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2BFD

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
A0009353cellular_componentobsolete mitochondrial oxoglutarate dehydrogenase complex
A0016491molecular_functionoxidoreductase activity
A0016624molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor
A0016831molecular_functioncarboxy-lyase activity
A0046872molecular_functionmetal ion binding
A0047101molecular_functionbranched-chain alpha-keto acid dehydrogenase activity
A0160120cellular_componentobsolete mitochondrial branched-chain alpha-keto acid 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
AHOH2117

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MN A 503
ChainResidue
ATPP601
AHOH2339
AGLU193
AASN222
ATYR224

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CL A 504
ChainResidue
APRO53
AGLU55
AGLN369
AHOH2071
BHOH2049

site_idAC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE K B 502
ChainResidue
BGLY128
BLEU130
BTHR131
BCYS178
BASP181
BASN183
BHOH2148

site_idAC5
Number of Residues23
DetailsBINDING SITE FOR RESIDUE TPP A 601
ChainResidue
AGLN112
AARG114
ASER162
ALEU164
AGLY192
AGLU193
AGLY194
AALA195
AGLU198
AARG220
AASN222
ATYR224
AALA225
AILE226
AMN503
AHOH2208
AHOH2339
AHOH2340
BGLU46
BLEU74
BGLU76
BGLN98
BTYR102

site_idAC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL B 701
ChainResidue
AGLN374
BTRP260
BTHR284
BGLU290
BTHR294
BARG309
BHOH2260

site_idAC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MPD B 901
ChainResidue
AILE73
AGLU76
AARG82
APHE349
AHOH2090
BVAL58
BHOH2261

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

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

218500

PDB entries from 2024-04-17

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