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Chlorine in PDB 6g9j: Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2

Enzymatic activity of Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2

All present enzymatic activity of Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2:
2.7.11.24;

Protein crystallography data

The structure of Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2, PDB code: 6g9j was solved by M.O'reilly, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 28.34 / 1.98
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 48.842, 70.258, 60.577, 90.00, 109.90, 90.00
R / Rfree (%) 15.9 / 21.2

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2 (pdb code 6g9j). 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 Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2, PDB code: 6g9j:

Chlorine binding site 1 out of 1 in 6g9j

Go back to Chlorine Binding Sites List in 6g9j
Chlorine binding site 1 out of 1 in the Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl403

b:35.9
occ:1.00
 CL3 A:ERK403 0.0 35.9 1.0
C29 A:ERK403 1.7 30.8 1.0
H48 A:ERK403 2.5 30.7 1.0
C28 A:ERK403 2.7 32.0 1.0
C17 A:ERK403 2.7 27.4 1.0
H59 A:ERK403 2.8 31.9 1.0
OE1 A:GLN105 2.9 25.1 1.0
C13 A:ERK403 3.0 31.0 1.0
C12 A:ERK403 3.1 27.6 1.0
CD A:GLN105 3.4 32.0 1.0
CB A:GLN105 3.5 31.2 1.0
O A:HOH634 3.6 39.4 1.0
N27 A:ERK403 4.0 31.9 1.0
N18 A:ERK403 4.0 25.9 1.0
CB A:ALA52 4.0 29.9 1.0
CG A:GLN105 4.1 26.9 1.0
CD1 A:LEU156 4.1 26.1 1.0
NE2 A:GLN105 4.2 24.8 1.0
C14 A:ERK403 4.2 32.4 1.0
CG1 A:ILE84 4.2 23.1 1.0
C11 A:ERK403 4.3 31.9 1.0
O A:ASP106 4.4 35.0 1.0
C19 A:ERK403 4.4 28.6 1.0
CD1 A:ILE84 4.7 34.7 1.0
CA A:GLN105 4.9 29.1 1.0
H47 A:ERK403 4.9 33.5 1.0

Reference:

T.D.Heightman, V.Berdini, H.Braithwaite, I.M.Buck, M.Cassidy, J.Castro, A.Courtin, J.E.H.Day, C.East, L.Fazal, B.Graham, C.M.Griffiths-Jones, J.F.Lyons, V.Martins, S.Muench, J.M.Munck, D.Norton, M.O'reilly, N.Palmer, P.Pathuri, M.Reader, D.C.Rees, S.J.Rich, C.Richardson, H.Saini, N.T.Thompson, N.G.Wallis, H.Walton, N.E.Wilsher, A.J.Woolford, M.Cooke, D.Cousin, S.Onions, J.Shannon, J.Watts, C.W.Murray. Fragment-Based Discovery of A Potent, Orally Bioavailable Inhibitor That Modulates the Phosphorylation and Catalytic Activity of ERK1/2. J. Med. Chem. V. 61 4978 2018.
ISSN: ISSN 1520-4804
PubMed: 29775310
DOI: 10.1021/ACS.JMEDCHEM.8B00421
Page generated: Sat Jul 27 23:53:48 2024

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