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Atomistry » Sodium » PDB 2xjr-2xzi » 2xjt » |
Sodium in PDB 2xjt: X-Ray Structure of the N-Terminal Domain of the Flocculin FLO5 From Saccharomyces Cerevisiae in Complex with Calcium and MAN5(D1)Protein crystallography data
The structure of X-Ray Structure of the N-Terminal Domain of the Flocculin FLO5 From Saccharomyces Cerevisiae in Complex with Calcium and MAN5(D1), PDB code: 2xjt
was solved by
M.Veelders,
S.Brueckner,
D.Ott,
C.Unverzagt,
H.-U.Moesch,
L.-O.Essen,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 2xjt:
The structure of X-Ray Structure of the N-Terminal Domain of the Flocculin FLO5 From Saccharomyces Cerevisiae in Complex with Calcium and MAN5(D1) also contains other interesting chemical elements:
Sodium Binding Sites:
The binding sites of Sodium atom in the X-Ray Structure of the N-Terminal Domain of the Flocculin FLO5 From Saccharomyces Cerevisiae in Complex with Calcium and MAN5(D1)
(pdb code 2xjt). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 2 binding sites of Sodium where determined in the X-Ray Structure of the N-Terminal Domain of the Flocculin FLO5 From Saccharomyces Cerevisiae in Complex with Calcium and MAN5(D1), PDB code: 2xjt: Jump to Sodium binding site number: 1; 2; Sodium binding site 1 out of 2 in 2xjtGo back to Sodium Binding Sites List in 2xjt
Sodium binding site 1 out
of 2 in the X-Ray Structure of the N-Terminal Domain of the Flocculin FLO5 From Saccharomyces Cerevisiae in Complex with Calcium and MAN5(D1)
Mono view Stereo pair view
Sodium binding site 2 out of 2 in 2xjtGo back to Sodium Binding Sites List in 2xjt
Sodium binding site 2 out
of 2 in the X-Ray Structure of the N-Terminal Domain of the Flocculin FLO5 From Saccharomyces Cerevisiae in Complex with Calcium and MAN5(D1)
Mono view Stereo pair view
Reference:
M.Veelders,
S.Brueckner,
D.Ott,
C.Unverzagt,
H.-U.Moesch,
L.-O.Essen.
Structural Basis of Flocculin-Mediated Social Behavior in Yeast Proc.Natl.Acad.Sci.Usa V. 107 22511 2010.
Page generated: Mon Oct 7 05:13:31 2024
ISSN: ISSN 0027-8424 PubMed: 21149680 DOI: 10.1073/PNAS.1013210108 |
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