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Bromine in PDB 8kh6: Crystal Structure of FGFR4 Kinase Domain with 8R

Enzymatic activity of Crystal Structure of FGFR4 Kinase Domain with 8R

All present enzymatic activity of Crystal Structure of FGFR4 Kinase Domain with 8R:
2.7.10.1;

Protein crystallography data

The structure of Crystal Structure of FGFR4 Kinase Domain with 8R, PDB code: 8kh6 was solved by Q.M.Lin, X.J.Chen, Y.H.Chen, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 27.27 / 1.62
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 41.78, 61.18, 60.72, 90, 97.76, 90
R / Rfree (%) 20.4 / 22.8

Other elements in 8kh6:

The structure of Crystal Structure of FGFR4 Kinase Domain with 8R also contains other interesting chemical elements:

Chlorine (Cl) 2 atoms

Bromine Binding Sites:

The binding sites of Bromine atom in the Crystal Structure of FGFR4 Kinase Domain with 8R (pdb code 8kh6). This binding sites where shown within 5.0 Angstroms radius around Bromine atom.
In total only one binding site of Bromine was determined in the Crystal Structure of FGFR4 Kinase Domain with 8R, PDB code: 8kh6:

Bromine binding site 1 out of 1 in 8kh6

Go back to Bromine Binding Sites List in 8kh6
Bromine binding site 1 out of 1 in the Crystal Structure of FGFR4 Kinase Domain with 8R


Mono view


Stereo pair view

A full contact list of Bromine with other atoms in the Br binding site number 1 of Crystal Structure of FGFR4 Kinase Domain with 8R within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Br802

b:126.2
occ:1.00
BRAG A:VVI802 0.0 126.2 1.0
CAB A:VVI802 1.9 55.1 1.0
CAC A:VVI802 2.8 52.2 1.0
CAA A:VVI802 2.9 50.5 1.0
CAH A:VVI802 3.1 41.2 1.0
NH1 A:ARG483 3.3 62.7 1.0
OAI A:VVI802 3.5 47.5 1.0
CZ A:ARG483 3.7 64.6 1.0
CD A:ARG483 3.8 55.2 1.0
NE A:ARG483 3.9 58.2 1.0
CG2 A:THR499 4.1 35.0 1.0
NAF A:VVI802 4.1 45.3 1.0
CAD A:VVI802 4.1 54.1 1.0
CG A:ARG483 4.4 44.2 1.0
NH2 A:ARG483 4.5 63.5 1.0
CAE A:VVI802 4.6 50.8 1.0
SG A:CYS552 4.7 39.1 1.0
CA A:ALA554 4.8 38.4 1.0
CB A:ALA554 4.9 41.0 1.0

Reference:

F.Yang, Q.Lin, X.Song, H.Huang, X.Chen, J.Tan, Y.Li, Y.Zhou, Z.Tu, H.Du, Z.M.Zhang, R.Ortega, X.Lin, A.V.Patterson, J.B.Smaill, Y.Chen, X.Lu. Discovery of 6-Formylpyridyl Urea Derivatives As Potent Reversible-Covalent Fibroblast Growth Factor Receptor 4 Inhibitors with Improved Anti-Hepatocellular Carcinoma Activity. J.Med.Chem. V. 67 2667 2024.
ISSN: ISSN 0022-2623
PubMed: 38348819
DOI: 10.1021/ACS.JMEDCHEM.3C01810
Page generated: Sat Sep 28 08:39:34 2024

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