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3DV0

Snapshots of catalysis in the E1 subunit of the pyruvate dehydrogenase multi-enzyme complex

Functional Information from GO Data
ChainGOidnamespacecontents
A0004739molecular_functionpyruvate dehydrogenase (acetyl-transferring) activity
A0005515molecular_functionprotein binding
A0009083biological_processbranched-chain amino acid catabolic process
A0016491molecular_functionoxidoreductase activity
A0016624molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor
B0003824molecular_functioncatalytic activity
B0004739molecular_functionpyruvate dehydrogenase (acetyl-transferring) activity
B0005515molecular_functionprotein binding
B0016491molecular_functionoxidoreductase activity
C0004739molecular_functionpyruvate dehydrogenase (acetyl-transferring) activity
C0005515molecular_functionprotein binding
C0009083biological_processbranched-chain amino acid catabolic process
C0016491molecular_functionoxidoreductase activity
C0016624molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor
D0003824molecular_functioncatalytic activity
D0004739molecular_functionpyruvate dehydrogenase (acetyl-transferring) activity
D0005515molecular_functionprotein binding
D0016491molecular_functionoxidoreductase activity
E0004739molecular_functionpyruvate dehydrogenase (acetyl-transferring) activity
E0005515molecular_functionprotein binding
E0009083biological_processbranched-chain amino acid catabolic process
E0016491molecular_functionoxidoreductase activity
E0016624molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor
F0003824molecular_functioncatalytic activity
F0004739molecular_functionpyruvate dehydrogenase (acetyl-transferring) activity
F0005515molecular_functionprotein binding
F0016491molecular_functionoxidoreductase activity
G0004739molecular_functionpyruvate dehydrogenase (acetyl-transferring) activity
G0005515molecular_functionprotein binding
G0009083biological_processbranched-chain amino acid catabolic process
G0016491molecular_functionoxidoreductase activity
G0016624molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor
H0003824molecular_functioncatalytic activity
H0004739molecular_functionpyruvate dehydrogenase (acetyl-transferring) activity
H0005515molecular_functionprotein binding
H0016491molecular_functionoxidoreductase activity
I0004742molecular_functiondihydrolipoyllysine-residue acetyltransferase activity
I0005515molecular_functionprotein binding
I0005737cellular_componentcytoplasm
I0016407molecular_functionacetyltransferase activity
I0016746molecular_functionacyltransferase activity
I0031405molecular_functionlipoic acid binding
J0004742molecular_functiondihydrolipoyllysine-residue acetyltransferase activity
J0005515molecular_functionprotein binding
J0005737cellular_componentcytoplasm
J0016407molecular_functionacetyltransferase activity
J0016746molecular_functionacyltransferase activity
J0031405molecular_functionlipoic acid binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG A1368
ChainResidue
AASP173
AASN202
APHE204
ATPW1370

site_idAC2
Number of Residues22
DetailsBINDING SITE FOR RESIDUE TPW A1370
ChainResidue
AASP173
AGLY174
AGLY175
AGLN178
AASN202
APHE204
AALA205
AILE206
AARG267
AMG1368
AHOH1489
DGLU28
DLEU57
DGLU59
DGLN81
DPHE85
DPYR502
ATYR102
AARG103
AILE142
AILE144
AGLY172

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE K B1325
ChainResidue
BILE112
BTHR113
BALA160
BASP163
BASP165
BHOH1344

site_idAC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG B1326
ChainResidue
AGLU183
AHOH1375
AHOH1436
BGLU88
BHOH1436
CHOH1421
DHOH1439

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE PYR B 502
ChainResidue
BPHE82
BHIS128
BHOH1379
CPHE74
CILE142
CTPW1370
CHOH1401

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG C1368
ChainResidue
CASP173
CASN202
CPHE204
CTPW1370

site_idAC7
Number of Residues22
DetailsBINDING SITE FOR RESIDUE TPW C1370
ChainResidue
BGLU28
BLEU57
BGLU59
BGLN81
BPHE85
BPYR502
CTYR102
CARG103
CILE142
CILE144
CGLY172
CASP173
CGLY174
CGLY175
CGLN178
CASN202
CPHE204
CALA205
CILE206
CHIS271
CMG1368
CHOH1442

site_idAC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE K D1325
ChainResidue
DILE112
DTHR113
DALA160
DASP163
DASP165
DHOH1328

site_idAC9
Number of Residues6
DetailsBINDING SITE FOR RESIDUE PYR D 502
ChainResidue
AILE142
ATPW1370
DGLN81
DPHE82
DPHE85
DHIS128

site_idBC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE TPW E1370
ChainResidue
HLEU57
HGLU59
HGLN81
HPHE85
HGLU88
ETYR102
EARG103
EILE142
EILE144
EGLY172
EASP173
EGLY174
EGLY175
EASN202
EPHE204
EALA205
EILE206
EMG1368
EHOH1462
HGLU28

site_idBC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG E1368
ChainResidue
EGLY172
EASP173
EGLN200
EASN202
ETPW1370

site_idBC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K F1325
ChainResidue
FILE112
FTHR113
FALA160
FASP163
FASP165

site_idBC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG G1326
ChainResidue
GASP180
GGLU183
HHOH1372
HHOH1376

site_idBC5
Number of Residues20
DetailsBINDING SITE FOR RESIDUE TPW G1370
ChainResidue
FGLU28
FLEU57
FGLU59
FGLN81
FPHE85
GTYR102
GARG103
GILE142
GILE144
GGLY172
GASP173
GGLY174
GGLY175
GGLN178
GASN202
GPHE204
GALA205
GILE206
GHIS271
GMG1367

site_idBC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG G1367
ChainResidue
GASP173
GASN202
GPHE204
GTPW1370

site_idBC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE K H1325
ChainResidue
HILE112
HTHR113
HALA160
HASP163
HASP165
HHOH1330

Functional Information from PROSITE/UniProt
site_idPS00189
Number of Residues30
DetailsLIPOYL 2-oxo acid dehydrogenases acyltransferase component lipoyl binding site. GdeVnedDVLceVQNdKAVveIpspvkGkV
ChainResidueDetails
IGLY27-VAL56

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: ACT_SITE => ECO:0000255
ChainResidueDetails
IHIS399
JHIS399
FGLU59
HGLU59

site_idSWS_FT_FI2
Number of Residues2
DetailsMOD_RES: N6-lipoyllysine => ECO:0000255|PROSITE-ProRule:PRU01066, ECO:0000269|PubMed:8445635
ChainResidueDetails
ILYS43
JLYS43

Catalytic Information from CSA
site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
AHIS271

site_idCSA10
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
FGLU59
FHIS128

site_idCSA11
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
HGLU59
HHIS128

site_idCSA2
Number of Residues1
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
CHIS271

site_idCSA3
Number of Residues1
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
GHIS271

site_idCSA4
Number of Residues1
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
BGLU59

site_idCSA5
Number of Residues1
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
DGLU59

site_idCSA6
Number of Residues1
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
FGLU59

site_idCSA7
Number of Residues1
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
HGLU59

site_idCSA8
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
BGLU59
BHIS128

site_idCSA9
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
DGLU59
DHIS128

site_idMCSA1
Number of Residues2
DetailsM-CSA 106
ChainResidueDetails
BGLU59proton acceptor, proton donor
BHIS128proton acceptor, proton donor
ATYR281electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues2
DetailsM-CSA 106
ChainResidueDetails
DGLU59proton acceptor, proton donor
DHIS128proton acceptor, proton donor
CTYR281electrostatic stabiliser, hydrogen bond donor

site_idMCSA3
Number of Residues2
DetailsM-CSA 106
ChainResidueDetails
FGLU59proton acceptor, proton donor
FHIS128proton acceptor, proton donor
ETYR281electrostatic stabiliser, hydrogen bond donor

site_idMCSA4
Number of Residues2
DetailsM-CSA 106
ChainResidueDetails
HGLU59proton acceptor, proton donor
HHIS128proton acceptor, proton donor
GTYR281electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2024-10-02

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