Phospholipid biosynthesis, acyl transferase lysophosphatidylglycerol acyl transferase
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0012505 | endomembrane system | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8IE09
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0036149 | phosphatidylinositol acyl-chain remodeling | 7 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.547 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.463 |
CLV_PCSK_FUR_1 | 460 | 464 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.354 |
CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.191 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.449 |
DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.312 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.264 |
DEG_MDM2_SWIB_1 | 415 | 423 | PF02201 | 0.314 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.610 |
DEG_SCF_FBW7_1 | 450 | 456 | PF00400 | 0.475 |
DOC_CDC14_PxL_1 | 164 | 172 | PF14671 | 0.464 |
DOC_CKS1_1 | 450 | 455 | PF01111 | 0.482 |
DOC_CYCLIN_RxL_1 | 106 | 114 | PF00134 | 0.512 |
DOC_CYCLIN_RxL_1 | 175 | 183 | PF00134 | 0.460 |
DOC_CYCLIN_RxL_1 | 332 | 343 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 293 | 299 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 387 | 395 | PF00069 | 0.500 |
DOC_MAPK_JIP1_4 | 280 | 286 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 134 | 140 | PF00149 | 0.437 |
DOC_PP1_RVXF_1 | 193 | 200 | PF00149 | 0.512 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.555 |
DOC_PP2B_PxIxI_1 | 206 | 212 | PF00149 | 0.446 |
DOC_USP7_UBL2_3 | 161 | 165 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.213 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 150 | 160 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 417 | 426 | PF00244 | 0.299 |
LIG_Actin_RPEL_3 | 410 | 429 | PF02755 | 0.213 |
LIG_Actin_WH2_2 | 435 | 451 | PF00022 | 0.436 |
LIG_APCC_ABBA_1 | 209 | 214 | PF00400 | 0.426 |
LIG_CaM_IQ_9 | 455 | 471 | PF13499 | 0.549 |
LIG_deltaCOP1_diTrp_1 | 138 | 146 | PF00928 | 0.409 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.436 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.439 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.422 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.396 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.480 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.437 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.389 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.534 |
LIG_LIR_Apic_2 | 273 | 277 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 108 | 117 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 78 | 87 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 142 | 146 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.531 |
LIG_MAD2 | 115 | 123 | PF02301 | 0.520 |
LIG_PCNA_PIPBox_1 | 193 | 202 | PF02747 | 0.460 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.434 |
LIG_Pex14_1 | 385 | 389 | PF04695 | 0.522 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.402 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.360 |
LIG_REV1ctd_RIR_1 | 412 | 421 | PF16727 | 0.322 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.586 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.566 |
LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.469 |
LIG_SH2_STAT3 | 389 | 392 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.371 |
LIG_SH3_2 | 120 | 125 | PF14604 | 0.513 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.475 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.429 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.409 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.579 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.208 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.573 |
LIG_SUMO_SIM_anti_2 | 205 | 212 | PF11976 | 0.446 |
LIG_SUMO_SIM_anti_2 | 26 | 33 | PF11976 | 0.237 |
LIG_SUMO_SIM_par_1 | 246 | 254 | PF11976 | 0.518 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.536 |
LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.454 |
LIG_UBA3_1 | 152 | 161 | PF00899 | 0.541 |
LIG_UBA3_1 | 30 | 37 | PF00899 | 0.292 |
LIG_UBA3_1 | 457 | 466 | PF00899 | 0.449 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.464 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.322 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.353 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.464 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.586 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.359 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.530 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.529 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.459 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.299 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.542 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.479 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.351 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.256 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.250 |
MOD_NEK2_2 | 96 | 101 | PF00069 | 0.543 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.576 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.487 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.439 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.235 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.584 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.561 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.537 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.313 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.503 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.523 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.466 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.512 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.512 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.213 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.482 |
MOD_SUMO_rev_2 | 162 | 167 | PF00179 | 0.491 |
TRG_AP2beta_CARGO_1 | 175 | 184 | PF09066 | 0.446 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_4 | 263 | 269 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.468 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.602 |
TRG_ER_diLys_1 | 472 | 477 | PF00400 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 109 | 114 | PF00026 | 0.347 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKC7 | Leptomonas seymouri | 59% | 100% |
A0A0S4J7G6 | Bodo saltans | 31% | 100% |
A0A1X0NU94 | Trypanosomatidae | 38% | 100% |
A0A422NH08 | Trypanosoma rangeli | 42% | 100% |
A4H937 | Leishmania braziliensis | 77% | 100% |
A4HXG9 | Leishmania infantum | 100% | 100% |
C9ZP55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AR64 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QE99 | Leishmania major | 96% | 100% |
Q5F3X0 | Gallus gallus | 28% | 100% |
V5BF39 | Trypanosoma cruzi | 39% | 100% |