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Atomistry » Magnesium » PDB 2amc-2b2k » 2az3 » |
Magnesium in PDB 2az3: Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum in Complex with CdpEnzymatic activity of Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum in Complex with Cdp
All present enzymatic activity of Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum in Complex with Cdp:
2.7.4.6; Protein crystallography data
The structure of Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum in Complex with Cdp, PDB code: 2az3
was solved by
H.Besir,
K.Zeth,
A.Bracher,
U.Heider,
M.Ishibashi,
M.Tokunaga,
D.Oesterhelt,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum in Complex with Cdp
(pdb code 2az3). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum in Complex with Cdp, PDB code: 2az3: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 2az3Go back to Magnesium Binding Sites List in 2az3
Magnesium binding site 1 out
of 2 in the Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum in Complex with Cdp
Mono view Stereo pair view
Magnesium binding site 2 out of 2 in 2az3Go back to Magnesium Binding Sites List in 2az3
Magnesium binding site 2 out
of 2 in the Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum in Complex with Cdp
Mono view Stereo pair view
Reference:
H.Besir,
K.Zeth,
A.Bracher,
U.Heider,
M.Ishibashi,
M.Tokunaga,
D.Oesterhelt.
Structure of A Halophilic Nucleoside Diphosphate Kinase From Halobacterium Salinarum Febs Lett. V. 579 6595 2005.
Page generated: Tue Aug 13 21:38:08 2024
ISSN: ISSN 0014-5793 PubMed: 16293253 DOI: 10.1016/J.FEBSLET.2005.10.052 |
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