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Ligands
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CE4 (2r)-2-[(R)-{[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}(carboxy)methyl]-5-methylidene-5,6-dihydro -2h-1,3-thiazine-4-carboxylic acid
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Code : 6CYU   PDBj   RCSB PDB   PDBe
Header : hydrolase/antibiotic
Title : Crystal structure of CTX-M-14 S70G/N106S/D240G beta-lactamase in complex with hydrolyzed cefotaxime
Release Data : 2018-10-10
Compound :
mol_id molecule chains
1 Beta-lactamase A
ec: 3.5.2.6
mutation: S70G, N106S, D240G
Source :
mol_id organism_scientific expression_system
1 Escherichia coli  (taxid:562) Escherichia coli BL21(DE3)  (taxid:469008)
gene: blaCTX-M-14, beta-lactamase CTX-M-14, bla-CTX-M-14a, blaCTX-M-14a, blaCTX-M-14b, blaCTX-M-14c, blaCTX-M-27b, blatoho-3, blaUOE-2, CTX-M-14, AM333_26030, APT94_14605, BET08_34355, BJJ90_27545, BK334_27290, BMR21_24310, BMR35_25520, BMR49_25760, BXT93_06855, CA268_29135, CDL37_21060, CR538_26855, ETN48_p0088, pCT_085, pHK01_011
Authors : Patel, M.P., Hu, L., Sankaran, B., Brown, C., Prasad, B.V.V., Palzkill, T.
Keywords : Beta-lactamase CTX-M-14, hydrolase-hydrolase inhibitor complex, hydrolase-antibiotic complex
Exp. method : X-RAY DIFFRACTION ( 1.820 Å )
Citation :

Synergistic effects of functionally distinct substitutions in beta-lactamase variants shed light on the evolution of bacterial drug resistance.

Patel, M.P.,Hu, L.,Brown, C.A.  et al.
(2018)  J. Biol. Chem.  293 : 17971 - 17984

PubMed: 30275013
DOI: 10.1074/jbc.RA118.003792

Chain : A
UniProt : Q9L5C7 (Q9L5C7_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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