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1M76

Crystal Structure of the S137C Mutant of L-3-HYDROXYACYL-COA Dehydrogenase in Complex with NAD and Acetoacetyl-COA

Functional Information from GO Data
ChainGOidnamespacecontents
A0003857molecular_function(3S)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity
A0005654cellular_componentnucleoplasm
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005759cellular_componentmitochondrial matrix
A0006629biological_processlipid metabolic process
A0006631biological_processfatty acid metabolic process
A0006635biological_processfatty acid beta-oxidation
A0007283biological_processspermatogenesis
A0009410biological_processresponse to xenobiotic stimulus
A0009725biological_processresponse to hormone
A0014823biological_processresponse to activity
A0016491molecular_functionoxidoreductase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0016740molecular_functiontransferase activity
A0030154biological_processcell differentiation
A0032868biological_processresponse to insulin
A0042802molecular_functionidentical protein binding
A0046676biological_processnegative regulation of insulin secretion
A0050796biological_processregulation of insulin secretion
A0070403molecular_functionNAD+ binding
A0120162biological_processpositive regulation of cold-induced thermogenesis
B0003857molecular_function(3S)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity
B0005654cellular_componentnucleoplasm
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005759cellular_componentmitochondrial matrix
B0006629biological_processlipid metabolic process
B0006631biological_processfatty acid metabolic process
B0006635biological_processfatty acid beta-oxidation
B0007283biological_processspermatogenesis
B0009410biological_processresponse to xenobiotic stimulus
B0009725biological_processresponse to hormone
B0014823biological_processresponse to activity
B0016491molecular_functionoxidoreductase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0016740molecular_functiontransferase activity
B0030154biological_processcell differentiation
B0032868biological_processresponse to insulin
B0042802molecular_functionidentical protein binding
B0046676biological_processnegative regulation of insulin secretion
B0050796biological_processregulation of insulin secretion
B0070403molecular_functionNAD+ binding
B0120162biological_processpositive regulation of cold-induced thermogenesis
Functional Information from PDB Data
site_idAC1
Number of Residues21
DetailsBINDING SITE FOR RESIDUE CAA A 351
ChainResidue
ASER61
APRO243
AMET244
ALEU249
ATYR252
ANAD350
AHOH801
AHOH911
AHOH1028
AHOH1040
AHOH1147
ACYS137
BGLY239
BALA240
APHE160
AASN161
APRO164
AVAL165
AMET166
AASN208
ALEU211

site_idAC2
Number of Residues22
DetailsBINDING SITE FOR RESIDUE CAA B 751
ChainResidue
AGLY239
AALA240
AHOH802
BSER61
BVAL65
BLYS68
BHIS158
BPHE160
BASN161
BPRO164
BVAL165
BMET166
BASN208
BLEU211
BPRO243
BMET244
BLEU249
BTYR252
BNAD750
BHOH1100
BHOH1242
BHOH1252

site_idAC3
Number of Residues26
DetailsBINDING SITE FOR RESIDUE NAD A 350
ChainResidue
AILE21
AGLY24
ALEU25
AMET26
AASP45
AGLN46
AALA107
AILE108
AGLU110
ALYS115
AASN135
ACYS137
AHIS158
APHE159
AASN161
AVAL253
ATHR257
ALYS293
ACAA351
AHOH804
AHOH863
AHOH878
AHOH1017
AHOH1020
AHOH1024
AHOH1146

site_idAC4
Number of Residues24
DetailsBINDING SITE FOR RESIDUE NAD B 750
ChainResidue
BGLY24
BLEU25
BMET26
BASP45
BGLN46
BALA107
BILE108
BGLU110
BLYS115
BASN135
BCYS137
BHIS158
BPHE159
BASN161
BVAL253
BLYS293
BCAA751
BHOH832
BHOH841
BHOH853
BHOH1021
BHOH1030
BHOH1038
BHOH1145

Functional Information from PROSITE/UniProt
site_idPS00067
Number of Residues25
Details3HCDH 3-hydroxyacyl-CoA dehydrogenase signature. DtpGFIvNRllvPYLmeair.LYerG
ChainResidueDetails
AASP201-GLY225

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues22
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"10231530","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"10840044","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"10840044","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues2
DetailsSite: {"description":"Important for catalytic activity","evidences":[{"evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsModified residue: {"description":"N6-succinyllysine","evidences":[{"source":"UniProtKB","id":"Q61425","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues18
DetailsModified residue: {"description":"N6-succinyllysine; alternate","evidences":[{"source":"UniProtKB","id":"Q61425","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues4
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"Q61425","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues2
DetailsModified residue: {"description":"N6-(2-hydroxyisobutyryl)lysine","evidences":[{"source":"PubMed","id":"29192674","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 336
ChainResidueDetails
ACYS137electrostatic stabiliser, hydrogen bond donor
AHIS158proton acceptor, proton donor
AGLU170electrostatic stabiliser, hydrogen bond acceptor, increase basicity
AASN208electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues4
DetailsM-CSA 336
ChainResidueDetails
BCYS137electrostatic stabiliser, hydrogen bond donor
BHIS158proton acceptor, proton donor
BGLU170electrostatic stabiliser, hydrogen bond acceptor, increase basicity
BASN208electrostatic stabiliser, hydrogen bond donor

242500

PDB entries from 2025-10-01

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