Structure of PDB 2q9n Chain A Binding Site BS01

Receptor Information
>2q9n Chain A (length=359) Species: 550 (Enterobacter cloacae) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
PVSEKQLAEVVANTITPLMKAQSVPGMAVAVIYQGKPHYYTFGKADIAAN
KPVTPQTLFELGSISKTFTGVLGGDAIARGEISLDDAVTRYWPQLTGKQW
QGIRMLDLATYTAGGLPLQVPDEVTDNASLLRFYQNWQPQWKPGTTRLYA
NASIGLFGALAVKPSGMPYEQAMTTRVLKPLKLDHTWINVPKAEEAHYAW
GYRDGKAVRVSPGMLDAQAYGVKTNVQDMANWVMANMAPENVADASLKQG
IALAQSRYWRIGSMYQGLGWEMLNWPVEANTVVEGSDSKVALAPLPVAEV
NPPAPPVKASWVHKTGSTGGFGSYVAFIPEKQIGIVMLANTSYPNPARVE
AAYHILEAL
Ligand information
Ligand IDLK5
InChIInChI=1S/C17H27NO4/c1-3-5-9-22-13-8-6-7-12-14(13)16(17(20)21)18-15(12)11(4-2)10-19/h10-13,15,18H,3-9H2,1-2H3,(H,20,21)/t11-,12+,13+,15+/m0/s1
InChIKeyWRBRCIHZCYLBFW-KYEXWDHISA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0CCCCOC1CCCC2C1=C(NC2C(CC)C=O)C(=O)O
ACDLabs 10.04O=CC(C2NC(=C1C(OCCCC)CCCC12)C(=O)O)CC
OpenEye OEToolkits 1.5.0CCCCO[C@@H]1CCC[C@@H]2C1=C(N[C@@H]2[C@@H](CC)C=O)C(=O)O
CACTVS 3.341CCCCO[CH]1CCC[CH]2[CH](NC(=C12)C(O)=O)[CH](CC)C=O
CACTVS 3.341CCCCO[C@@H]1CCC[C@H]2[C@H](NC(=C12)C(O)=O)[C@@H](CC)C=O
FormulaC17 H27 N O4
Name(1S,4R,7AR)-4-BUTOXY-1-[(1R)-1-FORMYLPROPYL]-2,4,5,6,7,7A-HEXAHYDRO-1H-ISOINDOLE-3-CARBOXYLIC ACID
ChEMBL
DrugBankDB08109
ZINCZINC000100036343
PDB chain2q9n Chain A Residue 0 [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]
PDB2q9n 4-Substituted Trinems as Broad Spectrum beta-Lactamase Inhibitors: Structure-Based Design, Synthesis, and Biological Activity
Resolution2.2 Å
Binding residue
(original residue number in PDB)
S64 L119 Q120 Y150 N152 R204 Y221 G317 S318 T319 G320
Binding residue
(residue number reindexed from 1)
S63 L118 Q119 Y149 N151 R203 Y220 G316 S317 T318 G319
Annotation score1
Binding affinityPDBbind-CN: -logKd/Ki=6.37,IC50=430nM
Enzymatic activity
Catalytic site (original residue number in PDB) S64 K67 Y112 V121 Y150 G156 E272 K315 S318
Catalytic site (residue number reindexed from 1) S63 K66 Y111 V120 Y149 G155 E271 K314 S317
Enzyme Commision number 3.5.2.6: beta-lactamase.
Gene Ontology
Molecular Function
GO:0008800 beta-lactamase activity
GO:0016787 hydrolase activity
Biological Process
GO:0017001 antibiotic catabolic process
GO:0046677 response to antibiotic
Cellular Component
GO:0030288 outer membrane-bounded periplasmic space
GO:0042597 periplasmic space

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:2q9n, PDBe:2q9n, PDBj:2q9n
PDBsum2q9n
PubMed17665896
UniProtP05364|AMPC_ENTCL Beta-lactamase (Gene Name=ampC)

[Back to BioLiP]