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5OIR

InhA (T2A mutant) complexed with 2,6-Dimethyl-3-(1-(pyrimidin-2-yl)piperidin-4-yl)pyridin-4(1H)-one

Functional Information from GO Data
ChainGOidnamespacecontents
A0004318molecular_functionenoyl-[acyl-carrier-protein] reductase (NADH) activity
A0005504molecular_functionfatty acid binding
A0005886cellular_componentplasma membrane
A0006629biological_processlipid metabolic process
A0006631biological_processfatty acid metabolic process
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
Functional Information from PDB Data
site_idAC1
Number of Residues33
Detailsbinding site for residue NAD A 301
ChainResidue
AGLY14
ASER94
AILE95
AGLY96
AILE122
AMET147
AASP148
APHE149
ALYS165
AGLY192
APRO193
AILE15
AILE194
ATHR196
A9W8302
AHOH406
AHOH416
AHOH417
AHOH481
AHOH504
AHOH511
AHOH519
AILE16
AHOH521
AHOH538
AHOH556
AHOH563
ASER20
AILE21
APHE41
ALEU63
AASP64
AVAL65

site_idAC2
Number of Residues9
Detailsbinding site for residue 9W8 A 302
ChainResidue
AGLY96
APHE97
AMET98
AMET103
ATYR158
AMET199
ANAD301
AETX303
AHOH417

site_idAC3
Number of Residues4
Detailsbinding site for residue ETX A 303
ChainResidue
AMET103
ATYR158
AILE215
A9W8302

site_idAC4
Number of Residues2
Detailsbinding site for residue ETX A 304
ChainResidue
AASP110
ALYS132

site_idAC5
Number of Residues5
Detailsbinding site for residue ETX A 305
ChainResidue
AASP150
ASER152
ASER152
AARG153
AHIS265

site_idAC6
Number of Residues4
Detailsbinding site for residue ETX A 306
ChainResidue
APHE97
APRO99
AGLN100
ALYS118

site_idAC7
Number of Residues9
Detailsbinding site for residue SO4 A 307
ChainResidue
ASER19
AHIS24
AILE194
AARG195
ATHR196
ALYS233
AALA235
AHOH439
AHOH454

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues5
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"10336454","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"16647717","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"7886450","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1BVR","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ENY","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2AQ8","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues1
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"10336454","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues1
DetailsSite: {"description":"May act as an intermediate that passes the hydride ion from NADH to the substrate","evidences":[{"source":"PubMed","id":"10336454","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues1
DetailsSite: {"description":"Transition state stabilizer","evidences":[{"source":"PubMed","id":"10521269","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues1
DetailsModified residue: {"description":"Phosphothreonine","evidences":[{"source":"PubMed","id":"20864541","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"21143326","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

247947

PDB entries from 2026-01-21

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