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1F0Y

L-3-HYDROXYACYL-COA DEHYDROGENASE COMPLEXED WITH ACETOACETYL-COA AND NAD+

Functional Information from GO Data
ChainGOidnamespacecontents
A0003857molecular_function3-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_function3-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 Residues24
DetailsBINDING SITE FOR RESIDUE CAA A 351
ChainResidue
ASER61
AVAL165
AASN208
ALEU211
APRO243
AMET244
ALEU249
ATYR252
AVAL253
ANAD350
AHOH801
AVAL65
AHOH1139
AHOH1186
AHOH1223
BGLY239
BALA240
ALYS68
ASER137
AHIS158
APHE160
AASN161
APRO162
APRO164

site_idAC2
Number of Residues22
DetailsBINDING SITE FOR RESIDUE CAA B 751
ChainResidue
AGLY239
BSER61
BVAL65
BLYS68
BSER137
BHIS158
BPHE160
BASN161
BPRO162
BPRO164
BVAL165
BASN208
BLEU211
BPRO243
BMET244
BLEU249
BTYR252
BNAD750
BHOH804
BHOH1079
BHOH1220
BHOH1246

site_idAC3
Number of Residues28
DetailsBINDING SITE FOR RESIDUE NAD A 350
ChainResidue
AILE21
AGLY24
ALEU25
AMET26
AASP45
AGLN46
AALA107
AILE108
AGLU110
ALYS115
AASN135
ASER137
AHIS158
APHE159
AASN161
AVAL253
ATHR257
ALYS293
ACAA351
AHOH818
AHOH879
AHOH885
AHOH908
AHOH926
AHOH975
AHOH1066
AHOH1087
AHOH1181

site_idAC4
Number of Residues25
DetailsBINDING SITE FOR RESIDUE NAD B 750
ChainResidue
BGLY24
BLEU25
BMET26
BASP45
BGLN46
BALA107
BILE108
BGLU110
BLYS115
BASN135
BSER137
BHIS158
BPHE159
BASN161
BVAL253
BTHR257
BLYS293
BCAA751
BHOH815
BHOH831
BHOH864
BHOH927
BHOH944
BHOH1042
BHOH1222

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 Residues14
DetailsBINDING: BINDING => ECO:0000269|PubMed:10231530, ECO:0000269|PubMed:10840044
ChainResidueDetails
AALA28
BASN116
BARG121
BSER143
BLYS167
BTYR299
ALEU51
AASN116
AARG121
ASER143
ALYS167
ATYR299
BALA28
BLEU51

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10840044
ChainResidueDetails
ALYS67
APRO74
BLYS67
BPRO74

site_idSWS_FT_FI3
Number of Residues2
DetailsSITE: Important for catalytic activity => ECO:0000305
ChainResidueDetails
APRO164
BPRO164

site_idSWS_FT_FI4
Number of Residues4
DetailsMOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:Q61425
ChainResidueDetails
APRO74
ALYS200
BPRO74
BLYS200

site_idSWS_FT_FI5
Number of Residues16
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:Q61425
ChainResidueDetails
ALYS75
BVAL81
BTHR130
BGLN179
BVAL186
BPRO196
BILE206
BALA235
AVAL81
ATHR130
AGLN179
AVAL186
APRO196
AILE206
AALA235
BLYS75

site_idSWS_FT_FI6
Number of Residues4
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:Q61425
ChainResidueDetails
APHE119
ALYS173
BPHE119
BLYS173

site_idSWS_FT_FI7
Number of Residues2
DetailsMOD_RES: N6-(2-hydroxyisobutyryl)lysine => ECO:0000269|PubMed:29192674
ChainResidueDetails
AARG121
BARG121

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 2hdh
ChainResidueDetails
AASN208
ASER137
AHIS158

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 2hdh
ChainResidueDetails
BASN208
BSER137
BHIS158

site_idMCSA1
Number of Residues4
DetailsM-CSA 336
ChainResidueDetails
ASER137electrostatic 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
BSER137electrostatic stabiliser, hydrogen bond donor
BHIS158proton acceptor, proton donor
BGLU170electrostatic stabiliser, hydrogen bond acceptor, increase basicity
BASN208electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2025-06-18

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