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Chlorine in PDB 2e9p: Structure of H-CHK1 Complexed with A771129

Enzymatic activity of Structure of H-CHK1 Complexed with A771129

All present enzymatic activity of Structure of H-CHK1 Complexed with A771129:
2.7.11.1;

Protein crystallography data

The structure of Structure of H-CHK1 Complexed with A771129, PDB code: 2e9p was solved by C.Park, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.65 / 2.60
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 44.948, 65.569, 58.267, 90.00, 94.03, 90.00
R / Rfree (%) n/a / n/a

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Structure of H-CHK1 Complexed with A771129 (pdb code 2e9p). 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 Structure of H-CHK1 Complexed with A771129, PDB code: 2e9p:

Chlorine binding site 1 out of 1 in 2e9p

Go back to Chlorine Binding Sites List in 2e9p
Chlorine binding site 1 out of 1 in the Structure of H-CHK1 Complexed with A771129


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of H-CHK1 Complexed with A771129 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1001

b:26.4
occ:1.00
CL10 A:77A1001 0.0 26.4 1.0
C4 A:77A1001 1.7 26.7 1.0
C3 A:77A1001 2.7 26.6 1.0
C5 A:77A1001 2.7 26.7 1.0
O A:HOH1105 3.4 35.4 1.0
O A:CYS87 3.5 26.8 1.0
O A:SER88 3.7 26.8 1.0
C A:SER88 3.9 26.6 1.0
O A:HOH1106 3.9 47.1 1.0
CA A:GLY90 3.9 25.6 1.0
N A:GLY90 4.0 25.9 1.0
CA A:SER88 4.1 26.8 1.0
C2 A:77A1001 4.1 27.1 1.0
C6 A:77A1001 4.1 27.1 1.0
C A:CYS87 4.3 27.1 1.0
CD2 A:LEU15 4.4 50.5 1.0
C A:GLY89 4.5 25.9 1.0
N A:SER88 4.6 26.9 1.0
C7 A:77A1001 4.6 27.1 1.0
N A:GLY89 4.6 26.4 1.0
CE1 A:TYR86 4.6 30.9 1.0
OH A:TYR86 4.7 31.0 1.0
O A:GLY89 4.9 25.9 1.0

Reference:

Y.Tong, A.Claiborne, K.D.Stewart, C.Park, P.Kovar, Z.Chen, R.B.Credo, S.L.Gwaltney, H.Zhang, S.H.Rosenberg, H.L.Sham, T.J.Sowin, N.H.Lin. Structure-Based Design, Synthesis and Biological Evaluation of Potent and Selective Macrocyclic CHK1 Inhibitors To Be Published.
Page generated: Sat Dec 12 09:03:47 2020

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