| 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: 5 |
| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0031201 | SNARE complex | 3 | 2 |
| GO:0032991 | protein-containing complex | 1 | 2 |
| GO:0098796 | membrane protein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q3F3
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 12 |
| GO:0006886 | intracellular protein transport | 4 | 12 |
| GO:0008104 | protein localization | 4 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0015031 | protein transport | 4 | 12 |
| GO:0033036 | macromolecule localization | 2 | 12 |
| GO:0045184 | establishment of protein localization | 3 | 12 |
| GO:0046907 | intracellular transport | 3 | 12 |
| GO:0051179 | localization | 1 | 12 |
| GO:0051234 | establishment of localization | 2 | 12 |
| GO:0051641 | cellular localization | 2 | 12 |
| GO:0051649 | establishment of localization in cell | 3 | 12 |
| GO:0070727 | cellular macromolecule localization | 3 | 12 |
| GO:0071702 | organic substance transport | 4 | 12 |
| GO:0071705 | nitrogen compound transport | 4 | 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000149 | SNARE binding | 3 | 2 |
| GO:0005483 | soluble NSF attachment protein activity | 3 | 2 |
| GO:0005488 | binding | 1 | 2 |
| GO:0005515 | protein binding | 2 | 2 |
| GO:0019905 | syntaxin binding | 4 | 2 |
| GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
| GO:0060090 | molecular adaptor activity | 1 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.682 |
| CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.562 |
| CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.562 |
| CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.367 |
| CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.402 |
| CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.367 |
| CLV_PCSK_PC1ET2_1 | 228 | 230 | PF00082 | 0.402 |
| CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.438 |
| CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.356 |
| CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.373 |
| DEG_SCF_FBW7_2 | 1 | 8 | PF00400 | 0.460 |
| DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.739 |
| DOC_CYCLIN_RxL_1 | 338 | 347 | PF00134 | 0.455 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 247 | 253 | PF00134 | 0.470 |
| DOC_MAPK_MEF2A_6 | 208 | 215 | PF00069 | 0.363 |
| DOC_MAPK_MEF2A_6 | 261 | 268 | PF00069 | 0.288 |
| DOC_PP1_RVXF_1 | 23 | 30 | PF00149 | 0.371 |
| DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.466 |
| DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.624 |
| DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.476 |
| DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.497 |
| DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.672 |
| DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.692 |
| DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.417 |
| DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.404 |
| DOC_USP7_UBL2_3 | 348 | 352 | PF12436 | 0.616 |
| DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.493 |
| DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.596 |
| LIG_14-3-3_CanoR_1 | 151 | 157 | PF00244 | 0.540 |
| LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.510 |
| LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.379 |
| LIG_FHA_1 | 105 | 111 | PF00498 | 0.622 |
| LIG_FHA_1 | 169 | 175 | PF00498 | 0.439 |
| LIG_FHA_2 | 165 | 171 | PF00498 | 0.624 |
| LIG_FHA_2 | 240 | 246 | PF00498 | 0.530 |
| LIG_FHA_2 | 271 | 277 | PF00498 | 0.510 |
| LIG_FHA_2 | 381 | 387 | PF00498 | 0.706 |
| LIG_LIR_Apic_2 | 155 | 161 | PF02991 | 0.491 |
| LIG_LIR_Apic_2 | 198 | 204 | PF02991 | 0.496 |
| LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.475 |
| LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.390 |
| LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.471 |
| LIG_LIR_Nem_3 | 280 | 284 | PF02991 | 0.469 |
| LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.395 |
| LIG_SH2_CRK | 158 | 162 | PF00017 | 0.517 |
| LIG_SH2_CRK | 178 | 182 | PF00017 | 0.433 |
| LIG_SH2_CRK | 47 | 51 | PF00017 | 0.508 |
| LIG_SH2_GRB2like | 47 | 50 | PF00017 | 0.500 |
| LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.453 |
| LIG_SH2_SRC | 122 | 125 | PF00017 | 0.454 |
| LIG_SH2_SRC | 243 | 246 | PF00017 | 0.517 |
| LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.416 |
| LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.480 |
| LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.368 |
| LIG_SUMO_SIM_anti_2 | 184 | 190 | PF11976 | 0.455 |
| LIG_SUMO_SIM_anti_2 | 265 | 270 | PF11976 | 0.276 |
| LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.382 |
| LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.453 |
| LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.379 |
| LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.229 |
| MOD_CDK_SPxK_1 | 1 | 7 | PF00069 | 0.471 |
| MOD_CK1_1 | 152 | 158 | PF00069 | 0.550 |
| MOD_CK1_1 | 164 | 170 | PF00069 | 0.506 |
| MOD_CK1_1 | 351 | 357 | PF00069 | 0.698 |
| MOD_CK1_1 | 94 | 100 | PF00069 | 0.576 |
| MOD_CK2_1 | 295 | 301 | PF00069 | 0.342 |
| MOD_CK2_1 | 380 | 386 | PF00069 | 0.653 |
| MOD_Cter_Amidation | 17 | 20 | PF01082 | 0.498 |
| MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.547 |
| MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.580 |
| MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.431 |
| MOD_GlcNHglycan | 365 | 369 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.593 |
| MOD_GSK3_1 | 104 | 111 | PF00069 | 0.512 |
| MOD_GSK3_1 | 160 | 167 | PF00069 | 0.584 |
| MOD_GSK3_1 | 239 | 246 | PF00069 | 0.498 |
| MOD_GSK3_1 | 344 | 351 | PF00069 | 0.533 |
| MOD_GSK3_1 | 378 | 385 | PF00069 | 0.781 |
| MOD_GSK3_1 | 93 | 100 | PF00069 | 0.580 |
| MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.542 |
| MOD_N-GLC_2 | 326 | 328 | PF02516 | 0.401 |
| MOD_NEK2_1 | 269 | 274 | PF00069 | 0.336 |
| MOD_PIKK_1 | 371 | 377 | PF00454 | 0.589 |
| MOD_PIKK_1 | 58 | 64 | PF00454 | 0.408 |
| MOD_PIKK_1 | 85 | 91 | PF00454 | 0.481 |
| MOD_PKA_1 | 341 | 347 | PF00069 | 0.493 |
| MOD_Plk_1 | 334 | 340 | PF00069 | 0.355 |
| MOD_Plk_2-3 | 382 | 388 | PF00069 | 0.695 |
| MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.482 |
| MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.594 |
| MOD_SUMO_rev_2 | 240 | 249 | PF00179 | 0.505 |
| TRG_DiLeu_BaEn_1 | 184 | 189 | PF01217 | 0.345 |
| TRG_DiLeu_BaEn_4 | 123 | 129 | PF01217 | 0.467 |
| TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.470 |
| TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.414 |
| TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.556 |
| TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.323 |
| TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.500 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I337 | Leptomonas seymouri | 66% | 99% |
| A0A0S4J5L6 | Bodo saltans | 30% | 100% |
| A0A1X0P9K4 | Trypanosomatidae | 37% | 100% |
| A0A3Q8IKP9 | Leishmania donovani | 92% | 100% |
| A0A422MZB1 | Trypanosoma rangeli | 37% | 100% |
| A4H7D4 | Leishmania braziliensis | 76% | 93% |
| A4I9M4 | Leishmania infantum | 92% | 100% |
| D0A1Z0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| E9B4M3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
| V5BRU6 | Trypanosoma cruzi | 36% | 100% |