| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I477
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006468 | protein phosphorylation | 5 | 5 |
| GO:0006793 | phosphorus metabolic process | 3 | 12 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0016310 | phosphorylation | 5 | 12 |
| GO:0019538 | protein metabolic process | 3 | 5 |
| GO:0036211 | protein modification process | 4 | 5 |
| GO:0043170 | macromolecule metabolic process | 3 | 5 |
| GO:0043412 | macromolecule modification | 4 | 5 |
| GO:0044237 | cellular metabolic process | 2 | 12 |
| GO:0044238 | primary metabolic process | 2 | 5 |
| GO:0071704 | organic substance metabolic process | 2 | 5 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
| GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
| GO:0042254 | ribosome biogenesis | 5 | 1 |
| GO:0044085 | cellular component biogenesis | 3 | 1 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 12 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004672 | protein kinase activity | 3 | 12 |
| GO:0004674 | protein serine/threonine kinase activity | 4 | 12 |
| GO:0005488 | binding | 1 | 12 |
| GO:0005524 | ATP binding | 5 | 12 |
| GO:0016301 | kinase activity | 4 | 12 |
| GO:0016740 | transferase activity | 2 | 12 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
| GO:0017076 | purine nucleotide binding | 4 | 12 |
| GO:0030554 | adenyl nucleotide binding | 5 | 12 |
| GO:0032553 | ribonucleotide binding | 3 | 12 |
| GO:0032555 | purine ribonucleotide binding | 4 | 12 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
| GO:0036094 | small molecule binding | 2 | 12 |
| GO:0043167 | ion binding | 2 | 12 |
| GO:0043168 | anion binding | 3 | 12 |
| GO:0097159 | organic cyclic compound binding | 2 | 12 |
| GO:0097367 | carbohydrate derivative binding | 2 | 12 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
| GO:1901265 | nucleoside phosphate binding | 3 | 12 |
| GO:1901363 | heterocyclic compound binding | 2 | 12 |
| GO:0106310 | protein serine kinase activity | 4 | 4 |
| GO:0016787 | hydrolase activity | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.762 |
| CLV_C14_Caspase3-7 | 483 | 487 | PF00656 | 0.700 |
| CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.195 |
| CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.206 |
| CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.195 |
| CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.424 |
| CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.429 |
| CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.588 |
| CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.666 |
| CLV_PCSK_FUR_1 | 519 | 523 | PF00082 | 0.439 |
| CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.195 |
| CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.418 |
| CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.565 |
| CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.505 |
| CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.304 |
| CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.587 |
| CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.262 |
| CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.303 |
| CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.424 |
| DEG_APCC_DBOX_1 | 151 | 159 | PF00400 | 0.295 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.550 |
| DEG_ODPH_VHL_1 | 247 | 260 | PF01847 | 0.406 |
| DOC_MAPK_gen_1 | 193 | 202 | PF00069 | 0.395 |
| DOC_MAPK_gen_1 | 233 | 241 | PF00069 | 0.492 |
| DOC_MAPK_gen_1 | 252 | 260 | PF00069 | 0.321 |
| DOC_MAPK_gen_1 | 319 | 327 | PF00069 | 0.403 |
| DOC_MAPK_gen_1 | 343 | 349 | PF00069 | 0.406 |
| DOC_MAPK_MEF2A_6 | 319 | 327 | PF00069 | 0.390 |
| DOC_MAPK_MEF2A_6 | 417 | 426 | PF00069 | 0.368 |
| DOC_PP1_RVXF_1 | 273 | 280 | PF00149 | 0.395 |
| DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.613 |
| DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.425 |
| DOC_USP7_UBL2_3 | 283 | 287 | PF12436 | 0.482 |
| DOC_USP7_UBL2_3 | 504 | 508 | PF12436 | 0.466 |
| DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.487 |
| DOC_USP7_UBL2_3 | 534 | 538 | PF12436 | 0.546 |
| DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.462 |
| DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.680 |
| LIG_14-3-3_CanoR_1 | 140 | 144 | PF00244 | 0.433 |
| LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.410 |
| LIG_APCC_ABBA_1 | 445 | 450 | PF00400 | 0.485 |
| LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.603 |
| LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.462 |
| LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.482 |
| LIG_eIF4E_1 | 300 | 306 | PF01652 | 0.419 |
| LIG_FHA_1 | 149 | 155 | PF00498 | 0.320 |
| LIG_FHA_1 | 195 | 201 | PF00498 | 0.395 |
| LIG_FHA_2 | 16 | 22 | PF00498 | 0.495 |
| LIG_FHA_2 | 171 | 177 | PF00498 | 0.332 |
| LIG_FHA_2 | 227 | 233 | PF00498 | 0.399 |
| LIG_FHA_2 | 361 | 367 | PF00498 | 0.333 |
| LIG_FHA_2 | 501 | 507 | PF00498 | 0.445 |
| LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.420 |
| LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.622 |
| LIG_LIR_Apic_2 | 330 | 336 | PF02991 | 0.441 |
| LIG_LIR_Gen_1 | 286 | 296 | PF02991 | 0.395 |
| LIG_LIR_Gen_1 | 311 | 318 | PF02991 | 0.395 |
| LIG_LIR_Gen_1 | 366 | 376 | PF02991 | 0.324 |
| LIG_LIR_Gen_1 | 420 | 429 | PF02991 | 0.349 |
| LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.424 |
| LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.395 |
| LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.529 |
| LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.395 |
| LIG_LIR_Nem_3 | 366 | 371 | PF02991 | 0.261 |
| LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.347 |
| LIG_REV1ctd_RIR_1 | 350 | 360 | PF16727 | 0.395 |
| LIG_RPA_C_Insects | 522 | 537 | PF08784 | 0.550 |
| LIG_SH2_CRK | 12 | 16 | PF00017 | 0.511 |
| LIG_SH2_CRK | 156 | 160 | PF00017 | 0.294 |
| LIG_SH2_CRK | 313 | 317 | PF00017 | 0.230 |
| LIG_SH2_SRC | 333 | 336 | PF00017 | 0.294 |
| LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.633 |
| LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.278 |
| LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.278 |
| LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.230 |
| LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.613 |
| LIG_SH3_3 | 143 | 149 | PF00018 | 0.358 |
| LIG_SH3_3 | 243 | 249 | PF00018 | 0.245 |
| LIG_SH3_3 | 274 | 280 | PF00018 | 0.230 |
| LIG_SUMO_SIM_par_1 | 321 | 326 | PF11976 | 0.230 |
| LIG_TRAF2_1 | 24 | 27 | PF00917 | 0.546 |
| LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.447 |
| LIG_TYR_ITIM | 154 | 159 | PF00017 | 0.285 |
| LIG_UBA3_1 | 392 | 397 | PF00899 | 0.488 |
| LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.375 |
| LIG_WRC_WIRS_1 | 349 | 354 | PF05994 | 0.304 |
| MOD_CDC14_SPxK_1 | 487 | 490 | PF00782 | 0.614 |
| MOD_CDK_SPxK_1 | 484 | 490 | PF00069 | 0.619 |
| MOD_CK1_1 | 198 | 204 | PF00069 | 0.399 |
| MOD_CK1_1 | 55 | 61 | PF00069 | 0.601 |
| MOD_CK2_1 | 170 | 176 | PF00069 | 0.339 |
| MOD_CK2_1 | 21 | 27 | PF00069 | 0.518 |
| MOD_CK2_1 | 226 | 232 | PF00069 | 0.235 |
| MOD_CK2_1 | 428 | 434 | PF00069 | 0.481 |
| MOD_CK2_1 | 500 | 506 | PF00069 | 0.482 |
| MOD_Cter_Amidation | 535 | 538 | PF01082 | 0.677 |
| MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.545 |
| MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.333 |
| MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.375 |
| MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.323 |
| MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.251 |
| MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.430 |
| MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.653 |
| MOD_GlcNHglycan | 462 | 467 | PF01048 | 0.731 |
| MOD_GlcNHglycan | 53 | 57 | PF01048 | 0.641 |
| MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.560 |
| MOD_GSK3_1 | 135 | 142 | PF00069 | 0.496 |
| MOD_GSK3_1 | 158 | 165 | PF00069 | 0.443 |
| MOD_GSK3_1 | 181 | 188 | PF00069 | 0.384 |
| MOD_GSK3_1 | 194 | 201 | PF00069 | 0.424 |
| MOD_GSK3_1 | 348 | 355 | PF00069 | 0.374 |
| MOD_GSK3_1 | 356 | 363 | PF00069 | 0.450 |
| MOD_GSK3_1 | 424 | 431 | PF00069 | 0.462 |
| MOD_GSK3_1 | 458 | 465 | PF00069 | 0.705 |
| MOD_LATS_1 | 335 | 341 | PF00433 | 0.251 |
| MOD_N-GLC_1 | 424 | 429 | PF02516 | 0.572 |
| MOD_N-GLC_1 | 500 | 505 | PF02516 | 0.591 |
| MOD_N-GLC_2 | 168 | 170 | PF02516 | 0.324 |
| MOD_NEK2_1 | 120 | 125 | PF00069 | 0.497 |
| MOD_NEK2_1 | 158 | 163 | PF00069 | 0.315 |
| MOD_NEK2_1 | 226 | 231 | PF00069 | 0.237 |
| MOD_NEK2_1 | 292 | 297 | PF00069 | 0.289 |
| MOD_NEK2_1 | 352 | 357 | PF00069 | 0.270 |
| MOD_NEK2_1 | 424 | 429 | PF00069 | 0.420 |
| MOD_PIKK_1 | 325 | 331 | PF00454 | 0.237 |
| MOD_PKA_2 | 139 | 145 | PF00069 | 0.473 |
| MOD_PKB_1 | 354 | 362 | PF00069 | 0.251 |
| MOD_Plk_1 | 118 | 124 | PF00069 | 0.460 |
| MOD_Plk_1 | 275 | 281 | PF00069 | 0.251 |
| MOD_Plk_1 | 424 | 430 | PF00069 | 0.575 |
| MOD_Plk_2-3 | 139 | 145 | PF00069 | 0.446 |
| MOD_Plk_2-3 | 477 | 483 | PF00069 | 0.609 |
| MOD_Plk_4 | 195 | 201 | PF00069 | 0.274 |
| MOD_Plk_4 | 337 | 343 | PF00069 | 0.373 |
| MOD_Plk_4 | 348 | 354 | PF00069 | 0.252 |
| MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.323 |
| MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.680 |
| MOD_SUMO_for_1 | 41 | 44 | PF00179 | 0.574 |
| TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.375 |
| TRG_DiLeu_BaEn_1 | 312 | 317 | PF01217 | 0.289 |
| TRG_DiLeu_BaEn_2 | 443 | 449 | PF01217 | 0.438 |
| TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.336 |
| TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.288 |
| TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.230 |
| TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.230 |
| TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.230 |
| TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.347 |
| TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.241 |
| TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.230 |
| TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.243 |
| TRG_ER_diLys_1 | 533 | 538 | PF00400 | 0.561 |
| TRG_NLS_Bipartite_1 | 521 | 538 | PF00514 | 0.632 |
| TRG_NLS_MonoCore_2 | 531 | 536 | PF00514 | 0.573 |
| TRG_NLS_MonoExtC_3 | 532 | 537 | PF00514 | 0.577 |
| TRG_NLS_MonoExtN_4 | 532 | 538 | PF00514 | 0.597 |
| TRG_Pf-PMV_PEXEL_1 | 112 | 116 | PF00026 | 0.499 |
| TRG_Pf-PMV_PEXEL_1 | 430 | 434 | PF00026 | 0.423 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IIE8 | Leptomonas seymouri | 82% | 97% |
| A0A0S4JDG4 | Bodo saltans | 54% | 97% |
| A0A1X0NZG1 | Trypanosomatidae | 65% | 97% |
| A0A3S7X229 | Leishmania donovani | 100% | 100% |
| A0A422NUW2 | Trypanosoma rangeli | 64% | 96% |
| A4HH32 | Leishmania braziliensis | 89% | 100% |
| C9ZKQ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 94% |
| E9ADM6 | Leishmania major | 96% | 100% |
| E9AM55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
| G0S3J5 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 38% | 100% |
| O14730 | Homo sapiens | 36% | 100% |
| O42650 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 41% | 100% |
| O44959 | Caenorhabditis elegans | 42% | 100% |
| Q12196 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 100% |
| Q1RMT7 | Bos taurus | 37% | 100% |
| Q922Q2 | Mus musculus | 41% | 95% |
| Q9BRS2 | Homo sapiens | 42% | 95% |
| Q9DBU3 | Mus musculus | 37% | 100% |
| V5BUJ3 | Trypanosoma cruzi | 64% | 99% |