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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A4HGS5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.424 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.431 |
CLV_PCSK_FUR_1 | 113 | 117 | PF00082 | 0.518 |
CLV_PCSK_FUR_1 | 376 | 380 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.420 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.433 |
CLV_PCSK_PC7_1 | 211 | 217 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.435 |
CLV_Separin_Metazoa | 150 | 154 | PF03568 | 0.515 |
CLV_Separin_Metazoa | 252 | 256 | PF03568 | 0.691 |
DEG_APCC_KENBOX_2 | 61 | 65 | PF00400 | 0.526 |
DOC_CYCLIN_RxL_1 | 54 | 63 | PF00134 | 0.612 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.516 |
DOC_USP7_UBL2_3 | 115 | 119 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.431 |
DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.588 |
DOC_USP7_UBL2_3 | 280 | 284 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 292 | 296 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 313 | 317 | PF12436 | 0.562 |
DOC_USP7_UBL2_3 | 77 | 81 | PF12436 | 0.509 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.458 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.469 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.562 |
LIG_LIR_Gen_1 | 363 | 374 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.548 |
LIG_PDZ_Class_2 | 398 | 403 | PF00595 | 0.489 |
LIG_SH2_NCK_1 | 366 | 370 | PF00017 | 0.562 |
LIG_SH2_SRC | 366 | 369 | PF00017 | 0.549 |
LIG_SxIP_EBH_1 | 47 | 58 | PF03271 | 0.548 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.654 |
LIG_TRAF2_1 | 385 | 388 | PF00917 | 0.446 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.555 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.626 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.624 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.533 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.635 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.547 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.624 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.613 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.579 |
MOD_NEK2_2 | 34 | 39 | PF00069 | 0.548 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.427 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.482 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.429 |
MOD_PKA_1 | 303 | 309 | PF00069 | 0.488 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.482 |
MOD_Plk_2-3 | 393 | 399 | PF00069 | 0.465 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.557 |
MOD_SUMO_for_1 | 76 | 79 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 111 | 121 | PF00179 | 0.515 |
MOD_SUMO_rev_2 | 212 | 221 | PF00179 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.637 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.567 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 229 | 232 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 356 | 358 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 74 | 76 | PF00400 | 0.441 |
TRG_NLS_Bipartite_1 | 161 | 179 | PF00514 | 0.511 |
TRG_NLS_Bipartite_1 | 263 | 284 | PF00514 | 0.513 |
TRG_NLS_Bipartite_1 | 292 | 306 | PF00514 | 0.425 |
TRG_NLS_MonoCore_2 | 174 | 179 | PF00514 | 0.512 |
TRG_NLS_MonoExtC_3 | 174 | 180 | PF00514 | 0.513 |
TRG_NLS_MonoExtC_3 | 279 | 284 | PF00514 | 0.519 |
TRG_NLS_MonoExtC_3 | 301 | 307 | PF00514 | 0.432 |
TRG_NLS_MonoExtN_4 | 278 | 284 | PF00514 | 0.430 |
TRG_NLS_MonoExtN_4 | 53 | 60 | PF00514 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 58 | 63 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 81 | 85 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IEZ7 | Leishmania donovani | 68% | 80% |
A4I3V1 | Leishmania infantum | 68% | 80% |