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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9B066
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.566 |
CLV_MEL_PAP_1 | 270 | 276 | PF00089 | 0.454 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.413 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.203 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.540 |
CLV_Separin_Metazoa | 14 | 18 | PF03568 | 0.408 |
DEG_APCC_DBOX_1 | 155 | 163 | PF00400 | 0.337 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.473 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.617 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.393 |
DOC_MAPK_DCC_7 | 357 | 367 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 17 | 27 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 195 | 204 | PF00069 | 0.339 |
DOC_MAPK_gen_1 | 242 | 251 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 68 | 75 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 94 | 102 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 18 | 27 | PF00069 | 0.290 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 95 | 104 | PF00069 | 0.365 |
DOC_PP1_RVXF_1 | 138 | 144 | PF00149 | 0.467 |
DOC_PP2B_LxvP_1 | 342 | 345 | PF13499 | 0.379 |
DOC_PP4_FxxP_1 | 372 | 375 | PF00568 | 0.280 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.375 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.532 |
DOC_USP7_UBL2_3 | 106 | 110 | PF12436 | 0.203 |
DOC_USP7_UBL2_3 | 134 | 138 | PF12436 | 0.203 |
DOC_USP7_UBL2_3 | 420 | 424 | PF12436 | 0.285 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.453 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 357 | 365 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 378 | 385 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 47 | 51 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 54 | 58 | PF00244 | 0.330 |
LIG_Actin_WH2_2 | 143 | 158 | PF00022 | 0.437 |
LIG_BRCT_BRCA1_1 | 260 | 264 | PF00533 | 0.357 |
LIG_CSL_BTD_1 | 342 | 345 | PF09270 | 0.379 |
LIG_deltaCOP1_diTrp_1 | 178 | 184 | PF00928 | 0.370 |
LIG_EH1_1 | 147 | 155 | PF00400 | 0.337 |
LIG_EH1_1 | 434 | 442 | PF00400 | 0.327 |
LIG_eIF4E_1 | 435 | 441 | PF01652 | 0.459 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.433 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.492 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.438 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.238 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.517 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.373 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.203 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.610 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.399 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.531 |
LIG_LIR_Apic_2 | 371 | 375 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 167 | 176 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 178 | 188 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 37 | 45 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.392 |
LIG_LYPXL_yS_3 | 425 | 428 | PF13949 | 0.544 |
LIG_MYND_1 | 340 | 344 | PF01753 | 0.545 |
LIG_MYND_1 | 450 | 454 | PF01753 | 0.390 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.434 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.413 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.393 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.397 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.590 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.675 |
LIG_SUMO_SIM_anti_2 | 267 | 272 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 476 | 483 | PF11976 | 0.483 |
LIG_TRAF2_1 | 172 | 175 | PF00917 | 0.203 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.583 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.436 |
LIG_WW_3 | 18 | 22 | PF00397 | 0.490 |
MOD_CDK_SPK_2 | 54 | 59 | PF00069 | 0.422 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.510 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.430 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.589 |
MOD_Cter_Amidation | 418 | 421 | PF01082 | 0.270 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.386 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.531 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.468 |
MOD_GlcNHglycan | 483 | 487 | PF01048 | 0.668 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.356 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.271 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.300 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.562 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.437 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.246 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.341 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.356 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.454 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.341 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.278 |
MOD_PK_1 | 424 | 430 | PF00069 | 0.426 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.601 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.282 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.331 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.440 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.473 |
MOD_Plk_2-3 | 230 | 236 | PF00069 | 0.203 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.301 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.393 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.431 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.518 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.390 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.556 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.535 |
TRG_DiLeu_BaEn_1 | 244 | 249 | PF01217 | 0.246 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.508 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.185 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 352 | 356 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3P6 | Leptomonas seymouri | 41% | 100% |
A0A1X0NR47 | Trypanosomatidae | 27% | 100% |
A0A3Q8IQU6 | Leishmania donovani | 67% | 100% |
A0A3R7K6Z5 | Trypanosoma rangeli | 28% | 100% |
A4HGU8 | Leishmania braziliensis | 51% | 100% |
A4I3X6 | Leishmania infantum | 67% | 100% |
D0A944 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |