8G5C
Structure of ACLY-D1026A-substrates, local refinement of ASH domain
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0003824 | molecular_function | catalytic activity |
A | 0003878 | molecular_function | ATP citrate synthase activity |
A | 0005515 | molecular_function | protein binding |
A | 0005524 | molecular_function | ATP binding |
A | 0005576 | cellular_component | extracellular region |
A | 0005654 | cellular_component | nucleoplasm |
A | 0005737 | cellular_component | cytoplasm |
A | 0005829 | cellular_component | cytosol |
A | 0006085 | biological_process | acetyl-CoA biosynthetic process |
A | 0006101 | biological_process | citrate metabolic process |
A | 0006107 | biological_process | oxaloacetate metabolic process |
A | 0006629 | biological_process | lipid metabolic process |
A | 0006633 | biological_process | fatty acid biosynthetic process |
A | 0006695 | biological_process | cholesterol biosynthetic process |
A | 0008610 | biological_process | lipid biosynthetic process |
A | 0015936 | biological_process | coenzyme A metabolic process |
A | 0016020 | cellular_component | membrane |
A | 0016740 | molecular_function | transferase activity |
A | 0035578 | cellular_component | azurophil granule lumen |
A | 0046872 | molecular_function | metal ion binding |
A | 0046912 | molecular_function | acyltransferase activity, acyl groups converted into alkyl on transfer |
A | 0070062 | cellular_component | extracellular exosome |
A | 1904813 | cellular_component | ficolin-1-rich granule lumen |
B | 0003824 | molecular_function | catalytic activity |
B | 0003878 | molecular_function | ATP citrate synthase activity |
B | 0005515 | molecular_function | protein binding |
B | 0005524 | molecular_function | ATP binding |
B | 0005576 | cellular_component | extracellular region |
B | 0005654 | cellular_component | nucleoplasm |
B | 0005737 | cellular_component | cytoplasm |
B | 0005829 | cellular_component | cytosol |
B | 0006085 | biological_process | acetyl-CoA biosynthetic process |
B | 0006101 | biological_process | citrate metabolic process |
B | 0006107 | biological_process | oxaloacetate metabolic process |
B | 0006629 | biological_process | lipid metabolic process |
B | 0006633 | biological_process | fatty acid biosynthetic process |
B | 0006695 | biological_process | cholesterol biosynthetic process |
B | 0008610 | biological_process | lipid biosynthetic process |
B | 0015936 | biological_process | coenzyme A metabolic process |
B | 0016020 | cellular_component | membrane |
B | 0016740 | molecular_function | transferase activity |
B | 0035578 | cellular_component | azurophil granule lumen |
B | 0046872 | molecular_function | metal ion binding |
B | 0046912 | molecular_function | acyltransferase activity, acyl groups converted into alkyl on transfer |
B | 0070062 | cellular_component | extracellular exosome |
B | 1904813 | cellular_component | ficolin-1-rich granule lumen |
C | 0003824 | molecular_function | catalytic activity |
C | 0003878 | molecular_function | ATP citrate synthase activity |
C | 0005515 | molecular_function | protein binding |
C | 0005524 | molecular_function | ATP binding |
C | 0005576 | cellular_component | extracellular region |
C | 0005654 | cellular_component | nucleoplasm |
C | 0005737 | cellular_component | cytoplasm |
C | 0005829 | cellular_component | cytosol |
C | 0006085 | biological_process | acetyl-CoA biosynthetic process |
C | 0006101 | biological_process | citrate metabolic process |
C | 0006107 | biological_process | oxaloacetate metabolic process |
C | 0006629 | biological_process | lipid metabolic process |
C | 0006633 | biological_process | fatty acid biosynthetic process |
C | 0006695 | biological_process | cholesterol biosynthetic process |
C | 0008610 | biological_process | lipid biosynthetic process |
C | 0015936 | biological_process | coenzyme A metabolic process |
C | 0016020 | cellular_component | membrane |
C | 0016740 | molecular_function | transferase activity |
C | 0035578 | cellular_component | azurophil granule lumen |
C | 0046872 | molecular_function | metal ion binding |
C | 0046912 | molecular_function | acyltransferase activity, acyl groups converted into alkyl on transfer |
C | 0070062 | cellular_component | extracellular exosome |
C | 1904813 | cellular_component | ficolin-1-rich granule lumen |
D | 0003824 | molecular_function | catalytic activity |
D | 0003878 | molecular_function | ATP citrate synthase activity |
D | 0005515 | molecular_function | protein binding |
D | 0005524 | molecular_function | ATP binding |
D | 0005576 | cellular_component | extracellular region |
D | 0005654 | cellular_component | nucleoplasm |
D | 0005737 | cellular_component | cytoplasm |
D | 0005829 | cellular_component | cytosol |
D | 0006085 | biological_process | acetyl-CoA biosynthetic process |
D | 0006101 | biological_process | citrate metabolic process |
D | 0006107 | biological_process | oxaloacetate metabolic process |
D | 0006629 | biological_process | lipid metabolic process |
D | 0006633 | biological_process | fatty acid biosynthetic process |
D | 0006695 | biological_process | cholesterol biosynthetic process |
D | 0008610 | biological_process | lipid biosynthetic process |
D | 0015936 | biological_process | coenzyme A metabolic process |
D | 0016020 | cellular_component | membrane |
D | 0016740 | molecular_function | transferase activity |
D | 0035578 | cellular_component | azurophil granule lumen |
D | 0046872 | molecular_function | metal ion binding |
D | 0046912 | molecular_function | acyltransferase activity, acyl groups converted into alkyl on transfer |
D | 0070062 | cellular_component | extracellular exosome |
D | 1904813 | cellular_component | ficolin-1-rich granule lumen |
Functional Information from PROSITE/UniProt
site_id | PS00399 |
Number of Residues | 17 |
Details | SUCCINYL_COA_LIG_2 ATP-citrate lyase / succinyl-CoA ligases family active site. GtcAtmfssevQFGHAG |
Chain | Residue | Details |
A | GLY746-GLY762 |
site_id | PS01216 |
Number of Residues | 30 |
Details | SUCCINYL_COA_LIG_1 ATP-citrate lyase / succinyl-CoA ligases family signature 1. SRSGGMSnElnniisrttdGvyegVAIGGD |
Chain | Residue | Details |
A | SER661-ASP690 |
site_id | PS01217 |
Number of Residues | 25 |
Details | SUCCINYL_COA_LIG_3 ATP-citrate lyase / succinyl-CoA ligases family signature 3. GrIwtMvAGGGASvvysDtIcdl.GG |
Chain | Residue | Details |
A | GLY273-GLY297 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 4 |
Details | ACT_SITE: Tele-phosphohistidine intermediate => ECO:0000305|PubMed:1371749 |
Chain | Residue | Details |
A | HIS760 | |
B | HIS760 | |
C | HIS760 | |
D | HIS760 |
site_id | SWS_FT_FI2 |
Number of Residues | 28 |
Details | BINDING: BINDING => ECO:0000305|PubMed:22102020 |
Chain | Residue | Details |
A | LYS58 | |
B | GLY67 | |
B | PRO109 | |
B | VAL111 | |
B | GLU118 | |
B | ASP216 | |
C | LYS58 | |
C | ARG66 | |
C | GLY67 | |
C | PRO109 | |
C | VAL111 | |
A | ARG66 | |
C | GLU118 | |
C | ASP216 | |
D | LYS58 | |
D | ARG66 | |
D | GLY67 | |
D | PRO109 | |
D | VAL111 | |
D | GLU118 | |
D | ASP216 | |
A | GLY67 | |
A | PRO109 | |
A | VAL111 | |
A | GLU118 | |
A | ASP216 | |
B | LYS58 | |
B | ARG66 |
site_id | SWS_FT_FI3 |
Number of Residues | 12 |
Details | BINDING: BINDING => ECO:0000269|PubMed:20558738, ECO:0000269|PubMed:22102020 |
Chain | Residue | Details |
A | ASP257 | |
D | ASP257 | |
D | SER260 | |
D | ALA262 | |
A | SER260 | |
A | ALA262 | |
B | ASP257 | |
B | SER260 | |
B | ALA262 | |
C | ASP257 | |
C | SER260 | |
C | ALA262 |
site_id | SWS_FT_FI4 |
Number of Residues | 20 |
Details | BINDING: BINDING => ECO:0000269|PubMed:20558738 |
Chain | Residue | Details |
A | GLY309 | |
B | ARG379 | |
C | GLY309 | |
C | ASN346 | |
C | THR348 | |
C | TYR364 | |
C | ARG379 | |
D | GLY309 | |
D | ASN346 | |
D | THR348 | |
D | TYR364 | |
A | ASN346 | |
D | ARG379 | |
A | THR348 | |
A | TYR364 | |
A | ARG379 | |
B | GLY309 | |
B | ASN346 | |
B | THR348 | |
B | TYR364 |
site_id | SWS_FT_FI5 |
Number of Residues | 4 |
Details | BINDING: BINDING => ECO:0000255 |
Chain | Residue | Details |
A | LEU779 | |
B | LEU779 | |
C | LEU779 | |
D | LEU779 |
site_id | SWS_FT_FI6 |
Number of Residues | 4 |
Details | MOD_RES: Phosphotyrosine => ECO:0007744|PubMed:15592455 |
Chain | Residue | Details |
A | TYR131 | |
B | TYR131 | |
C | TYR131 | |
D | TYR131 |
site_id | SWS_FT_FI7 |
Number of Residues | 4 |
Details | MOD_RES: Phosphoserine => ECO:0000250|UniProtKB:Q91V92 |
Chain | Residue | Details |
A | SER263 | |
B | SER263 | |
C | SER263 | |
D | SER263 |
site_id | SWS_FT_FI8 |
Number of Residues | 4 |
Details | MOD_RES: Phosphothreonine => ECO:0000250|UniProtKB:P16638 |
Chain | Residue | Details |
A | THR447 | |
B | THR447 | |
C | THR447 | |
D | THR447 |
site_id | SWS_FT_FI9 |
Number of Residues | 4 |
Details | MOD_RES: Phosphoserine => ECO:0000250|UniProtKB:P16638 |
Chain | Residue | Details |
A | SER451 | |
B | SER451 | |
C | SER451 | |
D | SER451 |
site_id | SWS_FT_FI10 |
Number of Residues | 4 |
Details | MOD_RES: Phosphoserine; by PKA and PKB/AKT1 or PKB/AKT2 or BCKDK => ECO:0000269|PubMed:29779826, ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:21406692, ECO:0007744|PubMed:23186163, ECO:0007744|PubMed:24275569 |
Chain | Residue | Details |
A | SER455 | |
B | SER455 | |
C | SER455 | |
D | SER455 |
site_id | SWS_FT_FI11 |
Number of Residues | 4 |
Details | MOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163 |
Chain | Residue | Details |
A | SER459 | |
B | SER459 | |
C | SER459 | |
D | SER459 |
site_id | SWS_FT_FI12 |
Number of Residues | 4 |
Details | MOD_RES: Phosphoserine => ECO:0007744|PubMed:17081983, ECO:0007744|PubMed:17924679, ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:18691976, ECO:0007744|PubMed:19369195, ECO:0007744|PubMed:19690332, ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:21406692, ECO:0007744|PubMed:23186163, ECO:0007744|PubMed:24275569 |
Chain | Residue | Details |
A | SER481 | |
B | SER481 | |
C | SER481 | |
D | SER481 |
site_id | SWS_FT_FI13 |
Number of Residues | 4 |
Details | MOD_RES: N6-acetyllysine; alternate => ECO:0000269|PubMed:23932781 |
Chain | Residue | Details |
A | LYS540 | |
B | LYS540 | |
C | LYS540 | |
D | LYS540 |
site_id | SWS_FT_FI14 |
Number of Residues | 8 |
Details | MOD_RES: N6-acetyllysine; alternate => ECO:0000269|PubMed:23932781, ECO:0007744|PubMed:19608861 |
Chain | Residue | Details |
A | LYS546 | |
A | LYS554 | |
B | LYS546 | |
B | LYS554 | |
C | LYS546 | |
C | LYS554 | |
D | LYS546 | |
D | LYS554 |
site_id | SWS_FT_FI15 |
Number of Residues | 4 |
Details | MOD_RES: Phosphothreonine => ECO:0007744|PubMed:19369195 |
Chain | Residue | Details |
A | THR639 | |
B | THR639 | |
C | THR639 | |
D | THR639 |
site_id | SWS_FT_FI16 |
Number of Residues | 8 |
Details | MOD_RES: Phosphoserine => ECO:0007744|PubMed:19369195 |
Chain | Residue | Details |
A | SER663 | |
A | SER839 | |
B | SER663 | |
B | SER839 | |
C | SER663 | |
C | SER839 | |
D | SER663 | |
D | SER839 |
site_id | SWS_FT_FI17 |
Number of Residues | 4 |
Details | MOD_RES: Phosphotyrosine => ECO:0007744|PubMed:15592455, ECO:0007744|PubMed:19369195 |
Chain | Residue | Details |
A | TYR682 | |
B | TYR682 | |
C | TYR682 | |
D | TYR682 |
site_id | SWS_FT_FI18 |
Number of Residues | 12 |
Details | MOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861 |
Chain | Residue | Details |
A | LYS948 | |
D | LYS948 | |
D | LYS968 | |
D | LYS1077 | |
A | LYS968 | |
A | LYS1077 | |
B | LYS948 | |
B | LYS968 | |
B | LYS1077 | |
C | LYS948 | |
C | LYS968 | |
C | LYS1077 |
site_id | SWS_FT_FI19 |
Number of Residues | 4 |
Details | MOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:Q91V92 |
Chain | Residue | Details |
A | LYS978 | |
B | LYS978 | |
C | LYS978 | |
D | LYS978 |
site_id | SWS_FT_FI20 |
Number of Residues | 4 |
Details | MOD_RES: Phosphoserine => ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:19369195 |
Chain | Residue | Details |
A | SER1100 | |
B | SER1100 | |
C | SER1100 | |
D | SER1100 |
site_id | SWS_FT_FI21 |
Number of Residues | 16 |
Details | CROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin); alternate => ECO:0000269|PubMed:27664236, ECO:0000305|PubMed:23932781 |
Chain | Residue | Details |
A | LYS540 | |
C | LYS546 | |
C | LYS554 | |
D | LYS540 | |
D | LYS546 | |
D | LYS554 | |
A | LYS546 | |
A | LYS554 | |
B | LYS540 | |
B | LYS546 | |
B | LYS554 | |
C | LYS540 |