Phosphatase, tyrosine specific phosphatase
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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4IDV1
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016311 | dephosphorylation | 5 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0036211 | protein modification process | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 8 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016791 | phosphatase activity | 5 | 8 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.424 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 484 | 488 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.783 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.468 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.410 |
DEG_APCC_KENBOX_2 | 140 | 144 | PF00400 | 0.387 |
DEG_SCF_FBW7_1 | 352 | 358 | PF00400 | 0.556 |
DOC_CKS1_1 | 352 | 357 | PF01111 | 0.632 |
DOC_CYCLIN_RxL_1 | 174 | 186 | PF00134 | 0.441 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.759 |
DOC_MAPK_DCC_7 | 99 | 109 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 282 | 289 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 7 | 16 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 99 | 106 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 101 | 109 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.376 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.765 |
DOC_PP2B_LxvP_1 | 428 | 431 | PF13499 | 0.749 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.376 |
DOC_SPAK_OSR1_1 | 11 | 15 | PF12202 | 0.506 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.692 |
DOC_USP7_MATH_2 | 364 | 370 | PF00917 | 0.705 |
DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.410 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 226 | 234 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 299 | 308 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 357 | 367 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 452 | 458 | PF00244 | 0.786 |
LIG_14-3-3_CanoR_1 | 467 | 472 | PF00244 | 0.572 |
LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.681 |
LIG_CtBP_PxDLS_1 | 397 | 401 | PF00389 | 0.573 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.410 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.720 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.595 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.346 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.419 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.707 |
LIG_Integrin_RGD_1 | 188 | 190 | PF01839 | 0.462 |
LIG_LIR_Apic_2 | 100 | 105 | PF02991 | 0.430 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.646 |
LIG_LYPXL_S_1 | 23 | 27 | PF13949 | 0.557 |
LIG_LYPXL_yS_3 | 24 | 27 | PF13949 | 0.559 |
LIG_OCRL_FandH_1 | 245 | 257 | PF00620 | 0.430 |
LIG_PCNA_yPIPBox_3 | 294 | 305 | PF02747 | 0.454 |
LIG_PDZ_Class_1 | 488 | 493 | PF00595 | 0.686 |
LIG_Pex14_1 | 123 | 127 | PF04695 | 0.376 |
LIG_Pex14_2 | 102 | 106 | PF04695 | 0.376 |
LIG_Pex14_2 | 488 | 492 | PF04695 | 0.681 |
LIG_PTB_Apo_2 | 89 | 96 | PF02174 | 0.376 |
LIG_PTB_Phospho_1 | 89 | 95 | PF10480 | 0.346 |
LIG_SH2_GRB2like | 127 | 130 | PF00017 | 0.430 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.376 |
LIG_SH2_PTP2 | 286 | 289 | PF00017 | 0.430 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.357 |
LIG_SH2_SRC | 95 | 98 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 195 | 198 | PF00017 | 0.353 |
LIG_SH2_STAT3 | 291 | 294 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.376 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.410 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.590 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.741 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.712 |
LIG_SUMO_SIM_anti_2 | 165 | 171 | PF11976 | 0.410 |
LIG_SUMO_SIM_anti_2 | 210 | 216 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 162 | 167 | PF11976 | 0.430 |
LIG_UBA3_1 | 214 | 223 | PF00899 | 0.376 |
LIG_WW_3 | 152 | 156 | PF00397 | 0.397 |
MOD_CDK_SPK_2 | 221 | 226 | PF00069 | 0.501 |
MOD_CDK_SPxK_1 | 351 | 357 | PF00069 | 0.554 |
MOD_CDK_SPxxK_3 | 460 | 467 | PF00069 | 0.726 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.411 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.309 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.720 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.713 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.716 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.692 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.754 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.738 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.689 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.485 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.430 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.670 |
MOD_DYRK1A_RPxSP_1 | 393 | 397 | PF00069 | 0.563 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.501 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.376 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.790 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.547 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.411 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.697 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.647 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.785 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.771 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.617 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.706 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.706 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.800 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.465 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.501 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.365 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.365 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.341 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.426 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.212 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.430 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.502 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.634 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.710 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.738 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.750 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.738 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.701 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.486 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.501 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.376 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.424 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.611 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.739 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.424 |
MOD_PK_1 | 174 | 180 | PF00069 | 0.410 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.501 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.725 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.807 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.792 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.545 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.501 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.365 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.741 |
MOD_Plk_2-3 | 383 | 389 | PF00069 | 0.685 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.376 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.430 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.430 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.430 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.746 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.520 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.349 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.295 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.390 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.644 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.438 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.699 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.711 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.719 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.697 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.749 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.677 |
MOD_SUMO_for_1 | 146 | 149 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 186 | 194 | PF00179 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 178 | 183 | PF01217 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.696 |
TRG_DiLeu_BaLyEn_6 | 461 | 466 | PF01217 | 0.682 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 4 | 8 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P9E1 | Leptomonas seymouri | 66% | 96% |
A0A3Q8ILM2 | Leishmania donovani | 99% | 100% |
A4HQ52 | Leishmania braziliensis | 77% | 100% |
E9ATX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q0M4 | Leishmania major | 95% | 100% |
V5B554 | Trypanosoma cruzi | 47% | 74% |