| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ASP3
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006470 | protein dephosphorylation | 5 | 7 |
| GO:0006793 | phosphorus metabolic process | 3 | 7 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
| GO:0008152 | metabolic process | 1 | 7 |
| GO:0009987 | cellular process | 1 | 7 |
| GO:0016311 | dephosphorylation | 5 | 7 |
| GO:0019538 | protein metabolic process | 3 | 7 |
| GO:0036211 | protein modification process | 4 | 7 |
| GO:0043170 | macromolecule metabolic process | 3 | 7 |
| GO:0043412 | macromolecule modification | 4 | 7 |
| GO:0044237 | cellular metabolic process | 2 | 7 |
| GO:0044238 | primary metabolic process | 2 | 7 |
| GO:0071704 | organic substance metabolic process | 2 | 7 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004721 | phosphoprotein phosphatase activity | 3 | 12 |
| GO:0004722 | protein serine/threonine phosphatase activity | 4 | 12 |
| GO:0016787 | hydrolase activity | 2 | 12 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
| GO:0016791 | phosphatase activity | 5 | 12 |
| GO:0042578 | phosphoric ester hydrolase activity | 4 | 12 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
| GO:0017018 | myosin phosphatase activity | 5 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 296 | 300 | PF00656 | 0.609 |
| CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.361 |
| CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.537 |
| CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.297 |
| CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.477 |
| CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.361 |
| CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.435 |
| CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.496 |
| CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.376 |
| CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.566 |
| CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.477 |
| CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.361 |
| CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.367 |
| CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.504 |
| CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.268 |
| CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.530 |
| CLV_PCSK_PC1ET2_1 | 572 | 574 | PF00082 | 0.530 |
| CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.636 |
| CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.541 |
| CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.494 |
| CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.481 |
| CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.606 |
| CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.430 |
| CLV_Separin_Metazoa | 550 | 554 | PF03568 | 0.563 |
| DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.421 |
| DEG_APCC_DBOX_1 | 519 | 527 | PF00400 | 0.475 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.601 |
| DOC_CYCLIN_RxL_1 | 408 | 417 | PF00134 | 0.278 |
| DOC_MAPK_DCC_7 | 13 | 21 | PF00069 | 0.491 |
| DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.435 |
| DOC_MAPK_gen_1 | 302 | 310 | PF00069 | 0.393 |
| DOC_MAPK_MEF2A_6 | 13 | 21 | PF00069 | 0.465 |
| DOC_MAPK_MEF2A_6 | 302 | 310 | PF00069 | 0.393 |
| DOC_MAPK_RevD_3 | 131 | 144 | PF00069 | 0.537 |
| DOC_PIKK_1 | 399 | 406 | PF02985 | 0.434 |
| DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.395 |
| DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.404 |
| DOC_PP2B_LxvP_1 | 416 | 419 | PF13499 | 0.362 |
| DOC_PP2B_PxIxI_1 | 16 | 22 | PF00149 | 0.482 |
| DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.387 |
| DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.574 |
| DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.524 |
| DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.356 |
| DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.511 |
| DOC_USP7_MATH_2 | 117 | 123 | PF00917 | 0.304 |
| DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.759 |
| DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.286 |
| DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.623 |
| DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.389 |
| DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.686 |
| DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.683 |
| LIG_14-3-3_CanoR_1 | 144 | 154 | PF00244 | 0.591 |
| LIG_14-3-3_CanoR_1 | 230 | 240 | PF00244 | 0.646 |
| LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.397 |
| LIG_14-3-3_CanoR_1 | 412 | 417 | PF00244 | 0.435 |
| LIG_14-3-3_CanoR_1 | 520 | 526 | PF00244 | 0.551 |
| LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.660 |
| LIG_14-3-3_CanoR_1 | 96 | 102 | PF00244 | 0.405 |
| LIG_Actin_WH2_2 | 303 | 318 | PF00022 | 0.362 |
| LIG_AP2alpha_2 | 78 | 80 | PF02296 | 0.294 |
| LIG_BRCT_BRCA1_1 | 279 | 283 | PF00533 | 0.402 |
| LIG_FHA_1 | 127 | 133 | PF00498 | 0.464 |
| LIG_FHA_1 | 21 | 27 | PF00498 | 0.454 |
| LIG_FHA_1 | 303 | 309 | PF00498 | 0.421 |
| LIG_FHA_1 | 68 | 74 | PF00498 | 0.623 |
| LIG_FHA_2 | 153 | 159 | PF00498 | 0.570 |
| LIG_FHA_2 | 331 | 337 | PF00498 | 0.362 |
| LIG_FHA_2 | 61 | 67 | PF00498 | 0.725 |
| LIG_IBAR_NPY_1 | 341 | 343 | PF08397 | 0.411 |
| LIG_LIR_Apic_2 | 469 | 473 | PF02991 | 0.427 |
| LIG_LIR_Gen_1 | 564 | 574 | PF02991 | 0.468 |
| LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.317 |
| LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.476 |
| LIG_LIR_Nem_3 | 376 | 380 | PF02991 | 0.341 |
| LIG_LIR_Nem_3 | 564 | 570 | PF02991 | 0.466 |
| LIG_Pex14_2 | 430 | 434 | PF04695 | 0.435 |
| LIG_PTAP_UEV_1 | 575 | 580 | PF05743 | 0.572 |
| LIG_PTB_Apo_2 | 262 | 269 | PF02174 | 0.280 |
| LIG_PTB_Apo_2 | 338 | 345 | PF02174 | 0.361 |
| LIG_PTB_Phospho_1 | 338 | 344 | PF10480 | 0.361 |
| LIG_REV1ctd_RIR_1 | 168 | 176 | PF16727 | 0.495 |
| LIG_SH2_CRK | 320 | 324 | PF00017 | 0.435 |
| LIG_SH2_GRB2like | 343 | 346 | PF00017 | 0.411 |
| LIG_SH2_PTP2 | 18 | 21 | PF00017 | 0.472 |
| LIG_SH2_SRC | 162 | 165 | PF00017 | 0.470 |
| LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.340 |
| LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.355 |
| LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.472 |
| LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.413 |
| LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.469 |
| LIG_SH3_1 | 125 | 131 | PF00018 | 0.567 |
| LIG_SH3_1 | 200 | 206 | PF00018 | 0.610 |
| LIG_SH3_1 | 573 | 579 | PF00018 | 0.526 |
| LIG_SH3_3 | 125 | 131 | PF00018 | 0.574 |
| LIG_SH3_3 | 177 | 183 | PF00018 | 0.453 |
| LIG_SH3_3 | 200 | 206 | PF00018 | 0.673 |
| LIG_SH3_3 | 555 | 561 | PF00018 | 0.501 |
| LIG_SH3_3 | 573 | 579 | PF00018 | 0.526 |
| LIG_SUMO_SIM_anti_2 | 522 | 527 | PF11976 | 0.487 |
| LIG_SUMO_SIM_par_1 | 305 | 311 | PF11976 | 0.410 |
| LIG_SUMO_SIM_par_1 | 367 | 373 | PF11976 | 0.365 |
| LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.553 |
| LIG_TRAF2_1 | 205 | 208 | PF00917 | 0.602 |
| LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.458 |
| LIG_TYR_ITIM | 16 | 21 | PF00017 | 0.486 |
| LIG_UBA3_1 | 10 | 15 | PF00899 | 0.478 |
| LIG_UBA3_1 | 368 | 375 | PF00899 | 0.420 |
| LIG_WRC_WIRS_1 | 35 | 40 | PF05994 | 0.393 |
| MOD_CDC14_SPxK_1 | 243 | 246 | PF00782 | 0.633 |
| MOD_CDK_SPK_2 | 54 | 59 | PF00069 | 0.644 |
| MOD_CDK_SPxK_1 | 240 | 246 | PF00069 | 0.627 |
| MOD_CK1_1 | 111 | 117 | PF00069 | 0.388 |
| MOD_CK1_1 | 152 | 158 | PF00069 | 0.547 |
| MOD_CK1_1 | 460 | 466 | PF00069 | 0.668 |
| MOD_CK2_1 | 152 | 158 | PF00069 | 0.467 |
| MOD_CK2_1 | 182 | 188 | PF00069 | 0.575 |
| MOD_CK2_1 | 359 | 365 | PF00069 | 0.402 |
| MOD_CK2_1 | 399 | 405 | PF00069 | 0.312 |
| MOD_CK2_1 | 460 | 466 | PF00069 | 0.605 |
| MOD_Cter_Amidation | 358 | 361 | PF01082 | 0.428 |
| MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.602 |
| MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.491 |
| MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.413 |
| MOD_GlcNHglycan | 207 | 211 | PF01048 | 0.449 |
| MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.401 |
| MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.508 |
| MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.594 |
| MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.559 |
| MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.661 |
| MOD_GSK3_1 | 111 | 118 | PF00069 | 0.312 |
| MOD_GSK3_1 | 145 | 152 | PF00069 | 0.547 |
| MOD_GSK3_1 | 195 | 202 | PF00069 | 0.757 |
| MOD_GSK3_1 | 214 | 221 | PF00069 | 0.483 |
| MOD_GSK3_1 | 240 | 247 | PF00069 | 0.442 |
| MOD_GSK3_1 | 298 | 305 | PF00069 | 0.489 |
| MOD_GSK3_1 | 446 | 453 | PF00069 | 0.525 |
| MOD_GSK3_1 | 54 | 61 | PF00069 | 0.573 |
| MOD_GSK3_1 | 67 | 74 | PF00069 | 0.739 |
| MOD_GSK3_1 | 96 | 103 | PF00069 | 0.411 |
| MOD_NEK2_1 | 101 | 106 | PF00069 | 0.356 |
| MOD_NEK2_1 | 216 | 221 | PF00069 | 0.348 |
| MOD_NEK2_1 | 277 | 282 | PF00069 | 0.313 |
| MOD_NEK2_1 | 29 | 34 | PF00069 | 0.540 |
| MOD_NEK2_1 | 48 | 53 | PF00069 | 0.362 |
| MOD_NEK2_1 | 89 | 94 | PF00069 | 0.429 |
| MOD_NEK2_2 | 351 | 356 | PF00069 | 0.337 |
| MOD_OFUCOSY | 269 | 276 | PF10250 | 0.207 |
| MOD_PIKK_1 | 71 | 77 | PF00454 | 0.601 |
| MOD_PKA_2 | 315 | 321 | PF00069 | 0.362 |
| MOD_PKA_2 | 519 | 525 | PF00069 | 0.536 |
| MOD_PKA_2 | 58 | 64 | PF00069 | 0.559 |
| MOD_Plk_1 | 302 | 308 | PF00069 | 0.435 |
| MOD_Plk_1 | 330 | 336 | PF00069 | 0.362 |
| MOD_Plk_1 | 398 | 404 | PF00069 | 0.318 |
| MOD_Plk_1 | 436 | 442 | PF00069 | 0.487 |
| MOD_Plk_1 | 498 | 504 | PF00069 | 0.427 |
| MOD_Plk_2-3 | 399 | 405 | PF00069 | 0.361 |
| MOD_Plk_4 | 111 | 117 | PF00069 | 0.341 |
| MOD_Plk_4 | 149 | 155 | PF00069 | 0.631 |
| MOD_Plk_4 | 220 | 226 | PF00069 | 0.515 |
| MOD_Plk_4 | 501 | 507 | PF00069 | 0.484 |
| MOD_Plk_4 | 521 | 527 | PF00069 | 0.269 |
| MOD_Plk_4 | 97 | 103 | PF00069 | 0.473 |
| MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.746 |
| MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.298 |
| MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.627 |
| MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.389 |
| MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.688 |
| MOD_SUMO_rev_2 | 362 | 369 | PF00179 | 0.359 |
| TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.553 |
| TRG_DiLeu_BaLyEn_6 | 128 | 133 | PF01217 | 0.529 |
| TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.479 |
| TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.435 |
| TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.427 |
| TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.573 |
| TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.356 |
| TRG_ER_diArg_1 | 487 | 490 | PF00400 | 0.503 |
| TRG_ER_diArg_1 | 506 | 509 | PF00400 | 0.272 |
| TRG_NES_CRM1_1 | 404 | 417 | PF08389 | 0.278 |
| TRG_Pf-PMV_PEXEL_1 | 121 | 126 | PF00026 | 0.548 |
| TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.581 |
| TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.397 |
| TRG_Pf-PMV_PEXEL_1 | 378 | 383 | PF00026 | 0.435 |
| TRG_Pf-PMV_PEXEL_1 | 412 | 417 | PF00026 | 0.345 |
| TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.553 |
| TRG_Pf-PMV_PEXEL_1 | 489 | 493 | PF00026 | 0.449 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5Q6 | Leptomonas seymouri | 61% | 100% |
| A0A0S4IM91 | Bodo saltans | 29% | 100% |
| A0A0S4IRQ5 | Bodo saltans | 29% | 100% |
| A0A1X0P810 | Trypanosomatidae | 45% | 97% |
| A0A3S7XAR2 | Leishmania donovani | 92% | 99% |
| A4HNY3 | Leishmania braziliensis | 79% | 100% |
| A4ICL1 | Leishmania infantum | 92% | 99% |
| D0A2U9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 97% |
| Q4Q1V3 | Leishmania major | 92% | 100% |
| V5BZP6 | Trypanosoma cruzi | 47% | 99% |