3DUF
Snapshots of catalysis in the E1 subunit of the pyruvate dehydrogenase multi-enzyme complex
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004739 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) activity |
A | 0005515 | molecular_function | protein binding |
A | 0009083 | biological_process | branched-chain amino acid catabolic process |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0016624 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor |
B | 0003824 | molecular_function | catalytic activity |
B | 0004739 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) activity |
B | 0005515 | molecular_function | protein binding |
B | 0016491 | molecular_function | oxidoreductase activity |
C | 0004739 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) activity |
C | 0005515 | molecular_function | protein binding |
C | 0009083 | biological_process | branched-chain amino acid catabolic process |
C | 0016491 | molecular_function | oxidoreductase activity |
C | 0016624 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor |
D | 0003824 | molecular_function | catalytic activity |
D | 0004739 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) activity |
D | 0005515 | molecular_function | protein binding |
D | 0016491 | molecular_function | oxidoreductase activity |
E | 0004739 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) activity |
E | 0005515 | molecular_function | protein binding |
E | 0009083 | biological_process | branched-chain amino acid catabolic process |
E | 0016491 | molecular_function | oxidoreductase activity |
E | 0016624 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor |
F | 0003824 | molecular_function | catalytic activity |
F | 0004739 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) activity |
F | 0005515 | molecular_function | protein binding |
F | 0016491 | molecular_function | oxidoreductase activity |
G | 0004739 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) activity |
G | 0005515 | molecular_function | protein binding |
G | 0009083 | biological_process | branched-chain amino acid catabolic process |
G | 0016491 | molecular_function | oxidoreductase activity |
G | 0016624 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor |
H | 0003824 | molecular_function | catalytic activity |
H | 0004739 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) activity |
H | 0005515 | molecular_function | protein binding |
H | 0016491 | molecular_function | oxidoreductase activity |
I | 0004742 | molecular_function | dihydrolipoyllysine-residue acetyltransferase activity |
I | 0005515 | molecular_function | protein binding |
I | 0005737 | cellular_component | cytoplasm |
I | 0016407 | molecular_function | acetyltransferase activity |
I | 0016746 | molecular_function | acyltransferase activity |
I | 0031405 | molecular_function | lipoic acid binding |
J | 0004742 | molecular_function | dihydrolipoyllysine-residue acetyltransferase activity |
J | 0005515 | molecular_function | protein binding |
J | 0005737 | cellular_component | cytoplasm |
J | 0016407 | molecular_function | acetyltransferase activity |
J | 0016746 | molecular_function | acyltransferase activity |
J | 0031405 | molecular_function | lipoic acid binding |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE MG A1368 |
Chain | Residue |
A | ASP173 |
A | ASN202 |
A | PHE204 |
A | R1T1370 |
A | HOH1374 |
site_id | AC2 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE K B1325 |
Chain | Residue |
B | ASP165 |
B | ILE112 |
B | THR113 |
B | ALA160 |
B | ASP163 |
site_id | AC3 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE MG D1326 |
Chain | Residue |
B | HOH1344 |
site_id | AC4 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE MG C1368 |
Chain | Residue |
C | ASP173 |
C | ASN202 |
C | PHE204 |
C | R1T1370 |
site_id | AC5 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE K D1325 |
Chain | Residue |
D | ILE112 |
D | THR113 |
D | ALA160 |
D | ASP163 |
D | ASP165 |
site_id | AC6 |
Number of Residues | 24 |
Details | BINDING SITE FOR RESIDUE R1T A1370 |
Chain | Residue |
A | TYR102 |
A | ARG103 |
A | ILE142 |
A | ILE144 |
A | GLY172 |
A | ASP173 |
A | GLY174 |
A | GLY175 |
A | GLN178 |
A | ASN202 |
A | PHE204 |
A | ALA205 |
A | ILE206 |
A | HIS271 |
A | MG1368 |
A | HOH1374 |
A | HOH1375 |
A | HOH1393 |
D | GLU28 |
D | LEU57 |
D | GLU59 |
D | GLN81 |
D | PHE85 |
D | HIS128 |
site_id | AC7 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE MG E1371 |
Chain | Residue |
E | ASP173 |
E | ASN202 |
E | PHE204 |
E | R1T1370 |
E | HOH1382 |
site_id | AC8 |
Number of Residues | 22 |
Details | BINDING SITE FOR RESIDUE R1T C1370 |
Chain | Residue |
B | GLU28 |
B | LEU57 |
B | GLU59 |
B | GLN81 |
B | PHE85 |
B | HIS128 |
C | TYR102 |
C | ARG103 |
C | ILE142 |
C | ILE144 |
C | GLY172 |
C | ASP173 |
C | GLY174 |
C | GLY175 |
C | GLN178 |
C | ASN202 |
C | PHE204 |
C | ALA205 |
C | ILE206 |
C | HIS271 |
C | MG1368 |
C | HOH1417 |
site_id | AC9 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE MG G1371 |
Chain | Residue |
G | ASP173 |
G | ASN202 |
G | PHE204 |
G | R1T1370 |
G | HOH1383 |
site_id | BC1 |
Number of Residues | 24 |
Details | BINDING SITE FOR RESIDUE R1T E1370 |
Chain | Residue |
H | HIS128 |
E | TYR102 |
E | ARG103 |
E | ILE142 |
E | ILE144 |
E | GLY172 |
E | ASP173 |
E | GLY174 |
E | GLY175 |
E | ASN202 |
E | PHE204 |
E | ALA205 |
E | ILE206 |
E | HIS271 |
E | MG1371 |
E | HOH1373 |
E | HOH1380 |
E | HOH1382 |
E | HOH1390 |
H | GLU28 |
H | LEU57 |
H | GLU59 |
H | GLN81 |
H | PHE85 |
site_id | BC2 |
Number of Residues | 22 |
Details | BINDING SITE FOR RESIDUE R1T G1370 |
Chain | Residue |
F | GLU28 |
F | LEU57 |
F | GLU59 |
F | GLN81 |
F | PHE85 |
F | HIS128 |
G | TYR102 |
G | ARG103 |
G | ILE142 |
G | ILE144 |
G | GLY172 |
G | ASP173 |
G | GLY174 |
G | GLY175 |
G | ASN202 |
G | PHE204 |
G | ALA205 |
G | ILE206 |
G | HIS271 |
G | MG1371 |
G | HOH1376 |
G | HOH1383 |
Functional Information from PROSITE/UniProt
site_id | PS00189 |
Number of Residues | 30 |
Details | LIPOYL 2-oxo acid dehydrogenases acyltransferase component lipoyl binding site. GdeVnedDVLceVQNdKAVveIpspvkGkV |
Chain | Residue | Details |
I | GLY27-VAL56 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | ACT_SITE: ACT_SITE => ECO:0000255 |
Chain | Residue | Details |
I | HIS399 | |
J | HIS399 | |
F | GLU59 | |
H | GLU59 |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | MOD_RES: N6-lipoyllysine => ECO:0000255|PROSITE-ProRule:PRU01066, ECO:0000269|PubMed:8445635 |
Chain | Residue | Details |
I | LYS43 | |
J | LYS43 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
A | HIS271 |
site_id | CSA10 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
D | GLU59 | |
D | HIS128 |
site_id | CSA11 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
F | GLU59 | |
F | HIS128 |
site_id | CSA12 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
H | GLU59 | |
H | HIS128 |
site_id | CSA2 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
C | HIS271 |
site_id | CSA3 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
E | HIS271 |
site_id | CSA4 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
G | HIS271 |
site_id | CSA5 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
B | GLU59 |
site_id | CSA6 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
D | GLU59 |
site_id | CSA7 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
F | GLU59 |
site_id | CSA8 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
H | GLU59 |
site_id | CSA9 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1dtw |
Chain | Residue | Details |
B | GLU59 | |
B | HIS128 |
site_id | MCSA1 |
Number of Residues | 2 |
Details | M-CSA 106 |
Chain | Residue | Details |
B | GLU59 | proton acceptor, proton donor |
B | HIS128 | proton acceptor, proton donor |
A | TYR281 | electrostatic stabiliser, hydrogen bond donor |
site_id | MCSA2 |
Number of Residues | 2 |
Details | M-CSA 106 |
Chain | Residue | Details |
D | GLU59 | proton acceptor, proton donor |
D | HIS128 | proton acceptor, proton donor |
C | TYR281 | electrostatic stabiliser, hydrogen bond donor |
site_id | MCSA3 |
Number of Residues | 2 |
Details | M-CSA 106 |
Chain | Residue | Details |
F | GLU59 | proton acceptor, proton donor |
F | HIS128 | proton acceptor, proton donor |
E | TYR281 | electrostatic stabiliser, hydrogen bond donor |
site_id | MCSA4 |
Number of Residues | 2 |
Details | M-CSA 106 |
Chain | Residue | Details |
H | GLU59 | proton acceptor, proton donor |
H | HIS128 | proton acceptor, proton donor |
G | TYR281 | electrostatic stabiliser, hydrogen bond donor |