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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HL03
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.433 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.484 |
DEG_SCF_TRCP1_1 | 109 | 114 | PF00400 | 0.270 |
DEG_SPOP_SBC_1 | 18 | 22 | PF00917 | 0.437 |
DOC_CYCLIN_RxL_1 | 399 | 409 | PF00134 | 0.468 |
DOC_MAPK_gen_1 | 247 | 253 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 303 | 311 | PF00069 | 0.285 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.415 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.351 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.498 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 258 | 268 | PF00244 | 0.247 |
LIG_Actin_WH2_2 | 88 | 103 | PF00022 | 0.378 |
LIG_deltaCOP1_diTrp_1 | 66 | 72 | PF00928 | 0.300 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.530 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.437 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.495 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.317 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.329 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.575 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.481 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.261 |
LIG_LIR_Gen_1 | 267 | 276 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.386 |
LIG_PDZ_Wminus1_1 | 423 | 425 | PF00595 | 0.459 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 138 | 142 | PF00017 | 0.261 |
LIG_SH2_NCK_1 | 15 | 19 | PF00017 | 0.424 |
LIG_SH2_NCK_1 | 189 | 193 | PF00017 | 0.402 |
LIG_SH2_SRC | 138 | 141 | PF00017 | 0.268 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.475 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.456 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.374 |
LIG_SUMO_SIM_anti_2 | 325 | 332 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 411 | 417 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 334 | 340 | PF11976 | 0.339 |
LIG_TRAF2_1 | 393 | 396 | PF00917 | 0.672 |
LIG_TRAF2_2 | 89 | 94 | PF00917 | 0.300 |
LIG_WW_3 | 375 | 379 | PF00397 | 0.475 |
MOD_CDC14_SPxK_1 | 363 | 366 | PF00782 | 0.482 |
MOD_CDC14_SPxK_1 | 375 | 378 | PF00782 | 0.474 |
MOD_CDK_SPK_2 | 52 | 57 | PF00069 | 0.371 |
MOD_CDK_SPxK_1 | 360 | 366 | PF00069 | 0.481 |
MOD_CDK_SPxK_1 | 372 | 378 | PF00069 | 0.445 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.580 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.497 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.492 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.410 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.466 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.478 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.318 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.605 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.586 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.453 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.428 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.322 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.366 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.557 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.402 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.737 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.476 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.201 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.550 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.507 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.419 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.376 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.435 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.352 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.652 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.322 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.485 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.389 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.410 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.405 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.448 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.437 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.437 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.263 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.399 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.444 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.336 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.462 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.403 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.350 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.315 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.448 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.355 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.572 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.305 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.481 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.445 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.662 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 179 | 184 | PF01217 | 0.254 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.214 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.771 |
TRG_NLS_MonoExtC_3 | 199 | 204 | PF00514 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5I9 | Leptomonas seymouri | 53% | 100% |
A0A1X0NRZ3 | Trypanosomatidae | 33% | 100% |
A0A3Q8IGJ4 | Leishmania donovani | 78% | 100% |
A0A422P320 | Trypanosoma rangeli | 38% | 100% |
A4I8I3 | Leishmania infantum | 78% | 100% |
D0AAN3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B3E4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q4Q8 | Leishmania major | 78% | 100% |
Q60525 | Mesocricetus auratus | 26% | 79% |
Q6NL34 | Drosophila melanogaster | 27% | 78% |
V5DMD9 | Trypanosoma cruzi | 36% | 100% |