Structure of PDB 1o07 Chain A Binding Site BS01
Receptor Information
>1o07 Chain A (length=355) Species:
562
(Escherichia coli) [
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APQQINDIVHRTITPLIEQQKIPGMAVAVIYQGKPYYFTWGYADIAKKQP
VTQQTLFELGSVSKTFTGVLGGDAIARGEIKLSDPTTKYWPELTAKQWNG
ITLLHLATYTAGGLPLLVPDEVKSSSDLLRFYQNWQPAWAPGTQRLEANS
SIGLFGALAVKPSGLSFEQAMQTRVFQPLKLNHTWINVPPAEEKNYAWGY
REGKAVHVSPGALDAEAYGVKSTIEDMARWVQSNLKPLDINEKTLQQGIQ
LAQSRYWQTGDMYQGLGWEMLDWPVNPDSISDNKIALAARPVKAITPPTP
AVRASWVHKTGATGGFGSYVAFIPEKELGIVMLANKNYPNPARVDAAWQI
LNALQ
Ligand information
Ligand ID
MXG
InChI
InChI=1S/C24H36N6O9S/c1-12-11-40-22(30-19(12)24(38)39)17(10-31)29-21(35)15(6-4-5-9-25)27-18(33)8-7-16(23(36)37)28-20(34)13(2)26-14(3)32/h10,13,15-17,22H,1,4-9,11,25H2,2-3H3,(H,26,32)(H,27,33)(H,28,34)(H,29,35)(H,36,37)(H,38,39)/t13-,15-,16+,17+,22+/m0/s1
InChIKey
BZBLEHRBZDVRSG-JKCYHXNASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C[C@@H](C(=O)N[C@H](CCC(=O)N[C@@H](CCCCN)C(=O)N[C@H](C=O)[C@@H]1N=C(C(=C)CS1)C(=O)O)C(=O)O)NC(=O)C
OpenEye OEToolkits 1.5.0
CC(C(=O)NC(CCC(=O)NC(CCCCN)C(=O)NC(C=O)C1N=C(C(=C)CS1)C(=O)O)C(=O)O)NC(=O)C
ACDLabs 10.04
O=C(NC(C(=O)NC(C(=O)O)CCC(=O)NC(C(=O)NC(C=O)C1N=C(\C(=C)CS1)C(=O)O)CCCCN)C)C
CACTVS 3.341
C[CH](NC(C)=O)C(=O)N[CH](CCC(=O)N[CH](CCCCN)C(=O)N[CH](C=O)[CH]1SCC(=C)C(=N1)C(O)=O)C(O)=O
CACTVS 3.341
C[C@H](NC(C)=O)C(=O)N[C@H](CCC(=O)N[C@@H](CCCCN)C(=O)N[C@H](C=O)[C@H]1SCC(=C)C(=N1)C(O)=O)C(O)=O
Formula
C24 H36 N6 O9 S
Name
2-(1-{2-[4-(2-ACETYLAMINO-PROPIONYLAMINO)-4-CARBOXY-BUTYRYLAMINO]-6-AMINO-HEXANOYLAMINO}-2-OXO-ETHYL)-5-METHYLENE-5,6-DIHYDRO-2H-[1,3]THIAZINE-4-CARBOXYLIC ACID
ChEMBL
DrugBank
ZINC
ZINC000015853296
PDB chain
1o07 Chain A Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
1o07
Structural Aspects for Evolution of beta-Lactamases from Penicillin-Binding Proteins
Resolution
1.71 Å
Binding residue
(original residue number in PDB)
S64 L119 E150 N152 R204 V211 S212 Y221 D288 A318 G320 N343
Binding residue
(residue number reindexed from 1)
S61 L116 E147 N149 R201 V208 S209 Y218 D282 A312 G314 N337
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S64 K67 Y112 A114 V121 E150 A151 G156 E272 K315 A318
Catalytic site (residue number reindexed from 1)
S61 K64 Y109 A111 V118 E147 A148 G153 E269 K309 A312
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
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1o07
,
PDBe:1o07
,
PDBj:1o07
PDBsum
1o07
PubMed
12904027
UniProt
P00811
|AMPC_ECOLI Beta-lactamase (Gene Name=ampC)
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