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Atomistry » Calcium » PDB 1m9i-1mr8 » 1mmq | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Calcium » PDB 1m9i-1mr8 » 1mmq » |
Calcium in PDB 1mmq: Matrilysin Complexed with Hydroxamate InhibitorEnzymatic activity of Matrilysin Complexed with Hydroxamate Inhibitor
All present enzymatic activity of Matrilysin Complexed with Hydroxamate Inhibitor:
3.4.24.23; Protein crystallography data
The structure of Matrilysin Complexed with Hydroxamate Inhibitor, PDB code: 1mmq
was solved by
M.F.Browner,
W.W.Smith,
A.L.Castelhano,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 1mmq:
The structure of Matrilysin Complexed with Hydroxamate Inhibitor also contains other interesting chemical elements:
Calcium Binding Sites:
The binding sites of Calcium atom in the Matrilysin Complexed with Hydroxamate Inhibitor
(pdb code 1mmq). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Matrilysin Complexed with Hydroxamate Inhibitor, PDB code: 1mmq: Jump to Calcium binding site number: 1; 2; Calcium binding site 1 out of 2 in 1mmqGo back to Calcium Binding Sites List in 1mmq
Calcium binding site 1 out
of 2 in the Matrilysin Complexed with Hydroxamate Inhibitor
Mono view Stereo pair view
Calcium binding site 2 out of 2 in 1mmqGo back to Calcium Binding Sites List in 1mmq
Calcium binding site 2 out
of 2 in the Matrilysin Complexed with Hydroxamate Inhibitor
Mono view Stereo pair view
Reference:
M.F.Browner,
W.W.Smith,
A.L.Castelhano.
Matrilysin-Inhibitor Complexes: Common Themes Among Metalloproteases. Biochemistry V. 34 6602 1995.
Page generated: Thu Jul 11 12:33:45 2024
ISSN: ISSN 0006-2960 PubMed: 7756291 DOI: 10.1021/BI00020A004 |
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