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PDBsum entry 8sdr

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protein ligands links
Hydrolase/hydrolase inhibitor PDB id
8sdr

 

 

 

 

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Contents
Protein chain
360 a.a.
Ligands
CB4
IMD
Waters ×593
PDB id:
8sdr
Name: Hydrolase/hydrolase inhibitor
Title: Crystal structure of pdc-3 beta-lactamase in complex with the boronic acid inhibitor lp-06
Structure: Beta-lactamase. Chain: a. Engineered: yes
Source: Pseudomonas aeruginosa. Organism_taxid: 287. Gene: ampc. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
1.35Å     R-factor:   0.131     R-free:   0.162
Authors: V.Kumar,F.Van Den Akker
Key ref: A.R.Mack et al. Natural protein engineering in the omega-Loop: the ro y221 in ceftazidime and ceftolozane resistance in pseudomonas-Derived cephalosporinase (pdc). To be published, . PubMed id: 37850746
Date:
07-Apr-23     Release date:   16-Aug-23    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P24735  (AMPC_PSEAE) -  Beta-lactamase from Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1)
Seq:
Struc:
397 a.a.
360 a.a.*
Key:    PfamA domain  Secondary structure
* PDB and UniProt seqs differ at 1 residue position (black cross)

 Enzyme reactions 
   Enzyme class: E.C.3.5.2.6  - beta-lactamase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

      Pathway:
Penicillin Biosynthesis and Metabolism
      Reaction: a beta-lactam + H2O = a substituted beta-amino acid
      Cofactor: Zn(2+)

 

 

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