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 |
Related structures:
AlphaFold database: A4IAR8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.534 |
CLV_PCSK_FUR_1 | 23 | 27 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.468 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.559 |
DOC_CYCLIN_RxL_1 | 128 | 138 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 261 | 268 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 45 | 52 | PF00149 | 0.523 |
DOC_PP1_SILK_1 | 318 | 323 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 321 | 324 | PF13499 | 0.617 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.461 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.450 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 224 | 234 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 322 | 332 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 46 | 52 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.486 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.633 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.515 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.443 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.451 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.567 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.451 |
LIG_GBD_Chelix_1 | 91 | 99 | PF00786 | 0.487 |
LIG_NRBOX | 12 | 18 | PF00104 | 0.479 |
LIG_NRBOX | 229 | 235 | PF00104 | 0.431 |
LIG_PCNA_yPIPBox_3 | 36 | 49 | PF02747 | 0.536 |
LIG_REV1ctd_RIR_1 | 220 | 228 | PF16727 | 0.440 |
LIG_SH2_NCK_1 | 273 | 277 | PF00017 | 0.463 |
LIG_SH2_SRC | 273 | 276 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.528 |
LIG_SUMO_SIM_anti_2 | 191 | 197 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 309 | 315 | PF11976 | 0.530 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.503 |
LIG_TRAF2_1 | 30 | 33 | PF00917 | 0.513 |
LIG_WRC_WIRS_1 | 127 | 132 | PF05994 | 0.487 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.537 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.366 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.581 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.453 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.623 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.568 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.615 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.464 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.412 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.416 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.429 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.458 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.538 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.593 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.470 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.586 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.476 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.541 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.386 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.529 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.484 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.403 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.406 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.538 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.424 |
MOD_SUMO_for_1 | 35 | 38 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 50 | 56 | PF00179 | 0.431 |
TRG_DiLeu_BaEn_1 | 12 | 17 | PF01217 | 0.541 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.381 |
TRG_DiLeu_BaEn_1 | 214 | 219 | PF01217 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 229 | 234 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.418 |
TRG_NES_CRM1_1 | 257 | 271 | PF08389 | 0.565 |
TRG_NES_CRM1_1 | 312 | 327 | PF08389 | 0.522 |
TRG_NLS_MonoExtN_4 | 23 | 28 | PF00514 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5M0 | Leptomonas seymouri | 38% | 100% |
A0A3Q8INY6 | Leishmania donovani | 99% | 100% |
A4HM56 | Leishmania braziliensis | 60% | 100% |
E9AEJ4 | Leishmania major | 87% | 100% |
E9B5Q5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |