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Atomistry » Calcium » PDB 1rc8-1rpk » 1rm8 » |
Calcium in PDB 1rm8: Crystal Structure of the Catalytic Domain of Mmp-16/MT3-Mmp: Characterization of Mt-Mmp Specific FeaturesProtein crystallography data
The structure of Crystal Structure of the Catalytic Domain of Mmp-16/MT3-Mmp: Characterization of Mt-Mmp Specific Features, PDB code: 1rm8
was solved by
R.Lang,
M.Braun,
N.E.Sounni,
A.Noel,
F.Frankenne,
J.-M.Foidart,
W.Bode,
K.Maskos,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Other elements in 1rm8:
The structure of Crystal Structure of the Catalytic Domain of Mmp-16/MT3-Mmp: Characterization of Mt-Mmp Specific Features also contains other interesting chemical elements:
Calcium Binding Sites:
The binding sites of Calcium atom in the Crystal Structure of the Catalytic Domain of Mmp-16/MT3-Mmp: Characterization of Mt-Mmp Specific Features
(pdb code 1rm8). This binding sites where shown within
5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Crystal Structure of the Catalytic Domain of Mmp-16/MT3-Mmp: Characterization of Mt-Mmp Specific Features, PDB code: 1rm8: Jump to Calcium binding site number: 1; 2; Calcium binding site 1 out of 2 in 1rm8Go back to![]() ![]()
Calcium binding site 1 out
of 2 in the Crystal Structure of the Catalytic Domain of Mmp-16/MT3-Mmp: Characterization of Mt-Mmp Specific Features
![]() Mono view ![]() Stereo pair view
Calcium binding site 2 out of 2 in 1rm8Go back to![]() ![]()
Calcium binding site 2 out
of 2 in the Crystal Structure of the Catalytic Domain of Mmp-16/MT3-Mmp: Characterization of Mt-Mmp Specific Features
![]() Mono view ![]() Stereo pair view
Reference:
R.Lang,
M.Braun,
N.E.Sounni,
A.Noel,
F.Frankenne,
J.M.Foidart,
W.Bode,
K.Maskos.
Crystal Structure of the Catalytic Domain of Mmp-16/MT3-Mmp: Characterization of Mt-Mmp Specific Features. J.Mol.Biol. V. 336 213 2004.
Page generated: Thu Jul 11 22:14:07 2024
ISSN: ISSN 0022-2836 PubMed: 14741217 DOI: 10.1016/J.JMB.2003.12.022 |
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