| 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: 9 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 1, no: 6 |
| NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q1W3
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.501 |
| CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.441 |
| CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.462 |
| CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.467 |
| CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.464 |
| CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.458 |
| CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.648 |
| CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.588 |
| DEG_APCC_DBOX_1 | 232 | 240 | PF00400 | 0.465 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.570 |
| DEG_SPOP_SBC_1 | 52 | 56 | PF00917 | 0.434 |
| DOC_CDC14_PxL_1 | 135 | 143 | PF14671 | 0.465 |
| DOC_CYCLIN_RxL_1 | 332 | 343 | PF00134 | 0.412 |
| DOC_CYCLIN_yCln2_LP_2 | 389 | 395 | PF00134 | 0.478 |
| DOC_CYCLIN_yCln2_LP_2 | 91 | 97 | PF00134 | 0.501 |
| DOC_MAPK_DCC_7 | 194 | 202 | PF00069 | 0.462 |
| DOC_MAPK_HePTP_8 | 191 | 203 | PF00069 | 0.411 |
| DOC_MAPK_HePTP_8 | 349 | 361 | PF00069 | 0.419 |
| DOC_MAPK_MEF2A_6 | 194 | 203 | PF00069 | 0.460 |
| DOC_MAPK_MEF2A_6 | 337 | 346 | PF00069 | 0.384 |
| DOC_MAPK_MEF2A_6 | 352 | 361 | PF00069 | 0.296 |
| DOC_PP2B_LxvP_1 | 91 | 94 | PF13499 | 0.533 |
| DOC_PP4_FxxP_1 | 177 | 180 | PF00568 | 0.476 |
| DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.441 |
| DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.499 |
| DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.599 |
| DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.433 |
| DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.441 |
| DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.579 |
| DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.475 |
| DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.546 |
| LIG_14-3-3_CanoR_1 | 188 | 198 | PF00244 | 0.584 |
| LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.544 |
| LIG_14-3-3_CanoR_1 | 6 | 16 | PF00244 | 0.515 |
| LIG_BIR_III_4 | 209 | 213 | PF00653 | 0.478 |
| LIG_BIR_III_4 | 43 | 47 | PF00653 | 0.403 |
| LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.347 |
| LIG_Clathr_ClatBox_1 | 359 | 363 | PF01394 | 0.416 |
| LIG_EH1_1 | 271 | 279 | PF00400 | 0.496 |
| LIG_eIF4E_1 | 272 | 278 | PF01652 | 0.455 |
| LIG_FHA_1 | 117 | 123 | PF00498 | 0.463 |
| LIG_FHA_1 | 242 | 248 | PF00498 | 0.551 |
| LIG_FHA_1 | 406 | 412 | PF00498 | 0.419 |
| LIG_FHA_2 | 190 | 196 | PF00498 | 0.553 |
| LIG_FHA_2 | 417 | 423 | PF00498 | 0.560 |
| LIG_FHA_2 | 52 | 58 | PF00498 | 0.453 |
| LIG_FHA_2 | 81 | 87 | PF00498 | 0.585 |
| LIG_LIR_Apic_2 | 28 | 33 | PF02991 | 0.455 |
| LIG_LIR_Gen_1 | 383 | 393 | PF02991 | 0.458 |
| LIG_LIR_LC3C_4 | 358 | 361 | PF02991 | 0.443 |
| LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.433 |
| LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.593 |
| LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.489 |
| LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.310 |
| LIG_LYPXL_yS_3 | 138 | 141 | PF13949 | 0.439 |
| LIG_MYND_3 | 434 | 438 | PF01753 | 0.456 |
| LIG_PDZ_Class_3 | 449 | 454 | PF00595 | 0.642 |
| LIG_Pex14_2 | 398 | 402 | PF04695 | 0.499 |
| LIG_SH2_CRK | 396 | 400 | PF00017 | 0.451 |
| LIG_SH2_GRB2like | 395 | 398 | PF00017 | 0.414 |
| LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.369 |
| LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.383 |
| LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.324 |
| LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.445 |
| LIG_SH3_3 | 133 | 139 | PF00018 | 0.447 |
| LIG_SH3_3 | 218 | 224 | PF00018 | 0.471 |
| LIG_SH3_3 | 307 | 313 | PF00018 | 0.450 |
| LIG_SH3_3 | 438 | 444 | PF00018 | 0.633 |
| LIG_SUMO_SIM_anti_2 | 358 | 363 | PF11976 | 0.424 |
| LIG_SUMO_SIM_par_1 | 295 | 301 | PF11976 | 0.440 |
| LIG_SUMO_SIM_par_1 | 337 | 343 | PF11976 | 0.396 |
| LIG_SUMO_SIM_par_1 | 358 | 363 | PF11976 | 0.380 |
| LIG_SxIP_EBH_1 | 423 | 436 | PF03271 | 0.478 |
| LIG_UBA3_1 | 385 | 394 | PF00899 | 0.464 |
| LIG_WRC_WIRS_1 | 399 | 404 | PF05994 | 0.438 |
| MOD_CK1_1 | 112 | 118 | PF00069 | 0.464 |
| MOD_CK1_1 | 25 | 31 | PF00069 | 0.411 |
| MOD_CK1_1 | 340 | 346 | PF00069 | 0.350 |
| MOD_CK2_1 | 190 | 196 | PF00069 | 0.574 |
| MOD_CK2_1 | 228 | 234 | PF00069 | 0.504 |
| MOD_CK2_1 | 443 | 449 | PF00069 | 0.611 |
| MOD_CK2_1 | 51 | 57 | PF00069 | 0.446 |
| MOD_CK2_1 | 80 | 86 | PF00069 | 0.569 |
| MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.468 |
| MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.471 |
| MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.434 |
| MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.466 |
| MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.607 |
| MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.609 |
| MOD_GSK3_1 | 105 | 112 | PF00069 | 0.475 |
| MOD_GSK3_1 | 146 | 153 | PF00069 | 0.389 |
| MOD_GSK3_1 | 237 | 244 | PF00069 | 0.526 |
| MOD_GSK3_1 | 322 | 329 | PF00069 | 0.467 |
| MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.455 |
| MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.420 |
| MOD_NEK2_1 | 158 | 163 | PF00069 | 0.399 |
| MOD_NEK2_1 | 203 | 208 | PF00069 | 0.403 |
| MOD_NEK2_1 | 238 | 243 | PF00069 | 0.432 |
| MOD_NEK2_1 | 322 | 327 | PF00069 | 0.408 |
| MOD_NEK2_1 | 34 | 39 | PF00069 | 0.405 |
| MOD_NEK2_1 | 398 | 403 | PF00069 | 0.439 |
| MOD_NEK2_1 | 8 | 13 | PF00069 | 0.480 |
| MOD_PIKK_1 | 158 | 164 | PF00454 | 0.385 |
| MOD_PIKK_1 | 238 | 244 | PF00454 | 0.476 |
| MOD_PIKK_1 | 254 | 260 | PF00454 | 0.410 |
| MOD_PIKK_1 | 405 | 411 | PF00454 | 0.452 |
| MOD_PIKK_1 | 416 | 422 | PF00454 | 0.447 |
| MOD_PKA_2 | 204 | 210 | PF00069 | 0.429 |
| MOD_Plk_1 | 180 | 186 | PF00069 | 0.453 |
| MOD_Plk_4 | 337 | 343 | PF00069 | 0.361 |
| MOD_Plk_4 | 355 | 361 | PF00069 | 0.540 |
| MOD_Plk_4 | 425 | 431 | PF00069 | 0.472 |
| MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.468 |
| MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.562 |
| MOD_SUMO_for_1 | 252 | 255 | PF00179 | 0.428 |
| MOD_SUMO_for_1 | 435 | 438 | PF00179 | 0.577 |
| TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.394 |
| TRG_DiLeu_BaEn_2 | 233 | 239 | PF01217 | 0.466 |
| TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.389 |
| TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.411 |
| TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.229 |
| TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.419 |
| TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.418 |
| TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.452 |
| TRG_NLS_MonoExtN_4 | 313 | 318 | PF00514 | 0.485 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5Q9 | Leptomonas seymouri | 53% | 88% |
| A0A0S4JAW3 | Bodo saltans | 27% | 100% |
| A4HNX3 | Leishmania braziliensis | 76% | 100% |
| A4ICM1 | Leishmania infantum | 93% | 100% |
| E9ASN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
| H2ALR9 | Leishmania donovani | 93% | 100% |