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Chlorine in PDB 7puj: Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus FaecalisEnzymatic activity of Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus Faecalis
All present enzymatic activity of Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus Faecalis:
3.2.1.52; Protein crystallography data
The structure of Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus Faecalis, PDB code: 7puj
was solved by
M.Garcia-Alija,
J.J.Du,
B.Trastoy,
E.J.Sundberg,
M.E.Guerin,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 7puj:
The structure of Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus Faecalis also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus Faecalis
(pdb code 7puj). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus Faecalis, PDB code: 7puj: Jump to Chlorine binding site number: 1; 2; Chlorine binding site 1 out of 2 in 7pujGo back to![]() ![]()
Chlorine binding site 1 out
of 2 in the Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus Faecalis
![]() Mono view ![]() Stereo pair view
Chlorine binding site 2 out of 2 in 7pujGo back to![]() ![]()
Chlorine binding site 2 out
of 2 in the Crystal Structure of Endoglycosidase E GH18 Domain From Enterococcus Faecalis
![]() Mono view ![]() Stereo pair view
Reference:
M.Garcia-Alija,
J.J.Du,
I.Ordonez,
A.Diz-Vallenilla,
A.Moraleda-Montoya,
N.Sultana,
C.G.Huynh,
C.Li,
T.C.Donahue,
L.X.Wang,
B.Trastoy,
E.J.Sundberg,
M.E.Guerin.
Mechanism of Cooperative N-Glycan Processing By the Multi-Modular Endoglycosidase Endoe. Nat Commun V. 13 1137 2022.
Page generated: Tue Jul 30 02:43:27 2024
ISSN: ESSN 2041-1723 PubMed: 35241669 DOI: 10.1038/S41467-022-28722-W |
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