| 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: 9 | 
| NetGPI | no | yes: 0, no: 9 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0000974 | Prp19 complex | 2 | 10 | 
| GO:0005681 | spliceosomal complex | 3 | 10 | 
| GO:0005840 | ribosome | 5 | 6 | 
| GO:0032991 | protein-containing complex | 1 | 10 | 
| GO:0043226 | organelle | 2 | 6 | 
| GO:0043228 | non-membrane-bounded organelle | 3 | 6 | 
| GO:0043229 | intracellular organelle | 3 | 6 | 
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 6 | 
| GO:0110165 | cellular anatomical entity | 1 | 6 | 
| GO:0140513 | nuclear protein-containing complex | 2 | 10 | 
| GO:1990904 | ribonucleoprotein complex | 2 | 10 | 
| GO:0005654 | nucleoplasm | 2 | 1 | 
| GO:0005684 | U2-type spliceosomal complex | 4 | 1 | 
| GO:0005730 | nucleolus | 5 | 1 | 
| GO:0005737 | cytoplasm | 2 | 1 | 
| GO:0071006 | U2-type catalytic step 1 spliceosome | 4 | 1 | 
| GO:0071012 | catalytic step 1 spliceosome | 3 | 1 | 
| GO:1902494 | catalytic complex | 2 | 1 | 
Related structures:
AlphaFold database: E9AZF7
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0000209 | protein polyubiquitination | 8 | 10 | 
| GO:0000375 | RNA splicing, via transesterification reactions | 8 | 10 | 
| GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 10 | 
| GO:0000398 | mRNA splicing, via spliceosome | 8 | 10 | 
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 | 
| GO:0006259 | DNA metabolic process | 4 | 10 | 
| GO:0006281 | DNA repair | 5 | 10 | 
| GO:0006396 | RNA processing | 6 | 10 | 
| GO:0006397 | mRNA processing | 7 | 10 | 
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 10 | 
| GO:0006950 | response to stress | 2 | 10 | 
| GO:0006974 | DNA damage response | 4 | 10 | 
| GO:0008152 | metabolic process | 1 | 10 | 
| GO:0008380 | RNA splicing | 7 | 10 | 
| GO:0009987 | cellular process | 1 | 10 | 
| GO:0016070 | RNA metabolic process | 5 | 10 | 
| GO:0016071 | mRNA metabolic process | 6 | 10 | 
| GO:0016567 | protein ubiquitination | 7 | 10 | 
| GO:0019538 | protein metabolic process | 3 | 10 | 
| GO:0032446 | protein modification by small protein conjugation | 6 | 10 | 
| GO:0033554 | cellular response to stress | 3 | 10 | 
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 | 
| GO:0036211 | protein modification process | 4 | 10 | 
| GO:0043170 | macromolecule metabolic process | 3 | 10 | 
| GO:0043412 | macromolecule modification | 4 | 10 | 
| GO:0044237 | cellular metabolic process | 2 | 10 | 
| GO:0044238 | primary metabolic process | 2 | 10 | 
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 | 
| GO:0046483 | heterocycle metabolic process | 3 | 10 | 
| GO:0050896 | response to stimulus | 1 | 10 | 
| GO:0051716 | cellular response to stimulus | 2 | 10 | 
| GO:0070534 | protein K63-linked ubiquitination | 9 | 10 | 
| GO:0070647 | protein modification by small protein conjugation or removal | 5 | 10 | 
| GO:0071704 | organic substance metabolic process | 2 | 10 | 
| GO:0090304 | nucleic acid metabolic process | 4 | 10 | 
| GO:1901360 | organic cyclic compound metabolic process | 3 | 10 | 
| GO:1901564 | organonitrogen compound metabolic process | 3 | 10 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 10 | 
| GO:0004842 | ubiquitin-protein transferase activity | 4 | 10 | 
| GO:0016740 | transferase activity | 2 | 10 | 
| GO:0019787 | ubiquitin-like protein transferase activity | 3 | 10 | 
| GO:0061630 | ubiquitin protein ligase activity | 5 | 10 | 
| GO:0061659 | ubiquitin-like protein ligase activity | 4 | 10 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 10 | 
| GO:0016746 | acyltransferase activity | 3 | 1 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.468 | 
| CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.397 | 
| CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.419 | 
| CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.422 | 
| CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.462 | 
| CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.471 | 
| DEG_APCC_DBOX_1 | 417 | 425 | PF00400 | 0.420 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.546 | 
| DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.433 | 
| DOC_ANK_TNKS_1 | 438 | 445 | PF00023 | 0.455 | 
| DOC_MAPK_DCC_7 | 418 | 426 | PF00069 | 0.426 | 
| DOC_MAPK_HePTP_8 | 6 | 18 | PF00069 | 0.465 | 
| DOC_MAPK_MEF2A_6 | 9 | 18 | PF00069 | 0.460 | 
| DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.382 | 
| DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.580 | 
| DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.523 | 
| DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.543 | 
| DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.605 | 
| DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.614 | 
| DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.334 | 
| DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.663 | 
| DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.398 | 
| DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.591 | 
| DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.435 | 
| LIG_14-3-3_CanoR_1 | 275 | 284 | PF00244 | 0.397 | 
| LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.445 | 
| LIG_14-3-3_CanoR_1 | 461 | 469 | PF00244 | 0.546 | 
| LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.499 | 
| LIG_Actin_WH2_2 | 116 | 133 | PF00022 | 0.484 | 
| LIG_Actin_WH2_2 | 465 | 480 | PF00022 | 0.458 | 
| LIG_BIR_III_2 | 432 | 436 | PF00653 | 0.408 | 
| LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.427 | 
| LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.433 | 
| LIG_FHA_1 | 10 | 16 | PF00498 | 0.479 | 
| LIG_FHA_1 | 249 | 255 | PF00498 | 0.483 | 
| LIG_FHA_1 | 271 | 277 | PF00498 | 0.305 | 
| LIG_FHA_1 | 330 | 336 | PF00498 | 0.490 | 
| LIG_FHA_1 | 429 | 435 | PF00498 | 0.309 | 
| LIG_FHA_1 | 472 | 478 | PF00498 | 0.435 | 
| LIG_FHA_1 | 490 | 496 | PF00498 | 0.305 | 
| LIG_FHA_2 | 317 | 323 | PF00498 | 0.433 | 
| LIG_FHA_2 | 343 | 349 | PF00498 | 0.471 | 
| LIG_FHA_2 | 465 | 471 | PF00498 | 0.454 | 
| LIG_FHA_2 | 74 | 80 | PF00498 | 0.517 | 
| LIG_LIR_Gen_1 | 189 | 200 | PF02991 | 0.396 | 
| LIG_LIR_LC3C_4 | 446 | 449 | PF02991 | 0.357 | 
| LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.364 | 
| LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.436 | 
| LIG_Rb_LxCxE_1 | 339 | 354 | PF01857 | 0.453 | 
| LIG_SH2_CRK | 352 | 356 | PF00017 | 0.322 | 
| LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.415 | 
| LIG_SH2_STAP1 | 506 | 510 | PF00017 | 0.454 | 
| LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.386 | 
| LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.446 | 
| LIG_SH3_3 | 145 | 151 | PF00018 | 0.450 | 
| LIG_SH3_3 | 417 | 423 | PF00018 | 0.421 | 
| LIG_SH3_3 | 8 | 14 | PF00018 | 0.386 | 
| LIG_SUMO_SIM_par_1 | 14 | 20 | PF11976 | 0.459 | 
| LIG_SUMO_SIM_par_1 | 315 | 322 | PF11976 | 0.445 | 
| LIG_SUMO_SIM_par_1 | 332 | 341 | PF11976 | 0.438 | 
| MOD_CK1_1 | 17 | 23 | PF00069 | 0.348 | 
| MOD_CK1_1 | 184 | 190 | PF00069 | 0.543 | 
| MOD_CK1_1 | 196 | 202 | PF00069 | 0.613 | 
| MOD_CK1_1 | 204 | 210 | PF00069 | 0.426 | 
| MOD_CK1_1 | 300 | 306 | PF00069 | 0.436 | 
| MOD_CK1_1 | 408 | 414 | PF00069 | 0.442 | 
| MOD_CK1_1 | 463 | 469 | PF00069 | 0.610 | 
| MOD_CK1_1 | 62 | 68 | PF00069 | 0.510 | 
| MOD_CK1_1 | 73 | 79 | PF00069 | 0.389 | 
| MOD_CK2_1 | 24 | 30 | PF00069 | 0.348 | 
| MOD_CK2_1 | 264 | 270 | PF00069 | 0.436 | 
| MOD_CK2_1 | 318 | 324 | PF00069 | 0.445 | 
| MOD_CK2_1 | 342 | 348 | PF00069 | 0.434 | 
| MOD_CK2_1 | 464 | 470 | PF00069 | 0.634 | 
| MOD_CK2_1 | 73 | 79 | PF00069 | 0.491 | 
| MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.525 | 
| MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.404 | 
| MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.534 | 
| MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.338 | 
| MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.414 | 
| MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.321 | 
| MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.448 | 
| MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.511 | 
| MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.351 | 
| MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.248 | 
| MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.234 | 
| MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.556 | 
| MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.475 | 
| MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.534 | 
| MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.528 | 
| MOD_GSK3_1 | 175 | 182 | PF00069 | 0.557 | 
| MOD_GSK3_1 | 196 | 203 | PF00069 | 0.612 | 
| MOD_GSK3_1 | 282 | 289 | PF00069 | 0.498 | 
| MOD_GSK3_1 | 318 | 325 | PF00069 | 0.442 | 
| MOD_GSK3_1 | 329 | 336 | PF00069 | 0.419 | 
| MOD_GSK3_1 | 338 | 345 | PF00069 | 0.428 | 
| MOD_GSK3_1 | 386 | 393 | PF00069 | 0.275 | 
| MOD_GSK3_1 | 460 | 467 | PF00069 | 0.487 | 
| MOD_GSK3_1 | 485 | 492 | PF00069 | 0.437 | 
| MOD_GSK3_1 | 59 | 66 | PF00069 | 0.535 | 
| MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.444 | 
| MOD_NEK2_1 | 24 | 29 | PF00069 | 0.440 | 
| MOD_NEK2_1 | 337 | 342 | PF00069 | 0.488 | 
| MOD_NEK2_1 | 462 | 467 | PF00069 | 0.516 | 
| MOD_NEK2_1 | 477 | 482 | PF00069 | 0.282 | 
| MOD_NEK2_1 | 505 | 510 | PF00069 | 0.420 | 
| MOD_NEK2_2 | 14 | 19 | PF00069 | 0.459 | 
| MOD_PIKK_1 | 181 | 187 | PF00454 | 0.429 | 
| MOD_PIKK_1 | 256 | 262 | PF00454 | 0.376 | 
| MOD_PIKK_1 | 297 | 303 | PF00454 | 0.442 | 
| MOD_PIKK_1 | 4 | 10 | PF00454 | 0.403 | 
| MOD_PIKK_1 | 97 | 103 | PF00454 | 0.437 | 
| MOD_PKA_2 | 121 | 127 | PF00069 | 0.553 | 
| MOD_PKA_2 | 460 | 466 | PF00069 | 0.439 | 
| MOD_Plk_1 | 24 | 30 | PF00069 | 0.348 | 
| MOD_Plk_1 | 270 | 276 | PF00069 | 0.342 | 
| MOD_Plk_1 | 59 | 65 | PF00069 | 0.560 | 
| MOD_Plk_4 | 282 | 288 | PF00069 | 0.562 | 
| MOD_Plk_4 | 374 | 380 | PF00069 | 0.407 | 
| MOD_Plk_4 | 408 | 414 | PF00069 | 0.388 | 
| MOD_Plk_4 | 73 | 79 | PF00069 | 0.499 | 
| MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.586 | 
| MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.445 | 
| TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.327 | 
| TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.543 | 
| TRG_NLS_Bipartite_1 | 156 | 173 | PF00514 | 0.416 | 
| TRG_NLS_MonoExtC_3 | 168 | 173 | PF00514 | 0.481 | 
| TRG_NLS_MonoExtN_4 | 166 | 173 | PF00514 | 0.481 | 
| TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.316 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1IMA9 | Leptomonas seymouri | 66% | 100% | 
| A0A0S4J7B3 | Bodo saltans | 35% | 100% | 
| A0A1X0NFA4 | Trypanosomatidae | 35% | 100% | 
| A0A3Q8IGJ0 | Leishmania donovani | 96% | 100% | 
| A0A3R7NBE4 | Trypanosoma rangeli | 35% | 100% | 
| A4HG28 | Leishmania braziliensis | 83% | 100% | 
| A4I350 | Leishmania infantum | 96% | 100% | 
| C9ZJM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% | 
| E9ACW8 | Leishmania major | 96% | 100% | 
| O22785 | Arabidopsis thaliana | 28% | 98% | 
| Q08E38 | Bos taurus | 30% | 100% | 
| Q10051 | Caenorhabditis elegans | 27% | 100% | 
| Q5ZMA2 | Gallus gallus | 32% | 100% | 
| Q7KWK5 | Dictyostelium discoideum | 26% | 100% | 
| Q94BR4 | Arabidopsis thaliana | 28% | 98% | 
| Q99KP6 | Mus musculus | 30% | 100% | 
| Q9AV81 | Oryza sativa subsp. japonica | 27% | 97% | 
| Q9JMJ4 | Rattus norvegicus | 30% | 100% | 
| Q9UMS4 | Homo sapiens | 31% | 100% |