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Atomistry » Calcium » PDB 2c5d-2cn3 » 2cel | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Calcium » PDB 2c5d-2cn3 » 2cel » |
Calcium in PDB 2cel: Active-Site Mutant E212Q Determined at pH 6.0 with No Ligand Bound in the Active SiteEnzymatic activity of Active-Site Mutant E212Q Determined at pH 6.0 with No Ligand Bound in the Active Site
All present enzymatic activity of Active-Site Mutant E212Q Determined at pH 6.0 with No Ligand Bound in the Active Site:
3.2.1.91; Protein crystallography data
The structure of Active-Site Mutant E212Q Determined at pH 6.0 with No Ligand Bound in the Active Site, PDB code: 2cel
was solved by
C.Divne,
J.Stahlberg,
T.A.Jones,
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 Active-Site Mutant E212Q Determined at pH 6.0 with No Ligand Bound in the Active Site
(pdb code 2cel). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Active-Site Mutant E212Q Determined at pH 6.0 with No Ligand Bound in the Active Site, PDB code: 2cel: Jump to Calcium binding site number: 1; 2; Calcium binding site 1 out of 2 in 2celGo back to![]() ![]()
Calcium binding site 1 out
of 2 in the Active-Site Mutant E212Q Determined at pH 6.0 with No Ligand Bound in the Active Site
![]() Mono view ![]() Stereo pair view
Calcium binding site 2 out of 2 in 2celGo back to![]() ![]()
Calcium binding site 2 out
of 2 in the Active-Site Mutant E212Q Determined at pH 6.0 with No Ligand Bound in the Active Site
![]() Mono view ![]() Stereo pair view
Reference:
J.Stahlberg,
C.Divne,
A.Koivula,
K.Piens,
M.Claeyssens,
T.T.Teeri,
T.A.Jones.
Activity Studies and Crystal Structures of Catalytically Deficient Mutants of Cellobiohydrolase I From Trichoderma Reesei. J.Mol.Biol. V. 264 337 1996.
Page generated: Tue Jul 8 04:49:19 2025
ISSN: ISSN 0022-2836 PubMed: 8951380 DOI: 10.1006/JMBI.1996.0644 |
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