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: 2 |
Silverman et al. | no | yes: 1 |
Pissara et al. | no | yes: 10 |
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. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
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:0005737 | cytoplasm | 2 | 3 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0005654 | nucleoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IGS1
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 16 |
GO:0006793 | phosphorus metabolic process | 3 | 16 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016311 | dephosphorylation | 5 | 16 |
GO:0019538 | protein metabolic process | 3 | 16 |
GO:0036211 | protein modification process | 4 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0043412 | macromolecule modification | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
GO:0035970 | peptidyl-threonine dephosphorylation | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 23 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 23 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 23 |
GO:0016787 | hydrolase activity | 2 | 23 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 23 |
GO:0016791 | phosphatase activity | 5 | 23 |
GO:0017018 | myosin phosphatase activity | 5 | 10 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 23 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 23 |
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.273 |
CLV_C14_Caspase3-7 | 522 | 526 | PF00656 | 0.732 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.218 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.212 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.519 |
CLV_PCSK_FUR_1 | 43 | 47 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.216 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.212 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.390 |
CLV_Separin_Metazoa | 109 | 113 | PF03568 | 0.370 |
DEG_APCC_DBOX_1 | 356 | 364 | PF00400 | 0.250 |
DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.339 |
DOC_CKS1_1 | 451 | 456 | PF01111 | 0.498 |
DOC_MAPK_gen_1 | 281 | 289 | PF00069 | 0.212 |
DOC_MAPK_gen_1 | 351 | 360 | PF00069 | 0.237 |
DOC_MAPK_MEF2A_6 | 51 | 59 | PF00069 | 0.334 |
DOC_PP2B_LxvP_1 | 6 | 9 | PF13499 | 0.435 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.250 |
DOC_PP4_MxPP_1 | 412 | 415 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.212 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.309 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.220 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.245 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 145 | 149 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.408 |
LIG_APCC_ABBA_1 | 226 | 231 | PF00400 | 0.250 |
LIG_Clathr_ClatBox_1 | 154 | 158 | PF01394 | 0.250 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.472 |
LIG_EH1_1 | 47 | 55 | PF00400 | 0.328 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.250 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.585 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.663 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.459 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.369 |
LIG_LIR_Apic_2 | 348 | 352 | PF02991 | 0.250 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.353 |
LIG_PCNA_yPIPBox_3 | 273 | 287 | PF02747 | 0.250 |
LIG_PCNA_yPIPBox_3 | 31 | 45 | PF02747 | 0.416 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.361 |
LIG_SH2_SRC | 211 | 214 | PF00017 | 0.244 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.175 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.250 |
LIG_SH2_STAT3 | 26 | 29 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.387 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.255 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.753 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.519 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 153 | 158 | PF11976 | 0.242 |
LIG_SUMO_SIM_anti_2 | 385 | 390 | PF11976 | 0.296 |
LIG_SUMO_SIM_anti_2 | 58 | 63 | PF11976 | 0.301 |
LIG_SUMO_SIM_par_1 | 152 | 158 | PF11976 | 0.250 |
LIG_SUMO_SIM_par_1 | 285 | 290 | PF11976 | 0.250 |
LIG_SUMO_SIM_par_1 | 57 | 63 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 72 | 77 | PF11976 | 0.292 |
LIG_UBA3_1 | 1 | 5 | PF00899 | 0.473 |
LIG_UBA3_1 | 154 | 159 | PF00899 | 0.250 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.237 |
LIG_WW_3 | 413 | 417 | PF00397 | 0.442 |
LIG_WW_3 | 7 | 11 | PF00397 | 0.464 |
MOD_CDK_SPK_2 | 487 | 492 | PF00069 | 0.525 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.280 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.542 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.485 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.596 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.507 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.512 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.294 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.373 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.258 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.415 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.315 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.529 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.518 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.754 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.597 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.689 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.523 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.533 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.315 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.533 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.546 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.616 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.696 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.540 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.555 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.625 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.753 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.220 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.355 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.573 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.534 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.318 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.786 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.353 |
MOD_NEK2_2 | 538 | 543 | PF00069 | 0.519 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.376 |
MOD_PK_1 | 249 | 255 | PF00069 | 0.220 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.357 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.253 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.457 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.570 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.355 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.651 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.267 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.289 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.359 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.534 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.245 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.573 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.558 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.585 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.548 |
MOD_SUMO_for_1 | 193 | 196 | PF00179 | 0.220 |
MOD_SUMO_rev_2 | 254 | 263 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 476 | 486 | PF00179 | 0.570 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.215 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.212 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.227 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.212 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.212 |
TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.460 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PET0 | Leptomonas seymouri | 73% | 97% |
A0A3Q8IFG7 | Leishmania donovani | 30% | 100% |
A0A3Q8IL63 | Leishmania donovani | 29% | 100% |
A0A3S7WTA2 | Leishmania donovani | 36% | 100% |
A0A3S7WZ14 | Leishmania donovani | 32% | 100% |
A4H7Y6 | Leishmania braziliensis | 36% | 100% |
A4HAW5 | Leishmania braziliensis | 30% | 100% |
A4HE10 | Leishmania braziliensis | 31% | 100% |
A4HHY5 | Leishmania braziliensis | 28% | 100% |
A4HKF6 | Leishmania braziliensis | 78% | 100% |
A4HWB4 | Leishmania infantum | 36% | 100% |
A4I1B7 | Leishmania infantum | 32% | 100% |
A4I565 | Leishmania infantum | 31% | 100% |
A4I7Y4 | Leishmania infantum | 100% | 100% |
A4IA25 | Leishmania infantum | 29% | 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) | 31% | 100% |
E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B2U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B540 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q2U6 | Leishmania major | 29% | 100% |
Q4Q5B1 | Leishmania major | 92% | 100% |
Q4Q7S1 | Leishmania major | 31% | 100% |
Q4QA19 | Leishmania major | 32% | 100% |
Q4QFG7 | Leishmania major | 35% | 100% |
Q6K5I0 | Oryza sativa subsp. japonica | 30% | 100% |
Q9CAJ0 | Arabidopsis thaliana | 28% | 100% |