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Bromine in PDB 4gr0: Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B

Enzymatic activity of Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B

All present enzymatic activity of Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B:
3.4.24.65;

Protein crystallography data

The structure of Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B, PDB code: 4gr0 was solved by E.A.Stura, L.Vera, F.Beau, L.Devel, E.Cassar-Lajeunesse, V.Dive, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 32.41 / 1.50
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 69.770, 62.760, 37.840, 90.00, 90.00, 90.00
R / Rfree (%) 18.6 / 21.8

Other elements in 4gr0:

The structure of Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B also contains other interesting chemical elements:

Chlorine (Cl) 1 atom
Calcium (Ca) 3 atoms
Zinc (Zn) 2 atoms

Bromine Binding Sites:

The binding sites of Bromine atom in the Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B (pdb code 4gr0). This binding sites where shown within 5.0 Angstroms radius around Bromine atom.
In total only one binding site of Bromine was determined in the Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B, PDB code: 4gr0:

Bromine binding site 1 out of 1 in 4gr0

Go back to Bromine Binding Sites List in 4gr0
Bromine binding site 1 out of 1 in the Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B


Mono view


Stereo pair view

A full contact list of Bromine with other atoms in the Br binding site number 1 of Crystal Structure of the Catalytic Domain of Human MMP12 in Complex with Selective Phosphinic Inhibitor RXP470B within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Br306

b:26.8
occ:1.00
BR1 A:R4B306 0.0 26.8 1.0
C22 A:R4B306 1.9 16.3 1.0
C21 A:R4B306 2.8 17.4 1.0
C23 A:R4B306 2.9 16.6 1.0
O A:HOH498 3.7 18.8 1.0
C20 A:R4B306 4.1 15.0 1.0
ND1 A:HIS172 4.1 20.9 1.0
CE1 A:HIS172 4.1 26.2 1.0
C24 A:R4B306 4.2 13.2 1.0
O A:HOH527 4.2 26.2 1.0
C19 A:R4B306 4.7 12.6 1.0
O A:HOH546 4.9 13.9 1.0

Reference:

B.Czarny, E.A.Stura, L.Devel, L.Vera, E.Cassar-Lajeunesse, F.Beau, V.Calderone, M.Fragai, C.Luchinat, V.Dive. Molecular Determinants of A Selective Matrix Metalloprotease-12 Inhibitor: Insights From Crystallography and Thermodynamic Studies. J.Med.Chem. V. 56 1149 2013.
ISSN: ISSN 0022-2623
PubMed: 23343195
DOI: 10.1021/JM301574D
Page generated: Wed Jul 10 21:23:34 2024

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