This conserved lipid acyltransferase has many re-entrant segments but only one true TM helix. Most closely related to bacterial acyltransferases.. Heavily expanded in kinetoplastids for unknown reasons. Localization: ER (by homology)
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: 45 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 31 |
NetGPI | no | yes: 0, no: 31 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
Related structures:
AlphaFold database: A4H420
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 4 |
GO:0006644 | phospholipid metabolic process | 4 | 4 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 4 |
GO:0006654 | phosphatidic acid biosynthetic process | 6 | 4 |
GO:0006793 | phosphorus metabolic process | 3 | 4 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0008610 | lipid biosynthetic process | 4 | 4 |
GO:0008654 | phospholipid biosynthetic process | 5 | 4 |
GO:0009058 | biosynthetic process | 2 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0019637 | organophosphate metabolic process | 3 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044249 | cellular biosynthetic process | 3 | 4 |
GO:0044255 | cellular lipid metabolic process | 3 | 4 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 4 |
GO:0046473 | phosphatidic acid metabolic process | 6 | 4 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 4 |
GO:0046486 | glycerolipid metabolic process | 4 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0090407 | organophosphate biosynthetic process | 4 | 4 |
GO:1901576 | organic substance biosynthetic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 32 |
GO:0016740 | transferase activity | 2 | 32 |
GO:0016746 | acyltransferase activity | 3 | 32 |
GO:0003841 | 1-acylglycerol-3-phosphate O-acyltransferase activity | 7 | 9 |
GO:0008374 | O-acyltransferase activity | 5 | 9 |
GO:0016411 | acylglycerol O-acyltransferase activity | 6 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
GO:0042171 | lysophosphatidic acid acyltransferase activity | 6 | 9 |
GO:0071617 | lysophospholipid acyltransferase activity | 5 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 175 | 181 | PF00089 | 0.544 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.593 |
CLV_PCSK_FUR_1 | 322 | 326 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.420 |
DOC_CDC14_PxL_1 | 76 | 84 | PF14671 | 0.427 |
DOC_CYCLIN_yCln2_LP_2 | 70 | 76 | PF00134 | 0.444 |
DOC_MAPK_DCC_7 | 75 | 84 | PF00069 | 0.619 |
DOC_MAPK_MEF2A_6 | 228 | 236 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 23 | 32 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 75 | 84 | PF00069 | 0.602 |
DOC_PP1_RVXF_1 | 95 | 102 | PF00149 | 0.399 |
DOC_PP2B_LxvP_1 | 342 | 345 | PF13499 | 0.343 |
DOC_PP2B_LxvP_1 | 60 | 63 | PF13499 | 0.430 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.584 |
DOC_PP4_FxxP_1 | 140 | 143 | PF00568 | 0.294 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.321 |
LIG_14-3-3_CanoR_1 | 325 | 335 | PF00244 | 0.399 |
LIG_AP2alpha_1 | 140 | 144 | PF02296 | 0.266 |
LIG_AP2alpha_2 | 142 | 144 | PF02296 | 0.297 |
LIG_APCC_ABBA_1 | 218 | 223 | PF00400 | 0.286 |
LIG_BIR_III_4 | 113 | 117 | PF00653 | 0.279 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.291 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.280 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.380 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.339 |
LIG_GBD_Chelix_1 | 295 | 303 | PF00786 | 0.561 |
LIG_LIR_Apic_2 | 138 | 143 | PF02991 | 0.175 |
LIG_LIR_Gen_1 | 142 | 151 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 240 | 249 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 275 | 285 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.213 |
LIG_MYND_1 | 17 | 21 | PF01753 | 0.451 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.342 |
LIG_PCNA_PIPBox_1 | 205 | 214 | PF02747 | 0.189 |
LIG_PDZ_Class_2 | 350 | 355 | PF00595 | 0.353 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.258 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.314 |
LIG_Pex14_2 | 182 | 186 | PF04695 | 0.304 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.385 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.423 |
LIG_SH2_PTP2 | 277 | 280 | PF00017 | 0.374 |
LIG_SH2_PTP2 | 36 | 39 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.552 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.611 |
LIG_SUMO_SIM_par_1 | 253 | 260 | PF11976 | 0.324 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.316 |
LIG_TRFH_1 | 69 | 73 | PF08558 | 0.237 |
LIG_TYR_ITIM | 74 | 79 | PF00017 | 0.607 |
LIG_WRC_WIRS_1 | 233 | 238 | PF05994 | 0.285 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.363 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.410 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.398 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.585 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.324 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.403 |
MOD_LATS_1 | 185 | 191 | PF00433 | 0.189 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.475 |
MOD_N-GLC_2 | 86 | 88 | PF02516 | 0.181 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.264 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.248 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.312 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.324 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.353 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.271 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.510 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.214 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.281 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.275 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.349 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.294 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.442 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.326 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.300 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.321 |
MOD_SUMO_rev_2 | 113 | 121 | PF00179 | 0.272 |
MOD_SUMO_rev_2 | 329 | 334 | PF00179 | 0.499 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.574 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 325 | 330 | PF00026 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.257 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P455 | Leptomonas seymouri | 60% | 100% |
A0A0N1HTP4 | Leptomonas seymouri | 54% | 100% |
A0A0N1I6V1 | Leptomonas seymouri | 35% | 100% |
A0A0S4IQ05 | Bodo saltans | 29% | 100% |
A0A0S4IR22 | Bodo saltans | 39% | 100% |
A0A0S4JRB2 | Bodo saltans | 32% | 100% |
A0A1X0NUQ7 | Trypanosomatidae | 27% | 100% |
A0A3Q8IFY7 | Leishmania donovani | 30% | 100% |
A0A3R7NKA0 | Trypanosoma rangeli | 34% | 100% |
A0A3S5H5E4 | Leishmania donovani | 54% | 82% |
A0A3S5H7L8 | Leishmania donovani | 33% | 100% |
A0A3S5IQW0 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WNW6 | Leishmania donovani | 70% | 100% |
A4H419 | Leishmania braziliensis | 75% | 100% |
A4HHM7 | Leishmania braziliensis | 34% | 100% |
A4HKI5 | Leishmania braziliensis | 30% | 100% |
A4HSA1 | Leishmania infantum | 53% | 100% |
A4HSA2 | Leishmania infantum | 70% | 100% |
A4I4U2 | Leishmania infantum | 33% | 100% |
A4I816 | Leishmania infantum | 30% | 100% |
C9ZLI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AE90 | Leishmania major | 32% | 100% |
E9AK86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9ALJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B2X4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4Q582 | Leishmania major | 31% | 100% |
Q9NF90 | Leishmania major | 71% | 100% |
Q9NF91 | Leishmania major | 55% | 100% |
V5ALB6 | Trypanosoma cruzi | 25% | 100% |
V5C201 | Trypanosoma cruzi | 32% | 100% |