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Atomistry » Magnesium » PDB 3efq-3eql » 3eqg » |
Magnesium in PDB 3eqg: X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Ternary Complex with Pd, Adp and MG2PEnzymatic activity of X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Ternary Complex with Pd, Adp and MG2P
All present enzymatic activity of X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Ternary Complex with Pd, Adp and MG2P:
2.7.12.2; Protein crystallography data
The structure of X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Ternary Complex with Pd, Adp and MG2P, PDB code: 3eqg
was solved by
T.O.Fischmann,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 3eqg:
The structure of X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Ternary Complex with Pd, Adp and MG2P also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Ternary Complex with Pd, Adp and MG2P
(pdb code 3eqg). 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 X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Ternary Complex with Pd, Adp and MG2P, PDB code: 3eqg: Magnesium binding site 1 out of 1 in 3eqgGo back to Magnesium Binding Sites List in 3eqg
Magnesium binding site 1 out
of 1 in the X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Ternary Complex with Pd, Adp and MG2P
Mono view Stereo pair view
Reference:
T.O.Fischmann,
C.K.Smith,
T.W.Mayhood,
J.E.Myers,
P.Reichert,
A.Mannarino,
D.Carr,
H.Zhu,
J.Wong,
R.S.Yang,
H.V.Le,
V.S.Madison.
Crystal Structures of MEK1 Binary and Ternary Complexes with Nucleotides and Inhibitors. Biochemistry V. 48 2661 2009.
Page generated: Wed Aug 14 13:16:40 2024
ISSN: ISSN 0006-2960 PubMed: 19161339 DOI: 10.1021/BI801898E |
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