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: 33 |
NetGPI | no | yes: 0, no: 33 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 34 |
GO:0110165 | cellular anatomical entity | 1 | 34 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005783 | endoplasmic reticulum | 5 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
Related structures:
AlphaFold database: E9AGT2
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.330 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.385 |
DEG_APCC_DBOX_1 | 484 | 492 | PF00400 | 0.398 |
DEG_MDM2_SWIB_1 | 17 | 24 | PF02201 | 0.301 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.257 |
DEG_SPOP_SBC_1 | 359 | 363 | PF00917 | 0.535 |
DOC_CDC14_PxL_1 | 389 | 397 | PF14671 | 0.398 |
DOC_CYCLIN_RxL_1 | 68 | 78 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 337 | 343 | PF00134 | 0.361 |
DOC_MAPK_DCC_7 | 485 | 495 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 246 | 253 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 483 | 490 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 483 | 490 | PF00069 | 0.551 |
DOC_PP1_RVXF_1 | 257 | 264 | PF00149 | 0.282 |
DOC_PP1_SILK_1 | 374 | 379 | PF00149 | 0.347 |
DOC_PP2B_LxvP_1 | 337 | 340 | PF13499 | 0.361 |
DOC_PP4_FxxP_1 | 167 | 170 | PF00568 | 0.304 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 123 | 128 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 254 | 259 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 358 | 366 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 378 | 387 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 404 | 408 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 485 | 491 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 71 | 77 | PF00244 | 0.575 |
LIG_Actin_WH2_2 | 244 | 261 | PF00022 | 0.299 |
LIG_Actin_WH2_2 | 410 | 426 | PF00022 | 0.288 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.286 |
LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.575 |
LIG_BRCT_BRCA1_1 | 524 | 528 | PF00533 | 0.398 |
LIG_CSL_BTD_1 | 110 | 113 | PF09270 | 0.588 |
LIG_CtBP_PxDLS_1 | 444 | 448 | PF00389 | 0.468 |
LIG_deltaCOP1_diTrp_1 | 43 | 49 | PF00928 | 0.313 |
LIG_deltaCOP1_diTrp_1 | 463 | 471 | PF00928 | 0.475 |
LIG_EH_1 | 26 | 30 | PF12763 | 0.304 |
LIG_eIF4E_1 | 332 | 338 | PF01652 | 0.335 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.673 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.425 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.435 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.344 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.415 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.462 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.292 |
LIG_LIR_Apic_2 | 144 | 148 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 18 | 29 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 326 | 335 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 348 | 357 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 382 | 392 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.231 |
LIG_LIR_Gen_1 | 432 | 443 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 382 | 387 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.210 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.473 |
LIG_NRBOX | 58 | 64 | PF00104 | 0.420 |
LIG_Pex14_1 | 219 | 223 | PF04695 | 0.390 |
LIG_Pex14_1 | 249 | 253 | PF04695 | 0.294 |
LIG_Pex14_1 | 464 | 468 | PF04695 | 0.468 |
LIG_Pex14_1 | 471 | 475 | PF04695 | 0.468 |
LIG_Pex14_2 | 17 | 21 | PF04695 | 0.302 |
LIG_Pex14_2 | 425 | 429 | PF04695 | 0.329 |
LIG_Pex14_2 | 460 | 464 | PF04695 | 0.470 |
LIG_Pex14_2 | 496 | 500 | PF04695 | 0.324 |
LIG_PTB_Apo_2 | 24 | 31 | PF02174 | 0.316 |
LIG_REV1ctd_RIR_1 | 27 | 36 | PF16727 | 0.318 |
LIG_SH2_CRK | 151 | 155 | PF00017 | 0.283 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.270 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.437 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.312 |
LIG_SH2_CRK | 475 | 479 | PF00017 | 0.468 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 151 | 155 | PF00017 | 0.301 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.301 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 332 | 336 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.468 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.615 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.388 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.433 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.398 |
LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.502 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.283 |
LIG_TRFH_1 | 335 | 339 | PF08558 | 0.438 |
LIG_TYR_ITIM | 418 | 423 | PF00017 | 0.414 |
LIG_TYR_ITIM | 473 | 478 | PF00017 | 0.466 |
LIG_UBA3_1 | 417 | 424 | PF00899 | 0.347 |
LIG_WRC_WIRS_1 | 347 | 352 | PF05994 | 0.333 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.294 |
LIG_WW_1 | 339 | 342 | PF00397 | 0.393 |
LIG_WW_3 | 112 | 116 | PF00397 | 0.537 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.596 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.613 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.636 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.346 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.482 |
MOD_CMANNOS | 461 | 464 | PF00535 | 0.270 |
MOD_Cter_Amidation | 539 | 542 | PF01082 | 0.357 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.496 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.575 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.335 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.329 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.438 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.549 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.395 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.444 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.728 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.464 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.648 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.593 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.603 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.600 |
MOD_LATS_1 | 356 | 362 | PF00433 | 0.446 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.550 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.286 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.295 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.240 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.475 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.633 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.537 |
MOD_PKA_1 | 541 | 547 | PF00069 | 0.567 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.558 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.326 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.292 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.591 |
MOD_PKB_1 | 121 | 129 | PF00069 | 0.560 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.328 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.478 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.415 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.344 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.389 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.317 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.405 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.597 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.255 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.620 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.590 |
TRG_DiLeu_BaEn_2 | 408 | 414 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.351 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.588 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 447 | 449 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.486 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRP6 | Bodo saltans | 42% | 92% |
A0A1X0P614 | Trypanosomatidae | 38% | 88% |
A0A1X0P616 | Trypanosomatidae | 48% | 90% |
A0A1X0P718 | Trypanosomatidae | 45% | 85% |
A0A3Q8IAC1 | Leishmania donovani | 99% | 71% |
A0A3Q8IBC3 | Leishmania donovani | 98% | 91% |
A0A3Q8IDD7 | Leishmania donovani | 99% | 71% |
A0A3S5H769 | Leishmania donovani | 98% | 80% |
A0A3S5IRW9 | Trypanosoma rangeli | 40% | 88% |
A0A3S7WVK4 | Leishmania donovani | 95% | 71% |
A0A3S7WVS3 | Leishmania donovani | 94% | 100% |
A4HA75 | Leishmania braziliensis | 62% | 100% |
A4HA76 | Leishmania braziliensis | 62% | 100% |
A4HA77 | Leishmania braziliensis | 65% | 100% |
A4HA79 | Leishmania braziliensis | 74% | 100% |
A4HA81 | Leishmania braziliensis | 68% | 100% |
A4HA82 | Leishmania braziliensis | 68% | 100% |
D0A0T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 90% |
E8NHJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AGS9 | Leishmania infantum | 100% | 100% |
E9AGT1 | Leishmania infantum | 95% | 100% |
E9AGT3 | Leishmania infantum | 96% | 71% |
E9AGT4 | Leishmania infantum | 100% | 71% |
E9AS84 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9AS85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AS86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 73% |
P53154 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 98% |
Q09758 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 94% |
Q4QD77 | Leishmania major | 28% | 75% |
Q4QD78 | Leishmania major | 92% | 100% |
Q4QD79 | Leishmania major | 88% | 100% |
Q4QD80 | Leishmania major | 88% | 100% |
Q4QD81 | Leishmania major | 71% | 100% |
Q4QD82 | Leishmania major | 89% | 100% |
Q5AKZ2 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 94% |
Q7Z877 | Candida tropicalis | 28% | 94% |