This protein is likely involved in lipid transfer processes, as judged by the presence of a VASt domain. . Modestly expanded family.
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: 18 |
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 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HKQ9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.417 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.671 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.504 |
CLV_Separin_Metazoa | 106 | 110 | PF03568 | 0.362 |
DEG_SCF_FBW7_1 | 373 | 380 | PF00400 | 0.365 |
DEG_SCF_TRCP1_1 | 234 | 239 | PF00400 | 0.500 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.386 |
DOC_CKS1_1 | 189 | 194 | PF01111 | 0.421 |
DOC_MAPK_gen_1 | 177 | 183 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 37 | 44 | PF00069 | 0.450 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.450 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.282 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 273 | 281 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 97 | 102 | PF00244 | 0.275 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.352 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.415 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.261 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.309 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.586 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.607 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.350 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.233 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.484 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.239 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.482 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.268 |
LIG_NRBOX | 258 | 264 | PF00104 | 0.447 |
LIG_Pex14_1 | 58 | 62 | PF04695 | 0.282 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.329 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.461 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.500 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.296 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.275 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.273 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.406 |
LIG_SUMO_SIM_anti_2 | 100 | 106 | PF11976 | 0.315 |
LIG_SUMO_SIM_anti_2 | 343 | 348 | PF11976 | 0.672 |
LIG_SUMO_SIM_par_1 | 100 | 106 | PF11976 | 0.293 |
LIG_TYR_ITIM | 200 | 205 | PF00017 | 0.249 |
LIG_UBA3_1 | 48 | 56 | PF00899 | 0.434 |
MOD_CDK_SPK_2 | 188 | 193 | PF00069 | 0.432 |
MOD_CDK_SPxxK_3 | 124 | 131 | PF00069 | 0.386 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.282 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.282 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.296 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.504 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.613 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.418 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.382 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.233 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.683 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.345 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.298 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.357 |
MOD_DYRK1A_RPxSP_1 | 109 | 113 | PF00069 | 0.362 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.487 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.562 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.583 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.683 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.669 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.432 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.648 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.471 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.379 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.513 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.624 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.598 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.584 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.438 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.299 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.292 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.629 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.388 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.560 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.389 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.433 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.629 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.574 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.406 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.586 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.475 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.296 |
MOD_NEK2_2 | 244 | 249 | PF00069 | 0.427 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.282 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.347 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.628 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.302 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.282 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.252 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.596 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.445 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.319 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.631 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.364 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.313 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.362 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.362 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.282 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.427 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.438 |
MOD_SUMO_rev_2 | 305 | 314 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 33 | 43 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 74 | 82 | PF00179 | 0.362 |
TRG_DiLeu_BaEn_1 | 310 | 315 | PF01217 | 0.704 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDN4 | Leptomonas seymouri | 71% | 98% |
A0A1X0NRK7 | Trypanosomatidae | 44% | 98% |
A0A3Q8IGC9 | Leishmania donovani | 84% | 99% |
A0A422NZS9 | Trypanosoma rangeli | 44% | 99% |
A4I889 | Leishmania infantum | 84% | 99% |
D0AAF9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 99% |
E9B347 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
Q4Q507 | Leishmania major | 83% | 100% |
V5DAU6 | Trypanosoma cruzi | 40% | 98% |