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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QEY7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.376 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.302 |
DEG_APCC_DBOX_1 | 216 | 224 | PF00400 | 0.349 |
DEG_SIAH_1 | 46 | 54 | PF03145 | 0.488 |
DOC_CKS1_1 | 178 | 183 | PF01111 | 0.656 |
DOC_CYCLIN_RxL_1 | 345 | 353 | PF00134 | 0.418 |
DOC_CYCLIN_yCln2_LP_2 | 164 | 170 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.486 |
DOC_MAPK_gen_1 | 348 | 356 | PF00069 | 0.404 |
DOC_PP1_RVXF_1 | 318 | 325 | PF00149 | 0.338 |
DOC_PP1_RVXF_1 | 346 | 353 | PF00149 | 0.414 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.485 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.683 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 203 | 211 | PF00244 | 0.554 |
LIG_BRCT_BRCA1_1 | 108 | 112 | PF00533 | 0.487 |
LIG_Clathr_ClatBox_1 | 326 | 330 | PF01394 | 0.427 |
LIG_eIF4E_1 | 120 | 126 | PF01652 | 0.537 |
LIG_FAT_LD_1 | 220 | 228 | PF03623 | 0.442 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.435 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.624 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.650 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.503 |
LIG_LIR_Gen_1 | 289 | 300 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.328 |
LIG_LYPXL_S_1 | 266 | 270 | PF13949 | 0.436 |
LIG_LYPXL_yS_3 | 267 | 270 | PF13949 | 0.434 |
LIG_MAD2 | 261 | 269 | PF02301 | 0.438 |
LIG_NRBOX | 110 | 116 | PF00104 | 0.400 |
LIG_NRBOX | 219 | 225 | PF00104 | 0.476 |
LIG_Pex14_2 | 192 | 196 | PF04695 | 0.547 |
LIG_Pex14_2 | 352 | 356 | PF04695 | 0.371 |
LIG_Rb_LxCxE_1 | 325 | 344 | PF01857 | 0.426 |
LIG_REV1ctd_RIR_1 | 315 | 324 | PF16727 | 0.383 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.435 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.399 |
LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.376 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.693 |
LIG_Sin3_3 | 112 | 119 | PF02671 | 0.413 |
LIG_TRAF2_1 | 377 | 380 | PF00917 | 0.460 |
MOD_CDK_SPK_2 | 177 | 182 | PF00069 | 0.659 |
MOD_CDK_SPxxK_3 | 17 | 24 | PF00069 | 0.604 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.719 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.537 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.499 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.620 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.375 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.465 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.633 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.630 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.663 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.449 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.411 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.596 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.589 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.733 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.618 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.568 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.490 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.623 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.562 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.457 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.437 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.629 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.591 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.698 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.449 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.544 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.482 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.447 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.604 |
MOD_NEK2_2 | 96 | 101 | PF00069 | 0.407 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.567 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.406 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.549 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.599 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.309 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.585 |
MOD_Plk_2-3 | 333 | 339 | PF00069 | 0.443 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.735 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.499 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.597 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.580 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.676 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.593 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.620 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.493 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 310 | 317 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 333 | 342 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 375 | 384 | PF00179 | 0.479 |
TRG_DiLeu_BaEn_1 | 219 | 224 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.429 |
TRG_DiLeu_BaEn_1 | 59 | 64 | PF01217 | 0.682 |
TRG_DiLeu_BaEn_4 | 337 | 343 | PF01217 | 0.426 |
TRG_DiLeu_BaEn_4 | 379 | 385 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 24 | 28 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 320 | 325 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 348 | 353 | PF00026 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7Y6 | Leptomonas seymouri | 49% | 90% |
A0A0S4JDY7 | Bodo saltans | 43% | 100% |
A0A1X0NZ18 | Trypanosomatidae | 47% | 100% |
A0A1X0NZ32 | Trypanosomatidae | 27% | 91% |
A0A3Q8IAF9 | Leishmania donovani | 94% | 100% |
A0A3R7KLW2 | Trypanosoma rangeli | 28% | 87% |
A0A422N3A0 | Trypanosoma rangeli | 46% | 100% |
A4H8F9 | Leishmania braziliensis | 81% | 98% |
A4HWT2 | Leishmania infantum | 94% | 100% |
C9ZW42 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZW43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 97% |
C9ZXL6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 90% |
E9AQJ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5AX32 | Trypanosoma cruzi | 28% | 73% |
V5D513 | Trypanosoma cruzi | 29% | 100% |