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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HPA2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 318 | 322 | PF00656 | 0.655 |
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.450 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.296 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 141 | 143 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.274 |
DEG_APCC_DBOX_1 | 166 | 174 | PF00400 | 0.459 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.542 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.308 |
DEG_SCF_FBW7_1 | 304 | 311 | PF00400 | 0.656 |
DEG_SCF_FBW7_1 | 396 | 403 | PF00400 | 0.351 |
DOC_CKS1_1 | 305 | 310 | PF01111 | 0.785 |
DOC_CKS1_1 | 397 | 402 | PF01111 | 0.468 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 154 | 163 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 124 | 130 | PF00134 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 159 | 165 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 270 | 279 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 44 | 50 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 167 | 174 | PF00069 | 0.502 |
DOC_MAPK_NFAT4_5 | 167 | 175 | PF00069 | 0.502 |
DOC_PP1_RVXF_1 | 389 | 396 | PF00149 | 0.438 |
DOC_PP1_RVXF_1 | 54 | 61 | PF00149 | 0.490 |
DOC_PP4_FxxP_1 | 384 | 387 | PF00568 | 0.452 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.728 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.478 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 326 | 336 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.477 |
LIG_Actin_WH2_2 | 63 | 78 | PF00022 | 0.502 |
LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.564 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.344 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.490 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.538 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.389 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.575 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.466 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.659 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.409 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.452 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.508 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.283 |
LIG_LIR_Apic_2 | 281 | 287 | PF02991 | 0.621 |
LIG_LIR_Apic_2 | 330 | 336 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 101 | 111 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 19 | 23 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.530 |
LIG_LYPXL_S_1 | 377 | 381 | PF13949 | 0.360 |
LIG_LYPXL_yS_3 | 378 | 381 | PF13949 | 0.360 |
LIG_MLH1_MIPbox_1 | 290 | 294 | PF16413 | 0.564 |
LIG_Pex14_2 | 384 | 388 | PF04695 | 0.447 |
LIG_REV1ctd_RIR_1 | 18 | 24 | PF16727 | 0.437 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.530 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.684 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.642 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.598 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.390 |
LIG_SUMO_SIM_anti_2 | 161 | 167 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 170 | 177 | PF11976 | 0.579 |
LIG_SUMO_SIM_par_1 | 2 | 7 | PF11976 | 0.203 |
LIG_SUMO_SIM_par_1 | 31 | 36 | PF11976 | 0.465 |
LIG_TYR_ITIM | 376 | 381 | PF00017 | 0.434 |
LIG_WRC_WIRS_1 | 17 | 22 | PF05994 | 0.361 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.361 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.389 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.406 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.266 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.361 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.617 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.743 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.662 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.363 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.360 |
MOD_CMANNOS | 12 | 15 | PF00535 | 0.284 |
MOD_Cter_Amidation | 42 | 45 | PF01082 | 0.400 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.438 |
MOD_GlcNHglycan | 148 | 152 | PF01048 | 0.448 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.538 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.682 |
MOD_GlcNHglycan | 321 | 325 | PF01048 | 0.707 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.491 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.221 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.437 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.565 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.549 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.308 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.602 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.562 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.659 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.400 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.519 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.329 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.291 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.200 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.346 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.579 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.249 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.348 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.203 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.319 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.415 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.309 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.371 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.606 |
MOD_PKB_1 | 24 | 32 | PF00069 | 0.447 |
MOD_PKB_1 | 326 | 334 | PF00069 | 0.483 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.223 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.304 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.220 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.347 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.529 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.323 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.342 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.321 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.360 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.288 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.626 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.597 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.258 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 250 | 258 | PF00179 | 0.637 |
TRG_DiLeu_BaLyEn_6 | 376 | 381 | PF01217 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 388 | 393 | PF01217 | 0.407 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.417 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 44 | 46 | PF00400 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 44 | 49 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7B0 | Leptomonas seymouri | 48% | 100% |
A0A1X0P7L9 | Trypanosomatidae | 30% | 100% |
A0A3Q8IQZ6 | Leishmania donovani | 75% | 99% |
A4IDK8 | Leishmania infantum | 75% | 99% |
D0A3A6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AT11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |
Q4Q1I7 | Leishmania major | 75% | 99% |
V5DCK9 | Trypanosoma cruzi | 29% | 100% |