Chlorine in PDB 7nig: 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008

Enzymatic activity of 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008

All present enzymatic activity of 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008:
5.2.1.8;

Protein crystallography data

The structure of 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008, PDB code: 7nig was solved by M.Wolter, L.V.Dijck, P.J.Cossar, C.Ottmann, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 41.68 / 1.90
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 82.089, 111.584, 62.692, 90, 90, 90
R / Rfree (%) 16.5 / 20.5

Other elements in 7nig:

The structure of 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008 also contains other interesting chemical elements:

Bromine (Br) 1 atom
Calcium (Ca) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008 (pdb code 7nig). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008, PDB code: 7nig:

Chlorine binding site 1 out of 1 in 7nig

Go back to Chlorine Binding Sites List in 7nig
Chlorine binding site 1 out of 1 in the 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of 14-3-3 Sigma with PIN1 Binding Site PS72 and Covalently Bound LVD1008 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl304

b:15.1
occ:0.89
NZ A:LYS9 3.1 12.0 1.0
CD A:LYS9 3.7 8.2 1.0
CE A:LYS9 3.7 9.3 1.0
CZ A:PHE25 4.3 7.4 1.0
CE1 A:PHE25 4.5 8.2 1.0
CE A:MET1 4.7 15.9 1.0
CG A:LYS9 5.0 7.3 1.0

Reference:

P.J.Cossar, M.Wolter, L.Van Dijck, D.Valenti, L.M.Levy, C.Ottmann, L.Brunsveld. Reversible Covalent Imine-Tethering For Selective Stabilization of 14-3-3 Hub Protein Interactions. J.Am.Chem.Soc. 2021.
ISSN: ESSN 1520-5126
PubMed: 34047554
DOI: 10.1021/JACS.1C03035
Page generated: Tue Jul 30 00:55:25 2024

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