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Atomistry » Magnesium » PDB 1l3r-1lny » 1l4u » |
Magnesium in PDB 1l4u: Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis in Complex with Mgadp and Pt(II) at 1.8 Angstrom ResolutionEnzymatic activity of Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis in Complex with Mgadp and Pt(II) at 1.8 Angstrom Resolution
All present enzymatic activity of Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis in Complex with Mgadp and Pt(II) at 1.8 Angstrom Resolution:
2.7.1.71; Protein crystallography data
The structure of Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis in Complex with Mgadp and Pt(II) at 1.8 Angstrom Resolution, PDB code: 1l4u
was solved by
Y.Gu,
L.Reshetnikova,
Y.Li,
Y.Wu,
H.Yan,
S.Singh,
X.Ji,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 1l4u:
The structure of Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis in Complex with Mgadp and Pt(II) at 1.8 Angstrom Resolution also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis in Complex with Mgadp and Pt(II) at 1.8 Angstrom Resolution
(pdb code 1l4u). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total only one binding site of Magnesium was determined in the Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis in Complex with Mgadp and Pt(II) at 1.8 Angstrom Resolution, PDB code: 1l4u: Magnesium binding site 1 out of 1 in 1l4uGo back to Magnesium Binding Sites List in 1l4u
Magnesium binding site 1 out
of 1 in the Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis in Complex with Mgadp and Pt(II) at 1.8 Angstrom Resolution
Mono view Stereo pair view
Reference:
Y.Gu,
L.Reshetnikova,
Y.Li,
Y.Wu,
H.Yan,
S.Singh,
X.Ji.
Crystal Structure of Shikimate Kinase From Mycobacterium Tuberculosis Reveals the Dynamic Role of the Lid Domain in Catalysis. J.Mol.Biol. V. 319 779 2002.
Page generated: Tue Aug 13 08:25:55 2024
ISSN: ISSN 0022-2836 PubMed: 12054870 DOI: 10.1016/S0022-2836(02)00339-X |
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