Structure of PDB 2ffy Chain B Binding Site BS01

Receptor Information
>2ffy Chain B (length=358) Species: 562 (Escherichia coli) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
APQQINDIVHRTITPLIEQQKIPGMAVAVIYQGKPYYFTWGYADIAKKQP
VTQQTLFELGSVSKTFTGVLGGDAIARGEIKLSDPTTKYWPELTAKQWNG
ITLLHLATYTAGGLPLQVPDEVKSSSDLLRFYQNWQPAWAPGTQRLYANS
SIGLFGALAVKPSGLSFEQAMQTRVFQPLKLNHTWINVPPAEEKNYAWGY
REGKAVHVSPGALDAEAYGVKSTIEDMARWVQSNLKPLDINEKTLQQGIQ
LAQSRYWQTGDMYQGLGWEMLDWPVNPDSIINGSDAKIALAARPVKAITP
PTPAVRASWVHKTGATGGFGSYVAFIPEKELGIVMLANKNYPNPARVDAA
WQILNALQ
Ligand information
Ligand IDSM3
InChIInChI=1S/C13H14BNO3S/c16-12(9-11-7-4-8-19-11)15-13(14(17)18)10-5-2-1-3-6-10/h1-8,13,17-18H,9H2,(H,15,16)/t13-/m0/s1
InChIKeyLGJCDEZMANATFA-ZDUSSCGKSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0B(C(c1ccccc1)NC(=O)Cc2cccs2)(O)O
ACDLabs 10.04O=C(NC(B(O)O)c1ccccc1)Cc2sccc2
CACTVS 3.341OB(O)[C@@H](NC(=O)Cc1sccc1)c2ccccc2
OpenEye OEToolkits 1.5.0B([C@H](c1ccccc1)NC(=O)Cc2cccs2)(O)O
CACTVS 3.341OB(O)[CH](NC(=O)Cc1sccc1)c2ccccc2
FormulaC13 H14 B N O3 S
Name(1R)-1-(2-THIENYLACETYLAMINO)-1-PHENYLMETHYLBORONIC ACID
ChEMBLCHEMBL404155
DrugBankDB08552
ZINCZINC000169748509
PDB chain2ffy Chain B Residue 9401 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2ffy The deacylation mechanism of AmpC beta-lactamase at ultrahigh resolution
Resolution1.07 Å
Binding residue
(original residue number in PDB)		S64 L119 Q120 Y150 Y221 G317 A318 T319 G320
Binding residue
(residue number reindexed from 1)		S61 L116 Q117 Y147 Y218 G314 A315 T316 G317
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) S64 K67 Y112 A114 V121 Y150 G156 E272 K315 A318
Catalytic site (residue number reindexed from 1) S61 K64 Y109 A111 V118 Y147 G153 E269 K312 A315
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:2ffy, PDBe:2ffy, PDBj:2ffy
PDBsum2ffy
PubMed16506777
UniProtP00811|AMPC_ECOLI Beta-lactamase (Gene Name=ampC)

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