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Atomistry » Calcium » PDB 4aqi-4ayp » 4avo | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Calcium » PDB 4aqi-4ayp » 4avo » |
Calcium in PDB 4avo: Thermobifida Fusca Cellobiohydrolase CEL6B Catalytic Mutant D274A Cocrystallized with CellobioseEnzymatic activity of Thermobifida Fusca Cellobiohydrolase CEL6B Catalytic Mutant D274A Cocrystallized with Cellobiose
All present enzymatic activity of Thermobifida Fusca Cellobiohydrolase CEL6B Catalytic Mutant D274A Cocrystallized with Cellobiose:
3.2.1.91; Protein crystallography data
The structure of Thermobifida Fusca Cellobiohydrolase CEL6B Catalytic Mutant D274A Cocrystallized with Cellobiose, PDB code: 4avo
was solved by
M.Wu,
T.V.Vuong,
D.B.Wilson,
M.Sandgren,
J.Stahlberg,
H.Hansson,
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 Thermobifida Fusca Cellobiohydrolase CEL6B Catalytic Mutant D274A Cocrystallized with Cellobiose
(pdb code 4avo). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total only one binding site of Calcium was determined in the Thermobifida Fusca Cellobiohydrolase CEL6B Catalytic Mutant D274A Cocrystallized with Cellobiose, PDB code: 4avo: Calcium binding site 1 out of 1 in 4avoGo back to Calcium Binding Sites List in 4avo
Calcium binding site 1 out
of 1 in the Thermobifida Fusca Cellobiohydrolase CEL6B Catalytic Mutant D274A Cocrystallized with Cellobiose
Mono view Stereo pair view
Reference:
M.Wu,
L.Bu,
T.V.Vuong,
D.B.Wilson,
M.F.Crowley,
M.Sandgren,
J.Stahlberg,
G.T.Beckham,
H.Hansson.
Loop Motions Important to Product Expulsion in the Thermobifida Fusca Glycoside Hydrolase Family 6 Cellobiohydrolase From Structural and Computational Studies. J.Biol.Chem. V. 288 33107 2013.
Page generated: Sat Jul 13 22:20:15 2024
ISSN: ISSN 0021-9258 PubMed: 24085303 DOI: 10.1074/JBC.M113.502765 |
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