| 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: 12 | 
| NetGPI | no | yes: 0, no: 12 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 13 | 
| GO:0110165 | cellular anatomical entity | 1 | 13 | 
Related structures:
AlphaFold database: Q4Q6R0
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006810 | transport | 3 | 1 | 
| GO:0008643 | carbohydrate transport | 5 | 1 | 
| GO:0051179 | localization | 1 | 1 | 
| GO:0051234 | establishment of localization | 2 | 1 | 
| GO:0071702 | organic substance transport | 4 | 1 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 579 | 583 | PF00656 | 0.670 | 
| CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.667 | 
| CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.432 | 
| CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.435 | 
| CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.585 | 
| CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.433 | 
| CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.348 | 
| CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.420 | 
| CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.596 | 
| CLV_PCSK_PC1ET2_1 | 317 | 319 | PF00082 | 0.392 | 
| CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.494 | 
| CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.314 | 
| CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.310 | 
| CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.425 | 
| DEG_APCC_DBOX_1 | 121 | 129 | PF00400 | 0.335 | 
| DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.600 | 
| DOC_CDC14_PxL_1 | 556 | 564 | PF14671 | 0.399 | 
| DOC_CYCLIN_RxL_1 | 48 | 59 | PF00134 | 0.620 | 
| DOC_CYCLIN_yCln2_LP_2 | 32 | 38 | PF00134 | 0.612 | 
| DOC_MAPK_gen_1 | 184 | 193 | PF00069 | 0.570 | 
| DOC_MAPK_MEF2A_6 | 184 | 193 | PF00069 | 0.584 | 
| DOC_MAPK_MEF2A_6 | 466 | 475 | PF00069 | 0.362 | 
| DOC_MAPK_MEF2A_6 | 485 | 494 | PF00069 | 0.387 | 
| DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.658 | 
| DOC_PP2B_PxIxI_1 | 188 | 194 | PF00149 | 0.529 | 
| DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.369 | 
| DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.613 | 
| DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.671 | 
| DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.395 | 
| DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.343 | 
| DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.425 | 
| DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.793 | 
| DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.567 | 
| DOC_USP7_UBL2_3 | 466 | 470 | PF12436 | 0.326 | 
| LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.702 | 
| LIG_14-3-3_CanoR_1 | 330 | 334 | PF00244 | 0.677 | 
| LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.641 | 
| LIG_14-3-3_CanoR_1 | 48 | 55 | PF00244 | 0.622 | 
| LIG_Actin_WH2_2 | 471 | 487 | PF00022 | 0.336 | 
| LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.599 | 
| LIG_deltaCOP1_diTrp_1 | 94 | 102 | PF00928 | 0.607 | 
| LIG_EH_1 | 435 | 439 | PF12763 | 0.520 | 
| LIG_eIF4E_1 | 294 | 300 | PF01652 | 0.269 | 
| LIG_FHA_1 | 127 | 133 | PF00498 | 0.369 | 
| LIG_FHA_1 | 206 | 212 | PF00498 | 0.488 | 
| LIG_FHA_1 | 227 | 233 | PF00498 | 0.436 | 
| LIG_FHA_1 | 27 | 33 | PF00498 | 0.828 | 
| LIG_FHA_1 | 489 | 495 | PF00498 | 0.438 | 
| LIG_FHA_1 | 50 | 56 | PF00498 | 0.628 | 
| LIG_FHA_1 | 591 | 597 | PF00498 | 0.644 | 
| LIG_FHA_1 | 60 | 66 | PF00498 | 0.615 | 
| LIG_FHA_2 | 349 | 355 | PF00498 | 0.619 | 
| LIG_FHA_2 | 83 | 89 | PF00498 | 0.672 | 
| LIG_LIR_Apic_2 | 40 | 46 | PF02991 | 0.594 | 
| LIG_LIR_Gen_1 | 161 | 172 | PF02991 | 0.419 | 
| LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.410 | 
| LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.323 | 
| LIG_LIR_Gen_1 | 367 | 376 | PF02991 | 0.478 | 
| LIG_LIR_Gen_1 | 99 | 110 | PF02991 | 0.654 | 
| LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.382 | 
| LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.565 | 
| LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.478 | 
| LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.436 | 
| LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.561 | 
| LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.396 | 
| LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.587 | 
| LIG_NRBOX | 405 | 411 | PF00104 | 0.369 | 
| LIG_Pex14_1 | 97 | 101 | PF04695 | 0.664 | 
| LIG_Pex14_2 | 356 | 360 | PF04695 | 0.426 | 
| LIG_Pex14_2 | 362 | 366 | PF04695 | 0.367 | 
| LIG_Pex14_2 | 450 | 454 | PF04695 | 0.346 | 
| LIG_PTB_Apo_2 | 376 | 383 | PF02174 | 0.371 | 
| LIG_SH2_CRK | 164 | 168 | PF00017 | 0.369 | 
| LIG_SH2_NCK_1 | 388 | 392 | PF00017 | 0.277 | 
| LIG_SH2_NCK_1 | 503 | 507 | PF00017 | 0.552 | 
| LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.416 | 
| LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.363 | 
| LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.369 | 
| LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.342 | 
| LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.552 | 
| LIG_SH2_STAP1 | 511 | 515 | PF00017 | 0.294 | 
| LIG_SH2_STAP1 | 594 | 598 | PF00017 | 0.665 | 
| LIG_SH2_STAT3 | 420 | 423 | PF00017 | 0.592 | 
| LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.394 | 
| LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.424 | 
| LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.313 | 
| LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.600 | 
| LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.381 | 
| LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.424 | 
| LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.615 | 
| LIG_SH3_3 | 304 | 310 | PF00018 | 0.359 | 
| LIG_SH3_3 | 31 | 37 | PF00018 | 0.617 | 
| LIG_SH3_3 | 468 | 474 | PF00018 | 0.404 | 
| LIG_SH3_3 | 554 | 560 | PF00018 | 0.408 | 
| LIG_SUMO_SIM_par_1 | 52 | 59 | PF11976 | 0.621 | 
| LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.398 | 
| LIG_Vh1_VBS_1 | 247 | 265 | PF01044 | 0.536 | 
| LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.385 | 
| LIG_WRC_WIRS_1 | 450 | 455 | PF05994 | 0.431 | 
| MOD_CK1_1 | 130 | 136 | PF00069 | 0.463 | 
| MOD_CK1_1 | 142 | 148 | PF00069 | 0.440 | 
| MOD_CK1_1 | 150 | 156 | PF00069 | 0.396 | 
| MOD_CK1_1 | 251 | 257 | PF00069 | 0.709 | 
| MOD_CK1_1 | 26 | 32 | PF00069 | 0.816 | 
| MOD_CK1_1 | 44 | 50 | PF00069 | 0.635 | 
| MOD_CK1_1 | 523 | 529 | PF00069 | 0.394 | 
| MOD_CK1_1 | 56 | 62 | PF00069 | 0.621 | 
| MOD_CK1_1 | 592 | 598 | PF00069 | 0.700 | 
| MOD_CK1_1 | 66 | 72 | PF00069 | 0.681 | 
| MOD_CK1_1 | 96 | 102 | PF00069 | 0.551 | 
| MOD_CK2_1 | 247 | 253 | PF00069 | 0.637 | 
| MOD_CK2_1 | 348 | 354 | PF00069 | 0.705 | 
| MOD_CK2_1 | 70 | 76 | PF00069 | 0.709 | 
| MOD_GlcNHglycan | 253 | 257 | PF01048 | 0.404 | 
| MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.390 | 
| MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.386 | 
| MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.389 | 
| MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.433 | 
| MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.444 | 
| MOD_GSK3_1 | 126 | 133 | PF00069 | 0.388 | 
| MOD_GSK3_1 | 139 | 146 | PF00069 | 0.383 | 
| MOD_GSK3_1 | 24 | 31 | PF00069 | 0.660 | 
| MOD_GSK3_1 | 247 | 254 | PF00069 | 0.627 | 
| MOD_GSK3_1 | 270 | 277 | PF00069 | 0.418 | 
| MOD_GSK3_1 | 37 | 44 | PF00069 | 0.645 | 
| MOD_GSK3_1 | 386 | 393 | PF00069 | 0.370 | 
| MOD_GSK3_1 | 398 | 405 | PF00069 | 0.336 | 
| MOD_GSK3_1 | 47 | 54 | PF00069 | 0.608 | 
| MOD_GSK3_1 | 474 | 481 | PF00069 | 0.302 | 
| MOD_GSK3_1 | 509 | 516 | PF00069 | 0.540 | 
| MOD_GSK3_1 | 519 | 526 | PF00069 | 0.368 | 
| MOD_GSK3_1 | 529 | 536 | PF00069 | 0.327 | 
| MOD_GSK3_1 | 56 | 63 | PF00069 | 0.594 | 
| MOD_GSK3_1 | 66 | 73 | PF00069 | 0.625 | 
| MOD_GSK3_1 | 93 | 100 | PF00069 | 0.655 | 
| MOD_LATS_1 | 51 | 57 | PF00433 | 0.624 | 
| MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.420 | 
| MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.442 | 
| MOD_NEK2_1 | 110 | 115 | PF00069 | 0.714 | 
| MOD_NEK2_1 | 126 | 131 | PF00069 | 0.352 | 
| MOD_NEK2_1 | 143 | 148 | PF00069 | 0.414 | 
| MOD_NEK2_1 | 149 | 154 | PF00069 | 0.433 | 
| MOD_NEK2_1 | 17 | 22 | PF00069 | 0.794 | 
| MOD_NEK2_1 | 24 | 29 | PF00069 | 0.611 | 
| MOD_NEK2_1 | 247 | 252 | PF00069 | 0.695 | 
| MOD_NEK2_1 | 274 | 279 | PF00069 | 0.424 | 
| MOD_NEK2_1 | 313 | 318 | PF00069 | 0.479 | 
| MOD_NEK2_1 | 364 | 369 | PF00069 | 0.418 | 
| MOD_NEK2_1 | 377 | 382 | PF00069 | 0.322 | 
| MOD_NEK2_1 | 460 | 465 | PF00069 | 0.490 | 
| MOD_NEK2_1 | 49 | 54 | PF00069 | 0.621 | 
| MOD_NEK2_1 | 502 | 507 | PF00069 | 0.603 | 
| MOD_NEK2_1 | 529 | 534 | PF00069 | 0.377 | 
| MOD_NEK2_2 | 449 | 454 | PF00069 | 0.353 | 
| MOD_PIKK_1 | 130 | 136 | PF00454 | 0.358 | 
| MOD_PIKK_1 | 260 | 266 | PF00454 | 0.511 | 
| MOD_PIKK_1 | 70 | 76 | PF00454 | 0.725 | 
| MOD_PKA_2 | 17 | 23 | PF00069 | 0.604 | 
| MOD_PKA_2 | 329 | 335 | PF00069 | 0.694 | 
| MOD_PKA_2 | 338 | 344 | PF00069 | 0.641 | 
| MOD_PKA_2 | 47 | 53 | PF00069 | 0.621 | 
| MOD_PKA_2 | 70 | 76 | PF00069 | 0.709 | 
| MOD_PKA_2 | 82 | 88 | PF00069 | 0.721 | 
| MOD_PKB_1 | 81 | 89 | PF00069 | 0.659 | 
| MOD_Plk_1 | 110 | 116 | PF00069 | 0.520 | 
| MOD_Plk_1 | 567 | 573 | PF00069 | 0.705 | 
| MOD_Plk_1 | 577 | 583 | PF00069 | 0.735 | 
| MOD_Plk_1 | 93 | 99 | PF00069 | 0.620 | 
| MOD_Plk_4 | 214 | 220 | PF00069 | 0.406 | 
| MOD_Plk_4 | 226 | 232 | PF00069 | 0.354 | 
| MOD_Plk_4 | 270 | 276 | PF00069 | 0.407 | 
| MOD_Plk_4 | 398 | 404 | PF00069 | 0.411 | 
| MOD_Plk_4 | 449 | 455 | PF00069 | 0.513 | 
| MOD_Plk_4 | 474 | 480 | PF00069 | 0.307 | 
| MOD_Plk_4 | 93 | 99 | PF00069 | 0.684 | 
| TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.398 | 
| TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.399 | 
| TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.377 | 
| TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.320 | 
| TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.387 | 
| TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.375 | 
| TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.653 | 
| TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.808 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1HYC7 | Leptomonas seymouri | 57% | 100% | 
| A0A0N1I3H1 | Leptomonas seymouri | 28% | 89% | 
| A0A3Q8IF44 | Leishmania donovani | 93% | 100% | 
| A0A3Q8ILR5 | Leishmania donovani | 26% | 100% | 
| A4HIW8 | Leishmania braziliensis | 77% | 100% | 
| A4HL09 | Leishmania braziliensis | 27% | 100% | 
| A4I8J0 | Leishmania infantum | 26% | 100% | 
| E9AHK6 | Leishmania infantum | 93% | 100% | 
| E9B1F2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% | 
| E9B3F0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% | 
| Q4Q4Q0 | Leishmania major | 26% | 100% |