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: E9ASB1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.646 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.724 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.589 |
DEG_APCC_DBOX_1 | 234 | 242 | PF00400 | 0.433 |
DEG_APCC_DBOX_1 | 59 | 67 | PF00400 | 0.591 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 248 | 254 | PF00134 | 0.623 |
DOC_MAPK_gen_1 | 232 | 240 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 37 | 45 | PF00069 | 0.450 |
DOC_PP4_FxxP_1 | 317 | 320 | PF00568 | 0.515 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.558 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 15 | 25 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 204 | 213 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 342 | 352 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 86 | 90 | PF00244 | 0.654 |
LIG_Actin_WH2_2 | 316 | 331 | PF00022 | 0.574 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.552 |
LIG_Clathr_ClatBox_1 | 68 | 72 | PF01394 | 0.636 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.459 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.597 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.492 |
LIG_GBD_Chelix_1 | 241 | 249 | PF00786 | 0.656 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 210 | 221 | PF02991 | 0.719 |
LIG_LIR_Gen_1 | 262 | 270 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.721 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.611 |
LIG_NRBOX | 65 | 71 | PF00104 | 0.644 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.580 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.569 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.560 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.587 |
LIG_SH3_4 | 73 | 80 | PF00018 | 0.464 |
LIG_SUMO_SIM_anti_2 | 168 | 174 | PF11976 | 0.560 |
LIG_SUMO_SIM_anti_2 | 64 | 70 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 117 | 122 | PF11976 | 0.690 |
LIG_SUMO_SIM_par_1 | 40 | 46 | PF11976 | 0.654 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.640 |
LIG_TRAF2_1 | 377 | 380 | PF00917 | 0.658 |
LIG_UBA3_1 | 385 | 390 | PF00899 | 0.416 |
LIG_UBA3_1 | 68 | 73 | PF00899 | 0.502 |
MOD_CDC14_SPxK_1 | 222 | 225 | PF00782 | 0.586 |
MOD_CDK_SPK_2 | 250 | 255 | PF00069 | 0.550 |
MOD_CDK_SPxK_1 | 219 | 225 | PF00069 | 0.588 |
MOD_CDK_SPxxK_3 | 335 | 342 | PF00069 | 0.587 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.609 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.595 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.462 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.702 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.562 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.656 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.538 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.573 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.558 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.595 |
MOD_GlcNHglycan | 289 | 293 | PF01048 | 0.773 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.597 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.625 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.670 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.565 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.514 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.577 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.632 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.662 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.431 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.493 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.641 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.619 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.457 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.666 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.578 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.551 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.473 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.697 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.549 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.589 |
TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.558 |
TRG_DiLeu_BaEn_1 | 64 | 69 | PF01217 | 0.648 |
TRG_DiLeu_BaLyEn_6 | 20 | 25 | PF01217 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.422 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.443 |
TRG_NES_CRM1_1 | 129 | 141 | PF08389 | 0.567 |
TRG_NES_CRM1_1 | 350 | 364 | PF08389 | 0.453 |
TRG_NLS_Bipartite_1 | 2 | 19 | PF00514 | 0.593 |
TRG_NLS_MonoExtN_4 | 14 | 19 | PF00514 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 30 | 34 | PF00026 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 342 | 347 | PF00026 | 0.621 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IB12 | Leptomonas seymouri | 33% | 100% |
A0A3S7WVS2 | Leishmania donovani | 88% | 100% |
A4HAA7 | Leishmania braziliensis | 72% | 100% |
A4HYI7 | Leishmania infantum | 87% | 100% |
Q4QD51 | Leishmania major | 86% | 100% |