| 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: 8 |
| NetGPI | no | yes: 0, no: 8 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0016604 | nuclear body | 2 | 1 |
| GO:0031422 | RecQ family helicase-topoisomerase III complex | 3 | 1 |
| GO:0031974 | membrane-enclosed lumen | 2 | 1 |
| GO:0031981 | nuclear lumen | 5 | 1 |
| GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0043233 | organelle lumen | 3 | 1 |
| GO:0070013 | intracellular organelle lumen | 4 | 1 |
| GO:0097014 | ciliary plasm | 5 | 1 |
| GO:0099568 | cytoplasmic region | 3 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
| GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9AXQ8
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000712 | resolution of meiotic recombination intermediates | 4 | 1 |
| GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
| GO:0000725 | recombinational repair | 6 | 1 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
| GO:0006259 | DNA metabolic process | 4 | 1 |
| GO:0006281 | DNA repair | 5 | 1 |
| GO:0006302 | double-strand break repair | 6 | 1 |
| GO:0006310 | DNA recombination | 5 | 1 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0006950 | response to stress | 2 | 1 |
| GO:0006974 | DNA damage response | 4 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0022402 | cell cycle process | 2 | 1 |
| GO:0022414 | reproductive process | 1 | 1 |
| GO:0033554 | cellular response to stress | 3 | 1 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
| GO:0046483 | heterocycle metabolic process | 3 | 1 |
| GO:0050896 | response to stimulus | 1 | 1 |
| GO:0051716 | cellular response to stimulus | 2 | 1 |
| GO:0061982 | meiosis I cell cycle process | 3 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0090304 | nucleic acid metabolic process | 4 | 1 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
| GO:1903046 | meiotic cell cycle process | 2 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 1 |
| GO:0004518 | nuclease activity | 4 | 1 |
| GO:0004519 | endonuclease activity | 5 | 1 |
| GO:0016787 | hydrolase activity | 2 | 1 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.464 |
| CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.473 |
| CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.745 |
| CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.448 |
| CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.448 |
| CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.512 |
| DEG_ODPH_VHL_1 | 37 | 49 | PF01847 | 0.524 |
| DOC_ANK_TNKS_1 | 465 | 472 | PF00023 | 0.418 |
| DOC_CKS1_1 | 40 | 45 | PF01111 | 0.491 |
| DOC_CYCLIN_RxL_1 | 160 | 171 | PF00134 | 0.453 |
| DOC_CYCLIN_RxL_1 | 426 | 437 | PF00134 | 0.448 |
| DOC_MAPK_gen_1 | 96 | 104 | PF00069 | 0.495 |
| DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.665 |
| DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.538 |
| DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.715 |
| DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.541 |
| DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.543 |
| DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.386 |
| DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.538 |
| DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.528 |
| LIG_14-3-3_CanoR_1 | 111 | 118 | PF00244 | 0.463 |
| LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.499 |
| LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.445 |
| LIG_14-3-3_CanoR_1 | 461 | 465 | PF00244 | 0.537 |
| LIG_APCC_ABBA_1 | 245 | 250 | PF00400 | 0.516 |
| LIG_APCC_ABBAyCdc20_2 | 63 | 69 | PF00400 | 0.614 |
| LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.516 |
| LIG_CtBP_PxDLS_1 | 197 | 203 | PF00389 | 0.452 |
| LIG_FHA_1 | 207 | 213 | PF00498 | 0.495 |
| LIG_FHA_1 | 331 | 337 | PF00498 | 0.391 |
| LIG_FHA_1 | 365 | 371 | PF00498 | 0.473 |
| LIG_FHA_1 | 407 | 413 | PF00498 | 0.431 |
| LIG_FHA_1 | 42 | 48 | PF00498 | 0.499 |
| LIG_FHA_1 | 442 | 448 | PF00498 | 0.493 |
| LIG_FHA_1 | 77 | 83 | PF00498 | 0.348 |
| LIG_LIR_Gen_1 | 170 | 179 | PF02991 | 0.448 |
| LIG_LIR_Gen_1 | 367 | 374 | PF02991 | 0.366 |
| LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.448 |
| LIG_LIR_Nem_3 | 246 | 251 | PF02991 | 0.378 |
| LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.374 |
| LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.367 |
| LIG_MYND_1 | 35 | 39 | PF01753 | 0.552 |
| LIG_SH2_CRK | 190 | 194 | PF00017 | 0.488 |
| LIG_SH2_CRK | 368 | 372 | PF00017 | 0.447 |
| LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.447 |
| LIG_SH2_STAT3 | 272 | 275 | PF00017 | 0.493 |
| LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.619 |
| LIG_SH3_2 | 306 | 311 | PF14604 | 0.481 |
| LIG_SH3_3 | 151 | 157 | PF00018 | 0.516 |
| LIG_SH3_3 | 25 | 31 | PF00018 | 0.580 |
| LIG_SH3_3 | 279 | 285 | PF00018 | 0.536 |
| LIG_SH3_3 | 303 | 309 | PF00018 | 0.425 |
| LIG_SH3_3 | 319 | 325 | PF00018 | 0.337 |
| LIG_SH3_3 | 418 | 424 | PF00018 | 0.466 |
| LIG_SH3_3 | 476 | 482 | PF00018 | 0.440 |
| LIG_SUMO_SIM_anti_2 | 439 | 444 | PF11976 | 0.420 |
| LIG_SUMO_SIM_anti_2 | 79 | 84 | PF11976 | 0.495 |
| LIG_SUMO_SIM_par_1 | 175 | 181 | PF11976 | 0.474 |
| LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.477 |
| MOD_CDK_SPxxK_3 | 388 | 395 | PF00069 | 0.488 |
| MOD_CK1_1 | 106 | 112 | PF00069 | 0.587 |
| MOD_CK1_1 | 183 | 189 | PF00069 | 0.495 |
| MOD_CK1_1 | 55 | 61 | PF00069 | 0.732 |
| MOD_CK1_1 | 72 | 78 | PF00069 | 0.467 |
| MOD_CK2_1 | 431 | 437 | PF00069 | 0.478 |
| MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.295 |
| MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.315 |
| MOD_GlcNHglycan | 180 | 185 | PF01048 | 0.315 |
| MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.636 |
| MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.701 |
| MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.492 |
| MOD_GSK3_1 | 103 | 110 | PF00069 | 0.550 |
| MOD_GSK3_1 | 2 | 9 | PF00069 | 0.675 |
| MOD_GSK3_1 | 208 | 215 | PF00069 | 0.482 |
| MOD_GSK3_1 | 258 | 265 | PF00069 | 0.617 |
| MOD_GSK3_1 | 283 | 290 | PF00069 | 0.673 |
| MOD_GSK3_1 | 330 | 337 | PF00069 | 0.447 |
| MOD_GSK3_1 | 342 | 349 | PF00069 | 0.539 |
| MOD_GSK3_1 | 386 | 393 | PF00069 | 0.634 |
| MOD_GSK3_1 | 55 | 62 | PF00069 | 0.739 |
| MOD_GSK3_1 | 68 | 75 | PF00069 | 0.496 |
| MOD_NEK2_1 | 103 | 108 | PF00069 | 0.495 |
| MOD_NEK2_1 | 208 | 213 | PF00069 | 0.456 |
| MOD_NEK2_1 | 257 | 262 | PF00069 | 0.586 |
| MOD_NEK2_1 | 287 | 292 | PF00069 | 0.632 |
| MOD_NEK2_1 | 366 | 371 | PF00069 | 0.435 |
| MOD_NEK2_1 | 431 | 436 | PF00069 | 0.426 |
| MOD_PIKK_1 | 381 | 387 | PF00454 | 0.538 |
| MOD_PIKK_1 | 55 | 61 | PF00454 | 0.615 |
| MOD_PKA_2 | 110 | 116 | PF00069 | 0.550 |
| MOD_PKA_2 | 155 | 161 | PF00069 | 0.474 |
| MOD_PKA_2 | 206 | 212 | PF00069 | 0.499 |
| MOD_PKA_2 | 262 | 268 | PF00069 | 0.654 |
| MOD_PKA_2 | 33 | 39 | PF00069 | 0.508 |
| MOD_PKA_2 | 381 | 387 | PF00069 | 0.500 |
| MOD_PKA_2 | 460 | 466 | PF00069 | 0.448 |
| MOD_Plk_1 | 134 | 140 | PF00069 | 0.509 |
| MOD_Plk_1 | 213 | 219 | PF00069 | 0.463 |
| MOD_Plk_1 | 6 | 12 | PF00069 | 0.573 |
| MOD_Plk_1 | 90 | 96 | PF00069 | 0.448 |
| MOD_Plk_2-3 | 406 | 412 | PF00069 | 0.343 |
| MOD_Plk_4 | 366 | 372 | PF00069 | 0.430 |
| MOD_Plk_4 | 78 | 84 | PF00069 | 0.283 |
| MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.552 |
| MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.387 |
| MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.541 |
| MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.531 |
| TRG_DiLeu_BaEn_1 | 397 | 402 | PF01217 | 0.485 |
| TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.619 |
| TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.488 |
| TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.378 |
| TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.451 |
| TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.494 |
| TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.395 |
| TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.495 |
| TRG_NES_CRM1_1 | 168 | 181 | PF08389 | 0.516 |
| TRG_NES_CRM1_1 | 236 | 250 | PF08389 | 0.516 |
| TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.315 |
| TRG_Pf-PMV_PEXEL_1 | 175 | 180 | PF00026 | 0.315 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I876 | Leptomonas seymouri | 55% | 100% |
| A0A3S7WZC3 | Leishmania donovani | 88% | 96% |
| A0A422NGJ8 | Trypanosoma rangeli | 28% | 100% |
| A4HEG6 | Leishmania braziliensis | 78% | 99% |
| A4I1M4 | Leishmania infantum | 89% | 96% |
| Q4Q9R3 | Leishmania major | 90% | 100% |
| V5DIU3 | Trypanosoma cruzi | 33% | 97% |