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Ligands
Code Name Style Show Link
JSD [(1,2,3,4,5-eta)-1-(4-{[(4-carboxy-5,5-dimethyl-1,3-thiazolidin-2-yl)methyl]amino}-4-oxobutanoyl)cyclopentadienyl][(1,2,3,4,5-eta)-cyclopentadienyl]ruthenium
JSC [(1,2,3,4,5-eta)-1-(4-{[carboxy(4-carboxy-5,5-dimethyl-1,3-thiazolidin-2-yl)methyl]amino}-4-oxobutanoyl)cyclopentadienyl][(1,2,3,4,5-eta)-cyclopentadienyl]ruthenium
JSE [(1,2,3,4,5-eta)-1-(4-{[carboxy(4-carboxy-5,5-dimethyl-1,3-thiazolidin-2-yl)methyl]amino}-4-oxobutanoyl)cyclopentadienyl][(1,2,3,4,5-eta)-cyclopentadienyl]ruthenium
K Potassium ion
RU Ruthenium ion
Non-standard Residues
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PCA Pyroglutamic acid
Glycosylation
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Modification
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Code : 5VLE   PDBj   RCSB PDB   PDBe
Header : HYDROLASE
Title : Ultrahigh Resolution X-Ray Crystal Structure of Ruthenocene Conjugated Penicilloate and Penilloate Products in Complex with CTX-M-14 E166A Beta-Lactamase
Release Data : 2017-11-08
Compound :
mol_id molecule chains
1 Beta-lactamase A,B
ec: 3.5.2.6
fragment: UNP residues 22-284
mutation: E166A
Source :
mol_id organism_scientific expression_system
1 Escherichia coli  (taxid:562) Escherichia coli  (taxid:562)
gene: CTX-M-14
Authors : Lewandowski, E.M., Chen, Y.
Keywords : Beta-Lactamase, organometallic, Ruthenocene, CTX-M-14, HYDROLASE
Exp. method : X-RAY DIFFRACTION ( 0.85 Å )
Citation :

Mechanisms of proton relay and product release by Class A beta-lactamase at ultrahigh resolution.

Lewandowski, E.M.,Lethbridge, K.G.,Sanishvili, R.  et al.
(2018)  FEBS J.  285 : 87 - 100

PubMed: 29095570
DOI: 10.1111/febs.14315

Chain : A, B
UniProt : H6UQI0 (H6UQI0_ECOLX)
Reaction: EC: Evidence:
Physiological Direction:
a beta-lactam + H2O = a substituted beta-amino acid 3.5.2.6 ARBA:ARBA00001526, RuleBase:RU361140
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