| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 2 |
| Forrest at al. (procyclic) | no | yes: 2 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | no | yes: 12 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 5 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | yes | yes: 5 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
| GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7WVP4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 1 |
| GO:0006457 | protein folding | 2 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
| GO:0018208 | peptidyl-proline modification | 6 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0036211 | protein modification process | 4 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043412 | macromolecule modification | 4 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 12 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0016853 | isomerase activity | 2 | 12 |
| GO:0016859 | cis-trans isomerase activity | 3 | 12 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 292 | 296 | PF00656 | 0.513 |
| CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.383 |
| CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.335 |
| CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.332 |
| CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.333 |
| CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.359 |
| CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.369 |
| CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.345 |
| CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.318 |
| CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.369 |
| CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.473 |
| CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.281 |
| CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.319 |
| CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.197 |
| CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.191 |
| CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.375 |
| CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.395 |
| CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.319 |
| DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.568 |
| DOC_MAPK_gen_1 | 153 | 161 | PF00069 | 0.461 |
| DOC_MAPK_gen_1 | 307 | 315 | PF00069 | 0.300 |
| DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.401 |
| DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.383 |
| DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.553 |
| DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.469 |
| DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.270 |
| DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.281 |
| DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.247 |
| DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.540 |
| LIG_14-3-3_CanoR_1 | 271 | 276 | PF00244 | 0.457 |
| LIG_14-3-3_CanoR_1 | 359 | 365 | PF00244 | 0.378 |
| LIG_14-3-3_CanoR_1 | 4 | 13 | PF00244 | 0.707 |
| LIG_Actin_WH2_2 | 375 | 392 | PF00022 | 0.191 |
| LIG_Actin_WH2_2 | 96 | 114 | PF00022 | 0.281 |
| LIG_APCC_ABBA_1 | 214 | 219 | PF00400 | 0.303 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.616 |
| LIG_BIR_III_2 | 242 | 246 | PF00653 | 0.480 |
| LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.391 |
| LIG_Clathr_ClatBox_1 | 135 | 139 | PF01394 | 0.281 |
| LIG_EH1_1 | 61 | 69 | PF00400 | 0.319 |
| LIG_FHA_1 | 100 | 106 | PF00498 | 0.220 |
| LIG_FHA_1 | 142 | 148 | PF00498 | 0.420 |
| LIG_FHA_1 | 176 | 182 | PF00498 | 0.355 |
| LIG_FHA_1 | 259 | 265 | PF00498 | 0.327 |
| LIG_FHA_1 | 367 | 373 | PF00498 | 0.391 |
| LIG_FHA_1 | 391 | 397 | PF00498 | 0.354 |
| LIG_FHA_1 | 41 | 47 | PF00498 | 0.374 |
| LIG_FHA_2 | 199 | 205 | PF00498 | 0.486 |
| LIG_FHA_2 | 64 | 70 | PF00498 | 0.377 |
| LIG_Integrin_RGD_1 | 79 | 81 | PF01839 | 0.391 |
| LIG_LIR_Apic_2 | 167 | 171 | PF02991 | 0.392 |
| LIG_LIR_Apic_2 | 246 | 250 | PF02991 | 0.415 |
| LIG_LIR_Gen_1 | 274 | 283 | PF02991 | 0.434 |
| LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.581 |
| LIG_LIR_Nem_3 | 204 | 208 | PF02991 | 0.424 |
| LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.450 |
| LIG_Pex14_2 | 427 | 431 | PF04695 | 0.521 |
| LIG_PTB_Apo_2 | 167 | 174 | PF02174 | 0.482 |
| LIG_SH2_CRK | 196 | 200 | PF00017 | 0.570 |
| LIG_SH2_CRK | 275 | 279 | PF00017 | 0.324 |
| LIG_SH2_CRK | 41 | 45 | PF00017 | 0.371 |
| LIG_SH2_GRB2like | 168 | 171 | PF00017 | 0.422 |
| LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.377 |
| LIG_SH2_SRC | 117 | 120 | PF00017 | 0.391 |
| LIG_SH2_SRC | 168 | 171 | PF00017 | 0.422 |
| LIG_SH2_SRC | 351 | 354 | PF00017 | 0.214 |
| LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.373 |
| LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.390 |
| LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.515 |
| LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.358 |
| LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.262 |
| LIG_SH3_3 | 123 | 129 | PF00018 | 0.247 |
| LIG_SH3_3 | 20 | 26 | PF00018 | 0.443 |
| LIG_SH3_3 | 28 | 34 | PF00018 | 0.375 |
| LIG_SUMO_SIM_par_1 | 261 | 268 | PF11976 | 0.368 |
| LIG_SUMO_SIM_par_1 | 360 | 367 | PF11976 | 0.327 |
| LIG_SUMO_SIM_par_1 | 393 | 399 | PF11976 | 0.307 |
| LIG_SUMO_SIM_par_1 | 42 | 47 | PF11976 | 0.445 |
| LIG_UBA3_1 | 158 | 163 | PF00899 | 0.462 |
| LIG_UBA3_1 | 372 | 377 | PF00899 | 0.391 |
| MOD_CDK_SPxK_1 | 194 | 200 | PF00069 | 0.536 |
| MOD_CK1_1 | 124 | 130 | PF00069 | 0.343 |
| MOD_CK1_1 | 175 | 181 | PF00069 | 0.427 |
| MOD_CK1_1 | 267 | 273 | PF00069 | 0.468 |
| MOD_CK1_1 | 363 | 369 | PF00069 | 0.272 |
| MOD_CK1_1 | 8 | 14 | PF00069 | 0.574 |
| MOD_CK2_1 | 248 | 254 | PF00069 | 0.348 |
| MOD_GlcNHglycan | 148 | 152 | PF01048 | 0.395 |
| MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.386 |
| MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.409 |
| MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.486 |
| MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.467 |
| MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.651 |
| MOD_GSK3_1 | 153 | 160 | PF00069 | 0.446 |
| MOD_GSK3_1 | 194 | 201 | PF00069 | 0.589 |
| MOD_GSK3_1 | 267 | 274 | PF00069 | 0.415 |
| MOD_GSK3_1 | 351 | 358 | PF00069 | 0.345 |
| MOD_GSK3_1 | 360 | 367 | PF00069 | 0.348 |
| MOD_GSK3_1 | 4 | 11 | PF00069 | 0.582 |
| MOD_GSK3_1 | 68 | 75 | PF00069 | 0.256 |
| MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.247 |
| MOD_NEK2_1 | 157 | 162 | PF00069 | 0.520 |
| MOD_NEK2_1 | 173 | 178 | PF00069 | 0.409 |
| MOD_NEK2_1 | 322 | 327 | PF00069 | 0.451 |
| MOD_NEK2_1 | 364 | 369 | PF00069 | 0.191 |
| MOD_NEK2_1 | 40 | 45 | PF00069 | 0.324 |
| MOD_NEK2_1 | 68 | 73 | PF00069 | 0.355 |
| MOD_NEK2_1 | 83 | 88 | PF00069 | 0.161 |
| MOD_NEK2_2 | 57 | 62 | PF00069 | 0.331 |
| MOD_NEK2_2 | 99 | 104 | PF00069 | 0.281 |
| MOD_PIKK_1 | 14 | 20 | PF00454 | 0.531 |
| MOD_PIKK_1 | 48 | 54 | PF00454 | 0.425 |
| MOD_PKA_1 | 227 | 233 | PF00069 | 0.421 |
| MOD_PKA_1 | 289 | 295 | PF00069 | 0.404 |
| MOD_PKA_2 | 227 | 233 | PF00069 | 0.336 |
| MOD_Plk_1 | 130 | 136 | PF00069 | 0.247 |
| MOD_Plk_1 | 153 | 159 | PF00069 | 0.323 |
| MOD_Plk_1 | 173 | 179 | PF00069 | 0.329 |
| MOD_Plk_1 | 258 | 264 | PF00069 | 0.397 |
| MOD_Plk_1 | 267 | 273 | PF00069 | 0.294 |
| MOD_Plk_1 | 322 | 328 | PF00069 | 0.485 |
| MOD_Plk_1 | 83 | 89 | PF00069 | 0.271 |
| MOD_Plk_4 | 130 | 136 | PF00069 | 0.300 |
| MOD_Plk_4 | 153 | 159 | PF00069 | 0.334 |
| MOD_Plk_4 | 258 | 264 | PF00069 | 0.331 |
| MOD_Plk_4 | 40 | 46 | PF00069 | 0.325 |
| MOD_Plk_4 | 422 | 428 | PF00069 | 0.521 |
| MOD_Plk_4 | 63 | 69 | PF00069 | 0.383 |
| MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.281 |
| MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.247 |
| MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.533 |
| MOD_SUMO_for_1 | 326 | 329 | PF00179 | 0.500 |
| MOD_SUMO_rev_2 | 276 | 284 | PF00179 | 0.332 |
| TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.408 |
| TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.393 |
| TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.365 |
| TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.384 |
| TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.318 |
| TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.449 |
| TRG_ER_diLys_1 | 428 | 432 | PF00400 | 0.488 |
| TRG_NES_CRM1_1 | 387 | 399 | PF08389 | 0.318 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PDU7 | Leptomonas seymouri | 74% | 100% |
| A0A0S4IT01 | Bodo saltans | 45% | 100% |
| A0A1X0P656 | Trypanosomatidae | 51% | 100% |
| A0A3R7L7K6 | Trypanosoma rangeli | 54% | 100% |
| A4HAA2 | Leishmania braziliensis | 87% | 100% |
| A4HYI1 | Leishmania infantum | 100% | 100% |
| D0A0V5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
| E9ASA6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
| P27124 | Oryctolagus cuniculus | 33% | 94% |
| P30416 | Mus musculus | 33% | 94% |
| Q02790 | Homo sapiens | 32% | 94% |
| Q13451 | Homo sapiens | 31% | 95% |
| Q38931 | Arabidopsis thaliana | 30% | 78% |
| Q43207 | Triticum aestivum | 30% | 77% |
| Q4QD56 | Leishmania major | 96% | 100% |
| Q5RF88 | Pongo abelii | 31% | 95% |
| Q64378 | Mus musculus | 32% | 95% |
| Q7DMA9 | Arabidopsis thaliana | 24% | 68% |
| Q95L05 | Chlorocebus aethiops | 31% | 95% |
| Q9FJL3 | Arabidopsis thaliana | 29% | 75% |
| Q9QVC8 | Rattus norvegicus | 32% | 94% |
| Q9TRY0 | Bos taurus | 33% | 94% |
| Q9VL78 | Drosophila melanogaster | 31% | 98% |
| Q9XSH5 | Saimiri boliviensis boliviensis | 30% | 95% |
| Q9XSI2 | Saguinus oedipus | 31% | 95% |
| Q9XT11 | Aotus nancymaae | 30% | 95% |
| V5AP12 | Trypanosoma cruzi | 50% | 90% |