATAAGGGTTCCGACAGACAAGAAGCC AAGCGAATAACAGATGCTGGTGGGTTCGTTTTAAGTGGACGCGTTAATGGAGTATTAGCCGTAACGAGAAGTTTG GGTGATTCGTCAATGAAAGAATTTGTTGTCGGTGCACCATATACTACTGAGACGGAGCTATGCAACGACGATGAA TTTTTGATTCTGGCTTGCGACGGACTCTGGGACGTCATTAATGACCAGCCGGCCGTTGACCTTGTCCGTGATATG CAAGACGCTCAAGCAGCCAGTGCCAAGCTCCTGAAGCACGCCCTTTCTCACCACACCACCGACAACGTCACGGTT ATCGTCATTCGTTTTAAACAGCCCGTGCGAAATTCATGA |
| Gene | >AgabiH97|045990 ATGGCCTTTACTGACTCCCCAAATGCGCGCTCAAAATCAATAACCTCGGCCGACCTCGAAACATATGGTGTATGC GCCCTGTTCTTCTCCCAGCTTGGTATTCACCTGTCGCCAGATCCTCAACCGCGTCTCCAACAACCACCCCACATT CTCCTTAGGGGTATCGGAGGACAAAGGAAGCAGGCGTACCATGGAAGATGCACATTCATTCGTAGTCGACTTTGA TTCCGTTCGCGGCCAAGGCTTCTATGCCATATTCGATGGCCACGCCGGCAAACACGCCGCCGAATGGTGCGGCCA GCACTTTCATGAGGTACCCAACAAGACATCCTAGCCGTGCCTCAGAGATTAAATCTCCCGTAGTATCTTTTGGAT GCCCTTCATCACAACCCAGACAAACCGATTCCCGACATCCTCAACAGCACCTTCCACAACGTCGACGGTAGCTTG TCGCGTATGTGTGAGGAGTCAGATGGGAAGATCCACTCTGGTTGCACCGCAGTGACGGCGTTCCTCCGGATTGAG GATGATGAGGGTCATCAATCTTTTATTAAAGACGCCGCGATGCATTCGCCTGATTCTGATGACGATGGCACCGGC AGCAATAAAGCAAGTAGTGGCGATAGCCTTTCGGTCAATGGTGATCCCAAAGACGGCAAGGAATTAAAGTCAAAA TCTCATCAGAGTCGGATTAAAGGTGCCTTCAGACACTTCTCTAATAAGCCTTCTGCTTCTTCGACTCTTGCTTCA CCATCTACGGCCAAAGTCTCTTCAGAAGGCGTCACAGTCGCAGTTCCTCCTCTAACGACCAGACGCGTTCTATAT TGTGCAAATGCCGGTGATGCTCGGGGCGTGCTCTGCCGGAAAGGAAAAGCAGTGCGTTTAACATATGACCATAAG GGTTCCGACAGACAAGAAGCCAAGCGAATAACAGATGCTGGTGGGTTCGTTTTAAGTGGACGCGTTAATGGAGTA TTAGCCGTAACGAGAAGTTTGGGTGATTCGTCAATGAAAGAATTTGTTGTCGGTGCACCATATACTACTGAGACG GAGCTATGCAACGACGATGAATTTTTGATTCTGGCTTGCGACGGAGTACGTTTTGTTCCTCTGCGTTGAGTTACC ATGCACCTAATTTTGCCATGTTACCTAGCTCTGGGACGTCATTAATGACCAGCCGGCCGTTGACCTTGTCCGTGA TATGCAAGACGCTCAAGCAGCCAGTGCCAAGCTCCTGAAGCACGCCCTTTCTCACCACACCACCGACAACGTCAC GGTTATCGTCATTCGTTTTAAACAGCCCGTGCGAAATTCATGA |