This large family encompasses many diverse protein phosphatases. Some appear to have evolved transmembrane segments. Very tentatively they might regulate transmembrane receptor kinases.. The TM and non-TM groups diverged early in Eukaryota and appear to be distinct enough that they probably should not be part of the same cluster. This latter group has not expanded.
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 0 |
| Forrest at al. (procyclic) | no | yes: 3 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | yes | yes: 16 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 16 |
| NetGPI | no | yes: 0, no: 16 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H7Y6
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006470 | protein dephosphorylation | 5 | 17 |
| GO:0006793 | phosphorus metabolic process | 3 | 17 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 17 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 17 |
| GO:0008152 | metabolic process | 1 | 17 |
| GO:0009987 | cellular process | 1 | 17 |
| GO:0016311 | dephosphorylation | 5 | 17 |
| GO:0019538 | protein metabolic process | 3 | 17 |
| GO:0036211 | protein modification process | 4 | 17 |
| GO:0043170 | macromolecule metabolic process | 3 | 17 |
| GO:0043412 | macromolecule modification | 4 | 17 |
| GO:0044237 | cellular metabolic process | 2 | 17 |
| GO:0044238 | primary metabolic process | 2 | 17 |
| GO:0071704 | organic substance metabolic process | 2 | 17 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 17 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 17 |
| GO:0004721 | phosphoprotein phosphatase activity | 3 | 17 |
| GO:0004722 | protein serine/threonine phosphatase activity | 4 | 17 |
| GO:0016787 | hydrolase activity | 2 | 17 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 17 |
| GO:0016791 | phosphatase activity | 5 | 17 |
| GO:0042578 | phosphoric ester hydrolase activity | 4 | 17 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 17 |
| GO:0017018 | myosin phosphatase activity | 5 | 3 |
| GO:0005488 | binding | 1 | 1 |
| GO:0043167 | ion binding | 2 | 1 |
| GO:0043169 | cation binding | 3 | 1 |
| GO:0046872 | metal ion binding | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.543 |
| CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.431 |
| CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.393 |
| CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.197 |
| CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.512 |
| CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.543 |
| CLV_PCSK_FUR_1 | 94 | 98 | PF00082 | 0.393 |
| CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.490 |
| CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.448 |
| CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.490 |
| CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.391 |
| CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.458 |
| CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.341 |
| CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.319 |
| CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.526 |
| CLV_Separin_Metazoa | 65 | 69 | PF03568 | 0.382 |
| DEG_APCC_DBOX_1 | 96 | 104 | PF00400 | 0.391 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.601 |
| DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.625 |
| DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.357 |
| DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.296 |
| LIG_14-3-3_CanoR_1 | 194 | 199 | PF00244 | 0.201 |
| LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.514 |
| LIG_BRCT_BRCA1_2 | 184 | 190 | PF00533 | 0.201 |
| LIG_FHA_1 | 229 | 235 | PF00498 | 0.284 |
| LIG_FHA_1 | 395 | 401 | PF00498 | 0.355 |
| LIG_FHA_1 | 48 | 54 | PF00498 | 0.596 |
| LIG_FHA_1 | 82 | 88 | PF00498 | 0.551 |
| LIG_FHA_2 | 124 | 130 | PF00498 | 0.522 |
| LIG_FHA_2 | 209 | 215 | PF00498 | 0.301 |
| LIG_Integrin_isoDGR_2 | 13 | 15 | PF01839 | 0.542 |
| LIG_LIR_Gen_1 | 193 | 199 | PF02991 | 0.317 |
| LIG_LIR_Gen_1 | 211 | 219 | PF02991 | 0.330 |
| LIG_LIR_Gen_1 | 332 | 343 | PF02991 | 0.314 |
| LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.521 |
| LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.347 |
| LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.291 |
| LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.313 |
| LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.313 |
| LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.527 |
| LIG_NRBOX | 99 | 105 | PF00104 | 0.540 |
| LIG_PCNA_yPIPBox_3 | 349 | 360 | PF02747 | 0.244 |
| LIG_PCNA_yPIPBox_3 | 94 | 108 | PF02747 | 0.512 |
| LIG_Pex14_2 | 208 | 212 | PF04695 | 0.384 |
| LIG_PTB_Apo_2 | 127 | 134 | PF02174 | 0.431 |
| LIG_PTB_Apo_2 | 151 | 158 | PF02174 | 0.305 |
| LIG_SH2_CRK | 195 | 199 | PF00017 | 0.305 |
| LIG_SH2_PTP2 | 236 | 239 | PF00017 | 0.441 |
| LIG_SH2_PTP2 | 335 | 338 | PF00017 | 0.441 |
| LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.288 |
| LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.471 |
| LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.441 |
| LIG_SH3_3 | 316 | 322 | PF00018 | 0.393 |
| LIG_SH3_3 | 377 | 383 | PF00018 | 0.305 |
| LIG_SUMO_SIM_anti_2 | 397 | 402 | PF11976 | 0.373 |
| LIG_SUMO_SIM_par_1 | 317 | 323 | PF11976 | 0.229 |
| LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.402 |
| LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.449 |
| LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.384 |
| LIG_UBA3_1 | 352 | 360 | PF00899 | 0.441 |
| LIG_UBA3_1 | 399 | 404 | PF00899 | 0.352 |
| MOD_CK1_1 | 228 | 234 | PF00069 | 0.351 |
| MOD_CK1_1 | 362 | 368 | PF00069 | 0.201 |
| MOD_CK1_1 | 44 | 50 | PF00069 | 0.548 |
| MOD_CK2_1 | 208 | 214 | PF00069 | 0.423 |
| MOD_CK2_1 | 345 | 351 | PF00069 | 0.330 |
| MOD_CK2_1 | 378 | 384 | PF00069 | 0.429 |
| MOD_CK2_1 | 80 | 86 | PF00069 | 0.618 |
| MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.592 |
| MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.349 |
| MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.277 |
| MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.316 |
| MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.357 |
| MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.253 |
| MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.201 |
| MOD_GSK3_1 | 113 | 120 | PF00069 | 0.534 |
| MOD_GSK3_1 | 173 | 180 | PF00069 | 0.506 |
| MOD_GSK3_1 | 182 | 189 | PF00069 | 0.456 |
| MOD_GSK3_1 | 323 | 330 | PF00069 | 0.471 |
| MOD_GSK3_1 | 362 | 369 | PF00069 | 0.336 |
| MOD_GSK3_1 | 390 | 397 | PF00069 | 0.447 |
| MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.354 |
| MOD_N-GLC_2 | 375 | 377 | PF02516 | 0.441 |
| MOD_NEK2_1 | 157 | 162 | PF00069 | 0.193 |
| MOD_NEK2_1 | 208 | 213 | PF00069 | 0.436 |
| MOD_NEK2_1 | 254 | 259 | PF00069 | 0.467 |
| MOD_NEK2_1 | 294 | 299 | PF00069 | 0.314 |
| MOD_NEK2_1 | 46 | 51 | PF00069 | 0.643 |
| MOD_PIKK_1 | 47 | 53 | PF00454 | 0.550 |
| MOD_PKA_1 | 359 | 365 | PF00069 | 0.281 |
| MOD_PKA_1 | 7 | 13 | PF00069 | 0.628 |
| MOD_PKA_2 | 14 | 20 | PF00069 | 0.571 |
| MOD_PKA_2 | 81 | 87 | PF00069 | 0.646 |
| MOD_Plk_1 | 394 | 400 | PF00069 | 0.353 |
| MOD_Plk_4 | 194 | 200 | PF00069 | 0.358 |
| MOD_Plk_4 | 208 | 214 | PF00069 | 0.206 |
| MOD_Plk_4 | 331 | 337 | PF00069 | 0.332 |
| MOD_Plk_4 | 394 | 400 | PF00069 | 0.353 |
| MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.357 |
| MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.296 |
| MOD_SUMO_for_1 | 62 | 65 | PF00179 | 0.515 |
| MOD_SUMO_rev_2 | 262 | 269 | PF00179 | 0.318 |
| TRG_DiLeu_BaEn_1 | 148 | 153 | PF01217 | 0.357 |
| TRG_DiLeu_BaEn_3 | 350 | 356 | PF01217 | 0.433 |
| TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.388 |
| TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.450 |
| TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.441 |
| TRG_NLS_Bipartite_1 | 57 | 76 | PF00514 | 0.525 |
| TRG_NLS_MonoExtC_3 | 71 | 77 | PF00514 | 0.596 |
| TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.692 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5C7 | Leptomonas seymouri | 69% | 100% |
| A0A0N0P8F8 | Leptomonas seymouri | 38% | 100% |
| A0A0N1I0H9 | Leptomonas seymouri | 39% | 100% |
| A0A0N1IHU6 | Leptomonas seymouri | 31% | 99% |
| A0A0N1PAL8 | Leptomonas seymouri | 33% | 100% |
| A0A0N1PET0 | Leptomonas seymouri | 36% | 69% |
| A0A0S4ILP4 | Bodo saltans | 26% | 77% |
| A0A0S4IY95 | Bodo saltans | 37% | 100% |
| A0A0S4J0A6 | Bodo saltans | 32% | 99% |
| A0A0S4J8Y7 | Bodo saltans | 29% | 78% |
| A0A0S4JHB4 | Bodo saltans | 35% | 100% |
| A0A0S4JPC3 | Bodo saltans | 44% | 100% |
| A0A0S4JPM8 | Bodo saltans | 48% | 100% |
| A0A0S4KIS4 | Bodo saltans | 36% | 89% |
| A0A0S4KJV9 | Bodo saltans | 39% | 93% |
| A0A1X0NRG3 | Trypanosomatidae | 35% | 100% |
| A0A1X0NVC4 | Trypanosomatidae | 54% | 98% |
| A0A1X0P568 | Trypanosomatidae | 33% | 99% |
| A0A1X0P991 | Trypanosomatidae | 42% | 100% |
| A0A1X0PAN4 | Trypanosomatidae | 28% | 100% |
| A0A3Q8IEK6 | Leishmania donovani | 39% | 100% |
| A0A3Q8IFG7 | Leishmania donovani | 33% | 100% |
| A0A3Q8IGS1 | Leishmania donovani | 36% | 72% |
| A0A3Q8IK65 | Leishmania donovani | 40% | 100% |
| A0A3Q8IL63 | Leishmania donovani | 26% | 100% |
| A0A3S7WTA2 | Leishmania donovani | 80% | 100% |
| A0A3S7WZ14 | Leishmania donovani | 31% | 100% |
| A0A3S7X808 | Leishmania donovani | 32% | 90% |
| A0A422N8D7 | Trypanosoma rangeli | 28% | 100% |
| A0A422NAJ1 | Trypanosoma rangeli | 36% | 100% |
| A0A422NL94 | Trypanosoma rangeli | 37% | 92% |
| A0A422NS77 | Trypanosoma rangeli | 50% | 98% |
| A0A422P293 | Trypanosoma rangeli | 39% | 100% |
| A0BLX0 | Paramecium tetraurelia | 34% | 100% |
| A0BQL0 | Paramecium tetraurelia | 36% | 100% |
| A0CUB5 | Paramecium tetraurelia | 34% | 100% |
| A0DSB3 | Paramecium tetraurelia | 35% | 100% |
| A0DTY1 | Paramecium tetraurelia | 35% | 100% |
| A3A8W2 | Oryza sativa subsp. japonica | 31% | 100% |
| A3A8W6 | Oryza sativa subsp. japonica | 27% | 70% |
| A4HAW6 | Leishmania braziliensis | 30% | 90% |
| A4HE10 | Leishmania braziliensis | 29% | 100% |
| A4HG10 | Leishmania braziliensis | 39% | 100% |
| A4HHY5 | Leishmania braziliensis | 34% | 100% |
| A4HKF6 | Leishmania braziliensis | 35% | 71% |
| A4HNR1 | Leishmania braziliensis | 40% | 100% |
| A4HWB4 | Leishmania infantum | 80% | 100% |
| A4I1B7 | Leishmania infantum | 31% | 100% |
| A4I329 | Leishmania infantum | 39% | 100% |
| A4I565 | Leishmania infantum | 33% | 100% |
| A4I7Y4 | Leishmania infantum | 36% | 72% |
| A4IA25 | Leishmania infantum | 26% | 100% |
| A4IA26 | Leishmania infantum | 31% | 90% |
| A4ICT4 | Leishmania infantum | 41% | 100% |
| A5PJZ2 | Bos taurus | 33% | 100% |
| C9ZJK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| C9ZMJ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
| C9ZNW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 95% |
| D0A2L9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
| D0A5L0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 99% |
| E9ACV0 | Leishmania major | 39% | 100% |
| E9AQ14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
| E9ASH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
| E9AXF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
| E9AZD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
| E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
| E9B2U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 72% |
| E9B540 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
| E9B541 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
| O62829 | Bos taurus | 35% | 100% |
| O62830 | Bos taurus | 36% | 83% |
| O75688 | Homo sapiens | 36% | 84% |
| O81716 | Arabidopsis thaliana | 34% | 100% |
| P20650 | Rattus norvegicus | 35% | 100% |
| P34221 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 86% |
| P35182 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
| P35813 | Homo sapiens | 35% | 100% |
| P35814 | Oryctolagus cuniculus | 35% | 100% |
| P35815 | Rattus norvegicus | 37% | 100% |
| P36982 | Leishmania chagasi | 31% | 100% |
| P36993 | Mus musculus | 36% | 100% |
| P38089 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
| P39966 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 87% |
| P49443 | Mus musculus | 35% | 100% |
| P49444 | Paramecium tetraurelia | 34% | 100% |
| P49593 | Homo sapiens | 30% | 89% |
| P49594 | Caenorhabditis elegans | 24% | 90% |
| P49596 | Caenorhabditis elegans | 40% | 100% |
| P49599 | Arabidopsis thaliana | 25% | 100% |
| Q09172 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 100% |
| Q09173 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 98% |
| Q0IIF0 | Bos taurus | 31% | 100% |
| Q0J2L7 | Oryza sativa subsp. japonica | 32% | 100% |
| Q0JL75 | Oryza sativa subsp. japonica | 30% | 100% |
| Q0JLP9 | Oryza sativa subsp. japonica | 32% | 87% |
| Q10MX1 | Oryza sativa subsp. japonica | 31% | 100% |
| Q19775 | Caenorhabditis elegans | 34% | 86% |
| Q2QWE3 | Oryza sativa subsp. japonica | 27% | 96% |
| Q2R637 | Oryza sativa subsp. japonica | 29% | 94% |
| Q4Q225 | Leishmania major | 39% | 100% |
| Q4Q2U5 | Leishmania major | 31% | 90% |
| Q4Q2U6 | Leishmania major | 26% | 100% |
| Q4Q5B1 | Leishmania major | 36% | 72% |
| Q4Q7S1 | Leishmania major | 32% | 100% |
| Q4QA19 | Leishmania major | 31% | 100% |
| Q4QFG7 | Leishmania major | 79% | 100% |
| Q53Q11 | Oryza sativa subsp. japonica | 27% | 100% |
| Q5SGD2 | Homo sapiens | 34% | 100% |
| Q5SMK6 | Oryza sativa subsp. japonica | 28% | 100% |
| Q5SN75 | Oryza sativa subsp. japonica | 33% | 100% |
| Q653S3 | Oryza sativa subsp. japonica | 34% | 100% |
| Q65XG6 | Oryza sativa subsp. japonica | 33% | 97% |
| Q67UP9 | Oryza sativa subsp. japonica | 34% | 100% |
| Q67UX7 | Oryza sativa subsp. japonica | 31% | 100% |
| Q69QZ0 | Oryza sativa subsp. japonica | 28% | 100% |
| Q69VD9 | Oryza sativa subsp. japonica | 31% | 100% |
| Q6AUQ4 | Oryza sativa subsp. japonica | 30% | 100% |
| Q6ETK3 | Oryza sativa subsp. japonica | 35% | 100% |
| Q6K1U4 | Oryza sativa subsp. japonica | 27% | 78% |
| Q6K5I0 | Oryza sativa subsp. japonica | 24% | 78% |
| Q6L4R7 | Oryza sativa subsp. japonica | 33% | 91% |
| Q6L5H6 | Oryza sativa subsp. japonica | 32% | 100% |
| Q7XJ53 | Arabidopsis thaliana | 26% | 100% |
| Q7XU84 | Oryza sativa subsp. japonica | 31% | 100% |
| Q84JI0 | Oryza sativa subsp. japonica | 32% | 100% |
| Q8BHN0 | Mus musculus | 33% | 100% |
| Q8CGA0 | Mus musculus | 32% | 89% |
| Q8GY60 | Arabidopsis thaliana | 29% | 86% |
| Q8N819 | Homo sapiens | 33% | 94% |
| Q8R0F6 | Mus musculus | 31% | 100% |
| Q9CAJ0 | Arabidopsis thaliana | 32% | 79% |
| Q9FXE4 | Arabidopsis thaliana | 31% | 91% |
| Q9H0C8 | Homo sapiens | 31% | 100% |
| Q9LMT1 | Arabidopsis thaliana | 27% | 100% |
| Q9LNF4 | Arabidopsis thaliana | 29% | 100% |
| Q9LNP9 | Arabidopsis thaliana | 32% | 79% |
| Q9M1V8 | Arabidopsis thaliana | 26% | 96% |
| Q9SA22 | Arabidopsis thaliana | 27% | 82% |
| Q9SZ53 | Arabidopsis thaliana | 34% | 100% |
| Q9WVR7 | Rattus norvegicus | 33% | 90% |
| Q9XEE8 | Arabidopsis thaliana | 28% | 100% |
| Q9Z1Z6 | Rattus norvegicus | 31% | 100% |
| V5BA03 | Trypanosoma cruzi | 41% | 100% |
| V5BCX6 | Trypanosoma cruzi | 35% | 100% |
| V5BH00 | Trypanosoma cruzi | 35% | 100% |
| V5DCR6 | Trypanosoma cruzi | 52% | 98% |