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: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
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:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AKB4
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:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 18 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 18 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 18 |
GO:0005488 | binding | 1 | 12 |
GO:0016787 | hydrolase activity | 2 | 18 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 18 |
GO:0016791 | phosphatase activity | 5 | 18 |
GO:0017018 | myosin phosphatase activity | 5 | 18 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 558 | 562 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.359 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.372 |
CLV_PCSK_PC7_1 | 171 | 177 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.354 |
DEG_APCC_DBOX_1 | 55 | 63 | PF00400 | 0.372 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.714 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.749 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.640 |
DOC_CYCLIN_yCln2_LP_2 | 162 | 168 | PF00134 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 326 | 332 | PF00134 | 0.388 |
DOC_MAPK_gen_1 | 427 | 436 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 88 | 98 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 319 | 326 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 430 | 438 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 347 | 354 | PF00149 | 0.372 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.712 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 54 | 58 | PF12436 | 0.485 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 374 | 380 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 564 | 572 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.237 |
LIG_Actin_WH2_2 | 343 | 361 | PF00022 | 0.372 |
LIG_Actin_WH2_2 | 375 | 391 | PF00022 | 0.372 |
LIG_APCC_ABBA_1 | 330 | 335 | PF00400 | 0.388 |
LIG_APCC_ABBA_1 | 540 | 545 | PF00400 | 0.372 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.402 |
LIG_deltaCOP1_diTrp_1 | 435 | 444 | PF00928 | 0.372 |
LIG_EH1_1 | 359 | 367 | PF00400 | 0.500 |
LIG_eIF4E_1 | 360 | 366 | PF01652 | 0.372 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.364 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.667 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.549 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.622 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.367 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.351 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.552 |
LIG_IRF3_LxIS_1 | 302 | 308 | PF10401 | 0.442 |
LIG_LIR_Apic_2 | 505 | 511 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 202 | 212 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 293 | 302 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 320 | 330 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 419 | 428 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 435 | 444 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.360 |
LIG_MLH1_MIPbox_1 | 63 | 67 | PF16413 | 0.388 |
LIG_MYND_1 | 137 | 141 | PF01753 | 0.618 |
LIG_OCRL_FandH_1 | 332 | 344 | PF00620 | 0.372 |
LIG_PTB_Apo_2 | 361 | 368 | PF02174 | 0.500 |
LIG_REV1ctd_RIR_1 | 64 | 73 | PF16727 | 0.359 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.372 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.496 |
LIG_SH2_CRK | 549 | 553 | PF00017 | 0.372 |
LIG_SH2_GRB2like | 265 | 268 | PF00017 | 0.622 |
LIG_SH2_GRB2like | 296 | 299 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 115 | 119 | PF00017 | 0.372 |
LIG_SH2_PTP2 | 205 | 208 | PF00017 | 0.690 |
LIG_SH2_SRC | 446 | 449 | PF00017 | 0.461 |
LIG_SH2_SRC | 549 | 552 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 360 | 363 | PF00017 | 0.500 |
LIG_SH2_STAT3 | 547 | 550 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.375 |
LIG_SH3_2 | 186 | 191 | PF14604 | 0.725 |
LIG_SH3_2 | 273 | 278 | PF14604 | 0.623 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.705 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.766 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.379 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.678 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.625 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.439 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.371 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.355 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.367 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.686 |
LIG_SH3_4 | 603 | 610 | PF00018 | 0.668 |
LIG_SUMO_SIM_anti_2 | 211 | 216 | PF11976 | 0.557 |
LIG_SUMO_SIM_anti_2 | 97 | 105 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 210 | 216 | PF11976 | 0.557 |
LIG_SUMO_SIM_par_1 | 305 | 311 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 570 | 579 | PF11976 | 0.447 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.372 |
LIG_TRAF2_2 | 514 | 519 | PF00917 | 0.500 |
LIG_TYR_ITSM | 111 | 118 | PF00017 | 0.372 |
LIG_UBA3_1 | 322 | 327 | PF00899 | 0.440 |
LIG_UBA3_1 | 385 | 389 | PF00899 | 0.403 |
LIG_WRC_WIRS_1 | 417 | 422 | PF05994 | 0.372 |
LIG_WRC_WIRS_1 | 532 | 537 | PF05994 | 0.372 |
MOD_CDK_SPK_2 | 229 | 234 | PF00069 | 0.642 |
MOD_CDK_SPK_2 | 615 | 620 | PF00069 | 0.672 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.631 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.619 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.419 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.677 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.388 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.688 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.365 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.395 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.369 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.497 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.430 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.793 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.382 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.752 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.619 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.433 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.670 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.461 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.411 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.372 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.682 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.372 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.521 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.665 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.504 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.822 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.756 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.500 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.202 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.409 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.556 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.573 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.618 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.417 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.441 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.720 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.700 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.649 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.627 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.423 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.382 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.705 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.668 |
MOD_SUMO_rev_2 | 452 | 458 | PF00179 | 0.372 |
MOD_SUMO_rev_2 | 468 | 475 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 608 | 616 | PF00179 | 0.689 |
TRG_DiLeu_BaEn_1 | 301 | 306 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_3 | 151 | 157 | PF01217 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 275 | 280 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.690 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.789 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.790 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.438 |
TRG_ER_diLys_1 | 634 | 637 | PF00400 | 0.768 |
TRG_NES_CRM1_1 | 152 | 164 | PF08389 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I548 | Leptomonas seymouri | 94% | 100% |
A0A0S4JP77 | Bodo saltans | 72% | 100% |
A0A1X0P2R2 | Trypanosomatidae | 81% | 100% |
A0A3Q8I8M6 | Leishmania donovani | 34% | 100% |
A0A3S5H5F8 | Leishmania donovani | 99% | 100% |
A0A422NYB5 | Trypanosoma rangeli | 78% | 100% |
A4H456 | Leishmania braziliensis | 97% | 100% |
A4HSD9 | Leishmania infantum | 99% | 100% |
A4HVT0 | Leishmania infantum | 33% | 100% |
C9ZPX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 78% | 100% |
D0A366 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9APH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q4QG03 | Leishmania major | 32% | 100% |
Q4QJJ3 | Leishmania major | 99% | 100% |
V5BAC7 | Trypanosoma cruzi | 81% | 100% |
V5BBS3 | Trypanosoma cruzi | 28% | 100% |