| 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:0016020 | membrane | 2 | 9 |
| GO:0031207 | Sec62/Sec63 complex | 3 | 2 |
| GO:0032991 | protein-containing complex | 1 | 2 |
| GO:0098796 | membrane protein complex | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 9 |
| GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: E9AFD3
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006605 | protein targeting | 5 | 2 |
| GO:0006612 | protein targeting to membrane | 5 | 2 |
| GO:0006613 | cotranslational protein targeting to membrane | 6 | 2 |
| GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 2 |
| GO:0006620 | post-translational protein targeting to endoplasmic reticulum membrane | 6 | 2 |
| GO:0006810 | transport | 3 | 2 |
| GO:0006886 | intracellular protein transport | 4 | 2 |
| GO:0008104 | protein localization | 4 | 2 |
| GO:0009987 | cellular process | 1 | 2 |
| GO:0015031 | protein transport | 4 | 2 |
| GO:0033036 | macromolecule localization | 2 | 2 |
| GO:0033365 | protein localization to organelle | 5 | 2 |
| GO:0045047 | protein targeting to ER | 6 | 2 |
| GO:0045184 | establishment of protein localization | 3 | 2 |
| GO:0046907 | intracellular transport | 3 | 2 |
| GO:0051179 | localization | 1 | 2 |
| GO:0051234 | establishment of localization | 2 | 2 |
| GO:0051641 | cellular localization | 2 | 2 |
| GO:0051649 | establishment of localization in cell | 3 | 2 |
| GO:0051668 | localization within membrane | 3 | 2 |
| GO:0070727 | cellular macromolecule localization | 3 | 2 |
| GO:0070972 | protein localization to endoplasmic reticulum | 6 | 2 |
| GO:0071702 | organic substance transport | 4 | 2 |
| GO:0071705 | nitrogen compound transport | 4 | 2 |
| GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
| GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 2 |
| GO:0072657 | protein localization to membrane | 4 | 2 |
| GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 2 |
| GO:0008320 | protein transmembrane transporter activity | 3 | 2 |
| GO:0022857 | transmembrane transporter activity | 2 | 2 |
| GO:0022884 | macromolecule transmembrane transporter activity | 3 | 2 |
| GO:0140318 | protein transporter activity | 2 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.438 |
| CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.462 |
| CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.320 |
| CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.691 |
| CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.636 |
| CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.633 |
| CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.416 |
| CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.562 |
| CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.568 |
| CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.601 |
| CLV_PCSK_FUR_1 | 133 | 137 | PF00082 | 0.488 |
| CLV_PCSK_FUR_1 | 97 | 101 | PF00082 | 0.611 |
| CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.454 |
| CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.622 |
| CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.637 |
| CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.627 |
| CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.562 |
| CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.642 |
| CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.325 |
| CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.568 |
| CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.598 |
| CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.581 |
| CLV_PCSK_PC1ET2_1 | 184 | 186 | PF00082 | 0.614 |
| CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.602 |
| CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.627 |
| CLV_PCSK_PC1ET2_1 | 45 | 47 | PF00082 | 0.325 |
| CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.525 |
| CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.428 |
| CLV_PCSK_PC7_1 | 95 | 101 | PF00082 | 0.530 |
| CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.476 |
| CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.691 |
| CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.637 |
| CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.528 |
| CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.533 |
| CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.639 |
| CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.581 |
| DEG_APCC_DBOX_1 | 140 | 148 | PF00400 | 0.653 |
| DEG_APCC_DBOX_1 | 184 | 192 | PF00400 | 0.450 |
| DEG_APCC_DBOX_1 | 2 | 10 | PF00400 | 0.793 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.773 |
| DEG_SCF_FBW7_1 | 418 | 424 | PF00400 | 0.382 |
| DEG_SCF_FBW7_2 | 29 | 35 | PF00400 | 0.510 |
| DOC_CKS1_1 | 29 | 34 | PF01111 | 0.517 |
| DOC_CKS1_1 | 418 | 423 | PF01111 | 0.382 |
| DOC_CYCLIN_RxL_1 | 361 | 371 | PF00134 | 0.428 |
| DOC_CYCLIN_yCln2_LP_2 | 195 | 201 | PF00134 | 0.492 |
| DOC_MAPK_gen_1 | 382 | 390 | PF00069 | 0.383 |
| DOC_PP1_RVXF_1 | 362 | 369 | PF00149 | 0.421 |
| DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.489 |
| DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.411 |
| DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.558 |
| DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.523 |
| DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.334 |
| DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.390 |
| DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.501 |
| DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.819 |
| DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.738 |
| LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.690 |
| LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.406 |
| LIG_14-3-3_CanoR_1 | 234 | 241 | PF00244 | 0.429 |
| LIG_14-3-3_CanoR_1 | 259 | 266 | PF00244 | 0.340 |
| LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.754 |
| LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.443 |
| LIG_EH1_1 | 174 | 182 | PF00400 | 0.448 |
| LIG_FHA_1 | 160 | 166 | PF00498 | 0.413 |
| LIG_FHA_1 | 355 | 361 | PF00498 | 0.393 |
| LIG_FHA_2 | 204 | 210 | PF00498 | 0.481 |
| LIG_FHA_2 | 211 | 217 | PF00498 | 0.470 |
| LIG_FHA_2 | 29 | 35 | PF00498 | 0.562 |
| LIG_FHA_2 | 339 | 345 | PF00498 | 0.313 |
| LIG_FHA_2 | 407 | 413 | PF00498 | 0.442 |
| LIG_FHA_2 | 418 | 424 | PF00498 | 0.500 |
| LIG_LIR_Apic_2 | 308 | 314 | PF02991 | 0.355 |
| LIG_LIR_Gen_1 | 172 | 182 | PF02991 | 0.381 |
| LIG_LIR_Gen_1 | 209 | 217 | PF02991 | 0.493 |
| LIG_LIR_Gen_1 | 246 | 255 | PF02991 | 0.350 |
| LIG_LIR_Gen_1 | 31 | 41 | PF02991 | 0.498 |
| LIG_LIR_Gen_1 | 337 | 348 | PF02991 | 0.340 |
| LIG_LIR_Gen_1 | 63 | 73 | PF02991 | 0.510 |
| LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.359 |
| LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.506 |
| LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.363 |
| LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.414 |
| LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.510 |
| LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.339 |
| LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.445 |
| LIG_NRBOX | 143 | 149 | PF00104 | 0.525 |
| LIG_PTB_Apo_2 | 362 | 369 | PF02174 | 0.335 |
| LIG_SH2_CRK | 174 | 178 | PF00017 | 0.457 |
| LIG_SH2_CRK | 211 | 215 | PF00017 | 0.482 |
| LIG_SH2_CRK | 295 | 299 | PF00017 | 0.400 |
| LIG_SH2_CRK | 66 | 70 | PF00017 | 0.476 |
| LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.417 |
| LIG_SH3_3 | 194 | 200 | PF00018 | 0.441 |
| LIG_SH3_3 | 247 | 253 | PF00018 | 0.373 |
| LIG_SH3_3 | 26 | 32 | PF00018 | 0.522 |
| LIG_SUMO_SIM_anti_2 | 162 | 168 | PF11976 | 0.381 |
| LIG_SUMO_SIM_par_1 | 164 | 170 | PF11976 | 0.368 |
| LIG_SUMO_SIM_par_1 | 199 | 204 | PF11976 | 0.477 |
| LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.687 |
| LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.558 |
| MOD_CDK_SPxxK_3 | 86 | 93 | PF00069 | 0.759 |
| MOD_CK1_1 | 13 | 19 | PF00069 | 0.738 |
| MOD_CK1_1 | 159 | 165 | PF00069 | 0.449 |
| MOD_CK1_1 | 28 | 34 | PF00069 | 0.476 |
| MOD_CK1_1 | 334 | 340 | PF00069 | 0.355 |
| MOD_CK1_1 | 89 | 95 | PF00069 | 0.760 |
| MOD_CK2_1 | 210 | 216 | PF00069 | 0.469 |
| MOD_CK2_1 | 28 | 34 | PF00069 | 0.577 |
| MOD_CK2_1 | 338 | 344 | PF00069 | 0.319 |
| MOD_CK2_1 | 406 | 412 | PF00069 | 0.447 |
| MOD_CK2_1 | 417 | 423 | PF00069 | 0.497 |
| MOD_GlcNHglycan | 14 | 18 | PF01048 | 0.546 |
| MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.637 |
| MOD_GlcNHglycan | 61 | 65 | PF01048 | 0.301 |
| MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.587 |
| MOD_GSK3_1 | 135 | 142 | PF00069 | 0.641 |
| MOD_GSK3_1 | 255 | 262 | PF00069 | 0.339 |
| MOD_GSK3_1 | 285 | 292 | PF00069 | 0.408 |
| MOD_GSK3_1 | 331 | 338 | PF00069 | 0.382 |
| MOD_GSK3_1 | 417 | 424 | PF00069 | 0.381 |
| MOD_GSK3_1 | 74 | 81 | PF00069 | 0.695 |
| MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.452 |
| MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.607 |
| MOD_N-GLC_1 | 349 | 354 | PF02516 | 0.544 |
| MOD_NEK2_1 | 2 | 7 | PF00069 | 0.778 |
| MOD_NEK2_1 | 368 | 373 | PF00069 | 0.451 |
| MOD_NEK2_2 | 421 | 426 | PF00069 | 0.562 |
| MOD_PIKK_1 | 234 | 240 | PF00454 | 0.436 |
| MOD_PKA_1 | 135 | 141 | PF00069 | 0.690 |
| MOD_PKA_1 | 234 | 240 | PF00069 | 0.436 |
| MOD_PKA_1 | 259 | 265 | PF00069 | 0.285 |
| MOD_PKA_1 | 7 | 13 | PF00069 | 0.632 |
| MOD_PKA_2 | 135 | 141 | PF00069 | 0.645 |
| MOD_PKA_2 | 2 | 8 | PF00069 | 0.753 |
| MOD_PKA_2 | 234 | 240 | PF00069 | 0.436 |
| MOD_PKA_2 | 264 | 270 | PF00069 | 0.380 |
| MOD_PKA_2 | 73 | 79 | PF00069 | 0.637 |
| MOD_PKB_1 | 133 | 141 | PF00069 | 0.667 |
| MOD_PKB_1 | 226 | 234 | PF00069 | 0.486 |
| MOD_Plk_1 | 203 | 209 | PF00069 | 0.453 |
| MOD_Plk_1 | 228 | 234 | PF00069 | 0.488 |
| MOD_Plk_4 | 159 | 165 | PF00069 | 0.459 |
| MOD_Plk_4 | 318 | 324 | PF00069 | 0.375 |
| MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.523 |
| MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.335 |
| MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.390 |
| MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.505 |
| MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.818 |
| MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.731 |
| TRG_DiLeu_BaEn_2 | 138 | 144 | PF01217 | 0.660 |
| TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.527 |
| TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.362 |
| TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.501 |
| TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.366 |
| TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.372 |
| TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.476 |
| TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.429 |
| TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.792 |
| TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.445 |
| TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.418 |
| TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.794 |
| TRG_Pf-PMV_PEXEL_1 | 179 | 183 | PF00026 | 0.632 |
| TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.677 |
| TRG_Pf-PMV_PEXEL_1 | 364 | 369 | PF00026 | 0.577 |
| TRG_Pf-PMV_PEXEL_1 | 395 | 399 | PF00026 | 0.657 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P559 | Leptomonas seymouri | 66% | 99% |
| A0A0S4JM78 | Bodo saltans | 28% | 100% |
| A0A1X0P5J7 | Trypanosomatidae | 48% | 97% |
| A0A3Q8IJK4 | Leishmania donovani | 94% | 100% |
| A0A422MXB6 | Trypanosoma rangeli | 45% | 100% |
| A4HMX6 | Leishmania braziliensis | 80% | 100% |
| A4IBK0 | Leishmania infantum | 94% | 100% |
| C9ZZ44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
| E9B6I8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
| V5DUR2 | Trypanosoma cruzi | 43% | 100% |