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PDBsum entry 3u2d

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protein ligands metals Protein-protein interface(s) links
Isomerase/isomerase inhibitor PDB id
3u2d

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
194 a.a.
Ligands
08B ×2
Metals
_MG ×4
Waters ×324
PDB id:
3u2d
Name: Isomerase/isomerase inhibitor
Title: S. Aureus gyrb atpase domain in complex with small molecule inhibitor
Structure: DNA gyrase subunit b. Chain: a, b. Fragment: atpase domain with loop deletion, unp residues 14-104 and 128-233. Engineered: yes
Source: Staphylococcus aureus. Organism_taxid: 1280. Gene: gyrb. Expressed in: escherichia coli. Expression_system_taxid: 469008.
Resolution:
1.85Å     R-factor:   0.202     R-free:   0.232
Authors: P.A.Boriack-Sjodin,D.B.Prince,A.E.Eakin,B.A.Sherer
Key ref: A.E.Eakin et al. (2012). Pyrrolamide DNA gyrase inhibitors: fragment-based nuclear magnetic resonance screening to identify antibacterial agents. Antimicrob Agents Chemother, 56, 1240-1246. PubMed id: 22183167
Date:
03-Oct-11     Release date:   11-Jan-12    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P0A0K8  (GYRB_STAAU) -  DNA gyrase subunit B from Staphylococcus aureus
Seq:
Struc:
 
Seq:
Struc:
644 a.a.
194 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.5.6.2.2  - Dna topoisomerase (ATP-hydrolyzing).
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

 

 
Antimicrob Agents Chemother 56:1240-1246 (2012)
PubMed id: 22183167  
 
 
Pyrrolamide DNA gyrase inhibitors: fragment-based nuclear magnetic resonance screening to identify antibacterial agents.
A.E.Eakin, O.Green, N.Hales, G.K.Walkup, S.Bist, A.Singh, G.Mullen, J.Bryant, K.Embrey, N.Gao, A.Breeze, D.Timms, B.Andrews, M.Uria-Nickelsen, J.Demeritt, J.T.Loch, K.Hull, A.Blodgett, R.N.Illingworth, B.Prince, P.A.Boriack-Sjodin, S.Hauck, L.J.MacPherson, H.Ni, B.Sherer.
 
  ABSTRACT  
 
No abstract given.

 

 

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