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Calcium in PDB 3fp7: Anionic Trypsin Variant S195A in Complex with Bovine Pancreatic Trypsin Inhibitor (Bpti) Cleaved at the Scissile Bond (LYS15-ALA16) Determined to the 1.46 A Resolution LimitEnzymatic activity of Anionic Trypsin Variant S195A in Complex with Bovine Pancreatic Trypsin Inhibitor (Bpti) Cleaved at the Scissile Bond (LYS15-ALA16) Determined to the 1.46 A Resolution Limit
All present enzymatic activity of Anionic Trypsin Variant S195A in Complex with Bovine Pancreatic Trypsin Inhibitor (Bpti) Cleaved at the Scissile Bond (LYS15-ALA16) Determined to the 1.46 A Resolution Limit:
3.4.21.4; Protein crystallography data
The structure of Anionic Trypsin Variant S195A in Complex with Bovine Pancreatic Trypsin Inhibitor (Bpti) Cleaved at the Scissile Bond (LYS15-ALA16) Determined to the 1.46 A Resolution Limit, PDB code: 3fp7
was solved by
E.Zakharova,
M.P.Horvath,
D.P.Goldenberg,
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 Anionic Trypsin Variant S195A in Complex with Bovine Pancreatic Trypsin Inhibitor (Bpti) Cleaved at the Scissile Bond (LYS15-ALA16) Determined to the 1.46 A Resolution Limit
(pdb code 3fp7). 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 Anionic Trypsin Variant S195A in Complex with Bovine Pancreatic Trypsin Inhibitor (Bpti) Cleaved at the Scissile Bond (LYS15-ALA16) Determined to the 1.46 A Resolution Limit, PDB code: 3fp7: Calcium binding site 1 out of 1 in 3fp7Go back to Calcium Binding Sites List in 3fp7
Calcium binding site 1 out
of 1 in the Anionic Trypsin Variant S195A in Complex with Bovine Pancreatic Trypsin Inhibitor (Bpti) Cleaved at the Scissile Bond (LYS15-ALA16) Determined to the 1.46 A Resolution Limit
Mono view Stereo pair view
Reference:
E.Zakharova,
M.P.Horvath,
D.P.Goldenberg.
Structure of A Serine Protease Poised to Resynthesize A Peptide Bond. Proc.Natl.Acad.Sci.Usa V. 106 11034 2009.
Page generated: Sat Jul 13 10:15:59 2024
ISSN: ISSN 0027-8424 PubMed: 19549826 DOI: 10.1073/PNAS.0902463106 |
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