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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9AY69
Term | Name | Level | Count |
---|---|---|---|
GO:0001653 | peptide receptor activity | 3 | 11 |
GO:0038023 | signaling receptor activity | 2 | 11 |
GO:0060089 | molecular transducer activity | 1 | 11 |
GO:0140625 | opioid growth factor receptor activity | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.399 |
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 293 | 297 | PF00656 | 0.771 |
CLV_C14_Caspase3-7 | 398 | 402 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.606 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.314 |
DEG_APCC_DBOX_1 | 262 | 270 | PF00400 | 0.392 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.557 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.696 |
DOC_CYCLIN_RxL_1 | 209 | 218 | PF00134 | 0.339 |
DOC_CYCLIN_RxL_1 | 331 | 338 | PF00134 | 0.302 |
DOC_CYCLIN_yCln2_LP_2 | 107 | 110 | PF00134 | 0.400 |
DOC_MAPK_gen_1 | 331 | 341 | PF00069 | 0.343 |
DOC_MAPK_MEF2A_6 | 138 | 147 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 334 | 341 | PF00069 | 0.367 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.344 |
DOC_PP1_RVXF_1 | 345 | 352 | PF00149 | 0.352 |
DOC_PP1_RVXF_1 | 358 | 364 | PF00149 | 0.293 |
DOC_PP2B_LxvP_1 | 107 | 110 | PF13499 | 0.400 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.547 |
DOC_PP4_FxxP_1 | 363 | 366 | PF00568 | 0.431 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.511 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.458 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 230 | 236 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.434 |
LIG_Actin_WH2_2 | 329 | 345 | PF00022 | 0.406 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.352 |
LIG_eIF4E_1 | 233 | 239 | PF01652 | 0.428 |
LIG_EVH1_1 | 312 | 316 | PF00568 | 0.472 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.647 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.634 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.617 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.680 |
LIG_GBD_Chelix_1 | 344 | 352 | PF00786 | 0.317 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 203 | 214 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 234 | 242 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 262 | 270 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 318 | 325 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 338 | 349 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 318 | 322 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.338 |
LIG_MYND_1 | 146 | 150 | PF01753 | 0.411 |
LIG_NRBOX | 204 | 210 | PF00104 | 0.495 |
LIG_NRBOX | 332 | 338 | PF00104 | 0.264 |
LIG_Pex14_1 | 260 | 264 | PF04695 | 0.352 |
LIG_REV1ctd_RIR_1 | 239 | 249 | PF16727 | 0.548 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.300 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.317 |
LIG_SH2_PTP2 | 235 | 238 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.300 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.290 |
LIG_SH3_1 | 310 | 316 | PF00018 | 0.477 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.295 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.334 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.624 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.486 |
LIG_SUMO_SIM_anti_2 | 216 | 224 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 234 | 240 | PF11976 | 0.463 |
LIG_SUMO_SIM_anti_2 | 96 | 102 | PF11976 | 0.554 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.465 |
LIG_TRAF2_1 | 188 | 191 | PF00917 | 0.504 |
LIG_TRAF2_1 | 259 | 262 | PF00917 | 0.399 |
LIG_TYR_ITIM | 231 | 236 | PF00017 | 0.303 |
LIG_WRC_WIRS_1 | 319 | 324 | PF05994 | 0.613 |
LIG_WW_1 | 316 | 319 | PF00397 | 0.575 |
MOD_CDK_SPxxK_3 | 87 | 94 | PF00069 | 0.446 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.428 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.374 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.595 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.487 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.491 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.402 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.744 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.640 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.468 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.727 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.391 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.456 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.522 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.705 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.490 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.652 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.398 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.495 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.584 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.579 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.470 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.508 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.330 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.491 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.580 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.558 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.450 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.602 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.439 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.393 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.472 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.464 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.307 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.483 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.379 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.360 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.529 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.491 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.748 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.596 |
TRG_DiLeu_BaEn_1 | 204 | 209 | PF01217 | 0.374 |
TRG_DiLeu_BaEn_1 | 249 | 254 | PF01217 | 0.544 |
TRG_DiLeu_BaEn_1 | 262 | 267 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_4 | 249 | 255 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 357 | 362 | PF01217 | 0.320 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.446 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.467 |
TRG_NES_CRM1_1 | 338 | 350 | PF08389 | 0.307 |
TRG_NLS_MonoExtN_4 | 389 | 395 | PF00514 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 212 | 216 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 334 | 338 | PF00026 | 0.303 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ78 | Leptomonas seymouri | 52% | 100% |
A0A1X0NT07 | Trypanosomatidae | 34% | 100% |
A0A3Q8IFS6 | Leishmania donovani | 87% | 100% |
A0A422MXD1 | Trypanosoma rangeli | 37% | 100% |
A4HEU6 | Leishmania braziliensis | 73% | 96% |
A4I220 | Leishmania infantum | 87% | 100% |
C9ZRY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4Q9A3 | Leishmania major | 88% | 99% |
V5BUN4 | Trypanosoma cruzi | 34% | 100% |