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:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q507
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.712 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.504 |
CLV_Separin_Metazoa | 106 | 110 | PF03568 | 0.362 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.386 |
DOC_CKS1_1 | 189 | 194 | PF01111 | 0.430 |
DOC_CYCLIN_RxL_1 | 373 | 383 | PF00134 | 0.440 |
DOC_MAPK_gen_1 | 177 | 183 | PF00069 | 0.345 |
DOC_MAPK_gen_1 | 37 | 44 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 75 | 83 | PF00069 | 0.270 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.297 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.453 |
DOC_USP7_UBL2_3 | 71 | 75 | PF12436 | 0.219 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.282 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 278 | 286 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 347 | 352 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 97 | 102 | PF00244 | 0.274 |
LIG_BIR_III_4 | 227 | 231 | PF00653 | 0.598 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.351 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.418 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.393 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.315 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.621 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.243 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.506 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.484 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.219 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.447 |
LIG_PDZ_Class_1 | 379 | 384 | PF00595 | 0.354 |
LIG_Pex14_1 | 58 | 62 | PF04695 | 0.282 |
LIG_REV1ctd_RIR_1 | 66 | 75 | PF16727 | 0.219 |
LIG_SH2_GRB2like | 124 | 127 | PF00017 | 0.302 |
LIG_SH2_PTP2 | 357 | 360 | PF00017 | 0.434 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.455 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.511 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.296 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.361 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.282 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.413 |
LIG_SUMO_SIM_anti_2 | 257 | 262 | PF11976 | 0.403 |
LIG_SUMO_SIM_anti_2 | 98 | 103 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 100 | 106 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 363 | 368 | PF11976 | 0.391 |
LIG_UBA3_1 | 48 | 56 | PF00899 | 0.434 |
MOD_CDK_SPK_2 | 188 | 193 | PF00069 | 0.438 |
MOD_CDK_SPxxK_3 | 124 | 131 | PF00069 | 0.386 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.281 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.270 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.265 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.623 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.437 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.419 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.295 |
MOD_DYRK1A_RPxSP_1 | 109 | 113 | PF00069 | 0.362 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.537 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.583 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.584 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.660 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.439 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.575 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.482 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.306 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.372 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.559 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.525 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.290 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.643 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.586 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.385 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.439 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.428 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.632 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.424 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.469 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.296 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.282 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.692 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.345 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.640 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.282 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.459 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.310 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.529 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.629 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.394 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.306 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.362 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.386 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.282 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.434 |
MOD_SUMO_rev_2 | 33 | 43 | PF00179 | 0.409 |
MOD_SUMO_rev_2 | 74 | 81 | PF00179 | 0.362 |
TRG_DiLeu_BaEn_1 | 315 | 320 | PF01217 | 0.709 |
TRG_DiLeu_BaEn_4 | 315 | 321 | PF01217 | 0.674 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDN4 | Leptomonas seymouri | 71% | 99% |
A0A1X0NRK7 | Trypanosomatidae | 43% | 99% |
A0A3Q8IGC9 | Leishmania donovani | 94% | 100% |
A0A422NZS9 | Trypanosoma rangeli | 45% | 100% |
A4HKQ9 | Leishmania braziliensis | 83% | 100% |
A4I889 | Leishmania infantum | 94% | 100% |
D0AAF9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9B347 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5DAU6 | Trypanosoma cruzi | 45% | 99% |