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: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005783 | endoplasmic reticulum | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
Related structures:
AlphaFold database: E9AS84
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016746 | acyltransferase activity | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.401 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.493 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.492 |
CLV_PCSK_PC7_1 | 380 | 386 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.579 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.548 |
DEG_APCC_DBOX_1 | 371 | 379 | PF00400 | 0.594 |
DEG_SCF_FBW7_1 | 450 | 455 | PF00400 | 0.389 |
DEG_SPOP_SBC_1 | 166 | 170 | PF00917 | 0.552 |
DOC_CDC14_PxL_1 | 196 | 204 | PF14671 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 144 | 150 | PF00134 | 0.378 |
DOC_MAPK_DCC_7 | 292 | 302 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 290 | 297 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 53 | 60 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 290 | 297 | PF00069 | 0.567 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.295 |
DOC_PP1_SILK_1 | 181 | 186 | PF00149 | 0.508 |
DOC_PP2B_LxvP_1 | 144 | 147 | PF13499 | 0.378 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.365 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.436 |
LIG_14-3-3_CanoR_1 | 165 | 173 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 185 | 194 | PF00244 | 0.171 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 371 | 375 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 380 | 388 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 477 | 483 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 61 | 66 | PF00244 | 0.345 |
LIG_Actin_WH2_2 | 217 | 233 | PF00022 | 0.305 |
LIG_Actin_WH2_2 | 51 | 68 | PF00022 | 0.358 |
LIG_BRCT_BRCA1_1 | 203 | 207 | PF00533 | 0.377 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.369 |
LIG_CtBP_PxDLS_1 | 251 | 255 | PF00389 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 266 | 275 | PF00928 | 0.472 |
LIG_eIF4E_1 | 139 | 145 | PF01652 | 0.425 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.489 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.485 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.528 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.636 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.492 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.394 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.618 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.375 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.308 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.435 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.403 |
LIG_LIR_Gen_1 | 133 | 142 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 480 | 489 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 480 | 485 | PF02991 | 0.576 |
LIG_PAM2_1 | 384 | 396 | PF00658 | 0.552 |
LIG_Pex14_1 | 271 | 275 | PF04695 | 0.475 |
LIG_Pex14_1 | 278 | 282 | PF04695 | 0.475 |
LIG_Pex14_1 | 56 | 60 | PF04695 | 0.356 |
LIG_Pex14_2 | 232 | 236 | PF04695 | 0.325 |
LIG_Pex14_2 | 267 | 271 | PF04695 | 0.476 |
LIG_Pex14_2 | 303 | 307 | PF04695 | 0.332 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.287 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.453 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.328 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.475 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.289 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.677 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.415 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.413 |
LIG_SUMO_SIM_anti_2 | 31 | 37 | PF11976 | 0.309 |
LIG_SUMO_SIM_anti_2 | 6 | 13 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 260 | 266 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 30 | 37 | PF11976 | 0.515 |
LIG_TRFH_1 | 142 | 146 | PF08558 | 0.455 |
LIG_TYR_ITIM | 225 | 230 | PF00017 | 0.402 |
LIG_TYR_ITIM | 27 | 32 | PF00017 | 0.363 |
LIG_TYR_ITIM | 280 | 285 | PF00017 | 0.312 |
LIG_UBA3_1 | 224 | 231 | PF00899 | 0.363 |
LIG_UBA3_1 | 485 | 490 | PF00899 | 0.493 |
LIG_WRC_WIRS_1 | 154 | 159 | PF05994 | 0.334 |
LIG_WW_1 | 146 | 149 | PF00397 | 0.411 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.524 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.665 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.455 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.346 |
MOD_CMANNOS | 268 | 271 | PF00535 | 0.318 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.499 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.425 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.499 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.464 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.701 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.366 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.550 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.498 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.565 |
MOD_LATS_1 | 163 | 169 | PF00433 | 0.295 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.534 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.323 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.223 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.330 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.482 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.317 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.343 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.458 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.386 |
MOD_NEK2_2 | 403 | 408 | PF00069 | 0.243 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.363 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.477 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.546 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.486 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.518 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.495 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.430 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.432 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.513 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.468 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.409 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.476 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.583 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.324 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.390 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.502 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.540 |
TRG_DiLeu_BaEn_2 | 215 | 221 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.239 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.352 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.545 |
TRG_NES_CRM1_1 | 252 | 266 | PF08389 | 0.245 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRP6 | Bodo saltans | 36% | 82% |
A0A1X0P614 | Trypanosomatidae | 35% | 79% |
A0A1X0P616 | Trypanosomatidae | 41% | 80% |
A0A3Q8IBC3 | Leishmania donovani | 81% | 81% |
A0A3R7NNW7 | Trypanosoma rangeli | 41% | 100% |
A0A3S5H769 | Leishmania donovani | 93% | 72% |
A0A3S5IRW9 | Trypanosoma rangeli | 36% | 79% |
A0A3S7WVS3 | Leishmania donovani | 79% | 100% |
A4HA75 | Leishmania braziliensis | 72% | 100% |
A4HA76 | Leishmania braziliensis | 73% | 78% |
A4HA79 | Leishmania braziliensis | 70% | 100% |
A4HA81 | Leishmania braziliensis | 72% | 75% |
D0A0T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 81% |
E8NHJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9AGS9 | Leishmania infantum | 81% | 100% |
E9AGT1 | Leishmania infantum | 90% | 85% |
E9AGT2 | Leishmania infantum | 92% | 89% |
Q4QD80 | Leishmania major | 88% | 66% |
Q4QD81 | Leishmania major | 77% | 100% |
Q4QD82 | Leishmania major | 88% | 100% |