2GCI
The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed by an asparte/histidine pair and involves a smooth, methionine-rich surface for binding the fatty acyl moiety
Functional Information from GO Data
| Chain | GOid | namespace | contents |
| A | 0003824 | molecular_function | catalytic activity |
| A | 0006629 | biological_process | lipid metabolic process |
| A | 0006637 | biological_process | acyl-CoA metabolic process |
| A | 0008111 | molecular_function | alpha-methylacyl-CoA racemase activity |
| A | 0016853 | molecular_function | isomerase activity |
| A | 0042803 | molecular_function | protein homodimerization activity |
| B | 0003824 | molecular_function | catalytic activity |
| B | 0006629 | biological_process | lipid metabolic process |
| B | 0006637 | biological_process | acyl-CoA metabolic process |
| B | 0008111 | molecular_function | alpha-methylacyl-CoA racemase activity |
| B | 0016853 | molecular_function | isomerase activity |
| B | 0042803 | molecular_function | protein homodimerization activity |
| C | 0003824 | molecular_function | catalytic activity |
| C | 0006629 | biological_process | lipid metabolic process |
| C | 0006637 | biological_process | acyl-CoA metabolic process |
| C | 0008111 | molecular_function | alpha-methylacyl-CoA racemase activity |
| C | 0016853 | molecular_function | isomerase activity |
| C | 0042803 | molecular_function | protein homodimerization activity |
| D | 0003824 | molecular_function | catalytic activity |
| D | 0006629 | biological_process | lipid metabolic process |
| D | 0006637 | biological_process | acyl-CoA metabolic process |
| D | 0008111 | molecular_function | alpha-methylacyl-CoA racemase activity |
| D | 0016853 | molecular_function | isomerase activity |
| D | 0042803 | molecular_function | protein homodimerization activity |
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 21 |
| Details | BINDING SITE FOR RESIDUE MRR A 1751 |
| Chain | Residue |
| A | ARG38 |
| A | LEU92 |
| A | GLY113 |
| A | GLY125 |
| A | HIS126 |
| A | ASP127 |
| A | TYR130 |
| A | ASP156 |
| A | HOH1845 |
| A | HOH1871 |
| A | HOH1915 |
| A | ALA59 |
| A | HOH1957 |
| B | TYR224 |
| A | LEU61 |
| A | LYS62 |
| A | GLY83 |
| A | TYR84 |
| A | ARG85 |
| A | VAL88 |
| A | ARG91 |
| site_id | AC2 |
| Number of Residues | 38 |
| Details | BINDING SITE FOR RESIDUE MRR B 1752 |
| Chain | Residue |
| A | MET207 |
| A | MET216 |
| A | TYR224 |
| A | ILE240 |
| A | GLU241 |
| A | GOL1306 |
| A | HOH1946 |
| B | ILE16 |
| B | ARG38 |
| B | ALA59 |
| B | ASP60 |
| B | LEU61 |
| B | LYS62 |
| B | GLY83 |
| B | TYR84 |
| B | ARG85 |
| B | VAL88 |
| B | ARG91 |
| B | LEU92 |
| B | GLY113 |
| B | GLY125 |
| B | HIS126 |
| B | ASP127 |
| B | TYR130 |
| B | ASP156 |
| B | MET188 |
| B | ASN263 |
| B | ASP264 |
| B | ARG265 |
| B | ALA266 |
| B | GOL1305 |
| B | HOH1778 |
| B | HOH1853 |
| B | HOH1856 |
| B | HOH1866 |
| B | HOH1954 |
| B | HOH1973 |
| B | HOH1981 |
| site_id | AC3 |
| Number of Residues | 25 |
| Details | BINDING SITE FOR RESIDUE MRR C 1753 |
| Chain | Residue |
| C | ARG38 |
| C | ALA59 |
| C | ASP60 |
| C | LEU61 |
| C | LYS62 |
| C | GLY83 |
| C | TYR84 |
| C | ARG85 |
| C | VAL88 |
| C | ARG91 |
| C | LEU92 |
| C | GLY113 |
| C | GLY125 |
| C | HIS126 |
| C | ASP127 |
| C | TYR130 |
| C | ASP156 |
| C | HOH1814 |
| C | HOH1819 |
| C | HOH1907 |
| C | HOH1946 |
| C | HOH1953 |
| C | HOH2015 |
| C | HOH2075 |
| D | TYR224 |
| site_id | AC4 |
| Number of Residues | 31 |
| Details | BINDING SITE FOR RESIDUE MRR D 1754 |
| Chain | Residue |
| D | GLY113 |
| D | GLY125 |
| D | HIS126 |
| D | ASP127 |
| D | TYR130 |
| D | ASP156 |
| D | PRO261 |
| D | ASP264 |
| D | HOH1808 |
| D | HOH1820 |
| D | HOH1929 |
| D | HOH1966 |
| D | HOH2011 |
| D | HOH2042 |
| D | HOH2094 |
| D | HOH2123 |
| C | TYR224 |
| C | GLU241 |
| C | PRO242 |
| C | GOL1302 |
| D | ARG38 |
| D | ALA59 |
| D | ASP60 |
| D | LEU61 |
| D | LYS62 |
| D | GLY83 |
| D | TYR84 |
| D | ARG85 |
| D | VAL88 |
| D | ARG91 |
| D | LEU92 |
| site_id | AC5 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE GOL C 1301 |
| Chain | Residue |
| C | ASP48 |
| C | HOH1810 |
| C | HOH2061 |
| C | HOH2102 |
| D | ALA201 |
| D | MET202 |
| site_id | AC6 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE GOL C 1302 |
| Chain | Residue |
| C | MET216 |
| C | TYR223 |
| C | ILE240 |
| C | GLN262 |
| C | ASN263 |
| C | HOH1930 |
| D | PRO261 |
| D | ASN263 |
| D | MRR1754 |
| D | HOH1816 |
| site_id | AC7 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE GOL D 1303 |
| Chain | Residue |
| C | HOH1820 |
| C | HOH1853 |
| D | MET216 |
| D | TYR223 |
| D | ILE240 |
| D | PRO242 |
| D | GLN262 |
| D | ASN263 |
| site_id | AC8 |
| Number of Residues | 9 |
| Details | BINDING SITE FOR RESIDUE GOL B 1304 |
| Chain | Residue |
| A | ASN263 |
| A | HOH1810 |
| A | HOH1864 |
| B | MET216 |
| B | TYR223 |
| B | ILE240 |
| B | PRO242 |
| B | GLN262 |
| B | ASN263 |
| site_id | AC9 |
| Number of Residues | 9 |
| Details | BINDING SITE FOR RESIDUE GOL B 1305 |
| Chain | Residue |
| A | MET198 |
| A | ALA201 |
| A | MET202 |
| A | MET207 |
| A | HOH1912 |
| B | ASP48 |
| B | MET50 |
| B | ALA266 |
| B | MRR1752 |
| site_id | BC1 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE GOL A 1306 |
| Chain | Residue |
| A | MET216 |
| A | TYR223 |
| A | ILE240 |
| A | GLN262 |
| A | ASN263 |
| B | PRO261 |
| B | ASN263 |
| B | MRR1752 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 4 |
| Details | Active site: {"description":"Proton acceptor","evidences":[{"source":"PubMed","id":"17320106","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"22360758","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 4 |
| Details | Active site: {"description":"Proton donor","evidences":[{"source":"PubMed","id":"17320106","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"22360758","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 48 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"17320106","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"22360758","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
Catalytic Information from CSA
| site_id | CSA1 |
| Number of Residues | 1 |
| Details | Annotated By Reference To The Literature 1xvt |
| Chain | Residue | Details |
| A | ASP156 |
| site_id | CSA2 |
| Number of Residues | 1 |
| Details | Annotated By Reference To The Literature 1xvt |
| Chain | Residue | Details |
| B | ASP156 |
| site_id | CSA3 |
| Number of Residues | 1 |
| Details | Annotated By Reference To The Literature 1xvt |
| Chain | Residue | Details |
| C | ASP156 |
| site_id | CSA4 |
| Number of Residues | 1 |
| Details | Annotated By Reference To The Literature 1xvt |
| Chain | Residue | Details |
| D | ASP156 |






