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: 1 |
| Forrest at al. (metacyclic) | no | yes: 1 |
| Forrest at al. (procyclic) | no | yes: 1 |
| Silverman et al. | no | yes: 1 |
| Pissara et al. | no | yes: 7 |
| 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: 8 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 17 |
| NetGPI | no | yes: 0, no: 17 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 6 |
| GO:0110165 | cellular anatomical entity | 1 | 9 |
| GO:0005783 | endoplasmic reticulum | 5 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0005654 | nucleoplasm | 2 | 1 |
| GO:0005737 | cytoplasm | 2 | 3 |
| GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
| GO:0097014 | ciliary plasm | 5 | 2 |
| GO:0099568 | cytoplasmic region | 3 | 2 |
| GO:0031974 | membrane-enclosed lumen | 2 | 1 |
| GO:0031981 | nuclear lumen | 5 | 1 |
| GO:0043233 | organelle lumen | 3 | 1 |
| GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A4HKF6
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006470 | protein dephosphorylation | 5 | 15 |
| GO:0006793 | phosphorus metabolic process | 3 | 15 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 15 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 15 |
| GO:0008152 | metabolic process | 1 | 15 |
| GO:0009987 | cellular process | 1 | 15 |
| GO:0016311 | dephosphorylation | 5 | 15 |
| GO:0019538 | protein metabolic process | 3 | 15 |
| GO:0036211 | protein modification process | 4 | 15 |
| GO:0043170 | macromolecule metabolic process | 3 | 15 |
| GO:0043412 | macromolecule modification | 4 | 15 |
| GO:0044237 | cellular metabolic process | 2 | 15 |
| GO:0044238 | primary metabolic process | 2 | 15 |
| GO:0071704 | organic substance metabolic process | 2 | 15 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 15 |
| GO:0035970 | peptidyl-threonine dephosphorylation | 6 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 18 |
| GO:0004721 | phosphoprotein phosphatase activity | 3 | 18 |
| GO:0004722 | protein serine/threonine phosphatase activity | 4 | 18 |
| GO:0016787 | hydrolase activity | 2 | 18 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 18 |
| GO:0016791 | phosphatase activity | 5 | 18 |
| GO:0042578 | phosphoric ester hydrolase activity | 4 | 18 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 18 |
| GO:0005488 | binding | 1 | 3 |
| GO:0043167 | ion binding | 2 | 3 |
| GO:0043169 | cation binding | 3 | 3 |
| GO:0046872 | metal ion binding | 4 | 3 |
| GO:0017018 | myosin phosphatase activity | 5 | 6 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.270 |
| CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.600 |
| CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.365 |
| CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.223 |
| CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.222 |
| CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.465 |
| CLV_PCSK_FUR_1 | 43 | 47 | PF00082 | 0.409 |
| CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.618 |
| CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.369 |
| CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.222 |
| CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.224 |
| CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.402 |
| CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.412 |
| CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.570 |
| CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.402 |
| CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.552 |
| CLV_PCSK_PC7_1 | 6 | 12 | PF00082 | 0.507 |
| CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.238 |
| CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.349 |
| CLV_Separin_Metazoa | 109 | 113 | PF03568 | 0.383 |
| DEG_APCC_DBOX_1 | 356 | 364 | PF00400 | 0.266 |
| DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.346 |
| DEG_SPOP_SBC_1 | 549 | 553 | PF00917 | 0.510 |
| DOC_MAPK_gen_1 | 281 | 289 | PF00069 | 0.222 |
| DOC_MAPK_gen_1 | 351 | 360 | PF00069 | 0.251 |
| DOC_MAPK_MEF2A_6 | 51 | 59 | PF00069 | 0.576 |
| DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.416 |
| DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.275 |
| DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.222 |
| DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.298 |
| DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.539 |
| DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.605 |
| DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.531 |
| DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.562 |
| DOC_USP7_MATH_2 | 447 | 453 | PF00917 | 0.465 |
| DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.236 |
| DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.411 |
| DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.261 |
| DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.566 |
| DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.540 |
| DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.570 |
| DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.509 |
| DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.499 |
| LIG_14-3-3_CanoR_1 | 145 | 149 | PF00244 | 0.318 |
| LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.405 |
| LIG_14-3-3_CanoR_1 | 507 | 511 | PF00244 | 0.465 |
| LIG_APCC_ABBA_1 | 226 | 231 | PF00400 | 0.266 |
| LIG_Clathr_ClatBox_1 | 154 | 158 | PF01394 | 0.266 |
| LIG_CtBP_PxDLS_1 | 556 | 560 | PF00389 | 0.459 |
| LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.514 |
| LIG_FHA_1 | 151 | 157 | PF00498 | 0.282 |
| LIG_FHA_1 | 45 | 51 | PF00498 | 0.438 |
| LIG_FHA_1 | 509 | 515 | PF00498 | 0.538 |
| LIG_FHA_1 | 56 | 62 | PF00498 | 0.431 |
| LIG_FHA_1 | 75 | 81 | PF00498 | 0.295 |
| LIG_FHA_2 | 145 | 151 | PF00498 | 0.246 |
| LIG_LIR_Apic_2 | 348 | 352 | PF02991 | 0.275 |
| LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.278 |
| LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.268 |
| LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.315 |
| LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.296 |
| LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.278 |
| LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.268 |
| LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.315 |
| LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.345 |
| LIG_MAD2 | 548 | 556 | PF02301 | 0.479 |
| LIG_PCNA_yPIPBox_3 | 273 | 287 | PF02747 | 0.266 |
| LIG_PCNA_yPIPBox_3 | 31 | 45 | PF02747 | 0.418 |
| LIG_SH2_CRK | 70 | 74 | PF00017 | 0.354 |
| LIG_SH2_SRC | 229 | 232 | PF00017 | 0.362 |
| LIG_SH2_SRC | 416 | 419 | PF00017 | 0.415 |
| LIG_SH2_SRC | 68 | 71 | PF00017 | 0.261 |
| LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.266 |
| LIG_SH2_STAT3 | 26 | 29 | PF00017 | 0.406 |
| LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.351 |
| LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.280 |
| LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.317 |
| LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.229 |
| LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.432 |
| LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.234 |
| LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.415 |
| LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.384 |
| LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.246 |
| LIG_SH3_1 | 6 | 12 | PF00018 | 0.479 |
| LIG_SH3_2 | 17 | 22 | PF14604 | 0.405 |
| LIG_SH3_3 | 14 | 20 | PF00018 | 0.471 |
| LIG_SH3_3 | 259 | 265 | PF00018 | 0.263 |
| LIG_SH3_3 | 485 | 491 | PF00018 | 0.514 |
| LIG_SH3_3 | 6 | 12 | PF00018 | 0.497 |
| LIG_SUMO_SIM_anti_2 | 153 | 158 | PF11976 | 0.228 |
| LIG_SUMO_SIM_anti_2 | 385 | 390 | PF11976 | 0.308 |
| LIG_SUMO_SIM_anti_2 | 58 | 63 | PF11976 | 0.293 |
| LIG_SUMO_SIM_par_1 | 152 | 158 | PF11976 | 0.266 |
| LIG_SUMO_SIM_par_1 | 285 | 290 | PF11976 | 0.266 |
| LIG_SUMO_SIM_par_1 | 555 | 560 | PF11976 | 0.460 |
| LIG_SUMO_SIM_par_1 | 57 | 63 | PF11976 | 0.475 |
| LIG_SUMO_SIM_par_1 | 72 | 77 | PF11976 | 0.270 |
| LIG_UBA3_1 | 1 | 5 | PF00899 | 0.514 |
| LIG_UBA3_1 | 154 | 159 | PF00899 | 0.266 |
| LIG_WW_3 | 7 | 11 | PF00397 | 0.496 |
| MOD_CDC14_SPxK_1 | 19 | 22 | PF00782 | 0.391 |
| MOD_CDK_SPK_2 | 487 | 492 | PF00069 | 0.519 |
| MOD_CDK_SPxK_1 | 16 | 22 | PF00069 | 0.404 |
| MOD_CK1_1 | 405 | 411 | PF00069 | 0.467 |
| MOD_CK1_1 | 422 | 428 | PF00069 | 0.501 |
| MOD_CK1_1 | 438 | 444 | PF00069 | 0.546 |
| MOD_CK1_1 | 490 | 496 | PF00069 | 0.521 |
| MOD_CK1_1 | 506 | 512 | PF00069 | 0.520 |
| MOD_CK1_1 | 536 | 542 | PF00069 | 0.472 |
| MOD_CK2_1 | 310 | 316 | PF00069 | 0.297 |
| MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.373 |
| MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.303 |
| MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.302 |
| MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.557 |
| MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.524 |
| MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.524 |
| MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.495 |
| MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.541 |
| MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.576 |
| MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.560 |
| MOD_GSK3_1 | 167 | 174 | PF00069 | 0.333 |
| MOD_GSK3_1 | 398 | 405 | PF00069 | 0.553 |
| MOD_GSK3_1 | 406 | 413 | PF00069 | 0.536 |
| MOD_GSK3_1 | 418 | 425 | PF00069 | 0.513 |
| MOD_GSK3_1 | 434 | 441 | PF00069 | 0.553 |
| MOD_GSK3_1 | 483 | 490 | PF00069 | 0.744 |
| MOD_GSK3_1 | 506 | 513 | PF00069 | 0.467 |
| MOD_GSK3_1 | 548 | 555 | PF00069 | 0.544 |
| MOD_LATS_1 | 546 | 552 | PF00433 | 0.480 |
| MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.236 |
| MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.222 |
| MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.352 |
| MOD_N-GLC_1 | 427 | 432 | PF02516 | 0.622 |
| MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.531 |
| MOD_NEK2_1 | 287 | 292 | PF00069 | 0.323 |
| MOD_NEK2_1 | 541 | 546 | PF00069 | 0.523 |
| MOD_NEK2_1 | 55 | 60 | PF00069 | 0.327 |
| MOD_NEK2_1 | 550 | 555 | PF00069 | 0.497 |
| MOD_PIKK_1 | 115 | 121 | PF00454 | 0.368 |
| MOD_PIKK_1 | 25 | 31 | PF00454 | 0.396 |
| MOD_PIKK_1 | 299 | 305 | PF00454 | 0.299 |
| MOD_PK_1 | 249 | 255 | PF00069 | 0.236 |
| MOD_PKA_2 | 144 | 150 | PF00069 | 0.351 |
| MOD_PKA_2 | 317 | 323 | PF00069 | 0.274 |
| MOD_PKA_2 | 44 | 50 | PF00069 | 0.441 |
| MOD_PKA_2 | 506 | 512 | PF00069 | 0.491 |
| MOD_Plk_1 | 299 | 305 | PF00069 | 0.235 |
| MOD_Plk_1 | 382 | 388 | PF00069 | 0.352 |
| MOD_Plk_1 | 427 | 433 | PF00069 | 0.647 |
| MOD_Plk_1 | 557 | 563 | PF00069 | 0.468 |
| MOD_Plk_4 | 150 | 156 | PF00069 | 0.264 |
| MOD_Plk_4 | 382 | 388 | PF00069 | 0.301 |
| MOD_Plk_4 | 410 | 416 | PF00069 | 0.525 |
| MOD_Plk_4 | 57 | 63 | PF00069 | 0.324 |
| MOD_Plk_4 | 74 | 80 | PF00069 | 0.490 |
| MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.409 |
| MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.261 |
| MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.563 |
| MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.542 |
| MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.569 |
| MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.511 |
| MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.498 |
| MOD_SUMO_for_1 | 193 | 196 | PF00179 | 0.236 |
| MOD_SUMO_rev_2 | 254 | 263 | PF00179 | 0.315 |
| MOD_SUMO_rev_2 | 476 | 486 | PF00179 | 0.581 |
| TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.223 |
| TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.357 |
| TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.343 |
| TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.225 |
| TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.238 |
| TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.239 |
| TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.550 |
| TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.222 |
| TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.462 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PET0 | Leptomonas seymouri | 63% | 97% |
| A0A3Q8IFG7 | Leishmania donovani | 30% | 100% |
| A0A3Q8IGS1 | Leishmania donovani | 78% | 100% |
| A0A3Q8IL63 | Leishmania donovani | 28% | 100% |
| A0A3S7WTA2 | Leishmania donovani | 35% | 100% |
| A0A3S7WZ14 | Leishmania donovani | 31% | 100% |
| A4H7Y6 | Leishmania braziliensis | 35% | 100% |
| A4HAW5 | Leishmania braziliensis | 29% | 100% |
| A4HE10 | Leishmania braziliensis | 30% | 100% |
| A4HHY5 | Leishmania braziliensis | 28% | 100% |
| A4HWB4 | Leishmania infantum | 36% | 100% |
| A4I1B7 | Leishmania infantum | 31% | 100% |
| A4I565 | Leishmania infantum | 30% | 100% |
| A4I7Y4 | Leishmania infantum | 78% | 100% |
| A4IA25 | Leishmania infantum | 28% | 100% |
| D0AA51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
| E9AQ14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
| E9AXF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
| E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
| E9B2U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
| E9B540 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
| Q4Q2U6 | Leishmania major | 28% | 100% |
| Q4Q5B1 | Leishmania major | 77% | 99% |
| Q4Q7S1 | Leishmania major | 31% | 100% |
| Q4QA19 | Leishmania major | 31% | 100% |
| Q4QFG7 | Leishmania major | 35% | 100% |
| Q4QFP5 | Leishmania major | 25% | 66% |
| Q6K1U0 | Oryza sativa subsp. japonica | 30% | 77% |
| Q6K1U4 | Oryza sativa subsp. japonica | 29% | 100% |
| Q6K5I0 | Oryza sativa subsp. japonica | 30% | 100% |
| Q9CAJ0 | Arabidopsis thaliana | 29% | 100% |