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2BFC

Reactivity modulation of human branched-chain alpha-ketoacid dehydrogenase by an internal molecular switch

Functional Information from GO Data
ChainGOidnamespacecontents
A0003863molecular_function3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) activity
A0005515molecular_functionprotein binding
A0005739cellular_componentmitochondrion
A0005759cellular_componentmitochondrial matrix
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
A0016831molecular_functioncarboxy-lyase activity
A0045252cellular_componentoxoglutarate dehydrogenase complex
A0046872molecular_functionmetal ion binding
A0047101molecular_functionbranched-chain alpha-keto acid dehydrogenase activity
A0160157cellular_componentbranched-chain alpha-ketoacid dehydrogenase complex
B0003824molecular_functioncatalytic activity
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE K A 501
ChainResidue
AGLN112
ASER161
APRO163
ATHR166
AGLN167
AHOH2115

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MN A 503
ChainResidue
ATZD601
AHOH2337
AGLU193
AASN222
ATYR224

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE K B 502
ChainResidue
BGLY128
BLEU130
BTHR131
BCYS178
BASP181
BASN183
BHOH2156

site_idAC4
Number of Residues27
DetailsBINDING SITE FOR RESIDUE TZD A 601
ChainResidue
AARG114
ASER162
APRO163
ALEU164
AGLY192
AGLU193
AGLY194
AALA195
AGLU198
AARG220
AASN222
ATYR224
AALA225
AILE226
AMN503
AHOH2337
AHOH2339
AHOH2340
AHOH2341
AHOH2342
AHOH2343
BGLU46
BLEU74
BGLU76
BGLN98
BTYR102
BHOH2137

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL B 701
ChainResidue
AGLN374
BTRP260
BTHR284
BGLU290
BTHR294
BARG309
BHOH2271

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues7
DetailsBINDING: BINDING => ECO:0000269|PubMed:10745006, ECO:0007744|PDB:1DTW
ChainResidueDetails
BTYR102
AALA195
AARG220
AASN222
ATYR224
AALA291
BGLY128
BLEU130
BTHR131
BCYS178
BASP181
BASN183
AGLU193
AGLY194

site_idSWS_FT_FI2
Number of Residues1
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:Q6P3A8
ChainResidueDetails
BLYS182

site_idSWS_FT_FI3
Number of Residues1
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
BLYS191

site_idSWS_FT_FI4
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:P50136
ChainResidueDetails
ASER294
ASER302

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:P50136
ChainResidueDetails
ALYS311

site_idSWS_FT_FI6
Number of Residues1
DetailsMOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:P50136
ChainResidueDetails
ALYS335

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 280
ChainResidueDetails
AGLU76activator, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, steric role
ASER162hydrogen bond acceptor, steric role
AALA291activator, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
ASER292hydrogen bond acceptor, hydrogen bond donor

site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
BGLU76

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dtw
ChainResidueDetails
BGLU76
BHIS146

219140

PDB entries from 2024-05-01

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