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Atomistry » Fluorine » PDB 7ugj-7v3s » 7uyw | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Fluorine » PDB 7ugj-7v3s » 7uyw » |
Fluorine in PDB 7uyw: Crystal Structure of JAK2 Kinase Domain in Complex with Compound 30Enzymatic activity of Crystal Structure of JAK2 Kinase Domain in Complex with Compound 30
All present enzymatic activity of Crystal Structure of JAK2 Kinase Domain in Complex with Compound 30:
2.7.10.2; Protein crystallography data
The structure of Crystal Structure of JAK2 Kinase Domain in Complex with Compound 30, PDB code: 7uyw
was solved by
A.V.Toms,
S.Leit,
J.R.Greenwood,
S.Mondal,
S.Carriero,
M.Dahlgren,
G.C.Harriman,
J.J.Kennedy-Smith,
R.Kapeller,
J.P.Lawson,
D.L.Romero,
M.Shelley,
R.T.Wester,
W.Westlin,
J.J.Mc Elwee,
W.Miao,
S.D.Edmondson,
C.E.Massee,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Crystal Structure of JAK2 Kinase Domain in Complex with Compound 30
(pdb code 7uyw). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 2 binding sites of Fluorine where determined in the Crystal Structure of JAK2 Kinase Domain in Complex with Compound 30, PDB code: 7uyw: Jump to Fluorine binding site number: 1; 2; Fluorine binding site 1 out of 2 in 7uywGo back to![]() ![]()
Fluorine binding site 1 out
of 2 in the Crystal Structure of JAK2 Kinase Domain in Complex with Compound 30
![]() Mono view ![]() Stereo pair view
Fluorine binding site 2 out of 2 in 7uywGo back to![]() ![]()
Fluorine binding site 2 out
of 2 in the Crystal Structure of JAK2 Kinase Domain in Complex with Compound 30
![]() Mono view ![]() Stereo pair view
Reference:
S.Leit,
J.R.Greenwood,
S.Mondal,
S.Carriero,
M.Dahlgren,
G.C.Harriman,
J.J.Kennedy-Smith,
R.Kapeller,
J.P.Lawson,
D.L.Romero,
A.V.Toms,
M.Shelley,
R.T.Wester,
W.Westlin,
J.J.Mcelwee,
W.Miao,
S.D.Edmondson,
C.E.Masse.
Potent and Selective TYK2-JH1 Inhibitors Highly Efficacious in Rodent Model of Psoriasis. Bioorg.Med.Chem.Lett. V. 73 28891 2022.
Page generated: Wed Jul 16 01:08:20 2025
ISSN: ESSN 1464-3405 PubMed: 35842205 DOI: 10.1016/J.BMCL.2022.128891 |
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