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3ZW9

CRYSTAL STRUCTURE OF RAT PEROXISOMAL MULTIFUNCTIONAL ENZYME TYPE 1 (RPMFE1) COMPLEXED WITH (2S,3S)-3-HYDROXY-2-METHYLBUTANOYL-COA

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0003857molecular_function(3S)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity
A0004165molecular_functiondelta(3)-delta(2)-enoyl-CoA isomerase activity
A0004300molecular_functionenoyl-CoA hydratase activity
A0005777cellular_componentperoxisome
A0005782cellular_componentperoxisomal matrix
A0005829cellular_componentcytosol
A0006629biological_processlipid metabolic process
A0006631biological_processfatty acid metabolic process
A0006633biological_processfatty acid biosynthetic process
A0006635biological_processfatty acid beta-oxidation
A0016491molecular_functionoxidoreductase activity
A0016509molecular_functionlong-chain (3S)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0016829molecular_functionlyase activity
A0016853molecular_functionisomerase activity
A0016863molecular_functionintramolecular oxidoreductase activity, transposing C=C bonds
A0018812molecular_function3-hydroxyacyl-CoA dehydratase activity
A0019899molecular_functionenzyme binding
A0033540biological_processfatty acid beta-oxidation using acyl-CoA oxidase
A0070403molecular_functionNAD+ binding
B0003824molecular_functioncatalytic activity
B0003857molecular_function(3S)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity
B0004165molecular_functiondelta(3)-delta(2)-enoyl-CoA isomerase activity
B0004300molecular_functionenoyl-CoA hydratase activity
B0005777cellular_componentperoxisome
B0005782cellular_componentperoxisomal matrix
B0005829cellular_componentcytosol
B0006629biological_processlipid metabolic process
B0006631biological_processfatty acid metabolic process
B0006633biological_processfatty acid biosynthetic process
B0006635biological_processfatty acid beta-oxidation
B0016491molecular_functionoxidoreductase activity
B0016509molecular_functionlong-chain (3S)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0016829molecular_functionlyase activity
B0016853molecular_functionisomerase activity
B0016863molecular_functionintramolecular oxidoreductase activity, transposing C=C bonds
B0018812molecular_function3-hydroxyacyl-CoA dehydratase activity
B0019899molecular_functionenzyme binding
B0033540biological_processfatty acid beta-oxidation using acyl-CoA oxidase
B0070403molecular_functionNAD+ binding
Functional Information from PDB Data
site_idAC1
Number of Residues18
DetailsBINDING SITE FOR RESIDUE NAD A 1721
ChainResidue
ALEU302
AALA380
AVAL381
APHE382
AGLU383
ALYS388
AASN408
ASER410
AHIS431
APHE432
AGLY303
AGLY305
ATHR306
AMET307
AVAL325
AGLU326
ASER327
AGLN331

site_idAC2
Number of Residues19
DetailsBINDING SITE FOR RESIDUE T1G A 1722
ChainResidue
AVAL21
AALA23
AALA59
AGLY60
AALA61
AASP62
AILE63
APHE66
ALEU98
AGLY99
AGLY100
AGLU103
APRO122
AGLU123
AILE128
APRO130
AGLY131
ATYR156
BLYS249

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 1723
ChainResidue
APRO191
AILE192
AGLU193
AARG196

site_idAC4
Number of Residues20
DetailsBINDING SITE FOR RESIDUE NAD B 1719
ChainResidue
ATHR597
BLEU302
BGLY303
BGLY305
BTHR306
BMET307
BVAL325
BGLU326
BSER327
BGLN331
BALA380
BVAL381
BPHE382
BGLU383
BLYS388
BVAL391
BASN408
BSER410
BHIS431
BHOH2028

site_idAC5
Number of Residues17
DetailsBINDING SITE FOR RESIDUE T1G B 1721
ChainResidue
BVAL21
BALA59
BGLY60
BALA61
BASP62
BILE63
BPHE66
BLEU98
BGLY100
BGLU103
BPRO122
BGLU123
BLEU129
BPRO130
BGLY131
BTYR156
BLYS275

site_idAC6
Number of Residues2
DetailsBINDING SITE FOR RESIDUE SO4 B 1720
ChainResidue
BARG440
BHIS651

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 B 1722
ChainResidue
BPRO191
BILE192
BGLU193
BARG196

Functional Information from PROSITE/UniProt
site_idPS00067
Number of Residues25
Details3HCDH 3-hydroxyacyl-CoA dehydrogenase signature. NcyGFVgNRmlaPYYnqgff.LLeeG
ChainResidueDetails
AASN474-GLY498

site_idPS00166
Number of Residues21
DetailsENOYL_COA_HYDRATASE Enoyl-CoA hydratase/isomerase signature. LAaIQGvalGGGlelaLgCHY
ChainResidueDetails
ALEU90-TYR110

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues560
DetailsRegion: {"description":"Enoyl-CoA hydratase / isomerase"}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues578
DetailsRegion: {"description":"3-hydroxyacyl-CoA dehydrogenase"}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues2
DetailsBinding site: {"evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsSite: {"description":"Important for catalytic activity","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues2
DetailsModified residue: {"description":"Blocked amino end (Ala)"}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues18
DetailsModified residue: {"description":"N6-succinyllysine","evidences":[{"source":"UniProtKB","id":"Q9DBM2","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues14
DetailsModified residue: {"description":"N6-succinyllysine; alternate","evidences":[{"source":"UniProtKB","id":"Q9DBM2","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues6
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"Q9DBM2","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI9
Number of Residues2
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"Q08426","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI10
Number of Residues2
DetailsModified residue: {"description":"Phosphothreonine","evidences":[{"source":"UniProtKB","id":"Q08426","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

250059

PDB entries from 2026-03-04

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