Structure of PDB 3rv9 Chain A Binding Site BS01

Receptor Information
>3rv9 Chain A (length=420) Species: 1773 (Mycobacterium tuberculosis) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
SSSIPMPAGVNPADLAAELAAVVTESVDEDYLLYECDGQWVLAAGVQAMV
ELDSDELRVIRDGVTRRQQWSGRPGAALGEAVDRLLLETDQAFGWVAFEF
GVHRYGLQQRLAPHTPLARVFSPRTRIMVSEKEIRLFDAGIRHREAIDRL
LATGVREVPQSRSVDVSDDPSGFRRRVAVAVDEIAAGRYHKVILSRCVEV
PFAIDFPLTYRLGRRHNTPVRSFLLQLGGIRALGYSPELVTAVRADGVVI
TEPLAGTLARDDLESNSKEIVEHAISVRSSLEEITDIAEPGSAAVIDFMT
VRQHLGSTIRARLDPSSDRMAALEALFPAVTASGIPKAAGVEAIFRLDEC
PRGLYSGAVVMLSADGGLDAALTLRAAYQVGGRTWLRAGAGIIEESEPER
EFEETCEKLSTLTPYLVARQ
Ligand information
Ligand IDRVD
InChIInChI=1S/C12H12O6/c1-2-4-9(12(16)17)18-8-6-3-5-7(10(8)13)11(14)15/h3-6,13H,2H2,1H3,(H,14,15)(H,16,17)/b9-4-
InChIKeyNMNSLXCRMLAOLT-WTKPLQERSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.7.2CC/C=C(/C(=O)O)\Oc1cccc(c1O)C(=O)O
CACTVS 3.370CCC=C(Oc1cccc(C(O)=O)c1O)C(O)=O
OpenEye OEToolkits 1.7.2CCC=C(C(=O)O)Oc1cccc(c1O)C(=O)O
ACDLabs 12.01O=C(O)c1cccc(O/C(C(=O)O)=C\CC)c1O
CACTVS 3.370CC\C=C(/Oc1cccc(C(O)=O)c1O)C(O)=O
FormulaC12 H12 O6
Name3-{[(1Z)-1-carboxybut-1-en-1-yl]oxy}-2-hydroxybenzoic acid
ChEMBL
DrugBank
ZINCZINC000095921036
PDB chain3rv9 Chain A Residue 451 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB3rv9 Implications of binding mode and active site flexibility for inhibitor potency against the salicylate synthase from Mycobacterium tuberculosis
Resolution2.14 Å
Binding residue
(original residue number in PDB)
T361 Y385 L404 R405 A418 G419 K438
Binding residue
(residue number reindexed from 1)
T331 Y355 L374 R375 A388 G389 K408
Annotation score1
Binding affinityMOAD: Ki=12uM
PDBbind-CN: -logKd/Ki=4.92,Ki=12uM
Enzymatic activity
Catalytic site (original residue number in PDB) K205 E252 A269 E297 H334 T361 Y385 R405 G421 E434 K438
Catalytic site (residue number reindexed from 1) K191 E238 A255 E272 H304 T331 Y355 R375 G391 E404 K408
Enzyme Commision number 4.2.99.21: isochorismate lyase.
5.4.4.2: isochorismate synthase.
5.4.99.5: chorismate mutase.
Gene Ontology
Molecular Function
GO:0000287 magnesium ion binding
GO:0004106 chorismate mutase activity
GO:0008909 isochorismate synthase activity
GO:0016829 lyase activity
GO:0016833 oxo-acid-lyase activity
GO:0016853 isomerase activity
GO:0043904 isochorismate pyruvate lyase activity
GO:0046872 metal ion binding
Biological Process
GO:0000162 tryptophan biosynthetic process
GO:0009058 biosynthetic process
GO:0009697 salicylic acid biosynthetic process
GO:0010106 cellular response to iron ion starvation
GO:0019540 catechol-containing siderophore biosynthetic process
GO:0052572 response to host immune response
Cellular Component
GO:0005886 plasma membrane

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:3rv9, PDBe:3rv9, PDBj:3rv9
PDBsum3rv9
PubMed22607697
UniProtP9WFX1|MBTI_MYCTU Salicylate synthase (Gene Name=mbtI)

[Back to BioLiP]