| 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: 6 |
| 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: 16 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 7 |
| NetGPI | no | yes: 0, no: 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q0P8
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 8 |
| GO:0006886 | intracellular protein transport | 4 | 8 |
| GO:0007034 | vacuolar transport | 4 | 8 |
| GO:0008104 | protein localization | 4 | 8 |
| GO:0009987 | cellular process | 1 | 8 |
| GO:0015031 | protein transport | 4 | 8 |
| GO:0016192 | vesicle-mediated transport | 4 | 8 |
| GO:0016197 | endosomal transport | 4 | 8 |
| GO:0032509 | endosome transport via multivesicular body sorting pathway | 5 | 8 |
| GO:0032511 | late endosome to vacuole transport via multivesicular body sorting pathway | 6 | 8 |
| GO:0033036 | macromolecule localization | 2 | 8 |
| GO:0033365 | protein localization to organelle | 5 | 8 |
| GO:0043328 | protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway | 5 | 8 |
| GO:0045184 | establishment of protein localization | 3 | 8 |
| GO:0045324 | late endosome to vacuole transport | 5 | 8 |
| GO:0046907 | intracellular transport | 3 | 8 |
| GO:0051179 | localization | 1 | 8 |
| GO:0051234 | establishment of localization | 2 | 8 |
| GO:0051641 | cellular localization | 2 | 8 |
| GO:0051649 | establishment of localization in cell | 3 | 8 |
| GO:0070727 | cellular macromolecule localization | 3 | 8 |
| GO:0071702 | organic substance transport | 4 | 8 |
| GO:0071705 | nitrogen compound transport | 4 | 8 |
| GO:0071985 | multivesicular body sorting pathway | 5 | 8 |
| GO:0072594 | establishment of protein localization to organelle | 4 | 8 |
| GO:0072665 | protein localization to vacuole | 6 | 8 |
| GO:0072666 | establishment of protein localization to vacuole | 5 | 8 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 8 |
| GO:0005515 | protein binding | 2 | 8 |
| GO:0005543 | phospholipid binding | 3 | 8 |
| GO:0008289 | lipid binding | 2 | 8 |
| GO:0032182 | ubiquitin-like protein binding | 3 | 8 |
| GO:0035091 | phosphatidylinositol binding | 4 | 8 |
| GO:0043130 | ubiquitin binding | 4 | 8 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.390 |
| CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.664 |
| CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.670 |
| CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.292 |
| CLV_PCSK_FUR_1 | 210 | 214 | PF00082 | 0.579 |
| CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.700 |
| CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.704 |
| CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.292 |
| CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.591 |
| CLV_PCSK_PC7_1 | 209 | 215 | PF00082 | 0.496 |
| CLV_PCSK_PC7_1 | 61 | 67 | PF00082 | 0.292 |
| CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.340 |
| CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.467 |
| CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.294 |
| DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.460 |
| DEG_SPOP_SBC_1 | 448 | 452 | PF00917 | 0.593 |
| DOC_CKS1_1 | 378 | 383 | PF01111 | 0.619 |
| DOC_CYCLIN_RxL_1 | 98 | 106 | PF00134 | 0.455 |
| DOC_MAPK_gen_1 | 172 | 180 | PF00069 | 0.500 |
| DOC_MAPK_gen_1 | 212 | 221 | PF00069 | 0.516 |
| DOC_MAPK_gen_1 | 51 | 59 | PF00069 | 0.357 |
| DOC_MAPK_MEF2A_6 | 124 | 132 | PF00069 | 0.351 |
| DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.308 |
| DOC_MAPK_MEF2A_6 | 172 | 180 | PF00069 | 0.498 |
| DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.576 |
| DOC_MAPK_MEF2A_6 | 268 | 276 | PF00069 | 0.486 |
| DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.353 |
| DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.472 |
| DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.632 |
| DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.685 |
| DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.668 |
| DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.658 |
| DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.614 |
| DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.612 |
| DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.688 |
| DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.488 |
| DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.639 |
| DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.636 |
| DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.565 |
| LIG_14-3-3_CanoR_1 | 290 | 299 | PF00244 | 0.543 |
| LIG_14-3-3_CanoR_1 | 309 | 316 | PF00244 | 0.502 |
| LIG_Actin_WH2_2 | 275 | 292 | PF00022 | 0.431 |
| LIG_BH_BH3_1 | 141 | 157 | PF00452 | 0.421 |
| LIG_BIR_III_2 | 195 | 199 | PF00653 | 0.537 |
| LIG_BIR_III_2 | 313 | 317 | PF00653 | 0.612 |
| LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.333 |
| LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.357 |
| LIG_EH_1 | 19 | 23 | PF12763 | 0.297 |
| LIG_FHA_1 | 129 | 135 | PF00498 | 0.388 |
| LIG_FHA_1 | 273 | 279 | PF00498 | 0.443 |
| LIG_FHA_1 | 378 | 384 | PF00498 | 0.808 |
| LIG_FHA_1 | 444 | 450 | PF00498 | 0.550 |
| LIG_FHA_1 | 54 | 60 | PF00498 | 0.458 |
| LIG_FHA_1 | 76 | 82 | PF00498 | 0.292 |
| LIG_FHA_2 | 149 | 155 | PF00498 | 0.355 |
| LIG_FHA_2 | 236 | 242 | PF00498 | 0.395 |
| LIG_FHA_2 | 289 | 295 | PF00498 | 0.397 |
| LIG_FHA_2 | 508 | 514 | PF00498 | 0.496 |
| LIG_GBD_Chelix_1 | 215 | 223 | PF00786 | 0.648 |
| LIG_HCF-1_HBM_1 | 270 | 273 | PF13415 | 0.422 |
| LIG_LIR_Gen_1 | 270 | 278 | PF02991 | 0.454 |
| LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.311 |
| LIG_LIR_Gen_1 | 506 | 512 | PF02991 | 0.566 |
| LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.453 |
| LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.460 |
| LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.352 |
| LIG_LIR_Nem_3 | 506 | 511 | PF02991 | 0.566 |
| LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.291 |
| LIG_SH2_CRK | 200 | 204 | PF00017 | 0.538 |
| LIG_SH2_GRB2like | 242 | 245 | PF00017 | 0.398 |
| LIG_SH2_PTP2 | 273 | 276 | PF00017 | 0.446 |
| LIG_SH2_SRC | 39 | 42 | PF00017 | 0.282 |
| LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.444 |
| LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.371 |
| LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.411 |
| LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.530 |
| LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.417 |
| LIG_SH3_3 | 177 | 183 | PF00018 | 0.554 |
| LIG_SH3_3 | 353 | 359 | PF00018 | 0.672 |
| LIG_SH3_3 | 424 | 430 | PF00018 | 0.614 |
| LIG_SH3_3 | 470 | 476 | PF00018 | 0.621 |
| LIG_SH3_3 | 491 | 497 | PF00018 | 0.679 |
| LIG_SUMO_SIM_anti_2 | 53 | 61 | PF11976 | 0.347 |
| LIG_SUMO_SIM_par_1 | 274 | 280 | PF11976 | 0.389 |
| LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.448 |
| LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.676 |
| LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.601 |
| LIG_TRAF2_2 | 190 | 195 | PF00917 | 0.629 |
| LIG_UBA3_1 | 81 | 87 | PF00899 | 0.351 |
| LIG_WRC_WIRS_1 | 508 | 513 | PF05994 | 0.494 |
| LIG_WW_3 | 357 | 361 | PF00397 | 0.681 |
| MOD_CDC14_SPxK_1 | 357 | 360 | PF00782 | 0.534 |
| MOD_CDK_SPxK_1 | 354 | 360 | PF00069 | 0.637 |
| MOD_CK1_1 | 262 | 268 | PF00069 | 0.444 |
| MOD_CK1_1 | 482 | 488 | PF00069 | 0.650 |
| MOD_CK1_1 | 53 | 59 | PF00069 | 0.289 |
| MOD_CK1_1 | 88 | 94 | PF00069 | 0.335 |
| MOD_CK2_1 | 2 | 8 | PF00069 | 0.453 |
| MOD_CK2_1 | 426 | 432 | PF00069 | 0.614 |
| MOD_CK2_1 | 507 | 513 | PF00069 | 0.676 |
| MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.368 |
| MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.432 |
| MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.451 |
| MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.681 |
| MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.654 |
| MOD_GlcNHglycan | 338 | 342 | PF01048 | 0.695 |
| MOD_GlcNHglycan | 343 | 347 | PF01048 | 0.659 |
| MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.605 |
| MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.662 |
| MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.724 |
| MOD_GSK3_1 | 128 | 135 | PF00069 | 0.332 |
| MOD_GSK3_1 | 223 | 230 | PF00069 | 0.462 |
| MOD_GSK3_1 | 272 | 279 | PF00069 | 0.446 |
| MOD_GSK3_1 | 288 | 295 | PF00069 | 0.442 |
| MOD_GSK3_1 | 330 | 337 | PF00069 | 0.779 |
| MOD_GSK3_1 | 402 | 409 | PF00069 | 0.608 |
| MOD_GSK3_1 | 416 | 423 | PF00069 | 0.759 |
| MOD_GSK3_1 | 426 | 433 | PF00069 | 0.786 |
| MOD_GSK3_1 | 443 | 450 | PF00069 | 0.612 |
| MOD_GSK3_1 | 479 | 486 | PF00069 | 0.670 |
| MOD_GSK3_1 | 81 | 88 | PF00069 | 0.377 |
| MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.338 |
| MOD_N-GLC_2 | 251 | 253 | PF02516 | 0.455 |
| MOD_NEK2_1 | 128 | 133 | PF00069 | 0.331 |
| MOD_NEK2_1 | 232 | 237 | PF00069 | 0.465 |
| MOD_NEK2_1 | 277 | 282 | PF00069 | 0.483 |
| MOD_NEK2_1 | 288 | 293 | PF00069 | 0.496 |
| MOD_NEK2_1 | 330 | 335 | PF00069 | 0.657 |
| MOD_NEK2_1 | 347 | 352 | PF00069 | 0.623 |
| MOD_NEK2_1 | 370 | 375 | PF00069 | 0.616 |
| MOD_NEK2_1 | 444 | 449 | PF00069 | 0.662 |
| MOD_NEK2_1 | 81 | 86 | PF00069 | 0.371 |
| MOD_PIKK_1 | 262 | 268 | PF00454 | 0.438 |
| MOD_PIKK_1 | 292 | 298 | PF00454 | 0.435 |
| MOD_PIKK_1 | 96 | 102 | PF00454 | 0.314 |
| MOD_PKA_2 | 171 | 177 | PF00069 | 0.656 |
| MOD_PKA_2 | 227 | 233 | PF00069 | 0.483 |
| MOD_Plk_1 | 132 | 138 | PF00069 | 0.335 |
| MOD_Plk_1 | 303 | 309 | PF00069 | 0.469 |
| MOD_Plk_1 | 342 | 348 | PF00069 | 0.615 |
| MOD_Plk_1 | 53 | 59 | PF00069 | 0.335 |
| MOD_Plk_2-3 | 507 | 513 | PF00069 | 0.495 |
| MOD_Plk_4 | 132 | 138 | PF00069 | 0.348 |
| MOD_Plk_4 | 2 | 8 | PF00069 | 0.394 |
| MOD_Plk_4 | 259 | 265 | PF00069 | 0.538 |
| MOD_Plk_4 | 272 | 278 | PF00069 | 0.354 |
| MOD_Plk_4 | 507 | 513 | PF00069 | 0.495 |
| MOD_Plk_4 | 81 | 87 | PF00069 | 0.305 |
| MOD_Plk_4 | 88 | 94 | PF00069 | 0.314 |
| MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.614 |
| MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.685 |
| MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.639 |
| MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.639 |
| MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.567 |
| MOD_SUMO_for_1 | 176 | 179 | PF00179 | 0.514 |
| MOD_SUMO_for_1 | 301 | 304 | PF00179 | 0.486 |
| TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.400 |
| TRG_DiLeu_BaEn_2 | 39 | 45 | PF01217 | 0.351 |
| TRG_DiLeu_BaEn_4 | 144 | 150 | PF01217 | 0.437 |
| TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.460 |
| TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.430 |
| TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.658 |
| TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.292 |
| TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.521 |
| TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.351 |
| TRG_Pf-PMV_PEXEL_1 | 65 | 69 | PF00026 | 0.272 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PB53 | Leptomonas seymouri | 53% | 96% |
| A0A3Q8IJX3 | Leishmania donovani | 87% | 100% |
| A4HQ30 | Leishmania braziliensis | 62% | 100% |
| A4IDT6 | Leishmania infantum | 87% | 100% |
| E9ATU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
| V5BM99 | Trypanosoma cruzi | 36% | 100% |