| 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: 6 |
| NetGPI | no | yes: 0, no: 6 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6H6
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006468 | protein phosphorylation | 5 | 7 |
| GO:0006793 | phosphorus metabolic process | 3 | 7 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
| GO:0008152 | metabolic process | 1 | 7 |
| GO:0009987 | cellular process | 1 | 7 |
| GO:0016310 | phosphorylation | 5 | 7 |
| GO:0019538 | protein metabolic process | 3 | 7 |
| GO:0036211 | protein modification process | 4 | 7 |
| GO:0043170 | macromolecule metabolic process | 3 | 7 |
| GO:0043412 | macromolecule modification | 4 | 7 |
| GO:0044237 | cellular metabolic process | 2 | 7 |
| GO:0044238 | primary metabolic process | 2 | 7 |
| GO:0071704 | organic substance metabolic process | 2 | 7 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 7 |
| GO:0003824 | catalytic activity | 1 | 7 |
| GO:0004672 | protein kinase activity | 3 | 7 |
| GO:0005488 | binding | 1 | 7 |
| GO:0005524 | ATP binding | 5 | 7 |
| GO:0016301 | kinase activity | 4 | 7 |
| GO:0016740 | transferase activity | 2 | 7 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
| GO:0017076 | purine nucleotide binding | 4 | 7 |
| GO:0030554 | adenyl nucleotide binding | 5 | 7 |
| GO:0032553 | ribonucleotide binding | 3 | 7 |
| GO:0032555 | purine ribonucleotide binding | 4 | 7 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
| GO:0036094 | small molecule binding | 2 | 7 |
| GO:0043167 | ion binding | 2 | 7 |
| GO:0043168 | anion binding | 3 | 7 |
| GO:0097159 | organic cyclic compound binding | 2 | 7 |
| GO:0097367 | carbohydrate derivative binding | 2 | 7 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
| GO:1901265 | nucleoside phosphate binding | 3 | 7 |
| GO:1901363 | heterocyclic compound binding | 2 | 7 |
| GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.523 |
| CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.511 |
| CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.344 |
| CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.287 |
| CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.287 |
| CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.453 |
| CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.344 |
| CLV_PCSK_PC1ET2_1 | 308 | 310 | PF00082 | 0.273 |
| CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.313 |
| CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.453 |
| CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.539 |
| CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.366 |
| CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.277 |
| CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.336 |
| CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.560 |
| CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.363 |
| CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.472 |
| DEG_MDM2_SWIB_1 | 178 | 186 | PF02201 | 0.321 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.477 |
| DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.627 |
| DOC_CKS1_1 | 373 | 378 | PF01111 | 0.363 |
| DOC_CYCLIN_RxL_1 | 34 | 41 | PF00134 | 0.308 |
| DOC_MAPK_gen_1 | 245 | 254 | PF00069 | 0.309 |
| DOC_MAPK_gen_1 | 35 | 42 | PF00069 | 0.395 |
| DOC_MAPK_MEF2A_6 | 103 | 111 | PF00069 | 0.451 |
| DOC_MAPK_MEF2A_6 | 247 | 256 | PF00069 | 0.254 |
| DOC_MAPK_MEF2A_6 | 522 | 530 | PF00069 | 0.363 |
| DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.200 |
| DOC_PP1_RVXF_1 | 491 | 497 | PF00149 | 0.206 |
| DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.529 |
| DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.638 |
| DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.206 |
| DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.212 |
| DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.464 |
| DOC_USP7_UBL2_3 | 148 | 152 | PF12436 | 0.663 |
| DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.533 |
| DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.363 |
| DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.347 |
| DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.320 |
| LIG_14-3-3_CanoR_1 | 203 | 210 | PF00244 | 0.471 |
| LIG_14-3-3_CanoR_1 | 35 | 40 | PF00244 | 0.385 |
| LIG_14-3-3_CanoR_1 | 453 | 459 | PF00244 | 0.300 |
| LIG_14-3-3_CanoR_1 | 479 | 483 | PF00244 | 0.238 |
| LIG_14-3-3_CanoR_1 | 559 | 565 | PF00244 | 0.381 |
| LIG_Actin_WH2_2 | 292 | 310 | PF00022 | 0.291 |
| LIG_APCC_ABBA_1 | 110 | 115 | PF00400 | 0.454 |
| LIG_APCC_ABBA_1 | 348 | 353 | PF00400 | 0.363 |
| LIG_BRCT_BRCA1_1 | 513 | 517 | PF00533 | 0.387 |
| LIG_BRCT_BRCA1_1 | 536 | 540 | PF00533 | 0.314 |
| LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.363 |
| LIG_Clathr_ClatBox_1 | 461 | 465 | PF01394 | 0.206 |
| LIG_deltaCOP1_diTrp_1 | 419 | 428 | PF00928 | 0.363 |
| LIG_eIF4E_1 | 456 | 462 | PF01652 | 0.206 |
| LIG_FHA_1 | 102 | 108 | PF00498 | 0.454 |
| LIG_FHA_1 | 204 | 210 | PF00498 | 0.441 |
| LIG_FHA_1 | 215 | 221 | PF00498 | 0.288 |
| LIG_FHA_1 | 298 | 304 | PF00498 | 0.363 |
| LIG_FHA_1 | 308 | 314 | PF00498 | 0.260 |
| LIG_FHA_1 | 430 | 436 | PF00498 | 0.287 |
| LIG_FHA_1 | 511 | 517 | PF00498 | 0.380 |
| LIG_FHA_2 | 19 | 25 | PF00498 | 0.447 |
| LIG_FHA_2 | 414 | 420 | PF00498 | 0.287 |
| LIG_FHA_2 | 480 | 486 | PF00498 | 0.324 |
| LIG_FHA_2 | 82 | 88 | PF00498 | 0.570 |
| LIG_GBD_Chelix_1 | 252 | 260 | PF00786 | 0.363 |
| LIG_LIR_Apic_2 | 400 | 406 | PF02991 | 0.287 |
| LIG_LIR_Gen_1 | 121 | 130 | PF02991 | 0.602 |
| LIG_LIR_Gen_1 | 211 | 220 | PF02991 | 0.427 |
| LIG_LIR_Gen_1 | 26 | 36 | PF02991 | 0.454 |
| LIG_LIR_Gen_1 | 355 | 365 | PF02991 | 0.301 |
| LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.482 |
| LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.560 |
| LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.418 |
| LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.454 |
| LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.384 |
| LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.301 |
| LIG_LIR_Nem_3 | 366 | 371 | PF02991 | 0.321 |
| LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.363 |
| LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.401 |
| LIG_LYPXL_yS_3 | 444 | 447 | PF13949 | 0.363 |
| LIG_Pex14_2 | 178 | 182 | PF04695 | 0.357 |
| LIG_PTAP_UEV_1 | 161 | 166 | PF05743 | 0.519 |
| LIG_SH2_CRK | 123 | 127 | PF00017 | 0.483 |
| LIG_SH2_CRK | 36 | 40 | PF00017 | 0.452 |
| LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.363 |
| LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.363 |
| LIG_SH2_STAT3 | 456 | 459 | PF00017 | 0.206 |
| LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.410 |
| LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.390 |
| LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.230 |
| LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.254 |
| LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.206 |
| LIG_SH3_3 | 159 | 165 | PF00018 | 0.526 |
| LIG_SH3_3 | 370 | 376 | PF00018 | 0.363 |
| LIG_SH3_3 | 433 | 439 | PF00018 | 0.320 |
| LIG_SH3_3 | 480 | 486 | PF00018 | 0.267 |
| LIG_SH3_3 | 550 | 556 | PF00018 | 0.370 |
| LIG_SUMO_SIM_anti_2 | 529 | 535 | PF11976 | 0.206 |
| LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.363 |
| LIG_SUMO_SIM_par_1 | 526 | 532 | PF11976 | 0.291 |
| LIG_WRC_WIRS_1 | 540 | 545 | PF05994 | 0.363 |
| MOD_CK1_1 | 101 | 107 | PF00069 | 0.727 |
| MOD_CK1_1 | 118 | 124 | PF00069 | 0.500 |
| MOD_CK1_1 | 134 | 140 | PF00069 | 0.571 |
| MOD_CK1_1 | 151 | 157 | PF00069 | 0.556 |
| MOD_CK1_1 | 38 | 44 | PF00069 | 0.372 |
| MOD_CK1_1 | 393 | 399 | PF00069 | 0.313 |
| MOD_CK1_1 | 405 | 411 | PF00069 | 0.275 |
| MOD_CK1_1 | 511 | 517 | PF00069 | 0.327 |
| MOD_CK1_1 | 535 | 541 | PF00069 | 0.298 |
| MOD_CK1_1 | 57 | 63 | PF00069 | 0.422 |
| MOD_CK1_1 | 80 | 86 | PF00069 | 0.613 |
| MOD_CK2_1 | 81 | 87 | PF00069 | 0.455 |
| MOD_Cter_Amidation | 188 | 191 | PF01082 | 0.381 |
| MOD_DYRK1A_RPxSP_1 | 479 | 483 | PF00069 | 0.206 |
| MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.436 |
| MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.651 |
| MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.501 |
| MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.290 |
| MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.230 |
| MOD_GlcNHglycan | 352 | 357 | PF01048 | 0.435 |
| MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.456 |
| MOD_GlcNHglycan | 498 | 502 | PF01048 | 0.306 |
| MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.535 |
| MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.637 |
| MOD_GSK3_1 | 130 | 137 | PF00069 | 0.712 |
| MOD_GSK3_1 | 148 | 155 | PF00069 | 0.491 |
| MOD_GSK3_1 | 160 | 167 | PF00069 | 0.545 |
| MOD_GSK3_1 | 216 | 223 | PF00069 | 0.300 |
| MOD_GSK3_1 | 295 | 302 | PF00069 | 0.457 |
| MOD_GSK3_1 | 393 | 400 | PF00069 | 0.363 |
| MOD_GSK3_1 | 419 | 426 | PF00069 | 0.314 |
| MOD_GSK3_1 | 471 | 478 | PF00069 | 0.464 |
| MOD_GSK3_1 | 497 | 504 | PF00069 | 0.326 |
| MOD_GSK3_1 | 535 | 542 | PF00069 | 0.477 |
| MOD_GSK3_1 | 56 | 63 | PF00069 | 0.481 |
| MOD_GSK3_1 | 77 | 84 | PF00069 | 0.605 |
| MOD_GSK3_1 | 97 | 104 | PF00069 | 0.488 |
| MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.648 |
| MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.325 |
| MOD_NEK2_1 | 157 | 162 | PF00069 | 0.603 |
| MOD_NEK2_1 | 295 | 300 | PF00069 | 0.324 |
| MOD_NEK2_1 | 307 | 312 | PF00069 | 0.446 |
| MOD_NEK2_1 | 351 | 356 | PF00069 | 0.287 |
| MOD_NEK2_1 | 423 | 428 | PF00069 | 0.292 |
| MOD_NEK2_1 | 496 | 501 | PF00069 | 0.311 |
| MOD_PIKK_1 | 43 | 49 | PF00454 | 0.493 |
| MOD_PIKK_1 | 511 | 517 | PF00454 | 0.363 |
| MOD_PKA_2 | 18 | 24 | PF00069 | 0.417 |
| MOD_PKA_2 | 478 | 484 | PF00069 | 0.304 |
| MOD_PKA_2 | 554 | 560 | PF00069 | 0.287 |
| MOD_Plk_1 | 118 | 124 | PF00069 | 0.637 |
| MOD_Plk_1 | 170 | 176 | PF00069 | 0.570 |
| MOD_Plk_1 | 235 | 241 | PF00069 | 0.363 |
| MOD_Plk_1 | 352 | 358 | PF00069 | 0.309 |
| MOD_Plk_1 | 49 | 55 | PF00069 | 0.475 |
| MOD_Plk_4 | 118 | 124 | PF00069 | 0.627 |
| MOD_Plk_4 | 170 | 176 | PF00069 | 0.676 |
| MOD_Plk_4 | 23 | 29 | PF00069 | 0.502 |
| MOD_Plk_4 | 265 | 271 | PF00069 | 0.477 |
| MOD_Plk_4 | 35 | 41 | PF00069 | 0.349 |
| MOD_Plk_4 | 390 | 396 | PF00069 | 0.308 |
| MOD_Plk_4 | 397 | 403 | PF00069 | 0.346 |
| MOD_Plk_4 | 443 | 449 | PF00069 | 0.287 |
| MOD_Plk_4 | 457 | 463 | PF00069 | 0.287 |
| MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.530 |
| MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.363 |
| MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.347 |
| MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.320 |
| MOD_SUMO_rev_2 | 379 | 388 | PF00179 | 0.225 |
| MOD_SUMO_rev_2 | 460 | 469 | PF00179 | 0.206 |
| MOD_SUMO_rev_2 | 563 | 573 | PF00179 | 0.316 |
| TRG_DiLeu_BaEn_1 | 334 | 339 | PF01217 | 0.206 |
| TRG_DiLeu_BaEn_2 | 538 | 544 | PF01217 | 0.363 |
| TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.484 |
| TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.447 |
| TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.394 |
| TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.311 |
| TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.390 |
| TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.363 |
| TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.287 |
| TRG_ER_diArg_1 | 492 | 495 | PF00400 | 0.399 |
| TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.455 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I436 | Leptomonas seymouri | 40% | 98% |
| A0A3Q8IB87 | Leishmania donovani | 77% | 100% |
| A4HUW6 | Leishmania infantum | 77% | 100% |
| E9ANJ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
| G5EEN4 | Caenorhabditis elegans | 25% | 97% |
| Q4QH29 | Leishmania major | 76% | 100% |