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1P45

Targeting tuberculosis and malaria through inhibition of enoyl reductase: compound activity and structural data

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
Functional Information from PDB Data
site_idAC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE NAD A 300
ChainResidue
AGLY14
ASER94
AILE95
AGLY96
AILE122
AMET147
AASP148
ALYS165
APRO193
AILE194
ATHR196
AILE15
ATCL400
AILE16
ASER20
AILE21
APHE41
ALEU63
AASP64
AVAL65

site_idAC2
Number of Residues20
DetailsBINDING SITE FOR RESIDUE NAD B 350
ChainResidue
BGLY14
BILE15
BILE16
BSER20
BILE21
BPHE41
BLEU63
BASP64
BVAL65
BSER94
BILE95
BGLY96
BMET147
BASP148
BLYS165
BPRO193
BILE194
BTHR196
BALA198
BTCL500

site_idAC3
Number of Residues8
DetailsBINDING SITE FOR RESIDUE TCL A 400
ChainResidue
AGLY96
AMET98
AMET103
APHE149
ATYR158
AMET199
ANAD300
ATCL450

site_idAC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE TCL A 450
ChainResidue
AGLN100
AMET103
AGLY104
ATYR158
AILE202
AILE215
ALEU218
ATCL400

site_idAC5
Number of Residues9
DetailsBINDING SITE FOR RESIDUE TCL B 500
ChainResidue
BGLY96
BMET98
BMET103
BPHE149
BTYR158
BMET161
BALA198
BILE202
BNAD350

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues10
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
ASER20
BILE194
AASP64
AILE95
ALYS165
AILE194
BSER20
BASP64
BILE95
BLYS165

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:10336454
ChainResidueDetails
ATYR158
BTYR158

site_idSWS_FT_FI3
Number of Residues2
DetailsSITE: May act as an intermediate that passes the hydride ion from NADH to the substrate => ECO:0000305|PubMed:10336454
ChainResidueDetails
APHE149
BPHE149

site_idSWS_FT_FI4
Number of Residues2
DetailsSITE: Transition state stabilizer => ECO:0000305|PubMed:10521269
ChainResidueDetails
ATYR158
BTYR158

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: Phosphothreonine => ECO:0000269|PubMed:20864541, ECO:0000269|PubMed:21143326
ChainResidueDetails
ATHR266
BTHR266

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1qsg
ChainResidueDetails
ATYR158
ALYS165

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1qsg
ChainResidueDetails
BTYR158
BLYS165

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1qsg
ChainResidueDetails
AMET161
ALYS165

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1qsg
ChainResidueDetails
BMET161
BLYS165

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PDB entries from 2024-10-30

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