Chlorine in PDB 6n79: Structure of the Human JAK1 Kinase Domain with Compound 20

Enzymatic activity of Structure of the Human JAK1 Kinase Domain with Compound 20

All present enzymatic activity of Structure of the Human JAK1 Kinase Domain with Compound 20:
2.7.10.2;

Protein crystallography data

The structure of Structure of the Human JAK1 Kinase Domain with Compound 20, PDB code: 6n79 was solved by P.J.Lupardus, D.Brown, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 44.83 / 2.27
Space group P 2 21 21
Cell size a, b, c (Å), α, β, γ (°) 44.830, 169.910, 42.710, 90.00, 90.00, 90.00
R / Rfree (%) 22.4 / 27

Other elements in 6n79:

The structure of Structure of the Human JAK1 Kinase Domain with Compound 20 also contains other interesting chemical elements:

Fluorine (F) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Structure of the Human JAK1 Kinase Domain with Compound 20 (pdb code 6n79). 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 the Human JAK1 Kinase Domain with Compound 20, PDB code: 6n79:

Chlorine binding site 1 out of 1 in 6n79

Go back to Chlorine Binding Sites List in 6n79
Chlorine binding site 1 out of 1 in the Structure of the Human JAK1 Kinase Domain with Compound 20


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of the Human JAK1 Kinase Domain with Compound 20 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1201

b:35.6
occ:1.00
CL A:KES1201 0.0 35.6 1.0
C12 A:KES1201 1.7 37.0 1.0
C11 A:KES1201 2.7 37.0 1.0
C13 A:KES1201 2.7 38.7 1.0
N A:GLY884 3.5 38.7 1.0
O A:GLY887 3.7 41.5 1.0
O A:GLY882 3.8 41.7 1.0
C A:GLY887 3.8 41.8 1.0
N A:LYS888 4.0 37.5 1.0
C A:GLU883 4.0 41.5 1.0
C14 A:KES1201 4.0 38.1 1.0
C10 A:KES1201 4.0 36.2 1.0
CA A:GLU883 4.0 38.5 1.0
CA A:LYS888 4.1 37.0 1.0
O1 A:GOL1202 4.1 72.0 1.0
N A:VAL889 4.1 27.3 1.0
C1 A:GOL1202 4.1 69.6 1.0
C A:GLY882 4.1 42.0 1.0
CG2 A:VAL889 4.1 26.5 1.0
N A:GLU883 4.2 38.6 1.0
C A:LYS888 4.2 33.8 1.0
CA A:GLY884 4.3 38.6 1.0
C15 A:KES1201 4.5 36.8 1.0
CA A:GLY887 4.5 39.0 1.0
CB A:VAL889 4.6 27.0 1.0
CE A:LYS908 4.7 28.0 1.0
O A:HOH1322 4.8 40.1 1.0
O3 A:GOL1202 4.9 57.3 1.0
O A:GLU883 4.9 40.0 1.0
CA A:VAL889 4.9 26.0 1.0

Reference:

M.Zak, E.J.Hanan, P.Lupardus, D.G.Brown, C.Robinson, M.Siu, J.P.Lyssikatos, F.A.Romero, G.Zhao, T.Kellar, R.Mendonca, N.C.Ray, S.C.Goodacre, P.H.Crackett, N.Mclean, C.A.Hurley, P.W.Yuen, Y.X.Cheng, X.Liu, M.Liimatta, P.B.Kohli, J.Nonomiya, G.Salmon, G.Buckley, J.Lloyd, P.Gibbons, N.Ghilardi, J.R.Kenny, A.Johnson. Discovery of A Class of Highly Potent Janus Kinase 1/2 (JAK1/2) Inhibitors Demonstrating Effective Cell-Based Blockade of Il-13 Signaling. Bioorg.Med.Chem.Lett. V. 29 1522 2019.
ISSN: ESSN 1464-3405
PubMed: 30981576
DOI: 10.1016/J.BMCL.2019.04.008
Page generated: Sat Dec 12 13:22:47 2020

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