| 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: 1, no: 24 |
| NetGPI | no | yes: 0, no: 25 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005929 | cilium | 4 | 26 |
| GO:0042995 | cell projection | 2 | 26 |
| GO:0043226 | organelle | 2 | 26 |
| GO:0043227 | membrane-bounded organelle | 3 | 26 |
| GO:0110165 | cellular anatomical entity | 1 | 26 |
| GO:0120025 | plasma membrane bounded cell projection | 3 | 26 |
| GO:0000151 | ubiquitin ligase complex | 3 | 1 |
| GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
| GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0140535 | intracellular protein-containing complex | 2 | 1 |
| GO:1902494 | catalytic complex | 2 | 1 |
| GO:1990234 | transferase complex | 3 | 1 |
| GO:0005743 | mitochondrial inner membrane | 5 | 1 |
| GO:0016020 | membrane | 2 | 1 |
| GO:0019866 | organelle inner membrane | 4 | 1 |
| GO:0031090 | organelle membrane | 3 | 1 |
| GO:0031966 | mitochondrial membrane | 4 | 1 |
Related structures:
AlphaFold database: E9AWC6
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006793 | phosphorus metabolic process | 3 | 3 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 3 |
| GO:0008152 | metabolic process | 1 | 4 |
| GO:0009987 | cellular process | 1 | 4 |
| GO:0016310 | phosphorylation | 5 | 3 |
| GO:0044237 | cellular metabolic process | 2 | 4 |
| GO:0006508 | proteolysis | 4 | 1 |
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0009056 | catabolic process | 2 | 1 |
| GO:0009057 | macromolecule catabolic process | 4 | 1 |
| GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
| GO:0030163 | protein catabolic process | 4 | 1 |
| GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
| GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044248 | cellular catabolic process | 3 | 1 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
| GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
| GO:1901575 | organic substance catabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005488 | binding | 1 | 1 |
| GO:0043167 | ion binding | 2 | 1 |
| GO:0043169 | cation binding | 3 | 1 |
| GO:0046872 | metal ion binding | 4 | 1 |
| GO:0003824 | catalytic activity | 1 | 3 |
| GO:0016301 | kinase activity | 4 | 3 |
| GO:0016740 | transferase activity | 2 | 3 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 152 | 156 | PF00656 | 0.458 |
| CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.597 |
| CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.383 |
| CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.563 |
| CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.597 |
| CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.373 |
| CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.441 |
| CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.396 |
| CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.373 |
| CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.420 |
| CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.636 |
| CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.381 |
| CLV_Separin_Metazoa | 22 | 26 | PF03568 | 0.637 |
| DEG_APCC_DBOX_1 | 30 | 38 | PF00400 | 0.562 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.634 |
| DEG_SCF_FBW7_1 | 266 | 273 | PF00400 | 0.503 |
| DOC_MAPK_gen_1 | 158 | 167 | PF00069 | 0.467 |
| DOC_MAPK_gen_1 | 308 | 315 | PF00069 | 0.479 |
| DOC_MAPK_MEF2A_6 | 160 | 169 | PF00069 | 0.499 |
| DOC_MAPK_MEF2A_6 | 441 | 450 | PF00069 | 0.492 |
| DOC_MAPK_MEF2A_6 | 465 | 474 | PF00069 | 0.337 |
| DOC_PP1_RVXF_1 | 306 | 313 | PF00149 | 0.431 |
| DOC_PP4_FxxP_1 | 129 | 132 | PF00568 | 0.535 |
| DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.499 |
| DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.430 |
| DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.453 |
| DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.475 |
| DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.680 |
| DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.427 |
| DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.482 |
| DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.624 |
| DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.560 |
| LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.455 |
| LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.575 |
| LIG_14-3-3_CanoR_1 | 337 | 346 | PF00244 | 0.415 |
| LIG_14-3-3_CanoR_1 | 42 | 51 | PF00244 | 0.675 |
| LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.620 |
| LIG_14-3-3_CanoR_1 | 94 | 104 | PF00244 | 0.584 |
| LIG_Actin_WH2_2 | 267 | 282 | PF00022 | 0.453 |
| LIG_Actin_WH2_2 | 435 | 451 | PF00022 | 0.406 |
| LIG_APCC_ABBA_1 | 211 | 216 | PF00400 | 0.339 |
| LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.463 |
| LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.691 |
| LIG_Clathr_ClatBox_1 | 370 | 374 | PF01394 | 0.415 |
| LIG_FHA_1 | 236 | 242 | PF00498 | 0.389 |
| LIG_FHA_1 | 260 | 266 | PF00498 | 0.452 |
| LIG_FHA_1 | 379 | 385 | PF00498 | 0.371 |
| LIG_FHA_1 | 9 | 15 | PF00498 | 0.608 |
| LIG_FHA_2 | 17 | 23 | PF00498 | 0.597 |
| LIG_FHA_2 | 242 | 248 | PF00498 | 0.460 |
| LIG_FHA_2 | 283 | 289 | PF00498 | 0.245 |
| LIG_FHA_2 | 329 | 335 | PF00498 | 0.438 |
| LIG_FHA_2 | 423 | 429 | PF00498 | 0.409 |
| LIG_IRF3_LxIS_1 | 384 | 391 | PF10401 | 0.343 |
| LIG_LIR_Apic_2 | 126 | 132 | PF02991 | 0.544 |
| LIG_LIR_Gen_1 | 226 | 236 | PF02991 | 0.461 |
| LIG_LIR_Gen_1 | 366 | 373 | PF02991 | 0.488 |
| LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.409 |
| LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.464 |
| LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.438 |
| LIG_LIR_Nem_3 | 366 | 371 | PF02991 | 0.493 |
| LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.664 |
| LIG_MLH1_MIPbox_1 | 225 | 229 | PF16413 | 0.342 |
| LIG_NRBOX | 260 | 266 | PF00104 | 0.462 |
| LIG_PCNA_yPIPBox_3 | 460 | 469 | PF02747 | 0.368 |
| LIG_PTB_Apo_2 | 124 | 131 | PF02174 | 0.407 |
| LIG_PTB_Apo_2 | 342 | 349 | PF02174 | 0.410 |
| LIG_SH2_CRK | 107 | 111 | PF00017 | 0.602 |
| LIG_SH2_CRK | 368 | 372 | PF00017 | 0.521 |
| LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.479 |
| LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.449 |
| LIG_SH3_2 | 54 | 59 | PF14604 | 0.512 |
| LIG_SH3_3 | 168 | 174 | PF00018 | 0.424 |
| LIG_SH3_3 | 45 | 51 | PF00018 | 0.571 |
| LIG_SUMO_SIM_anti_2 | 141 | 146 | PF11976 | 0.504 |
| LIG_SUMO_SIM_anti_2 | 163 | 169 | PF11976 | 0.468 |
| LIG_SUMO_SIM_anti_2 | 316 | 323 | PF11976 | 0.542 |
| LIG_SUMO_SIM_anti_2 | 471 | 478 | PF11976 | 0.494 |
| LIG_SUMO_SIM_par_1 | 237 | 242 | PF11976 | 0.430 |
| LIG_SUMO_SIM_par_1 | 380 | 385 | PF11976 | 0.359 |
| LIG_TRAF2_1 | 425 | 428 | PF00917 | 0.502 |
| LIG_TRAF2_1 | 478 | 481 | PF00917 | 0.442 |
| LIG_TYR_ITSM | 364 | 371 | PF00017 | 0.508 |
| MOD_CK1_1 | 194 | 200 | PF00069 | 0.488 |
| MOD_CK1_1 | 230 | 236 | PF00069 | 0.407 |
| MOD_CK1_1 | 260 | 266 | PF00069 | 0.427 |
| MOD_CK1_1 | 282 | 288 | PF00069 | 0.246 |
| MOD_CK1_1 | 3 | 9 | PF00069 | 0.622 |
| MOD_CK1_1 | 316 | 322 | PF00069 | 0.402 |
| MOD_CK1_1 | 50 | 56 | PF00069 | 0.614 |
| MOD_CK1_1 | 82 | 88 | PF00069 | 0.601 |
| MOD_CK2_1 | 125 | 131 | PF00069 | 0.478 |
| MOD_CK2_1 | 16 | 22 | PF00069 | 0.605 |
| MOD_CK2_1 | 282 | 288 | PF00069 | 0.228 |
| MOD_CK2_1 | 328 | 334 | PF00069 | 0.392 |
| MOD_CK2_1 | 422 | 428 | PF00069 | 0.406 |
| MOD_CK2_1 | 475 | 481 | PF00069 | 0.492 |
| MOD_Cter_Amidation | 92 | 95 | PF01082 | 0.591 |
| MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.469 |
| MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.440 |
| MOD_GlcNHglycan | 300 | 304 | PF01048 | 0.397 |
| MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.666 |
| MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.605 |
| MOD_GSK3_1 | 223 | 230 | PF00069 | 0.434 |
| MOD_GSK3_1 | 231 | 238 | PF00069 | 0.411 |
| MOD_GSK3_1 | 241 | 248 | PF00069 | 0.375 |
| MOD_GSK3_1 | 260 | 267 | PF00069 | 0.391 |
| MOD_GSK3_1 | 275 | 282 | PF00069 | 0.312 |
| MOD_GSK3_1 | 299 | 306 | PF00069 | 0.402 |
| MOD_GSK3_1 | 378 | 385 | PF00069 | 0.360 |
| MOD_GSK3_1 | 418 | 425 | PF00069 | 0.410 |
| MOD_GSK3_1 | 43 | 50 | PF00069 | 0.659 |
| MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.518 |
| MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.447 |
| MOD_N-GLC_2 | 452 | 454 | PF02516 | 0.392 |
| MOD_NEK2_1 | 180 | 185 | PF00069 | 0.443 |
| MOD_NEK2_1 | 2 | 7 | PF00069 | 0.654 |
| MOD_NEK2_1 | 239 | 244 | PF00069 | 0.370 |
| MOD_NEK2_1 | 245 | 250 | PF00069 | 0.362 |
| MOD_NEK2_1 | 279 | 284 | PF00069 | 0.446 |
| MOD_NEK2_1 | 313 | 318 | PF00069 | 0.338 |
| MOD_NEK2_1 | 358 | 363 | PF00069 | 0.438 |
| MOD_NEK2_1 | 388 | 393 | PF00069 | 0.385 |
| MOD_NEK2_1 | 431 | 436 | PF00069 | 0.388 |
| MOD_NEK2_2 | 303 | 308 | PF00069 | 0.303 |
| MOD_PIKK_1 | 248 | 254 | PF00454 | 0.487 |
| MOD_PIKK_1 | 328 | 334 | PF00454 | 0.410 |
| MOD_PKA_1 | 186 | 192 | PF00069 | 0.487 |
| MOD_PKA_2 | 30 | 36 | PF00069 | 0.587 |
| MOD_PKA_2 | 316 | 322 | PF00069 | 0.430 |
| MOD_PKA_2 | 468 | 474 | PF00069 | 0.491 |
| MOD_PKA_2 | 80 | 86 | PF00069 | 0.581 |
| MOD_Plk_1 | 125 | 131 | PF00069 | 0.461 |
| MOD_Plk_1 | 154 | 160 | PF00069 | 0.402 |
| MOD_Plk_1 | 299 | 305 | PF00069 | 0.492 |
| MOD_Plk_1 | 313 | 319 | PF00069 | 0.265 |
| MOD_Plk_1 | 344 | 350 | PF00069 | 0.528 |
| MOD_Plk_1 | 366 | 372 | PF00069 | 0.457 |
| MOD_Plk_2-3 | 16 | 22 | PF00069 | 0.638 |
| MOD_Plk_2-3 | 288 | 294 | PF00069 | 0.341 |
| MOD_Plk_2-3 | 422 | 428 | PF00069 | 0.511 |
| MOD_Plk_2-3 | 468 | 474 | PF00069 | 0.531 |
| MOD_Plk_4 | 125 | 131 | PF00069 | 0.465 |
| MOD_Plk_4 | 163 | 169 | PF00069 | 0.434 |
| MOD_Plk_4 | 206 | 212 | PF00069 | 0.456 |
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.465 |
| MOD_Plk_4 | 260 | 266 | PF00069 | 0.460 |
| MOD_Plk_4 | 316 | 322 | PF00069 | 0.467 |
| MOD_Plk_4 | 366 | 372 | PF00069 | 0.402 |
| MOD_Plk_4 | 378 | 384 | PF00069 | 0.345 |
| MOD_Plk_4 | 453 | 459 | PF00069 | 0.448 |
| MOD_Plk_4 | 82 | 88 | PF00069 | 0.657 |
| MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.433 |
| MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.475 |
| MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.615 |
| MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.563 |
| MOD_SUMO_rev_2 | 427 | 434 | PF00179 | 0.420 |
| TRG_DiLeu_BaEn_4 | 296 | 302 | PF01217 | 0.521 |
| TRG_DiLeu_BaEn_4 | 374 | 380 | PF01217 | 0.498 |
| TRG_DiLeu_BaLyEn_6 | 462 | 467 | PF01217 | 0.355 |
| TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.592 |
| TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.510 |
| TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.417 |
| TRG_NES_CRM1_1 | 256 | 268 | PF08389 | 0.529 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P2F4 | Leptomonas seymouri | 70% | 100% |
| A0A0N0P8N9 | Leptomonas seymouri | 25% | 74% |
| A0A0S4IS80 | Bodo saltans | 33% | 95% |
| A0A0S4JR29 | Bodo saltans | 28% | 95% |
| A0A0S4JR64 | Bodo saltans | 23% | 75% |
| A0A0S4KN43 | Bodo saltans | 27% | 83% |
| A0A1X0NEN5 | Trypanosomatidae | 27% | 84% |
| A0A1X0NG16 | Trypanosomatidae | 27% | 84% |
| A0A1X0NPF4 | Trypanosomatidae | 25% | 100% |
| A0A1X0NXB3 | Trypanosomatidae | 53% | 100% |
| A0A1X0P4M6 | Trypanosomatidae | 28% | 84% |
| A0A3S5H7C2 | Leishmania donovani | 96% | 100% |
| A0A422NP39 | Trypanosoma rangeli | 51% | 100% |
| A4HCY0 | Leishmania braziliensis | 88% | 100% |
| A4HJE4 | Leishmania braziliensis | 26% | 100% |
| A4I0G3 | Leishmania infantum | 96% | 100% |
| C9ZS86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 90% |
| C9ZV75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
| D0A0X4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 72% |
| E9AIU4 | Leishmania braziliensis | 26% | 88% |
| P23799 | Trypanosoma brucei brucei | 25% | 77% |
| P26337 | Trypanosoma equiperdum | 25% | 77% |
| Q4QB46 | Leishmania major | 96% | 100% |
| V5BD47 | Trypanosoma cruzi | 27% | 100% |
| V5BMQ2 | Trypanosoma cruzi | 23% | 87% |
| V5DFL9 | Trypanosoma cruzi | 51% | 100% |