Chlorine in PDB 7bje: Crystal Structure of CHK1-10PT-Mutant Complex with Adenine

Enzymatic activity of Crystal Structure of CHK1-10PT-Mutant Complex with Adenine

All present enzymatic activity of Crystal Structure of CHK1-10PT-Mutant Complex with Adenine:
2.7.11.1;

Protein crystallography data

The structure of Crystal Structure of CHK1-10PT-Mutant Complex with Adenine, PDB code: 7bje was solved by P.Dokurno, A.E.Surgenor, D.S.Williamson, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 1.80
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 45.035, 65.815, 54.227, 90, 101.17, 90
R / Rfree (%) 17.2 / 19.9

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of CHK1-10PT-Mutant Complex with Adenine (pdb code 7bje). 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 Crystal Structure of CHK1-10PT-Mutant Complex with Adenine, PDB code: 7bje:

Chlorine binding site 1 out of 1 in 7bje

Go back to Chlorine Binding Sites List in 7bje
Chlorine binding site 1 out of 1 in the Crystal Structure of CHK1-10PT-Mutant Complex with Adenine


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of CHK1-10PT-Mutant Complex with Adenine within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl302

b:71.4
occ:1.00
O A:HOH597 2.2 64.5 1.0
O A:HOH604 2.3 55.8 1.0
O A:HOH589 3.3 54.4 1.0
C A:GLY204 3.9 25.3 1.0
N A:GLU205 4.0 24.8 1.0
CB A:ALA200 4.0 18.8 1.0
O A:GLY204 4.1 23.4 1.0
CA A:GLU205 4.2 28.2 1.0
CG2 A:ILE96 4.3 24.6 1.0
CG A:LEU206 4.3 28.4 1.0
CD2 A:LEU206 4.4 28.2 1.0
C A:GLU205 4.4 26.2 1.0
N A:LEU206 4.4 22.5 1.0
CA A:GLY204 4.5 24.3 1.0
O A:HOH509 4.6 31.5 1.0
CA A:ALA200 4.6 19.3 1.0
O A:ALA200 4.9 18.1 1.0
O A:GLU205 4.9 25.0 1.0

Reference:

D.S.Williamson, G.P.Smith, G.K.Mikkelsen, T.Jensen, P.Acheson-Dossang, L.Badolo, S.T.Bedford, V.Chell, I.J.Chen, P.Dokurno, M.Hentzer, S.Newland, S.C.Ray, T.Shaw, A.E.Surgenor, L.Terry, Y.Wang, K.V.Christensen. Design and Synthesis of Pyrrolo[2,3- D ]Pyrimidine-Derived Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitors Using A Checkpoint Kinase 1 (CHK1)-Derived Crystallographic Surrogate. J.Med.Chem. 2021.
ISSN: ISSN 0022-2623
PubMed: 34184879
DOI: 10.1021/ACS.JMEDCHEM.1C00720
Page generated: Sat Jul 10 12:34:07 2021

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