A large collection of various protein phosphatases. Very highly expanded in kinetoplastids.
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: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005955 | calcineurin complex | 3 | 1 |
GO:0008287 | protein serine/threonine phosphatase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1903293 | phosphatase complex | 3 | 1 |
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4H7E7
Term | Name | Level | Count |
---|---|---|---|
GO:0007165 | signal transduction | 2 | 5 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019722 | calcium-mediated signaling | 5 | 5 |
GO:0019932 | second-messenger-mediated signaling | 4 | 5 |
GO:0035556 | intracellular signal transduction | 3 | 5 |
GO:0050789 | regulation of biological process | 2 | 5 |
GO:0050794 | regulation of cellular process | 3 | 5 |
GO:0065007 | biological regulation | 1 | 5 |
GO:0097720 | calcineurin-mediated signaling | 6 | 5 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 2 |
GO:0000725 | recombinational repair | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 16 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 16 |
GO:0016791 | phosphatase activity | 5 | 16 |
GO:0017018 | myosin phosphatase activity | 5 | 16 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
GO:0004723 | calcium-dependent protein serine/threonine phosphatase activity | 5 | 5 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
GO:0033192 | calmodulin-dependent protein phosphatase activity | 6 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 51 | 55 | PF00656 | 0.619 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.243 |
CLV_PCSK_FUR_1 | 336 | 340 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.238 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.584 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.513 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.521 |
DEG_SPOP_SBC_1 | 31 | 35 | PF00917 | 0.523 |
DOC_CYCLIN_RxL_1 | 174 | 184 | PF00134 | 0.512 |
DOC_CYCLIN_yClb1_LxF_4 | 504 | 510 | PF00134 | 0.266 |
DOC_CYCLIN_yCln2_LP_2 | 414 | 420 | PF00134 | 0.304 |
DOC_MAPK_gen_1 | 208 | 214 | PF00069 | 0.719 |
DOC_MAPK_gen_1 | 503 | 509 | PF00069 | 0.221 |
DOC_MAPK_HePTP_8 | 286 | 298 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 289 | 298 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 349 | 358 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 411 | 418 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 569 | 578 | PF00069 | 0.475 |
DOC_MAPK_NFAT4_5 | 411 | 419 | PF00069 | 0.357 |
DOC_PP2B_LxvP_1 | 414 | 417 | PF13499 | 0.304 |
DOC_PP4_FxxP_1 | 533 | 536 | PF00568 | 0.373 |
DOC_SPAK_OSR1_1 | 428 | 432 | PF12202 | 0.357 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.542 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 135 | 145 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 225 | 231 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 349 | 355 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 428 | 438 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 528 | 533 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 569 | 574 | PF00244 | 0.537 |
LIG_BIR_III_2 | 56 | 60 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 232 | 236 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 497 | 501 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 580 | 584 | PF00533 | 0.556 |
LIG_BRCT_BRCA1_2 | 497 | 503 | PF00533 | 0.221 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.619 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.392 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.283 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.560 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.234 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.357 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.267 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.286 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.547 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.514 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.584 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.485 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.342 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.575 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.606 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.421 |
LIG_Integrin_RGD_1 | 249 | 251 | PF01839 | 0.469 |
LIG_LIR_Apic_2 | 531 | 536 | PF02991 | 0.370 |
LIG_LIR_Apic_2 | 568 | 574 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 316 | 326 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 424 | 431 | PF02991 | 0.413 |
LIG_LIR_LC3C_4 | 302 | 306 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 316 | 321 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.209 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.413 |
LIG_LYPXL_yS_3 | 367 | 370 | PF13949 | 0.357 |
LIG_MAD2 | 528 | 536 | PF02301 | 0.324 |
LIG_MLH1_MIPbox_1 | 580 | 584 | PF16413 | 0.478 |
LIG_PCNA_PIPBox_1 | 515 | 524 | PF02747 | 0.394 |
LIG_PCNA_yPIPBox_3 | 512 | 522 | PF02747 | 0.368 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.436 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.304 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.391 |
LIG_SH2_NCK_1 | 571 | 575 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 318 | 322 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.581 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.582 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.449 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 295 | 300 | PF11976 | 0.522 |
LIG_SUMO_SIM_anti_2 | 302 | 309 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 117 | 124 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 176 | 184 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 292 | 297 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 302 | 309 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 526 | 534 | PF11976 | 0.446 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.601 |
LIG_TRAF2_1 | 257 | 260 | PF00917 | 0.445 |
LIG_TRAF2_2 | 126 | 131 | PF00917 | 0.526 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.357 |
LIG_UBA3_1 | 358 | 364 | PF00899 | 0.471 |
MOD_CDK_SPK_2 | 227 | 232 | PF00069 | 0.416 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.518 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.555 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.603 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.503 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.581 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.587 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.556 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.551 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.494 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.352 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.546 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.239 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.550 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.562 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.504 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.426 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.378 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.444 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.524 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.742 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.555 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.558 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.371 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.575 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.373 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.564 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.314 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.269 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.304 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.296 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.542 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.581 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.533 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.526 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.460 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.477 |
MOD_N-GLC_2 | 537 | 539 | PF02516 | 0.414 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.586 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.613 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.566 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.532 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.606 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.499 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.327 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.357 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.539 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.576 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.502 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.535 |
MOD_NEK2_2 | 574 | 579 | PF00069 | 0.500 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.579 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.526 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.516 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.300 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.596 |
MOD_PKB_1 | 46 | 54 | PF00069 | 0.563 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.526 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.581 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.332 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.447 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.221 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.453 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.524 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.229 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.472 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.355 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.221 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.344 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.586 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.514 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.610 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.493 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.464 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.350 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.601 |
MOD_SUMO_for_1 | 363 | 366 | PF00179 | 0.357 |
MOD_SUMO_rev_2 | 217 | 226 | PF00179 | 0.530 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.294 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.282 |
TRG_DiLeu_LyEn_5 | 235 | 240 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.193 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.241 |
TRG_Pf-PMV_PEXEL_1 | 177 | 182 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I8M6 | Leishmania donovani | 72% | 100% |
A0A3Q8II54 | Leishmania donovani | 68% | 100% |
A0A3S7XAY3 | Leishmania donovani | 31% | 100% |
A0A422N1U7 | Trypanosoma rangeli | 32% | 98% |
A4HP65 | Leishmania braziliensis | 32% | 100% |
A4HVT0 | Leishmania infantum | 72% | 100% |
A4HVT6 | Leishmania infantum | 68% | 100% |
A4IDH0 | Leishmania infantum | 31% | 100% |
E9APH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9API1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 99% |
E9ASX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4Q1M5 | Leishmania major | 30% | 100% |
Q4QFZ7 | Leishmania major | 67% | 100% |
Q4QG03 | Leishmania major | 72% | 100% |