| 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. | yes | yes: 25 |
| 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: 8 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 8 |
| NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q6WRI4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006082 | organic acid metabolic process | 3 | 5 |
| GO:0006520 | amino acid metabolic process | 3 | 5 |
| GO:0006558 | L-phenylalanine metabolic process | 5 | 2 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
| GO:0008152 | metabolic process | 1 | 5 |
| GO:0009072 | aromatic amino acid metabolic process | 4 | 5 |
| GO:0009987 | cellular process | 1 | 5 |
| GO:0019752 | carboxylic acid metabolic process | 5 | 5 |
| GO:0043436 | oxoacid metabolic process | 4 | 5 |
| GO:0044237 | cellular metabolic process | 2 | 5 |
| GO:0044238 | primary metabolic process | 2 | 5 |
| GO:0044281 | small molecule metabolic process | 2 | 5 |
| GO:0071704 | organic substance metabolic process | 2 | 5 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
| GO:1901605 | alpha-amino acid metabolic process | 4 | 2 |
| GO:1902221 | erythrose 4-phosphate/phosphoenolpyruvate family amino acid metabolic process | 5 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 9 |
| GO:0004497 | monooxygenase activity | 3 | 9 |
| GO:0004505 | phenylalanine 4-monooxygenase activity | 5 | 6 |
| GO:0005488 | binding | 1 | 9 |
| GO:0005506 | iron ion binding | 6 | 9 |
| GO:0016491 | oxidoreductase activity | 2 | 9 |
| GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 9 |
| GO:0016714 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen | 4 | 9 |
| GO:0043167 | ion binding | 2 | 9 |
| GO:0043169 | cation binding | 3 | 9 |
| GO:0046872 | metal ion binding | 4 | 9 |
| GO:0046914 | transition metal ion binding | 5 | 9 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.447 |
| CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.249 |
| CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.298 |
| CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.298 |
| CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.288 |
| CLV_PCSK_FUR_1 | 165 | 169 | PF00082 | 0.314 |
| CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.249 |
| CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.298 |
| CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.291 |
| CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.631 |
| CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.546 |
| CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.268 |
| CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.223 |
| CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.314 |
| CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.552 |
| CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.350 |
| DEG_APCC_DBOX_1 | 261 | 269 | PF00400 | 0.514 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.573 |
| DOC_CDC14_PxL_1 | 298 | 306 | PF14671 | 0.514 |
| DOC_CKS1_1 | 286 | 291 | PF01111 | 0.447 |
| DOC_MAPK_gen_1 | 165 | 174 | PF00069 | 0.554 |
| DOC_MAPK_gen_1 | 176 | 186 | PF00069 | 0.465 |
| DOC_MAPK_gen_1 | 36 | 46 | PF00069 | 0.412 |
| DOC_MAPK_MEF2A_6 | 39 | 48 | PF00069 | 0.383 |
| DOC_PP1_RVXF_1 | 331 | 337 | PF00149 | 0.447 |
| DOC_USP7_UBL2_3 | 32 | 36 | PF12436 | 0.604 |
| DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.400 |
| DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.449 |
| DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.447 |
| DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.514 |
| LIG_14-3-3_CanoR_1 | 195 | 200 | PF00244 | 0.514 |
| LIG_14-3-3_CanoR_1 | 271 | 279 | PF00244 | 0.447 |
| LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.386 |
| LIG_14-3-3_CanoR_1 | 429 | 435 | PF00244 | 0.510 |
| LIG_14-3-3_CterR_2 | 448 | 453 | PF00244 | 0.593 |
| LIG_APCC_ABBAyCdc20_2 | 4 | 10 | PF00400 | 0.503 |
| LIG_BRCT_BRCA1_1 | 260 | 264 | PF00533 | 0.447 |
| LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.471 |
| LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.528 |
| LIG_eIF4E_1 | 218 | 224 | PF01652 | 0.514 |
| LIG_FHA_1 | 232 | 238 | PF00498 | 0.518 |
| LIG_FHA_1 | 254 | 260 | PF00498 | 0.466 |
| LIG_FHA_1 | 274 | 280 | PF00498 | 0.355 |
| LIG_FHA_1 | 311 | 317 | PF00498 | 0.514 |
| LIG_FHA_1 | 86 | 92 | PF00498 | 0.437 |
| LIG_FHA_2 | 188 | 194 | PF00498 | 0.447 |
| LIG_FHA_2 | 258 | 264 | PF00498 | 0.514 |
| LIG_LIR_Apic_2 | 119 | 125 | PF02991 | 0.363 |
| LIG_LIR_Gen_1 | 198 | 209 | PF02991 | 0.455 |
| LIG_LIR_Gen_1 | 306 | 316 | PF02991 | 0.451 |
| LIG_LIR_Gen_1 | 438 | 446 | PF02991 | 0.511 |
| LIG_LIR_Gen_1 | 88 | 97 | PF02991 | 0.412 |
| LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.455 |
| LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.451 |
| LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.398 |
| LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.449 |
| LIG_LIR_Nem_3 | 438 | 442 | PF02991 | 0.398 |
| LIG_LIR_Nem_3 | 61 | 66 | PF02991 | 0.380 |
| LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.404 |
| LIG_NRBOX | 55 | 61 | PF00104 | 0.369 |
| LIG_PCNA_yPIPBox_3 | 406 | 418 | PF02747 | 0.482 |
| LIG_PDZ_Class_2 | 448 | 453 | PF00595 | 0.593 |
| LIG_Pex14_1 | 197 | 201 | PF04695 | 0.514 |
| LIG_SH2_CRK | 216 | 220 | PF00017 | 0.514 |
| LIG_SH2_CRK | 24 | 28 | PF00017 | 0.405 |
| LIG_SH2_CRK | 392 | 396 | PF00017 | 0.398 |
| LIG_SH2_GRB2like | 80 | 83 | PF00017 | 0.608 |
| LIG_SH2_NCK_1 | 24 | 28 | PF00017 | 0.405 |
| LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.514 |
| LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.471 |
| LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.447 |
| LIG_SH2_STAP1 | 427 | 431 | PF00017 | 0.447 |
| LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.398 |
| LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.478 |
| LIG_SH2_STAT3 | 274 | 277 | PF00017 | 0.471 |
| LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.447 |
| LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.514 |
| LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.447 |
| LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.447 |
| LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.447 |
| LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.494 |
| LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.408 |
| LIG_SH3_3 | 122 | 128 | PF00018 | 0.316 |
| LIG_SH3_3 | 149 | 155 | PF00018 | 0.453 |
| LIG_SH3_3 | 373 | 379 | PF00018 | 0.447 |
| LIG_SH3_3 | 59 | 65 | PF00018 | 0.401 |
| LIG_SUMO_SIM_par_1 | 220 | 225 | PF11976 | 0.501 |
| LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.514 |
| LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.447 |
| LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.501 |
| LIG_TYR_ITIM | 199 | 204 | PF00017 | 0.501 |
| LIG_UBA3_1 | 327 | 333 | PF00899 | 0.514 |
| LIG_WRPW_2 | 63 | 66 | PF00400 | 0.363 |
| MOD_CDK_SPxxK_3 | 231 | 238 | PF00069 | 0.449 |
| MOD_CK1_1 | 26 | 32 | PF00069 | 0.469 |
| MOD_CK1_1 | 47 | 53 | PF00069 | 0.548 |
| MOD_CK2_1 | 187 | 193 | PF00069 | 0.447 |
| MOD_CK2_1 | 357 | 363 | PF00069 | 0.447 |
| MOD_CK2_1 | 411 | 417 | PF00069 | 0.501 |
| MOD_Cter_Amidation | 347 | 350 | PF01082 | 0.298 |
| MOD_GSK3_1 | 227 | 234 | PF00069 | 0.477 |
| MOD_GSK3_1 | 253 | 260 | PF00069 | 0.514 |
| MOD_GSK3_1 | 317 | 324 | PF00069 | 0.471 |
| MOD_GSK3_1 | 35 | 42 | PF00069 | 0.487 |
| MOD_GSK3_1 | 419 | 426 | PF00069 | 0.456 |
| MOD_GSK3_1 | 64 | 71 | PF00069 | 0.562 |
| MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.271 |
| MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.249 |
| MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.388 |
| MOD_NEK2_1 | 137 | 142 | PF00069 | 0.447 |
| MOD_NEK2_1 | 2 | 7 | PF00069 | 0.509 |
| MOD_NEK2_1 | 229 | 234 | PF00069 | 0.485 |
| MOD_NEK2_1 | 273 | 278 | PF00069 | 0.457 |
| MOD_NEK2_1 | 312 | 317 | PF00069 | 0.514 |
| MOD_NEK2_1 | 44 | 49 | PF00069 | 0.422 |
| MOD_NEK2_1 | 446 | 451 | PF00069 | 0.573 |
| MOD_NEK2_2 | 16 | 21 | PF00069 | 0.547 |
| MOD_NEK2_2 | 419 | 424 | PF00069 | 0.514 |
| MOD_NEK2_2 | 85 | 90 | PF00069 | 0.485 |
| MOD_PIKK_1 | 273 | 279 | PF00454 | 0.447 |
| MOD_PIKK_1 | 310 | 316 | PF00454 | 0.514 |
| MOD_PIKK_1 | 412 | 418 | PF00454 | 0.501 |
| MOD_PIKK_1 | 68 | 74 | PF00454 | 0.506 |
| MOD_PK_1 | 64 | 70 | PF00069 | 0.472 |
| MOD_PKA_2 | 40 | 46 | PF00069 | 0.468 |
| MOD_Plk_1 | 137 | 143 | PF00069 | 0.447 |
| MOD_Plk_1 | 68 | 74 | PF00069 | 0.397 |
| MOD_Plk_1 | 98 | 104 | PF00069 | 0.579 |
| MOD_Plk_4 | 118 | 124 | PF00069 | 0.383 |
| MOD_Plk_4 | 419 | 425 | PF00069 | 0.571 |
| MOD_Plk_4 | 58 | 64 | PF00069 | 0.564 |
| MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.397 |
| MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.449 |
| MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.447 |
| MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.514 |
| MOD_SUMO_rev_2 | 29 | 38 | PF00179 | 0.577 |
| TRG_DiLeu_BaEn_1 | 55 | 60 | PF01217 | 0.445 |
| TRG_DiLeu_BaLyEn_6 | 218 | 223 | PF01217 | 0.514 |
| TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.514 |
| TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.489 |
| TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.395 |
| TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.398 |
| TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.514 |
| TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.566 |
| TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.488 |
| TRG_NES_CRM1_1 | 292 | 306 | PF08389 | 0.514 |
| TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.284 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A060X6Z0 | Oncorhynchus mykiss | 43% | 93% |
| A0A0N1HZV2 | Leptomonas seymouri | 82% | 100% |
| A0A0S4JDM5 | Bodo saltans | 56% | 100% |
| A0A3S5H7J2 | Leishmania donovani | 98% | 100% |
| A4HGH5 | Leishmania braziliensis | 91% | 100% |
| A4I3K7 | Leishmania infantum | 98% | 100% |
| A8X3V8 | Caenorhabditis briggsae | 45% | 88% |
| B6DT73 | Bodo saltans | 56% | 100% |
| E9AZU7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| O17446 | Schistosoma mansoni | 42% | 97% |
| O42091 | Anguilla anguilla | 43% | 93% |
| P00439 | Homo sapiens | 44% | 100% |
| P04176 | Rattus norvegicus | 44% | 100% |
| P04177 | Rattus norvegicus | 43% | 91% |
| P07101 | Homo sapiens | 42% | 86% |
| P09810 | Rattus norvegicus | 43% | 100% |
| P11982 | Phasianidae sp. | 43% | 92% |
| P16331 | Mus musculus | 44% | 100% |
| P17276 | Drosophila melanogaster | 43% | 100% |
| P17289 | Bos taurus | 42% | 92% |
| P17290 | Oryctolagus cuniculus | 43% | 100% |
| P17532 | Mus musculus | 44% | 100% |
| P17752 | Homo sapiens | 44% | 100% |
| P18459 | Drosophila melanogaster | 48% | 78% |
| P24529 | Mus musculus | 43% | 91% |
| P70080 | Gallus gallus | 44% | 100% |
| P90925 | Caenorhabditis elegans | 45% | 99% |
| P90986 | Caenorhabditis elegans | 46% | 87% |
| Q0EAB8 | Equus caballus | 47% | 92% |
| Q2HZ26 | Macaca mulatta | 47% | 92% |
| Q2KIH7 | Bos taurus | 45% | 100% |
| Q54XS1 | Dictyostelium discoideum | 47% | 100% |
| Q76IQ3 | Canis lupus familiaris | 41% | 92% |
| Q8CGU9 | Rattus norvegicus | 42% | 93% |
| Q8CGV2 | Mus musculus | 41% | 93% |
| Q8IWU9 | Homo sapiens | 47% | 92% |
| Q92142 | Xenopus laevis | 42% | 94% |