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% |