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Zinc in PDB 2vh9: Crystal Structure of NXG1-Deltayniig in Complex with Xllg, A Xyloglucan Derived OligosaccharideEnzymatic activity of Crystal Structure of NXG1-Deltayniig in Complex with Xllg, A Xyloglucan Derived Oligosaccharide
All present enzymatic activity of Crystal Structure of NXG1-Deltayniig in Complex with Xllg, A Xyloglucan Derived Oligosaccharide:
3.2.1.151; 3.2.1.4; Protein crystallography data
The structure of Crystal Structure of NXG1-Deltayniig in Complex with Xllg, A Xyloglucan Derived Oligosaccharide, PDB code: 2vh9
was solved by
M.Czjzek,
P.Mark,
M.J.Baumann,
J.M.Eklof,
G.Michel,
H.Brumer,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of NXG1-Deltayniig in Complex with Xllg, A Xyloglucan Derived Oligosaccharide
(pdb code 2vh9). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Crystal Structure of NXG1-Deltayniig in Complex with Xllg, A Xyloglucan Derived Oligosaccharide, PDB code: 2vh9: Jump to Zinc binding site number: 1; 2; Zinc binding site 1 out of 2 in 2vh9Go back to![]() ![]()
Zinc binding site 1 out
of 2 in the Crystal Structure of NXG1-Deltayniig in Complex with Xllg, A Xyloglucan Derived Oligosaccharide
![]() Mono view ![]() Stereo pair view
Zinc binding site 2 out of 2 in 2vh9Go back to![]() ![]()
Zinc binding site 2 out
of 2 in the Crystal Structure of NXG1-Deltayniig in Complex with Xllg, A Xyloglucan Derived Oligosaccharide
![]() Mono view ![]() Stereo pair view
Reference:
P.Mark,
M.J.Baumann,
J.M.Eklof,
F.Gullfot,
G.Michel,
A.M.Kallas,
T.T.Teeri,
H.Brumer,
M.Czjzek.
Analysis of Nasturtium TMNXG1 Complexes By Crystallography and Molecular Dynamics Provides Detailed Insight Into Substrate Recognition By Family GH16 Xyloglucan Endo-Transglycosylases and Endo-Hydrolases. Proteins V. 75 820 2009.
Page generated: Thu Oct 17 04:18:31 2024
ISSN: ISSN 0887-3585 PubMed: 19004021 DOI: 10.1002/PROT.22291 |
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