Chlorine in PDB 7suh: Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15

All present enzymatic activity of Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15:
2.7.11.1;

The structure of Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15, PDB code: 7suh was solved by R.L.Palte, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	43.81 / 2.46
Space group	P 1 21 1
Cell size a, b, c (Å), α, β, γ (°)	44.8, 65.04, 53.55, 90, 102.08, 90
R / Rfree (%)	17.6 / 24.2

The binding sites of Chlorine atom in the Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15 (pdb code 7suh). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15, PDB code: 7suh:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in the Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15 within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl301 b:65.9 occ:1.00 CL1 A:BXI301 0.0 65.9 1.0 C11 A:BXI301 1.7 60.0 1.0 C10 A:BXI301 2.7 57.9 1.0 C12 A:BXI301 2.7 54.7 1.0 C13 A:BXI301 3.1 54.0 1.0 C14 A:BXI301 3.6 52.3 1.0 SD A:MET84 3.7 76.7 1.0 N A:ASP148 3.7 44.5 1.0 CB A:ALA147 4.0 39.8 1.0 C21 A:BXI301 4.0 52.2 1.0 C9 A:BXI301 4.0 57.4 1.0 CG2 A:VAL23 4.1 73.2 1.0 CA A:ASP148 4.2 46.0 1.0 CE A:MET84 4.3 73.7 1.0 CB A:ASP148 4.4 49.4 1.0 C20 A:BXI301 4.5 55.1 1.0 C22 A:BXI301 4.5 55.0 1.0 C15 A:BXI301 4.5 56.5 1.0 C A:ALA147 4.7 45.5 1.0 CA A:ALA147 4.8 39.6 1.0 O A:HOH411 4.8 61.1 1.0 CG1 A:VAL23 4.8 73.1 1.0

Chlorine binding site 2 out of 2 in the Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Structure of CHK1 10-Pt. Mutant Complex with LRRK2 Inhibitor 15 within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl301 b:76.0 occ:1.00 CL A:BXI301 0.0 76.0 1.0 C7 A:BXI301 1.7 75.5 1.0 N2 A:BXI301 2.7 78.3 1.0 C1 A:BXI301 2.8 71.5 1.0 C3 A:BXI301 3.1 82.2 1.0 N A:BXI301 3.2 64.7 1.0 O A:SER88 3.2 61.1 1.0 O A:ALA87 3.3 62.4 1.0 CA A:SER88 3.4 58.0 1.0 C A:SER88 3.6 60.2 1.0 C2 A:BXI301 3.9 75.2 1.0 N1 A:BXI301 3.9 77.8 1.0 C A:ALA87 4.0 62.4 1.0 N A:SER88 4.1 58.5 1.0 CD2 A:LEU15 4.3 81.6 1.0 CD1 A:LEU86 4.3 64.6 1.0 N A:GLY90 4.4 46.2 1.0 CB A:SER88 4.5 61.0 1.0 C A:BXI301 4.5 59.6 1.0 C4 A:BXI301 4.6 84.8 1.0 N A:GLY89 4.6 52.9 1.0 CG A:LEU86 4.7 64.6 1.0 CD2 A:LEU86 4.8 64.9 1.0 CA A:GLY90 4.9 45.0 1.0 CD1 A:LEU25 4.9 73.4 1.0

M.H.Keylor, A.Gulati, S.D.Kattar, R.E.Johnson, R.W.Chau, K.A.Margrey, M.J.Ardolino, C.Zarate, K.E.Poremba, V.Simov, G.J.Morriello, J.J.Acton, B.Pio, X.Yan, R.L.Palte, S.E.Mcminn, L.Nogle, C.A.Lesburg, D.Adpressa, S.Lin, S.Neelamkavil, P.Liu, J.Su, L.G.Hegde, J.D.Woodhouse, R.Faltus, T.Xiong, P.J.Ciaccio, J.Piesvaux, K.M.Otte, H.B.Wood, M.E.Kennedy, D.J.Bennett, E.F.Dimauro, M.J.Fell, P.H.Fuller. Structure-Guided Discovery of Aminoquinazolines As Brain-Penetrant and Selective LRRK2 Inhibitors. J.Med.Chem. V. 65 838 2022.
ISSN: ISSN 0022-2623
PubMed: 34967623
DOI: 10.1021/ACS.JMEDCHEM.1C01968