| 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 | 10 | 
| GO:0110165 | cellular anatomical entity | 1 | 10 | 
Related structures:
AlphaFold database: Q4QGW4
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006810 | transport | 3 | 2 | 
| GO:0006839 | mitochondrial transport | 4 | 2 | 
| GO:0006886 | intracellular protein transport | 4 | 2 | 
| GO:0006996 | organelle organization | 4 | 2 | 
| GO:0007005 | mitochondrion organization | 5 | 2 | 
| GO:0007006 | mitochondrial membrane organization | 5 | 2 | 
| GO:0008104 | protein localization | 4 | 2 | 
| GO:0009987 | cellular process | 1 | 2 | 
| GO:0015031 | protein transport | 4 | 2 | 
| GO:0016043 | cellular component organization | 3 | 2 | 
| GO:0032978 | protein insertion into membrane from inner side | 6 | 2 | 
| GO:0032979 | protein insertion into mitochondrial inner membrane from matrix | 5 | 2 | 
| GO:0033036 | macromolecule localization | 2 | 2 | 
| GO:0033365 | protein localization to organelle | 5 | 2 | 
| GO:0045184 | establishment of protein localization | 3 | 2 | 
| GO:0046907 | intracellular transport | 3 | 2 | 
| GO:0051179 | localization | 1 | 2 | 
| GO:0051205 | protein insertion into membrane | 5 | 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:0061024 | membrane organization | 4 | 2 | 
| GO:0070585 | protein localization to mitochondrion | 6 | 2 | 
| GO:0070727 | cellular macromolecule localization | 3 | 2 | 
| GO:0071702 | organic substance transport | 4 | 2 | 
| GO:0071705 | nitrogen compound transport | 4 | 2 | 
| GO:0071840 | cellular component organization or biogenesis | 2 | 2 | 
| GO:0072594 | establishment of protein localization to organelle | 4 | 2 | 
| GO:0072655 | establishment of protein localization to mitochondrion | 5 | 2 | 
| GO:0072657 | protein localization to membrane | 4 | 2 | 
| GO:0090150 | establishment of protein localization to membrane | 4 | 2 | 
| GO:0090151 | establishment of protein localization to mitochondrial membrane | 4 | 2 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0032977 | membrane insertase activity | 3 | 12 | 
| GO:0140104 | molecular carrier activity | 1 | 12 | 
| GO:0140597 | protein carrier chaperone | 2 | 12 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.734 | 
| CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.476 | 
| CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.713 | 
| CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.406 | 
| CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.276 | 
| CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.734 | 
| CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.476 | 
| CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.713 | 
| CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.276 | 
| CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.350 | 
| CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.276 | 
| CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.276 | 
| CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.276 | 
| CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.501 | 
| CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.354 | 
| CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.568 | 
| CLV_Separin_Metazoa | 106 | 110 | PF03568 | 0.367 | 
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.525 | 
| DOC_CDC14_PxL_1 | 138 | 146 | PF14671 | 0.386 | 
| DOC_CDC14_PxL_1 | 233 | 241 | PF14671 | 0.287 | 
| DOC_CYCLIN_RxL_1 | 133 | 143 | PF00134 | 0.449 | 
| DOC_CYCLIN_yCln2_LP_2 | 211 | 217 | PF00134 | 0.372 | 
| DOC_CYCLIN_yCln2_LP_2 | 317 | 323 | PF00134 | 0.344 | 
| DOC_MAPK_FxFP_2 | 332 | 335 | PF00069 | 0.564 | 
| DOC_MAPK_gen_1 | 109 | 119 | PF00069 | 0.394 | 
| DOC_MAPK_gen_1 | 19 | 29 | PF00069 | 0.502 | 
| DOC_MAPK_gen_1 | 273 | 283 | PF00069 | 0.476 | 
| DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.501 | 
| DOC_MAPK_MEF2A_6 | 288 | 297 | PF00069 | 0.386 | 
| DOC_PP1_RVXF_1 | 34 | 41 | PF00149 | 0.443 | 
| DOC_PP2B_LxvP_1 | 211 | 214 | PF13499 | 0.372 | 
| DOC_PP2B_LxvP_1 | 244 | 247 | PF13499 | 0.276 | 
| DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.553 | 
| DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.364 | 
| DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.642 | 
| DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.378 | 
| DOC_USP7_UBL2_3 | 181 | 185 | PF12436 | 0.476 | 
| LIG_14-3-3_CanoR_1 | 136 | 141 | PF00244 | 0.322 | 
| LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.456 | 
| LIG_14-3-3_CanoR_1 | 174 | 184 | PF00244 | 0.490 | 
| LIG_14-3-3_CanoR_1 | 22 | 29 | PF00244 | 0.527 | 
| LIG_14-3-3_CanoR_1 | 273 | 283 | PF00244 | 0.476 | 
| LIG_14-3-3_CanoR_1 | 288 | 293 | PF00244 | 0.329 | 
| LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.395 | 
| LIG_14-3-3_CanoR_1 | 376 | 384 | PF00244 | 0.693 | 
| LIG_AP2alpha_1 | 328 | 332 | PF02296 | 0.567 | 
| LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.287 | 
| LIG_Clathr_ClatBox_1 | 262 | 266 | PF01394 | 0.363 | 
| LIG_deltaCOP1_diTrp_1 | 88 | 97 | PF00928 | 0.359 | 
| LIG_EVH1_1 | 334 | 338 | PF00568 | 0.557 | 
| LIG_FHA_1 | 210 | 216 | PF00498 | 0.329 | 
| LIG_FHA_1 | 248 | 254 | PF00498 | 0.276 | 
| LIG_FHA_1 | 312 | 318 | PF00498 | 0.344 | 
| LIG_FHA_2 | 229 | 235 | PF00498 | 0.292 | 
| LIG_FHA_2 | 243 | 249 | PF00498 | 0.241 | 
| LIG_FHA_2 | 359 | 365 | PF00498 | 0.630 | 
| LIG_FHA_2 | 384 | 390 | PF00498 | 0.673 | 
| LIG_FHA_2 | 69 | 75 | PF00498 | 0.488 | 
| LIG_LIR_Apic_2 | 248 | 254 | PF02991 | 0.276 | 
| LIG_LIR_Apic_2 | 330 | 335 | PF02991 | 0.567 | 
| LIG_LIR_Apic_2 | 74 | 79 | PF02991 | 0.427 | 
| LIG_LIR_Apic_2 | 96 | 100 | PF02991 | 0.376 | 
| LIG_LIR_Gen_1 | 114 | 121 | PF02991 | 0.463 | 
| LIG_LIR_Gen_1 | 186 | 195 | PF02991 | 0.487 | 
| LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.367 | 
| LIG_LIR_Gen_1 | 353 | 360 | PF02991 | 0.652 | 
| LIG_LIR_Gen_1 | 389 | 398 | PF02991 | 0.642 | 
| LIG_LIR_Gen_1 | 8 | 13 | PF02991 | 0.508 | 
| LIG_LIR_Gen_1 | 82 | 90 | PF02991 | 0.353 | 
| LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.419 | 
| LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.539 | 
| LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.228 | 
| LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.568 | 
| LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.656 | 
| LIG_LIR_Nem_3 | 389 | 393 | PF02991 | 0.630 | 
| LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.517 | 
| LIG_LIR_Nem_3 | 8 | 12 | PF02991 | 0.506 | 
| LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.355 | 
| LIG_NRP_CendR_1 | 406 | 407 | PF00754 | 0.611 | 
| LIG_Pex14_1 | 124 | 128 | PF04695 | 0.276 | 
| LIG_Pex14_1 | 93 | 97 | PF04695 | 0.361 | 
| LIG_Pex14_2 | 261 | 265 | PF04695 | 0.329 | 
| LIG_Pex14_2 | 328 | 332 | PF04695 | 0.542 | 
| LIG_SH2_CRK | 251 | 255 | PF00017 | 0.363 | 
| LIG_SH2_NCK_1 | 251 | 255 | PF00017 | 0.476 | 
| LIG_SH2_NCK_1 | 390 | 394 | PF00017 | 0.685 | 
| LIG_SH2_PTP2 | 76 | 79 | PF00017 | 0.485 | 
| LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.276 | 
| LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.657 | 
| LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.622 | 
| LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.411 | 
| LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.476 | 
| LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.328 | 
| LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.485 | 
| LIG_SH3_3 | 332 | 338 | PF00018 | 0.559 | 
| LIG_SxIP_EBH_1 | 134 | 148 | PF03271 | 0.363 | 
| LIG_TRAF2_1 | 360 | 363 | PF00917 | 0.551 | 
| LIG_UBA3_1 | 345 | 350 | PF00899 | 0.631 | 
| LIG_WRC_WIRS_1 | 116 | 121 | PF05994 | 0.401 | 
| MOD_CK1_1 | 143 | 149 | PF00069 | 0.476 | 
| MOD_CK1_1 | 161 | 167 | PF00069 | 0.431 | 
| MOD_CK1_1 | 206 | 212 | PF00069 | 0.347 | 
| MOD_CK1_1 | 68 | 74 | PF00069 | 0.504 | 
| MOD_CK2_1 | 174 | 180 | PF00069 | 0.469 | 
| MOD_CK2_1 | 228 | 234 | PF00069 | 0.278 | 
| MOD_CK2_1 | 350 | 356 | PF00069 | 0.568 | 
| MOD_CK2_1 | 358 | 364 | PF00069 | 0.571 | 
| MOD_CK2_1 | 79 | 85 | PF00069 | 0.370 | 
| MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.317 | 
| MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.756 | 
| MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.329 | 
| MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.713 | 
| MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.305 | 
| MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.490 | 
| MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.508 | 
| MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.559 | 
| MOD_GSK3_1 | 136 | 143 | PF00069 | 0.329 | 
| MOD_GSK3_1 | 17 | 24 | PF00069 | 0.487 | 
| MOD_GSK3_1 | 199 | 206 | PF00069 | 0.506 | 
| MOD_GSK3_1 | 209 | 216 | PF00069 | 0.292 | 
| MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.289 | 
| MOD_NEK2_1 | 207 | 212 | PF00069 | 0.384 | 
| MOD_NEK2_2 | 219 | 224 | PF00069 | 0.329 | 
| MOD_NEK2_2 | 79 | 84 | PF00069 | 0.392 | 
| MOD_PIKK_1 | 199 | 205 | PF00454 | 0.516 | 
| MOD_PIKK_1 | 358 | 364 | PF00454 | 0.640 | 
| MOD_PIKK_1 | 65 | 71 | PF00454 | 0.365 | 
| MOD_PK_1 | 288 | 294 | PF00069 | 0.406 | 
| MOD_PKA_1 | 36 | 42 | PF00069 | 0.439 | 
| MOD_PKA_2 | 147 | 153 | PF00069 | 0.510 | 
| MOD_PKA_2 | 21 | 27 | PF00069 | 0.530 | 
| MOD_PKA_2 | 287 | 293 | PF00069 | 0.414 | 
| MOD_PKA_2 | 36 | 42 | PF00069 | 0.502 | 
| MOD_PKA_2 | 400 | 406 | PF00069 | 0.615 | 
| MOD_Plk_1 | 172 | 178 | PF00069 | 0.476 | 
| MOD_Plk_1 | 199 | 205 | PF00069 | 0.489 | 
| MOD_Plk_1 | 242 | 248 | PF00069 | 0.281 | 
| MOD_Plk_1 | 363 | 369 | PF00069 | 0.684 | 
| MOD_Plk_1 | 79 | 85 | PF00069 | 0.380 | 
| MOD_Plk_4 | 136 | 142 | PF00069 | 0.335 | 
| MOD_Plk_4 | 203 | 209 | PF00069 | 0.489 | 
| MOD_Plk_4 | 288 | 294 | PF00069 | 0.362 | 
| MOD_Plk_4 | 350 | 356 | PF00069 | 0.573 | 
| MOD_Plk_4 | 383 | 389 | PF00069 | 0.533 | 
| MOD_Plk_4 | 79 | 85 | PF00069 | 0.387 | 
| MOD_Plk_4 | 93 | 99 | PF00069 | 0.342 | 
| MOD_SUMO_rev_2 | 343 | 352 | PF00179 | 0.640 | 
| TRG_DiLeu_BaEn_2 | 233 | 239 | PF01217 | 0.276 | 
| TRG_DiLeu_BaEn_4 | 363 | 369 | PF01217 | 0.630 | 
| TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.487 | 
| TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.656 | 
| TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.623 | 
| TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.545 | 
| TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.276 | 
| TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.528 | 
| TRG_Pf-PMV_PEXEL_1 | 109 | 114 | PF00026 | 0.569 | 
| TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.287 | 
| TRG_Pf-PMV_PEXEL_1 | 81 | 85 | PF00026 | 0.653 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P2Y9 | Leptomonas seymouri | 84% | 90% | 
| A0A0S4IZY1 | Bodo saltans | 60% | 93% | 
| A0A1X0NWK5 | Trypanosomatidae | 70% | 100% | 
| A0A3R7NUU3 | Trypanosoma rangeli | 71% | 91% | 
| A0A3S7WRQ0 | Leishmania donovani | 97% | 92% | 
| A4H6P4 | Leishmania braziliensis | 89% | 100% | 
| A4HV25 | Leishmania infantum | 97% | 92% | 
| D0A7C4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 97% | 
| E9ANQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 91% | 
| V5C1D0 | Trypanosoma cruzi | 74% | 95% |