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 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: E8NHJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016746 | acyltransferase activity | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 542 | 546 | PF00656 | 0.408 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.471 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 487 | 493 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.564 |
DEG_APCC_DBOX_1 | 398 | 406 | PF00400 | 0.403 |
DEG_APCC_DBOX_1 | 478 | 486 | PF00400 | 0.588 |
DEG_Nend_UBRbox_2 | 1 | 2 | PF02207 | 0.573 |
DEG_SCF_FBW7_1 | 557 | 562 | PF00400 | 0.351 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.543 |
DOC_CDC14_PxL_1 | 303 | 311 | PF14671 | 0.396 |
DOC_CYCLIN_yCln2_LP_2 | 251 | 257 | PF00134 | 0.378 |
DOC_MAPK_DCC_7 | 399 | 409 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 160 | 167 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 397 | 404 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 171 | 178 | PF00149 | 0.293 |
DOC_PP1_SILK_1 | 288 | 293 | PF00149 | 0.510 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.378 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.335 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.524 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.421 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 272 | 280 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 292 | 301 | PF00244 | 0.247 |
LIG_14-3-3_CanoR_1 | 318 | 322 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 399 | 405 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 478 | 482 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 487 | 495 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 584 | 590 | PF00244 | 0.522 |
LIG_Actin_WH2_2 | 158 | 175 | PF00022 | 0.323 |
LIG_Actin_WH2_2 | 324 | 340 | PF00022 | 0.311 |
LIG_BRCT_BRCA1_1 | 163 | 167 | PF00533 | 0.340 |
LIG_BRCT_BRCA1_1 | 310 | 314 | PF00533 | 0.302 |
LIG_BRCT_BRCA1_1 | 438 | 442 | PF00533 | 0.403 |
LIG_deltaCOP1_diTrp_1 | 373 | 382 | PF00928 | 0.483 |
LIG_eIF4E_1 | 246 | 252 | PF01652 | 0.407 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.483 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.527 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.502 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.352 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.493 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.641 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.700 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.417 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.605 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.310 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.429 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.423 |
LIG_LIR_Apic_2 | 58 | 62 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 240 | 249 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 262 | 271 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 296 | 306 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 311 | 322 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 387 | 395 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 587 | 596 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 512 | 518 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 587 | 592 | PF02991 | 0.572 |
LIG_PAM2_1 | 491 | 503 | PF00658 | 0.533 |
LIG_Pex14_1 | 163 | 167 | PF04695 | 0.322 |
LIG_Pex14_1 | 378 | 382 | PF04695 | 0.488 |
LIG_Pex14_1 | 385 | 389 | PF04695 | 0.488 |
LIG_Pex14_2 | 339 | 343 | PF04695 | 0.337 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.489 |
LIG_Pex14_2 | 410 | 414 | PF04695 | 0.341 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.308 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.290 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.459 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.334 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 65 | 69 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 570 | 574 | PF00017 | 0.292 |
LIG_SH2_STAT3 | 132 | 135 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.385 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.625 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.419 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.396 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.409 |
LIG_SUMO_SIM_anti_2 | 113 | 120 | PF11976 | 0.321 |
LIG_SUMO_SIM_anti_2 | 138 | 144 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 120 | 126 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 137 | 144 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 366 | 373 | PF11976 | 0.430 |
LIG_TRFH_1 | 249 | 253 | PF08558 | 0.459 |
LIG_TYR_ITIM | 134 | 139 | PF00017 | 0.344 |
LIG_TYR_ITIM | 332 | 337 | PF00017 | 0.403 |
LIG_UBA3_1 | 331 | 338 | PF00899 | 0.362 |
LIG_UBA3_1 | 348 | 356 | PF00899 | 0.208 |
LIG_UBA3_1 | 592 | 597 | PF00899 | 0.511 |
LIG_WRC_WIRS_1 | 261 | 266 | PF05994 | 0.347 |
LIG_WW_1 | 253 | 256 | PF00397 | 0.412 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.520 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.681 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.475 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.462 |
MOD_CMANNOS | 375 | 378 | PF00535 | 0.331 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.506 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.407 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.667 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.495 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.435 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.705 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.375 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.725 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.540 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.662 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.505 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.526 |
MOD_LATS_1 | 270 | 276 | PF00433 | 0.309 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.350 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.487 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.386 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.366 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.344 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.248 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.352 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.481 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.505 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.357 |
MOD_NEK2_2 | 378 | 383 | PF00069 | 0.191 |
MOD_NEK2_2 | 510 | 515 | PF00069 | 0.275 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.420 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.409 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.472 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.362 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.552 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.429 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.461 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.431 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.399 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.505 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.196 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.477 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.501 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.448 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.388 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.423 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.565 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.340 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.372 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.482 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.503 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.508 |
TRG_DiLeu_BaEn_2 | 322 | 328 | PF01217 | 0.392 |
TRG_DiLeu_BaLyEn_6 | 170 | 175 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.238 |
TRG_DiLeu_BaLyEn_6 | 81 | 86 | PF01217 | 0.365 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 160 | 163 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.575 |
TRG_NES_CRM1_1 | 359 | 373 | PF08389 | 0.254 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRP6 | Bodo saltans | 35% | 100% |
A0A1X0P614 | Trypanosomatidae | 33% | 96% |
A0A1X0P616 | Trypanosomatidae | 40% | 98% |
A0A3Q8IAC1 | Leishmania donovani | 91% | 77% |
A0A3Q8IBC3 | Leishmania donovani | 81% | 99% |
A0A3Q8IBE0 | Leishmania donovani | 81% | 72% |
A0A3Q8IDD7 | Leishmania donovani | 91% | 77% |
A0A3R7NNW7 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H769 | Leishmania donovani | 91% | 87% |
A0A3S5IRW9 | Trypanosoma rangeli | 34% | 96% |
A0A3S7WVJ2 | Leishmania donovani | 81% | 71% |
A0A3S7WVK4 | Leishmania donovani | 89% | 77% |
A0A3S7WVS3 | Leishmania donovani | 77% | 100% |
A4HA75 | Leishmania braziliensis | 71% | 100% |
A4HA76 | Leishmania braziliensis | 72% | 100% |
A4HA79 | Leishmania braziliensis | 69% | 100% |
A4HA81 | Leishmania braziliensis | 69% | 100% |
A4HA82 | Leishmania braziliensis | 70% | 100% |
D0A0T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 98% |
E9AGS9 | Leishmania infantum | 79% | 100% |
E9AGT0 | Leishmania infantum | 81% | 71% |
E9AGT1 | Leishmania infantum | 88% | 100% |
E9AGT2 | Leishmania infantum | 90% | 100% |
E9AGT3 | Leishmania infantum | 89% | 77% |
E9AGT4 | Leishmania infantum | 91% | 77% |
E9AS84 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9AS85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 77% |
E9AS86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 79% |
Q4QD78 | Leishmania major | 89% | 100% |
Q4QD79 | Leishmania major | 87% | 100% |
Q4QD80 | Leishmania major | 87% | 100% |
Q4QD81 | Leishmania major | 75% | 100% |