Membrane-bound O-acyltransferase involved in the remodeling of glycosylphosphatidylinositol (GPI) anchors. Related to fungal GUP1 proteins.
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QD82
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016746 | acyltransferase activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.376 |
CLV_MEL_PAP_1 | 331 | 337 | PF00089 | 0.281 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.250 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.402 |
DEG_APCC_DBOX_1 | 177 | 185 | PF00400 | 0.401 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.529 |
DEG_SPOP_SBC_1 | 166 | 170 | PF00917 | 0.541 |
DOC_CDC14_PxL_1 | 196 | 204 | PF14671 | 0.419 |
DOC_CYCLIN_yCln2_LP_2 | 144 | 150 | PF00134 | 0.300 |
DOC_MAPK_DCC_7 | 292 | 302 | PF00069 | 0.294 |
DOC_MAPK_gen_1 | 174 | 183 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 290 | 297 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 51 | 60 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 290 | 297 | PF00069 | 0.511 |
DOC_PP1_RVXF_1 | 33 | 40 | PF00149 | 0.354 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.273 |
DOC_PP1_SILK_1 | 181 | 186 | PF00149 | 0.377 |
DOC_PP2B_LxvP_1 | 144 | 147 | PF13499 | 0.300 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.250 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.300 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.456 |
LIG_14-3-3_CanoR_1 | 165 | 173 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 185 | 194 | PF00244 | 0.146 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 358 | 367 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 61 | 66 | PF00244 | 0.283 |
LIG_Actin_WH2_2 | 217 | 233 | PF00022 | 0.249 |
LIG_Actin_WH2_2 | 51 | 68 | PF00022 | 0.317 |
LIG_BRCT_BRCA1_1 | 203 | 207 | PF00533 | 0.311 |
LIG_BRCT_BRCA1_1 | 238 | 242 | PF00533 | 0.531 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.278 |
LIG_CtBP_PxDLS_1 | 251 | 255 | PF00389 | 0.456 |
LIG_deltaCOP1_diTrp_1 | 270 | 278 | PF00928 | 0.467 |
LIG_eIF4E_1 | 139 | 145 | PF01652 | 0.341 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.580 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.360 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.315 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.311 |
LIG_LIR_Gen_1 | 133 | 142 | PF02991 | 0.256 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.187 |
LIG_LIR_Gen_1 | 239 | 250 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.187 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.524 |
LIG_Pex14_1 | 26 | 30 | PF04695 | 0.444 |
LIG_Pex14_1 | 271 | 275 | PF04695 | 0.452 |
LIG_Pex14_1 | 278 | 282 | PF04695 | 0.452 |
LIG_Pex14_1 | 56 | 60 | PF04695 | 0.335 |
LIG_Pex14_2 | 232 | 236 | PF04695 | 0.300 |
LIG_Pex14_2 | 267 | 271 | PF04695 | 0.456 |
LIG_Pex14_2 | 303 | 307 | PF04695 | 0.319 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.256 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.432 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.377 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.196 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.364 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.546 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.326 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.419 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.358 |
LIG_SUMO_SIM_anti_2 | 6 | 13 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.388 |
LIG_TRFH_1 | 142 | 146 | PF08558 | 0.419 |
LIG_TYR_ITIM | 161 | 166 | PF00017 | 0.540 |
LIG_TYR_ITIM | 225 | 230 | PF00017 | 0.325 |
LIG_TYR_ITIM | 280 | 285 | PF00017 | 0.452 |
LIG_UBA3_1 | 224 | 231 | PF00899 | 0.377 |
LIG_WRC_WIRS_1 | 154 | 159 | PF05994 | 0.300 |
LIG_WW_1 | 146 | 149 | PF00397 | 0.419 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.583 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.256 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.308 |
MOD_CMANNOS | 268 | 271 | PF00535 | 0.256 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.609 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.341 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.326 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.264 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.592 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.247 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.156 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.452 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.281 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.342 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.315 |
MOD_NEK2_2 | 365 | 370 | PF00069 | 0.535 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.572 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.311 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.749 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.319 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.321 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.377 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.308 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.403 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.401 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.377 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.331 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.402 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.585 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.310 |
TRG_DiLeu_BaEn_2 | 215 | 221 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.360 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.421 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3R7KT56 | Trypanosoma rangeli | 51% | 94% |
A0A3R7NNW7 | Trypanosoma rangeli | 48% | 86% |
A0A3S7WVS3 | Leishmania donovani | 94% | 92% |
A4HA77 | Leishmania braziliensis | 75% | 67% |
A4HA79 | Leishmania braziliensis | 77% | 77% |
E9AGS9 | Leishmania infantum | 88% | 92% |
E9AGT2 | Leishmania infantum | 89% | 69% |
E9AS84 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 77% |
P53154 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 68% |