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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HQ52
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016311 | dephosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 9 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0016791 | phosphatase activity | 5 | 9 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 1 |
GO:0017018 | myosin phosphatase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.445 |
CLV_PCSK_FUR_1 | 484 | 488 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.501 |
DEG_SCF_FBW7_1 | 317 | 323 | PF00400 | 0.504 |
DEG_SCF_FBW7_1 | 327 | 334 | PF00400 | 0.474 |
DOC_CKS1_1 | 317 | 322 | PF01111 | 0.502 |
DOC_CKS1_1 | 372 | 377 | PF01111 | 0.522 |
DOC_CYCLIN_RxL_1 | 177 | 186 | PF00134 | 0.382 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.648 |
DOC_CYCLIN_yCln2_LP_2 | 433 | 439 | PF00134 | 0.490 |
DOC_MAPK_DCC_7 | 99 | 109 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 226 | 234 | PF00069 | 0.212 |
DOC_MAPK_gen_1 | 282 | 289 | PF00069 | 0.341 |
DOC_MAPK_gen_1 | 99 | 106 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 101 | 109 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.294 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.748 |
DOC_PP2B_LxvP_1 | 433 | 436 | PF13499 | 0.600 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.294 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.800 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.370 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.212 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 299 | 308 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 357 | 363 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 467 | 472 | PF00244 | 0.591 |
LIG_BRCT_BRCA1_1 | 102 | 106 | PF00533 | 0.212 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.510 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.673 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.739 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.612 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.267 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.445 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.405 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.346 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.695 |
LIG_Integrin_RGD_1 | 188 | 190 | PF01839 | 0.349 |
LIG_LIR_Apic_2 | 100 | 105 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 103 | 114 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.544 |
LIG_LYPXL_S_1 | 23 | 27 | PF13949 | 0.523 |
LIG_LYPXL_yS_3 | 24 | 27 | PF13949 | 0.526 |
LIG_OCRL_FandH_1 | 245 | 257 | PF00620 | 0.329 |
LIG_PCNA_yPIPBox_3 | 294 | 305 | PF02747 | 0.419 |
LIG_Pex14_1 | 123 | 127 | PF04695 | 0.294 |
LIG_Pex14_2 | 102 | 106 | PF04695 | 0.294 |
LIG_PTB_Apo_2 | 89 | 96 | PF02174 | 0.294 |
LIG_PTB_Phospho_1 | 89 | 95 | PF10480 | 0.267 |
LIG_SH2_GRB2like | 127 | 130 | PF00017 | 0.388 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.294 |
LIG_SH2_PTP2 | 286 | 289 | PF00017 | 0.329 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.330 |
LIG_SH2_SRC | 95 | 98 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 291 | 294 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.330 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.632 |
LIG_SUMO_SIM_anti_2 | 210 | 216 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 162 | 167 | PF11976 | 0.388 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.212 |
LIG_UBA3_1 | 214 | 223 | PF00899 | 0.294 |
LIG_UBA3_1 | 352 | 360 | PF00899 | 0.489 |
MOD_CDC14_SPxK_1 | 113 | 116 | PF00782 | 0.212 |
MOD_CDK_SPK_2 | 221 | 226 | PF00069 | 0.374 |
MOD_CDK_SPK_2 | 371 | 376 | PF00069 | 0.529 |
MOD_CDK_SPxK_1 | 110 | 116 | PF00069 | 0.212 |
MOD_CDK_SPxxK_3 | 371 | 378 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 460 | 467 | PF00069 | 0.660 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.369 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.234 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.654 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.623 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.592 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.729 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.693 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.737 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.701 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.395 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.388 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.533 |
MOD_Cter_Amidation | 280 | 283 | PF01082 | 0.212 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.389 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.326 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.251 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.745 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.583 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.522 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.338 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.747 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.687 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.487 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.676 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.720 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.740 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.631 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.727 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.778 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.379 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.449 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.287 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.658 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.287 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.308 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.415 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.366 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.401 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.454 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.603 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.636 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.747 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.428 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.429 |
MOD_NEK2_2 | 271 | 276 | PF00069 | 0.212 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.294 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.510 |
MOD_PK_1 | 368 | 374 | PF00069 | 0.560 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.374 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.560 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.613 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.659 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.713 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.523 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.449 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.287 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.212 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.345 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.388 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.388 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.515 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.630 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.514 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.311 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.403 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.212 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.396 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.642 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.645 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.660 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.694 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.680 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.713 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.654 |
MOD_SUMO_for_1 | 146 | 149 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 186 | 194 | PF00179 | 0.378 |
TRG_DiLeu_BaEn_4 | 474 | 480 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.695 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.473 |
TRG_NLS_MonoExtC_3 | 2 | 7 | PF00514 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P9E1 | Leptomonas seymouri | 63% | 98% |
A0A3Q8ILM2 | Leishmania donovani | 77% | 100% |
A0A3R7L1Z6 | Trypanosoma rangeli | 47% | 81% |
A4IDV1 | Leishmania infantum | 77% | 100% |
E9ATX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q0M4 | Leishmania major | 75% | 100% |
V5B554 | Trypanosoma cruzi | 41% | 75% |