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5OVK

Crystal structure MabA bound to NADPH from M. smegmatis

Functional Information from GO Data
ChainGOidnamespacecontents
A0004316molecular_function3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
A0005576cellular_componentextracellular region
A0006633biological_processfatty acid biosynthetic process
A0016491molecular_functionoxidoreductase activity
A0018454molecular_functionacetoacetyl-CoA reductase activity
A0030497biological_processfatty acid elongation
A0050661molecular_functionNADP binding
B0004316molecular_function3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
B0005576cellular_componentextracellular region
B0006633biological_processfatty acid biosynthetic process
B0016491molecular_functionoxidoreductase activity
B0018454molecular_functionacetoacetyl-CoA reductase activity
B0030497biological_processfatty acid elongation
B0050661molecular_functionNADP binding
C0004316molecular_function3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
C0005576cellular_componentextracellular region
C0006633biological_processfatty acid biosynthetic process
C0016491molecular_functionoxidoreductase activity
C0018454molecular_functionacetoacetyl-CoA reductase activity
C0030497biological_processfatty acid elongation
C0050661molecular_functionNADP binding
D0004316molecular_function3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
D0005576cellular_componentextracellular region
D0006633biological_processfatty acid biosynthetic process
D0016491molecular_functionoxidoreductase activity
D0018454molecular_functionacetoacetyl-CoA reductase activity
D0030497biological_processfatty acid elongation
D0050661molecular_functionNADP binding
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue NDP A 301
ChainResidue
AGLY30
ATHR119
AHOH403
AHOH410
AHOH424
AHOH430
AHOH436
AHOH479
AASN32
AARG33
AARG55
ACYS68
AASP69
AVAL70
AALA97
AGLY98

site_idAC2
Number of Residues29
Detailsbinding site for residue NDP B 301
ChainResidue
BGLY30
BASN32
BARG33
BILE35
BARG55
BCYS68
BASP69
BVAL70
BASN96
BALA97
BGLY98
BILE99
BTHR119
BILE146
BGLY147
BTYR161
BLYS165
BPRO191
BGLY192
BILE194
BTHR196
BHOH405
BHOH406
BHOH424
BHOH433
BHOH474
BHOH490
BHOH493
BHOH499

site_idAC3
Number of Residues13
Detailsbinding site for residue NDP C 301
ChainResidue
CGLY30
CASN32
CARG33
CILE35
CARG55
CCYS68
CASP69
CVAL70
CALA97
CGLY98
CTHR119
CHOH445
CHOH465

site_idAC4
Number of Residues15
Detailsbinding site for residue NDP D 301
ChainResidue
DGLY30
DASN32
DARG33
DARG55
DCYS68
DASP69
DVAL70
DALA97
DGLY98
DTHR119
DGLU197
DHOH422
DHOH431
DHOH491
DHOH561

Functional Information from PROSITE/UniProt
site_idPS00061
Number of Residues29
DetailsADH_SHORT Short-chain dehydrogenases/reductases family signature. SvsgmwgignQanYAAAKAGLiGMArSIS
ChainResidueDetails
ASER148-SER176

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU10001
ChainResidueDetails
ATYR161
BTYR161
CTYR161
DTYR161

site_idSWS_FT_FI2
Number of Residues28
DetailsBINDING: BINDING => ECO:0000269|PubMed:29717709
ChainResidueDetails
AASN32
BASP69
BTYR161
BLYS165
BILE194
BARG205
CASN32
CARG55
CASP69
CTYR161
CLYS165
AARG55
CILE194
CARG205
DASN32
DARG55
DASP69
DTYR161
DLYS165
DILE194
DARG205
AASP69
ATYR161
ALYS165
AILE194
AARG205
BASN32
BARG55

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P9WGT3
ChainResidueDetails
AGLY98
BGLY98
CGLY98
DGLY98

site_idSWS_FT_FI4
Number of Residues4
DetailsSITE: Important for activity => ECO:0000250|UniProtKB:P9WGT3
ChainResidueDetails
ASER148
BSER148
CSER148
DSER148

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PDB entries from 2024-10-09

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