| 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: 4 |
| Pissara et al. | yes | yes: 20 |
| 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: 12 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 7 |
| NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HK65
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 8 |
| GO:0005488 | binding | 1 | 8 |
| GO:0097159 | organic cyclic compound binding | 2 | 8 |
| GO:1901363 | heterocyclic compound binding | 2 | 8 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 25 | 31 | PF00089 | 0.421 |
| CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.439 |
| CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.421 |
| CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.439 |
| CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.421 |
| CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.466 |
| CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.530 |
| CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.421 |
| CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.506 |
| CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.348 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.751 |
| DOC_CKS1_1 | 56 | 61 | PF01111 | 0.421 |
| DOC_MAPK_gen_1 | 339 | 345 | PF00069 | 0.465 |
| DOC_MAPK_gen_1 | 42 | 50 | PF00069 | 0.421 |
| DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.718 |
| DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.615 |
| DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.727 |
| DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.577 |
| DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.700 |
| DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.519 |
| DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.538 |
| DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.502 |
| LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.352 |
| LIG_14-3-3_CanoR_1 | 381 | 391 | PF00244 | 0.502 |
| LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.429 |
| LIG_14-3-3_CanoR_1 | 446 | 455 | PF00244 | 0.608 |
| LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.421 |
| LIG_AP2alpha_1 | 72 | 76 | PF02296 | 0.421 |
| LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.574 |
| LIG_EVH1_2 | 301 | 305 | PF00568 | 0.526 |
| LIG_FHA_1 | 100 | 106 | PF00498 | 0.582 |
| LIG_FHA_1 | 187 | 193 | PF00498 | 0.671 |
| LIG_FHA_1 | 20 | 26 | PF00498 | 0.353 |
| LIG_FHA_1 | 202 | 208 | PF00498 | 0.567 |
| LIG_FHA_1 | 301 | 307 | PF00498 | 0.452 |
| LIG_FHA_1 | 312 | 318 | PF00498 | 0.348 |
| LIG_FHA_1 | 35 | 41 | PF00498 | 0.353 |
| LIG_FHA_1 | 452 | 458 | PF00498 | 0.433 |
| LIG_FHA_1 | 64 | 70 | PF00498 | 0.488 |
| LIG_FHA_2 | 320 | 326 | PF00498 | 0.401 |
| LIG_FHA_2 | 425 | 431 | PF00498 | 0.578 |
| LIG_FHA_2 | 446 | 452 | PF00498 | 0.579 |
| LIG_LIR_Apic_2 | 201 | 206 | PF02991 | 0.717 |
| LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.429 |
| LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.733 |
| LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.417 |
| LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.435 |
| LIG_Pex14_2 | 72 | 76 | PF04695 | 0.421 |
| LIG_SH2_GRB2like | 436 | 439 | PF00017 | 0.540 |
| LIG_SH2_SRC | 436 | 439 | PF00017 | 0.540 |
| LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.577 |
| LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.560 |
| LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.608 |
| LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.682 |
| LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.542 |
| LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.560 |
| LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.467 |
| LIG_SH3_3 | 135 | 141 | PF00018 | 0.752 |
| LIG_SH3_3 | 144 | 150 | PF00018 | 0.791 |
| LIG_SH3_3 | 153 | 159 | PF00018 | 0.608 |
| LIG_SH3_3 | 162 | 168 | PF00018 | 0.568 |
| LIG_SH3_3 | 171 | 177 | PF00018 | 0.586 |
| LIG_SH3_3 | 185 | 191 | PF00018 | 0.594 |
| LIG_SH3_3 | 230 | 236 | PF00018 | 0.817 |
| LIG_SH3_3 | 310 | 316 | PF00018 | 0.488 |
| LIG_SH3_3 | 387 | 393 | PF00018 | 0.570 |
| LIG_SH3_3 | 454 | 460 | PF00018 | 0.472 |
| LIG_SH3_3 | 484 | 490 | PF00018 | 0.680 |
| LIG_SUMO_SIM_anti_2 | 307 | 312 | PF11976 | 0.434 |
| LIG_SUMO_SIM_anti_2 | 351 | 358 | PF11976 | 0.503 |
| LIG_WRC_WIRS_1 | 324 | 329 | PF05994 | 0.321 |
| MOD_CDK_SPxxK_3 | 404 | 411 | PF00069 | 0.506 |
| MOD_CK1_1 | 186 | 192 | PF00069 | 0.572 |
| MOD_CK1_1 | 201 | 207 | PF00069 | 0.566 |
| MOD_CK1_1 | 51 | 57 | PF00069 | 0.403 |
| MOD_CK2_1 | 121 | 127 | PF00069 | 0.623 |
| MOD_CK2_1 | 319 | 325 | PF00069 | 0.404 |
| MOD_CK2_1 | 445 | 451 | PF00069 | 0.567 |
| MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.707 |
| MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.549 |
| MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.557 |
| MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.418 |
| MOD_GSK3_1 | 15 | 22 | PF00069 | 0.668 |
| MOD_GSK3_1 | 201 | 208 | PF00069 | 0.566 |
| MOD_GSK3_1 | 23 | 30 | PF00069 | 0.320 |
| MOD_GSK3_1 | 300 | 307 | PF00069 | 0.483 |
| MOD_GSK3_1 | 319 | 326 | PF00069 | 0.320 |
| MOD_GSK3_1 | 400 | 407 | PF00069 | 0.599 |
| MOD_GSK3_1 | 420 | 427 | PF00069 | 0.427 |
| MOD_GSK3_1 | 428 | 435 | PF00069 | 0.484 |
| MOD_GSK3_1 | 44 | 51 | PF00069 | 0.532 |
| MOD_GSK3_1 | 447 | 454 | PF00069 | 0.504 |
| MOD_GSK3_1 | 95 | 102 | PF00069 | 0.489 |
| MOD_NEK2_1 | 121 | 126 | PF00069 | 0.726 |
| MOD_NEK2_1 | 229 | 234 | PF00069 | 0.704 |
| MOD_NEK2_1 | 323 | 328 | PF00069 | 0.319 |
| MOD_NEK2_1 | 400 | 405 | PF00069 | 0.705 |
| MOD_NEK2_1 | 99 | 104 | PF00069 | 0.407 |
| MOD_PIKK_1 | 15 | 21 | PF00454 | 0.687 |
| MOD_PIKK_1 | 186 | 192 | PF00454 | 0.669 |
| MOD_PKA_2 | 239 | 245 | PF00069 | 0.598 |
| MOD_PKA_2 | 27 | 33 | PF00069 | 0.348 |
| MOD_PKA_2 | 445 | 451 | PF00069 | 0.567 |
| MOD_Plk_1 | 64 | 70 | PF00069 | 0.356 |
| MOD_Plk_2-3 | 451 | 457 | PF00069 | 0.549 |
| MOD_Plk_4 | 100 | 106 | PF00069 | 0.482 |
| MOD_Plk_4 | 198 | 204 | PF00069 | 0.719 |
| MOD_Plk_4 | 300 | 306 | PF00069 | 0.456 |
| MOD_Plk_4 | 355 | 361 | PF00069 | 0.521 |
| MOD_Plk_4 | 432 | 438 | PF00069 | 0.457 |
| MOD_Plk_4 | 64 | 70 | PF00069 | 0.383 |
| MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.701 |
| MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.515 |
| MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.537 |
| MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.502 |
| MOD_SUMO_rev_2 | 475 | 482 | PF00179 | 0.603 |
| MOD_SUMO_rev_2 | 492 | 502 | PF00179 | 0.536 |
| TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.619 |
| TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.663 |
| TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.838 |
| TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.419 |
| TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.421 |
| TRG_Pf-PMV_PEXEL_1 | 467 | 471 | PF00026 | 0.506 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3Q8IFS5 | Leishmania donovani | 82% | 100% |
| A0A422N8U4 | Trypanosoma rangeli | 42% | 100% |
| A4I7Q0 | Leishmania infantum | 82% | 100% |
| E9B2K8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
| Q4Q5J8 | Leishmania major | 79% | 100% |
| V5B118 | Trypanosoma cruzi | 43% | 100% |