3GPC
Crystal structure of human Acyl-CoA synthetase medium-chain family member 2A (L64P mutation) in a complex with CoA
Replaces: 3EYNFunctional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004321 | molecular_function | fatty-acyl-CoA synthase activity |
A | 0005524 | molecular_function | ATP binding |
A | 0005739 | cellular_component | mitochondrion |
A | 0005759 | cellular_component | mitochondrial matrix |
A | 0006631 | biological_process | fatty acid metabolic process |
A | 0006633 | biological_process | fatty acid biosynthetic process |
A | 0006637 | biological_process | acyl-CoA metabolic process |
A | 0015645 | molecular_function | fatty acid ligase activity |
A | 0016405 | molecular_function | CoA-ligase activity |
A | 0016874 | molecular_function | ligase activity |
A | 0016878 | molecular_function | acid-thiol ligase activity |
A | 0018858 | molecular_function | benzoate-CoA ligase activity |
A | 0031956 | molecular_function | medium-chain fatty acid-CoA ligase activity |
A | 0036112 | biological_process | medium-chain fatty-acyl-CoA metabolic process |
A | 0042593 | biological_process | glucose homeostasis |
A | 0046872 | molecular_function | metal ion binding |
A | 0070328 | biological_process | triglyceride homeostasis |
A | 0102391 | molecular_function | decanoate-CoA ligase activity |
B | 0004321 | molecular_function | fatty-acyl-CoA synthase activity |
B | 0005524 | molecular_function | ATP binding |
B | 0005739 | cellular_component | mitochondrion |
B | 0005759 | cellular_component | mitochondrial matrix |
B | 0006631 | biological_process | fatty acid metabolic process |
B | 0006633 | biological_process | fatty acid biosynthetic process |
B | 0006637 | biological_process | acyl-CoA metabolic process |
B | 0015645 | molecular_function | fatty acid ligase activity |
B | 0016405 | molecular_function | CoA-ligase activity |
B | 0016874 | molecular_function | ligase activity |
B | 0016878 | molecular_function | acid-thiol ligase activity |
B | 0018858 | molecular_function | benzoate-CoA ligase activity |
B | 0031956 | molecular_function | medium-chain fatty acid-CoA ligase activity |
B | 0036112 | biological_process | medium-chain fatty-acyl-CoA metabolic process |
B | 0042593 | biological_process | glucose homeostasis |
B | 0046872 | molecular_function | metal ion binding |
B | 0070328 | biological_process | triglyceride homeostasis |
B | 0102391 | molecular_function | decanoate-CoA ligase activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE MG A 901 |
Chain | Residue |
A | MET483 |
A | HIS485 |
A | VAL488 |
A | HOH957 |
site_id | AC2 |
Number of Residues | 25 |
Details | BINDING SITE FOR RESIDUE COA A 578 |
Chain | Residue |
A | TYR361 |
A | GLY362 |
A | GLN363 |
A | THR364 |
A | LEU444 |
A | ASP446 |
A | PHE458 |
A | ARG461 |
A | THR553 |
A | THR555 |
A | LYS557 |
A | GLN559 |
A | HOH590 |
A | HOH687 |
A | HOH697 |
A | HOH780 |
A | HOH781 |
A | HOH785 |
A | HOH918 |
A | HOH1143 |
A | GLY338 |
A | GLU339 |
A | SER340 |
A | GLU359 |
A | SER360 |
site_id | AC3 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE MG B 901 |
Chain | Residue |
B | MET483 |
B | HIS485 |
B | VAL488 |
B | HOH611 |
site_id | AC4 |
Number of Residues | 19 |
Details | BINDING SITE FOR RESIDUE COA B 902 |
Chain | Residue |
B | TRP265 |
B | GLY338 |
B | GLU339 |
B | SER340 |
B | GLU359 |
B | SER360 |
B | TYR361 |
B | GLY362 |
B | GLN363 |
B | THR364 |
B | ASP446 |
B | PHE458 |
B | ARG461 |
B | THR555 |
B | HOH718 |
B | HOH787 |
B | HOH788 |
B | HOH794 |
B | HOH1192 |
Functional Information from PROSITE/UniProt
site_id | PS00455 |
Number of Residues | 12 |
Details | AMP_BINDING Putative AMP-binding domain signature. IYFTSGTSGlPK |
Chain | Residue | Details |
A | ILE218-LYS229 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 14 |
Details | BINDING: BINDING => ECO:0000269|PubMed:19345228 |
Chain | Residue | Details |
A | GLN139 | |
B | SER469 | |
B | ARG472 | |
B | ARG501 | |
B | LYS532 | |
B | TYR540 | |
A | THR364 | |
A | SER469 | |
A | ARG472 | |
A | ARG501 | |
A | LYS532 | |
A | TYR540 | |
B | GLN139 | |
B | THR364 |
site_id | SWS_FT_FI2 |
Number of Residues | 10 |
Details | BINDING: BINDING => ECO:0000269|PubMed:19345228, ECO:0000269|Ref.7 |
Chain | Residue | Details |
A | THR221 | |
B | LYS557 | |
A | GLU359 | |
A | ASP446 | |
A | ARG461 | |
A | LYS557 | |
B | THR221 | |
B | GLU359 | |
B | ASP446 | |
B | ARG461 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | MOD_RES: Phosphoserine => ECO:0000250|UniProtKB:Q68CK6 |
Chain | Residue | Details |
A | SER513 | |
B | SER513 |