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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 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 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H5M4
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 15 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 15 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 15 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 15 |
GO:0016791 | phosphatase activity | 5 | 15 |
GO:0017018 | myosin phosphatase activity | 5 | 15 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 15 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 582 | 586 | PF00656 | 0.402 |
CLV_C14_Caspase3-7 | 639 | 643 | PF00656 | 0.675 |
CLV_MEL_PAP_1 | 93 | 99 | PF00089 | 0.497 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.557 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.342 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 248 | 257 | PF00134 | 0.455 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.502 |
DOC_PP1_RVXF_1 | 253 | 260 | PF00149 | 0.646 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.588 |
DOC_PP4_FxxP_1 | 510 | 513 | PF00568 | 0.289 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.717 |
DOC_USP7_MATH_2 | 535 | 541 | PF00917 | 0.313 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 161 | 165 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.313 |
LIG_Actin_WH2_2 | 365 | 381 | PF00022 | 0.325 |
LIG_AP2alpha_1 | 362 | 366 | PF02296 | 0.289 |
LIG_AP2alpha_1 | 567 | 571 | PF02296 | 0.406 |
LIG_BIR_III_2 | 176 | 180 | PF00653 | 0.605 |
LIG_BRCT_BRCA1_1 | 460 | 464 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.406 |
LIG_deltaCOP1_diTrp_1 | 454 | 464 | PF00928 | 0.272 |
LIG_EH1_1 | 366 | 374 | PF00400 | 0.348 |
LIG_eIF4E_1 | 367 | 373 | PF01652 | 0.272 |
LIG_EVH1_1 | 100 | 104 | PF00568 | 0.532 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.525 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.580 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.514 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.294 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.437 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.597 |
LIG_LIR_Apic_2 | 507 | 513 | PF02991 | 0.290 |
LIG_LIR_Apic_2 | 529 | 535 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 374 | 382 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 461 | 471 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.308 |
LIG_NRP_CendR_1 | 645 | 646 | PF00754 | 0.586 |
LIG_OCRL_FandH_1 | 354 | 366 | PF00620 | 0.272 |
LIG_Pex14_2 | 279 | 283 | PF04695 | 0.483 |
LIG_Pex14_2 | 362 | 366 | PF04695 | 0.289 |
LIG_Pex14_2 | 567 | 571 | PF04695 | 0.363 |
LIG_Pex14_2 | 573 | 577 | PF04695 | 0.331 |
LIG_PTB_Apo_2 | 277 | 284 | PF02174 | 0.547 |
LIG_PTB_Apo_2 | 295 | 302 | PF02174 | 0.420 |
LIG_PTB_Apo_2 | 434 | 441 | PF02174 | 0.406 |
LIG_PTB_Phospho_1 | 295 | 301 | PF10480 | 0.416 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.368 |
LIG_SH2_CRK | 523 | 527 | PF00017 | 0.406 |
LIG_SH2_STAT3 | 133 | 136 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.741 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.672 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.615 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.406 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.302 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.622 |
LIG_SUMO_SIM_anti_2 | 111 | 116 | PF11976 | 0.412 |
LIG_SUMO_SIM_anti_2 | 398 | 403 | PF11976 | 0.302 |
LIG_SUMO_SIM_anti_2 | 492 | 500 | PF11976 | 0.353 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 111 | 116 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 15 | 23 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 612 | 618 | PF11976 | 0.327 |
LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.272 |
LIG_TRAF2_1 | 630 | 633 | PF00917 | 0.639 |
LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.533 |
LIG_UBA3_1 | 328 | 336 | PF00899 | 0.439 |
LIG_UBA3_1 | 405 | 409 | PF00899 | 0.300 |
LIG_WRC_WIRS_1 | 305 | 310 | PF05994 | 0.512 |
LIG_WRC_WIRS_1 | 372 | 377 | PF05994 | 0.272 |
LIG_WRC_WIRS_1 | 506 | 511 | PF05994 | 0.289 |
MOD_CDC14_SPxK_1 | 192 | 195 | PF00782 | 0.597 |
MOD_CDK_SPxK_1 | 189 | 195 | PF00069 | 0.598 |
MOD_CDK_SPxK_1 | 378 | 384 | PF00069 | 0.289 |
MOD_CDK_SPxxK_3 | 514 | 521 | PF00069 | 0.313 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.619 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.576 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.584 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.393 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.633 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.364 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.774 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.620 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.745 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.544 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.668 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.634 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.705 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.759 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.729 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.276 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.276 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.370 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.652 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.402 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.408 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.390 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.716 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.675 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.517 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.444 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.557 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.562 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.589 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.447 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.643 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.384 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.322 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.747 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.406 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.383 |
MOD_N-GLC_1 | 537 | 542 | PF02516 | 0.417 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.742 |
MOD_N-GLC_2 | 312 | 314 | PF02516 | 0.463 |
MOD_N-GLC_2 | 330 | 332 | PF02516 | 0.405 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.584 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.566 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.577 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.691 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.337 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.201 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.289 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.390 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.335 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.741 |
MOD_NEK2_2 | 404 | 409 | PF00069 | 0.406 |
MOD_NEK2_2 | 436 | 441 | PF00069 | 0.289 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.702 |
MOD_PK_1 | 344 | 350 | PF00069 | 0.372 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.523 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.586 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.528 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.660 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.518 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.505 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.313 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.365 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.335 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.652 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.493 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.533 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.478 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.646 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.289 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.277 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.348 |
MOD_Plk_2-3 | 537 | 543 | PF00069 | 0.351 |
MOD_Plk_2-3 | 635 | 641 | PF00069 | 0.496 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.508 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.399 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.593 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.285 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.289 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.607 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.535 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.519 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.530 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.682 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.604 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.448 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.441 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.336 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.289 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.730 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.342 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.538 |
MOD_SUMO_rev_2 | 333 | 338 | PF00179 | 0.378 |
TRG_DiLeu_BaEn_3 | 333 | 339 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 619 | 624 | PF01217 | 0.382 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 261 | 266 | PF00026 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5U5 | Leptomonas seymouri | 73% | 95% |
A0A0S4IYE4 | Bodo saltans | 55% | 100% |
A0A1X0NPA5 | Trypanosomatidae | 63% | 100% |
A0A3Q8I8M6 | Leishmania donovani | 33% | 100% |
A0A3R7NXP6 | Trypanosoma rangeli | 56% | 100% |
A0A3S5H6D4 | Leishmania donovani | 85% | 99% |
A4HTW1 | Leishmania infantum | 85% | 99% |
A4HVT0 | Leishmania infantum | 33% | 100% |
D0A9C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AMP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
E9APH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
Q4QG03 | Leishmania major | 33% | 100% |
Q4QHX7 | Leishmania major | 85% | 100% |