This protein is likely involved in lipid transfer processes, as judged by the presence of a VASt domain. . Modestly expanded family.
Uncharacterized Protein, Uncharacterized
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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IGC9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.322 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.403 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.499 |
CLV_Separin_Metazoa | 106 | 110 | PF03568 | 0.350 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.338 |
DOC_CKS1_1 | 189 | 194 | PF01111 | 0.410 |
DOC_CYCLIN_RxL_1 | 373 | 383 | PF00134 | 0.415 |
DOC_MAPK_gen_1 | 177 | 183 | PF00069 | 0.332 |
DOC_MAPK_gen_1 | 37 | 44 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 75 | 83 | PF00069 | 0.253 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.278 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.631 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.145 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.184 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 278 | 286 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 347 | 352 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 97 | 102 | PF00244 | 0.254 |
LIG_BIR_III_4 | 227 | 231 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.335 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.405 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.257 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.395 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.277 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.600 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.650 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.336 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.428 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.432 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.260 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.389 |
LIG_Pex14_1 | 58 | 62 | PF04695 | 0.265 |
LIG_SH2_GRB2like | 124 | 127 | PF00017 | 0.270 |
LIG_SH2_PTP2 | 357 | 360 | PF00017 | 0.418 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.451 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.461 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.279 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.265 |
LIG_SUMO_SIM_anti_2 | 100 | 106 | PF11976 | 0.299 |
LIG_SUMO_SIM_anti_2 | 257 | 262 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 348 | 353 | PF11976 | 0.637 |
LIG_SUMO_SIM_par_1 | 100 | 106 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 363 | 368 | PF11976 | 0.371 |
LIG_UBA3_1 | 48 | 56 | PF00899 | 0.384 |
MOD_CDK_SPK_2 | 188 | 193 | PF00069 | 0.417 |
MOD_CDK_SPxxK_3 | 124 | 131 | PF00069 | 0.338 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.284 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.270 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.342 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.602 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.375 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.399 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.275 |
MOD_DYRK1A_RPxSP_1 | 109 | 113 | PF00069 | 0.350 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.523 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.563 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.548 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.629 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.430 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.557 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.463 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.362 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.606 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.287 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.580 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.535 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.372 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.431 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.389 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.609 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.392 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.580 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.427 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.279 |
MOD_NEK2_2 | 249 | 254 | PF00069 | 0.406 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.265 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.671 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.329 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.620 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.265 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.441 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.230 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.521 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.608 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.342 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.297 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.350 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.145 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.184 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.414 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.424 |
MOD_SUMO_rev_2 | 33 | 43 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 74 | 81 | PF00179 | 0.325 |
TRG_DiLeu_BaEn_1 | 315 | 320 | PF01217 | 0.699 |
TRG_DiLeu_BaEn_4 | 315 | 321 | PF01217 | 0.639 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDN4 | Leptomonas seymouri | 71% | 99% |
A0A1X0NRK7 | Trypanosomatidae | 44% | 99% |
A0A422NZS9 | Trypanosoma rangeli | 46% | 100% |
A4HKQ9 | Leishmania braziliensis | 84% | 99% |
A4I889 | Leishmania infantum | 100% | 100% |
D0AAF9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9B347 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q507 | Leishmania major | 94% | 100% |
V5BE10 | Trypanosoma cruzi | 25% | 100% |
V5DAU6 | Trypanosoma cruzi | 43% | 99% |