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Atomistry » Zinc » PDB 3u6q-3uec » 3u7l » |
Zinc in PDB 3u7l: Crystal Structures of the Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New InhibitorsEnzymatic activity of Crystal Structures of the Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New Inhibitors
All present enzymatic activity of Crystal Structures of the Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New Inhibitors:
3.5.1.88; Protein crystallography data
The structure of Crystal Structures of the Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New Inhibitors, PDB code: 3u7l
was solved by
S.J.Lee,
S.-J.Lee,
S.K.Lee,
H.-J.Yoon,
H.H.Lee,
K.K.Kim,
B.J.Lee,
S.W.Suh,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 3u7l:
The structure of Crystal Structures of the Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New Inhibitors also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structures of the Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New Inhibitors
(pdb code 3u7l). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total only one binding site of Zinc was determined in the Crystal Structures of the Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New Inhibitors, PDB code: 3u7l: Zinc binding site 1 out of 1 in 3u7lGo back to![]() ![]()
Zinc binding site 1 out
of 1 in the Crystal Structures of the Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New Inhibitors
![]() Mono view ![]() Stereo pair view
Reference:
S.J.Lee,
S.-J.Lee,
S.K.Lee,
H.-J.Yoon,
H.H.Lee,
K.K.Kim,
B.J.Lee,
B.I.Lee,
S.W.Suh.
Structures of Staphylococcus Aureus Peptide Deformylase in Complex with Two Classes of New Inhibitors Acta Crystallogr.,Sect.D V. 68 784 2012.
Page generated: Sat Oct 26 17:03:07 2024
ISSN: ISSN 0907-4449 PubMed: 22751663 DOI: 10.1107/S0907444912011912 |
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