| 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: 8 |
| NetGPI | no | yes: 0, no: 8 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQ30
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 9 |
| GO:0006886 | intracellular protein transport | 4 | 9 |
| GO:0007034 | vacuolar transport | 4 | 9 |
| GO:0008104 | protein localization | 4 | 9 |
| GO:0009987 | cellular process | 1 | 9 |
| GO:0015031 | protein transport | 4 | 9 |
| GO:0016192 | vesicle-mediated transport | 4 | 9 |
| GO:0016197 | endosomal transport | 4 | 9 |
| GO:0032509 | endosome transport via multivesicular body sorting pathway | 5 | 9 |
| GO:0032511 | late endosome to vacuole transport via multivesicular body sorting pathway | 6 | 9 |
| GO:0033036 | macromolecule localization | 2 | 9 |
| GO:0033365 | protein localization to organelle | 5 | 9 |
| GO:0043328 | protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway | 5 | 9 |
| GO:0045184 | establishment of protein localization | 3 | 9 |
| GO:0045324 | late endosome to vacuole transport | 5 | 9 |
| GO:0046907 | intracellular transport | 3 | 9 |
| GO:0051179 | localization | 1 | 9 |
| GO:0051234 | establishment of localization | 2 | 9 |
| GO:0051641 | cellular localization | 2 | 9 |
| GO:0051649 | establishment of localization in cell | 3 | 9 |
| GO:0070727 | cellular macromolecule localization | 3 | 9 |
| GO:0071702 | organic substance transport | 4 | 9 |
| GO:0071705 | nitrogen compound transport | 4 | 9 |
| GO:0071985 | multivesicular body sorting pathway | 5 | 9 |
| GO:0072594 | establishment of protein localization to organelle | 4 | 9 |
| GO:0072665 | protein localization to vacuole | 6 | 9 |
| GO:0072666 | establishment of protein localization to vacuole | 5 | 9 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 9 |
| GO:0005515 | protein binding | 2 | 9 |
| GO:0005543 | phospholipid binding | 3 | 9 |
| GO:0008289 | lipid binding | 2 | 9 |
| GO:0032182 | ubiquitin-like protein binding | 3 | 9 |
| GO:0035091 | phosphatidylinositol binding | 4 | 9 |
| GO:0043130 | ubiquitin binding | 4 | 9 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.400 |
| CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.777 |
| CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.291 |
| CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.784 |
| CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.291 |
| CLV_PCSK_PC7_1 | 61 | 67 | PF00082 | 0.291 |
| CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.291 |
| CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.512 |
| DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.450 |
| DEG_SCF_FBW7_2 | 17 | 24 | PF00400 | 0.356 |
| DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.537 |
| DEG_SPOP_SBC_1 | 410 | 414 | PF00917 | 0.535 |
| DOC_CKS1_1 | 18 | 23 | PF01111 | 0.313 |
| DOC_MAPK_gen_1 | 51 | 59 | PF00069 | 0.367 |
| DOC_MAPK_MEF2A_6 | 124 | 132 | PF00069 | 0.370 |
| DOC_MAPK_MEF2A_6 | 268 | 276 | PF00069 | 0.465 |
| DOC_MAPK_MEF2A_6 | 65 | 74 | PF00069 | 0.305 |
| DOC_PP1_RVXF_1 | 1 | 7 | PF00149 | 0.320 |
| DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.325 |
| DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.548 |
| DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.309 |
| DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.469 |
| DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.549 |
| DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.582 |
| DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.630 |
| DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.621 |
| DOC_USP7_MATH_2 | 409 | 415 | PF00917 | 0.633 |
| DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.329 |
| DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.581 |
| DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.700 |
| DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.779 |
| LIG_14-3-3_CterR_2 | 507 | 510 | PF00244 | 0.505 |
| LIG_Actin_WH2_2 | 275 | 292 | PF00022 | 0.474 |
| LIG_AP_GAE_1 | 497 | 503 | PF02883 | 0.495 |
| LIG_BH_BH3_1 | 141 | 157 | PF00452 | 0.462 |
| LIG_BIR_III_2 | 217 | 221 | PF00653 | 0.494 |
| LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.335 |
| LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.415 |
| LIG_EVH1_1 | 322 | 326 | PF00568 | 0.490 |
| LIG_FHA_1 | 129 | 135 | PF00498 | 0.356 |
| LIG_FHA_1 | 13 | 19 | PF00498 | 0.490 |
| LIG_FHA_1 | 273 | 279 | PF00498 | 0.492 |
| LIG_FHA_1 | 413 | 419 | PF00498 | 0.734 |
| LIG_FHA_1 | 431 | 437 | PF00498 | 0.760 |
| LIG_FHA_1 | 76 | 82 | PF00498 | 0.291 |
| LIG_FHA_2 | 149 | 155 | PF00498 | 0.396 |
| LIG_FHA_2 | 289 | 295 | PF00498 | 0.441 |
| LIG_FHA_2 | 53 | 59 | PF00498 | 0.351 |
| LIG_HCF-1_HBM_1 | 270 | 273 | PF13415 | 0.466 |
| LIG_LIR_Apic_2 | 404 | 410 | PF02991 | 0.684 |
| LIG_LIR_Gen_1 | 20 | 26 | PF02991 | 0.328 |
| LIG_LIR_Gen_1 | 270 | 278 | PF02991 | 0.474 |
| LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.369 |
| LIG_LIR_Gen_1 | 497 | 504 | PF02991 | 0.562 |
| LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.340 |
| LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.490 |
| LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.458 |
| LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.390 |
| LIG_LIR_Nem_3 | 497 | 503 | PF02991 | 0.562 |
| LIG_MYND_1 | 354 | 358 | PF01753 | 0.525 |
| LIG_SH2_GRB2like | 242 | 245 | PF00017 | 0.446 |
| LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.522 |
| LIG_SH2_PTP2 | 273 | 276 | PF00017 | 0.463 |
| LIG_SH2_PTP2 | 407 | 410 | PF00017 | 0.518 |
| LIG_SH2_SRC | 39 | 42 | PF00017 | 0.285 |
| LIG_SH2_SRC | 407 | 410 | PF00017 | 0.518 |
| LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.482 |
| LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.411 |
| LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.462 |
| LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.549 |
| LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.448 |
| LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.518 |
| LIG_SH3_3 | 320 | 326 | PF00018 | 0.562 |
| LIG_SH3_3 | 375 | 381 | PF00018 | 0.654 |
| LIG_SH3_3 | 420 | 426 | PF00018 | 0.656 |
| LIG_SH3_3 | 433 | 439 | PF00018 | 0.605 |
| LIG_SUMO_SIM_anti_2 | 54 | 61 | PF11976 | 0.363 |
| LIG_SUMO_SIM_par_1 | 219 | 227 | PF11976 | 0.436 |
| LIG_SUMO_SIM_par_1 | 274 | 280 | PF11976 | 0.430 |
| LIG_SxIP_EBH_1 | 345 | 355 | PF03271 | 0.528 |
| LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.466 |
| LIG_TYR_ITSM | 18 | 25 | PF00017 | 0.356 |
| LIG_UBA3_1 | 81 | 87 | PF00899 | 0.385 |
| LIG_WW_3 | 352 | 356 | PF00397 | 0.624 |
| MOD_CK1_1 | 262 | 268 | PF00069 | 0.573 |
| MOD_CK1_1 | 342 | 348 | PF00069 | 0.687 |
| MOD_CK1_1 | 365 | 371 | PF00069 | 0.539 |
| MOD_CK1_1 | 385 | 391 | PF00069 | 0.617 |
| MOD_CK1_1 | 412 | 418 | PF00069 | 0.563 |
| MOD_CK1_1 | 477 | 483 | PF00069 | 0.571 |
| MOD_CK1_1 | 88 | 94 | PF00069 | 0.440 |
| MOD_CK2_1 | 2 | 8 | PF00069 | 0.485 |
| MOD_CK2_1 | 235 | 241 | PF00069 | 0.323 |
| MOD_CK2_1 | 250 | 256 | PF00069 | 0.493 |
| MOD_CK2_1 | 410 | 416 | PF00069 | 0.670 |
| MOD_CK2_1 | 440 | 446 | PF00069 | 0.746 |
| MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.627 |
| MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.424 |
| MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.505 |
| MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.659 |
| MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.612 |
| MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.704 |
| MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.606 |
| MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.773 |
| MOD_GSK3_1 | 128 | 135 | PF00069 | 0.438 |
| MOD_GSK3_1 | 143 | 150 | PF00069 | 0.352 |
| MOD_GSK3_1 | 223 | 230 | PF00069 | 0.511 |
| MOD_GSK3_1 | 272 | 279 | PF00069 | 0.482 |
| MOD_GSK3_1 | 288 | 295 | PF00069 | 0.364 |
| MOD_GSK3_1 | 326 | 333 | PF00069 | 0.625 |
| MOD_GSK3_1 | 339 | 346 | PF00069 | 0.676 |
| MOD_GSK3_1 | 365 | 372 | PF00069 | 0.614 |
| MOD_GSK3_1 | 381 | 388 | PF00069 | 0.604 |
| MOD_GSK3_1 | 412 | 419 | PF00069 | 0.635 |
| MOD_GSK3_1 | 441 | 448 | PF00069 | 0.678 |
| MOD_GSK3_1 | 477 | 484 | PF00069 | 0.710 |
| MOD_GSK3_1 | 81 | 88 | PF00069 | 0.431 |
| MOD_LATS_1 | 360 | 366 | PF00433 | 0.543 |
| MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.332 |
| MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.432 |
| MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.586 |
| MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.538 |
| MOD_NEK2_1 | 128 | 133 | PF00069 | 0.356 |
| MOD_NEK2_1 | 277 | 282 | PF00069 | 0.470 |
| MOD_NEK2_1 | 288 | 293 | PF00069 | 0.485 |
| MOD_NEK2_1 | 330 | 335 | PF00069 | 0.767 |
| MOD_NEK2_1 | 45 | 50 | PF00069 | 0.294 |
| MOD_NEK2_1 | 81 | 86 | PF00069 | 0.388 |
| MOD_NEK2_2 | 89 | 94 | PF00069 | 0.307 |
| MOD_PIKK_1 | 202 | 208 | PF00454 | 0.515 |
| MOD_PIKK_1 | 262 | 268 | PF00454 | 0.485 |
| MOD_PIKK_1 | 292 | 298 | PF00454 | 0.398 |
| MOD_PIKK_1 | 96 | 102 | PF00454 | 0.325 |
| MOD_PKA_1 | 318 | 324 | PF00069 | 0.505 |
| MOD_PKA_2 | 192 | 198 | PF00069 | 0.538 |
| MOD_PKA_2 | 227 | 233 | PF00069 | 0.489 |
| MOD_Plk_1 | 132 | 138 | PF00069 | 0.330 |
| MOD_Plk_1 | 143 | 149 | PF00069 | 0.378 |
| MOD_Plk_1 | 250 | 256 | PF00069 | 0.422 |
| MOD_Plk_1 | 342 | 348 | PF00069 | 0.611 |
| MOD_Plk_1 | 441 | 447 | PF00069 | 0.527 |
| MOD_Plk_4 | 132 | 138 | PF00069 | 0.361 |
| MOD_Plk_4 | 143 | 149 | PF00069 | 0.421 |
| MOD_Plk_4 | 2 | 8 | PF00069 | 0.426 |
| MOD_Plk_4 | 259 | 265 | PF00069 | 0.578 |
| MOD_Plk_4 | 272 | 278 | PF00069 | 0.391 |
| MOD_Plk_4 | 326 | 332 | PF00069 | 0.615 |
| MOD_Plk_4 | 402 | 408 | PF00069 | 0.536 |
| MOD_Plk_4 | 52 | 58 | PF00069 | 0.210 |
| MOD_Plk_4 | 81 | 87 | PF00069 | 0.300 |
| MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.321 |
| MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.585 |
| MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.695 |
| MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.782 |
| MOD_SUMO_for_1 | 168 | 171 | PF00179 | 0.436 |
| MOD_SUMO_for_1 | 176 | 179 | PF00179 | 0.500 |
| MOD_SUMO_for_1 | 301 | 304 | PF00179 | 0.562 |
| MOD_SUMO_for_1 | 469 | 472 | PF00179 | 0.528 |
| MOD_SUMO_rev_2 | 191 | 200 | PF00179 | 0.593 |
| MOD_SUMO_rev_2 | 313 | 321 | PF00179 | 0.514 |
| TRG_AP2beta_CARGO_1 | 497 | 507 | PF09066 | 0.480 |
| TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.432 |
| TRG_DiLeu_BaEn_2 | 39 | 45 | PF01217 | 0.385 |
| TRG_DiLeu_BaEn_4 | 144 | 150 | PF01217 | 0.458 |
| TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.349 |
| TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.382 |
| TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.481 |
| TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.460 |
| TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.291 |
| TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.385 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PB53 | Leptomonas seymouri | 63% | 94% |
| A0A0S4JSH6 | Bodo saltans | 34% | 100% |
| A0A3Q8IJX3 | Leishmania donovani | 65% | 98% |
| A4IDT6 | Leishmania infantum | 65% | 98% |
| E9ATU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
| Q4Q0P8 | Leishmania major | 62% | 100% |
| V5BM99 | Trypanosoma cruzi | 36% | 100% |