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Atomistry » Magnesium » PDB 6cpu-6cu1 » 6cr5 » |
Magnesium in PDB 6cr5: Ternary Complex Crystal Structure of Dna Polymerase Beta with A Dideoxy Terminated Primer with CH2-Beta, Gamma Datp AnalogueEnzymatic activity of Ternary Complex Crystal Structure of Dna Polymerase Beta with A Dideoxy Terminated Primer with CH2-Beta, Gamma Datp Analogue
All present enzymatic activity of Ternary Complex Crystal Structure of Dna Polymerase Beta with A Dideoxy Terminated Primer with CH2-Beta, Gamma Datp Analogue:
2.7.7.7; Protein crystallography data
The structure of Ternary Complex Crystal Structure of Dna Polymerase Beta with A Dideoxy Terminated Primer with CH2-Beta, Gamma Datp Analogue, PDB code: 6cr5
was solved by
V.K.Batra,
S.H.Wilson,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 6cr5:
The structure of Ternary Complex Crystal Structure of Dna Polymerase Beta with A Dideoxy Terminated Primer with CH2-Beta, Gamma Datp Analogue also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Ternary Complex Crystal Structure of Dna Polymerase Beta with A Dideoxy Terminated Primer with CH2-Beta, Gamma Datp Analogue
(pdb code 6cr5). 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 Ternary Complex Crystal Structure of Dna Polymerase Beta with A Dideoxy Terminated Primer with CH2-Beta, Gamma Datp Analogue, PDB code: 6cr5: Magnesium binding site 1 out of 1 in 6cr5Go back to Magnesium Binding Sites List in 6cr5
Magnesium binding site 1 out
of 1 in the Ternary Complex Crystal Structure of Dna Polymerase Beta with A Dideoxy Terminated Primer with CH2-Beta, Gamma Datp Analogue
Mono view Stereo pair view
Reference:
V.K.Batra,
K.Oertell,
W.A.Beard,
B.A.Kashemirov,
C.E.Mckenna,
M.F.Goodman,
S.H.Wilson.
Mapping Functional Substrate-Enzyme Interactions in the Pol Beta Active Site Through Chemical Biology: Structural Responses to Acidity Modification of Incoming Dntps. Biochemistry V. 57 3934 2018.
Page generated: Mon Sep 30 22:41:20 2024
ISSN: ISSN 1520-4995 PubMed: 29874056 DOI: 10.1021/ACS.BIOCHEM.8B00418 |
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