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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S5H6V7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 398 | 404 | PF00089 | 0.592 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.736 |
CLV_PCSK_FUR_1 | 239 | 243 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.739 |
CLV_PCSK_PC7_1 | 234 | 240 | PF00082 | 0.367 |
CLV_PCSK_PC7_1 | 241 | 247 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.190 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.337 |
DEG_APCC_DBOX_1 | 215 | 223 | PF00400 | 0.345 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.198 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.554 |
DOC_CYCLIN_RxL_1 | 47 | 59 | PF00134 | 0.403 |
DOC_MAPK_DCC_7 | 87 | 96 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 189 | 195 | PF00069 | 0.471 |
DOC_MAPK_HePTP_8 | 84 | 96 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 87 | 96 | PF00069 | 0.488 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.592 |
DOC_USP7_UBL2_3 | 83 | 87 | PF12436 | 0.353 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 133 | 140 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 270 | 279 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 313 | 320 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 47 | 55 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 58 | 63 | PF00244 | 0.462 |
LIG_APCC_ABBA_1 | 258 | 263 | PF00400 | 0.555 |
LIG_APCC_ABBA_1 | 36 | 41 | PF00400 | 0.384 |
LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.260 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.451 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.522 |
LIG_BRCT_BRCA1_2 | 7 | 13 | PF00533 | 0.500 |
LIG_CaM_IQ_9 | 208 | 223 | PF13499 | 0.452 |
LIG_eIF4E_1 | 230 | 236 | PF01652 | 0.506 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.412 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.313 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.454 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.454 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.317 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.487 |
LIG_LIR_Gen_1 | 152 | 158 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 183 | 191 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.542 |
LIG_MLH1_MIPbox_1 | 23 | 27 | PF16413 | 0.260 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.404 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.328 |
LIG_PTB_Apo_2 | 200 | 207 | PF02174 | 0.463 |
LIG_REV1ctd_RIR_1 | 24 | 32 | PF16727 | 0.269 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.533 |
LIG_SH3_5 | 226 | 230 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 255 | 260 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 326 | 332 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 326 | 332 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 76 | 82 | PF11976 | 0.400 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.399 |
LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.438 |
LIG_TYR_ITIM | 259 | 264 | PF00017 | 0.341 |
MOD_CDK_SPxxK_3 | 149 | 156 | PF00069 | 0.464 |
MOD_CDK_SPxxK_3 | 385 | 392 | PF00069 | 0.613 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.581 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.288 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.485 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.381 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.538 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.362 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.217 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.482 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.591 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.299 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.371 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.421 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.456 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.653 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.439 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.360 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.661 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.427 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.734 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.564 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.330 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.332 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.274 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.273 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.303 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.410 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.536 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.459 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.489 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.327 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.533 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.407 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.361 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.637 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.330 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.468 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.725 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.450 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.494 |
MOD_Plk_2-3 | 326 | 332 | PF00069 | 0.482 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.371 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.340 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.303 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.462 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.759 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.511 |
MOD_SUMO_for_1 | 206 | 209 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 369 | 378 | PF00179 | 0.618 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.368 |
TRG_DiLeu_BaEn_4 | 363 | 369 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 358 | 360 | PF00400 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.340 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILL6 | Leptomonas seymouri | 68% | 100% |
A0A0S4JNX3 | Bodo saltans | 50% | 100% |
A0A1X0P9L0 | Trypanosomatidae | 60% | 100% |
A4H888 | Leishmania braziliensis | 86% | 100% |
A4HWL1 | Leishmania infantum | 100% | 100% |
C9ZMN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AQB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QF56 | Leishmania major | 94% | 100% |
V5BKH7 | Trypanosoma cruzi | 62% | 100% |