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Atomistry » Calcium » PDB 6ry5-6sau » 6ryn | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Calcium » PDB 6ry5-6sau » 6ryn » |
Calcium in PDB 6ryn: Structure of Conglutinin Carbohydrate Recognition Domain with Glcnac- Alpha-1-Phosphate BoundProtein crystallography data
The structure of Structure of Conglutinin Carbohydrate Recognition Domain with Glcnac- Alpha-1-Phosphate Bound, PDB code: 6ryn
was solved by
A.K.Shrive,
T.J.Greenhough,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Calcium Binding Sites:
The binding sites of Calcium atom in the Structure of Conglutinin Carbohydrate Recognition Domain with Glcnac- Alpha-1-Phosphate Bound
(pdb code 6ryn). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Structure of Conglutinin Carbohydrate Recognition Domain with Glcnac- Alpha-1-Phosphate Bound, PDB code: 6ryn: Jump to Calcium binding site number: 1; 2; Calcium binding site 1 out of 2 in 6rynGo back to Calcium Binding Sites List in 6ryn
Calcium binding site 1 out
of 2 in the Structure of Conglutinin Carbohydrate Recognition Domain with Glcnac- Alpha-1-Phosphate Bound
Mono view Stereo pair view
Calcium binding site 2 out of 2 in 6rynGo back to Calcium Binding Sites List in 6ryn
Calcium binding site 2 out
of 2 in the Structure of Conglutinin Carbohydrate Recognition Domain with Glcnac- Alpha-1-Phosphate Bound
Mono view Stereo pair view
Reference:
J.M.Paterson,
A.J.Shaw,
I.Burns,
A.W.Dodds,
A.Prasad,
K.B.Reid,
T.J.Greenhough,
A.K.Shrive.
Atomic-Resolution Crystal Structures of the Immune Protein Conglutinin From Cow Reveal Specific Interactions of Its Binding Site Withn-Acetylglucosamine. J.Biol.Chem. V. 294 17155 2019.
Page generated: Tue Jul 16 14:28:47 2024
ISSN: ESSN 1083-351X PubMed: 31562242 DOI: 10.1074/JBC.RA119.010271 |
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