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3FNE

Crystal structure of InhA bound to triclosan derivative 17

Functional Information from GO Data
ChainGOidnamespacecontents
A0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
A0005504molecular_functionfatty acid binding
A0005886cellular_componentplasma membrane
A0006633biological_processfatty acid biosynthetic process
A0009274cellular_componentpeptidoglycan-based cell wall
A0016491molecular_functionoxidoreductase activity
A0030497biological_processfatty acid elongation
A0046677biological_processresponse to antibiotic
A0050343molecular_functiontrans-2-enoyl-CoA reductase (NADH) activity
A0070403molecular_functionNAD+ binding
A0071768biological_processmycolic acid biosynthetic process
B0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
B0005504molecular_functionfatty acid binding
B0005886cellular_componentplasma membrane
B0006633biological_processfatty acid biosynthetic process
B0009274cellular_componentpeptidoglycan-based cell wall
B0016491molecular_functionoxidoreductase activity
B0030497biological_processfatty acid elongation
B0046677biological_processresponse to antibiotic
B0050343molecular_functiontrans-2-enoyl-CoA reductase (NADH) activity
B0070403molecular_functionNAD+ binding
B0071768biological_processmycolic acid biosynthetic process
C0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
C0005504molecular_functionfatty acid binding
C0005886cellular_componentplasma membrane
C0006633biological_processfatty acid biosynthetic process
C0009274cellular_componentpeptidoglycan-based cell wall
C0016491molecular_functionoxidoreductase activity
C0030497biological_processfatty acid elongation
C0046677biological_processresponse to antibiotic
C0050343molecular_functiontrans-2-enoyl-CoA reductase (NADH) activity
C0070403molecular_functionNAD+ binding
C0071768biological_processmycolic acid biosynthetic process
D0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
D0005504molecular_functionfatty acid binding
D0005886cellular_componentplasma membrane
D0006633biological_processfatty acid biosynthetic process
D0009274cellular_componentpeptidoglycan-based cell wall
D0016491molecular_functionoxidoreductase activity
D0030497biological_processfatty acid elongation
D0046677biological_processresponse to antibiotic
D0050343molecular_functiontrans-2-enoyl-CoA reductase (NADH) activity
D0070403molecular_functionNAD+ binding
D0071768biological_processmycolic acid biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues34
DetailsBINDING SITE FOR RESIDUE NAD A 300
ChainResidue
AGLY14
ASER94
AILE95
AGLY96
AILE122
AMET147
AASP148
APHE149
ALYS165
AALA191
AGLY192
AILE15
APRO193
AILE194
ATHR196
AALA198
AHOH271
AHOH275
AHOH279
AHOH311
AHOH322
AHOH356
AILE16
AHOH357
AHOH363
A8PC400
AHOH648
AHOH683
ASER20
AILE21
APHE41
ALEU63
AASP64
AVAL65

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE 8PC A 400
ChainResidue
AGLY96
AMET98
APHE149
ATYR158
AMET161
AALA198
AMET199
ANAD300
AHOH362

site_idAC3
Number of Residues29
DetailsBINDING SITE FOR RESIDUE NAD B 310
ChainResidue
BGLY14
BILE16
BSER20
BILE21
BPHE41
BLEU63
BASP64
BVAL65
BSER94
BILE95
BGLY96
BILE122
BMET147
BASP148
BPHE149
BMET161
BLYS165
BALA191
BGLY192
BPRO193
BILE194
BTHR196
BALA198
BHOH270
BHOH360
BHOH362
BHOH392
B8PC410
BHOH538

site_idAC4
Number of Residues9
DetailsBINDING SITE FOR RESIDUE 8PC B 410
ChainResidue
BGLY96
BMET98
BMET103
BPHE149
BTYR158
BALA198
BLEU218
BGLU219
BNAD310

site_idAC5
Number of Residues31
DetailsBINDING SITE FOR RESIDUE NAD C 320
ChainResidue
CPRO193
CILE194
CTHR196
CALA198
CHOH281
CHOH282
CHOH296
CHOH302
CHOH330
CHOH335
CHOH341
CHOH358
C8PC420
CGLY14
CILE15
CILE16
CSER20
CILE21
CPHE41
CLEU63
CASP64
CVAL65
CSER94
CILE95
CGLY96
CILE122
CMET147
CASP148
CLYS165
CALA191
CGLY192

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE 8PC C 420
ChainResidue
CGLY96
CMET98
CMET103
CPHE149
CTYR158
CMET161
CLYS165
CALA198
CILE202
CLEU218
CNAD320

site_idAC7
Number of Residues28
DetailsBINDING SITE FOR RESIDUE NAD D 330
ChainResidue
DGLY14
DILE15
DILE16
DSER20
DILE21
DPHE41
DLEU63
DASP64
DVAL65
DSER94
DILE95
DGLY96
DILE122
DMET147
DASP148
DPHE149
DMET161
DLYS165
DALA191
DGLY192
DPRO193
DILE194
DTHR196
DALA198
DHOH272
DHOH306
D8PC430
DHOH504

site_idAC8
Number of Residues10
DetailsBINDING SITE FOR RESIDUE 8PC D 430
ChainResidue
DGLY96
DMET98
DMET103
DPHE149
DTYR158
DALA198
DMET199
DILE215
DNAD330
DHOH673

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues20
DetailsBINDING: BINDING => ECO:0000269|PubMed:10336454, ECO:0000269|PubMed:16647717, ECO:0000269|PubMed:7886450, ECO:0007744|PDB:1BVR, ECO:0007744|PDB:1ENY, ECO:0007744|PDB:2AQ8
ChainResidueDetails
CILE95
CLYS165
CILE194
DSER20
DASP64
DILE95
DLYS165
DILE194
ASER20
AASP64
AILE95
ALYS165
AILE194
BSER20
BASP64
BILE95
BLYS165
BILE194
CSER20
CASP64

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10336454
ChainResidueDetails
ATYR158
BTYR158
CTYR158
DTYR158

site_idSWS_FT_FI3
Number of Residues4
DetailsSITE: May act as an intermediate that passes the hydride ion from NADH to the substrate => ECO:0000305|PubMed:10336454
ChainResidueDetails
APHE149
BPHE149
CPHE149
DPHE149

site_idSWS_FT_FI4
Number of Residues4
DetailsSITE: Transition state stabilizer => ECO:0000305|PubMed:10521269
ChainResidueDetails
ATYR158
BTYR158
CTYR158
DTYR158

site_idSWS_FT_FI5
Number of Residues4
DetailsMOD_RES: Phosphothreonine => ECO:0000269|PubMed:20864541, ECO:0000269|PubMed:21143326
ChainResidueDetails
ATHR266
BTHR266
CTHR266
DTHR266

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PDB entries from 2024-06-12

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