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Atomistry » Magnesium » PDB 5c29-5ca1 » 5c2o | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Magnesium » PDB 5c29-5ca1 » 5c2o » |
Magnesium in PDB 5c2o: Crystal Structure of Streptococcus Mutans Deoxycytidylate Deaminase Complexed with DttpProtein crystallography data
The structure of Crystal Structure of Streptococcus Mutans Deoxycytidylate Deaminase Complexed with Dttp, PDB code: 5c2o
was solved by
Y.H.Li,
Z.Q.Gao,
H.F.Hou,
Y.H.Dong,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 5c2o:
The structure of Crystal Structure of Streptococcus Mutans Deoxycytidylate Deaminase Complexed with Dttp also contains other interesting chemical elements:
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Crystal Structure of Streptococcus Mutans Deoxycytidylate Deaminase Complexed with Dttp
(pdb code 5c2o). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Crystal Structure of Streptococcus Mutans Deoxycytidylate Deaminase Complexed with Dttp, PDB code: 5c2o: Jump to Magnesium binding site number: 1; 2; Magnesium binding site 1 out of 2 in 5c2oGo back to![]() ![]()
Magnesium binding site 1 out
of 2 in the Crystal Structure of Streptococcus Mutans Deoxycytidylate Deaminase Complexed with Dttp
![]() Mono view ![]() Stereo pair view
Magnesium binding site 2 out of 2 in 5c2oGo back to![]() ![]()
Magnesium binding site 2 out
of 2 in the Crystal Structure of Streptococcus Mutans Deoxycytidylate Deaminase Complexed with Dttp
![]() Mono view ![]() Stereo pair view
Reference:
Y.Li,
Z.Guo,
L.Jin,
D.Wang,
Z.Gao,
X.Su,
H.Hou,
Y.Dong.
Mechanism of the Allosteric Regulation of Streptococcus Mutans 2'-Deoxycytidylate Deaminase Acta Crystallogr.,Sect.D V. 72 883 2016.
Page generated: Tue Aug 12 06:15:26 2025
ISSN: ESSN 1399-0047 DOI: 10.1107/S2059798316009153 |
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