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4KUG

Crystal structure of 3-hydroxybutylryl-CoA dehydrogenase with NAD from Clostridium butyricum

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0006631biological_processfatty acid metabolic process
A0008691molecular_function3-hydroxybutyryl-CoA dehydrogenase activity
A0016491molecular_functionoxidoreductase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0019605biological_processbutyrate metabolic process
A0044248biological_processcellular catabolic process
A0070403molecular_functionNAD+ binding
B0000166molecular_functionnucleotide binding
B0006631biological_processfatty acid metabolic process
B0008691molecular_function3-hydroxybutyryl-CoA dehydrogenase activity
B0016491molecular_functionoxidoreductase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0019605biological_processbutyrate metabolic process
B0044248biological_processcellular catabolic process
B0070403molecular_functionNAD+ binding
C0000166molecular_functionnucleotide binding
C0006631biological_processfatty acid metabolic process
C0008691molecular_function3-hydroxybutyryl-CoA dehydrogenase activity
C0016491molecular_functionoxidoreductase activity
C0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
C0019605biological_processbutyrate metabolic process
C0044248biological_processcellular catabolic process
C0070403molecular_functionNAD+ binding
D0000166molecular_functionnucleotide binding
D0006631biological_processfatty acid metabolic process
D0008691molecular_function3-hydroxybutyryl-CoA dehydrogenase activity
D0016491molecular_functionoxidoreductase activity
D0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
D0019605biological_processbutyrate metabolic process
D0044248biological_processcellular catabolic process
D0070403molecular_functionNAD+ binding
Functional Information from PDB Data
site_idAC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE NAD A 301
ChainResidue
AGLY8
ALYS95
AILE98
AASN115
ATHR116
ASER117
AHIS138
APHE139
AHOH418
AHOH426
AHOH438
AGLY10
AHOH439
ATHR11
AMET12
AARG30
AASP31
AALA87
AALA88
AGLU90

site_idAC2
Number of Residues19
DetailsBINDING SITE FOR RESIDUE NAD B 301
ChainResidue
BGLY8
BGLY10
BTHR11
BMET12
BARG30
BASP31
BILE32
BALA87
BALA88
BGLU90
BLYS95
BILE98
BASN115
BTHR116
BSER117
BHIS138
BPHE139
BASN141
BHOH416

site_idAC3
Number of Residues19
DetailsBINDING SITE FOR RESIDUE NAD C 301
ChainResidue
CALA9
CGLY10
CTHR11
CMET12
CARG30
CASP31
CILE32
CPHE36
CALA87
CALA88
CILE89
CGLU90
CLYS95
CASN115
CTHR116
CSER117
CHIS138
CPHE139
CASN141

site_idAC4
Number of Residues19
DetailsBINDING SITE FOR RESIDUE NAD D 301
ChainResidue
DGLY8
DGLY10
DTHR11
DMET12
DARG30
DASP31
DILE32
DALA87
DALA88
DGLU90
DLYS95
DILE98
DASN115
DTHR116
DSER117
DHIS138
DPHE139
DASN141
DHOH454

Functional Information from PROSITE/UniProt
site_idPS00067
Number of Residues25
Details3HCDH 3-hydroxyacyl-CoA dehydrogenase signature. EapGFVvNRiliPMIneatf.ILqeG
ChainResidueDetails
AGLU181-GLY205

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PDB entries from 2024-07-10

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