Fluorine in PDB 5am6: Native FGFR1 with An Inhibitor

All present enzymatic activity of Native FGFR1 with An Inhibitor:
2.7.10.1;

The structure of Native FGFR1 with An Inhibitor, PDB code: 5am6 was solved by T.D.Bunney, S.Wan, N.Thiyagarajan, L.Sutto, S.V.Williams, P.Ashford, H.Koss, M.A.Knowles, F.L.Gervasio, P.V.Coveney, M.Katan, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	43.26 / 1.96
Space group	C 1 2 1
Cell size a, b, c (Å), α, β, γ (°)	208.670, 57.590, 65.560, 90.00, 107.39, 90.00
R / Rfree (%)	21.367 / 25.179

The structure of Native FGFR1 with An Inhibitor also contains other interesting chemical elements:

Chlorine

(Cl)

3 atoms

The binding sites of Fluorine atom in the Native FGFR1 with An Inhibitor (pdb code 5am6). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 2 binding sites of Fluorine where determined in the Native FGFR1 with An Inhibitor, PDB code: 5am6:
Jump to Fluorine binding site number: 1; 2;

Fluorine binding site 1 out of 2 in the Native FGFR1 with An Inhibitor


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Native FGFR1 with An Inhibitor within 5.0Å range: probe atom residue distance (Å) B Occ A:F1766 b:38.2 occ:0.98 F22 A:38O1766 0.0 38.2 1.0 C21 A:38O1766 1.3 37.7 1.0 C23 A:38O1766 2.4 34.8 1.0 C20 A:38O1766 2.4 36.5 1.0 N19 A:38O1766 2.7 40.6 1.0 O A:HOH2157 2.9 53.1 1.0 C18 A:38O1766 3.0 37.5 1.0 O A:HOH2030 3.4 59.1 1.0 C24 A:38O1766 3.7 34.4 1.0 C26 A:38O1766 3.8 34.6 1.0 O A:HOH2087 3.8 36.9 1.0 CG2 A:VAL492 3.9 45.7 1.0 C25 A:38O1766 4.2 33.8 1.0 CG1 A:VAL492 4.4 44.9 1.0 C17 A:38O1766 4.4 36.8 1.0 OD2 A:ASP641 4.5 47.6 1.0 CB A:VAL492 4.6 45.5 1.0 OD1 A:ASP641 4.7 44.8 1.0 CD1 A:LEU630 4.8 33.5 1.0 N27 A:38O1766 4.9 33.3 1.0 CG A:ASP641 5.0 40.6 1.0

Fluorine binding site 2 out of 2 in the Native FGFR1 with An Inhibitor


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Native FGFR1 with An Inhibitor within 5.0Å range: probe atom residue distance (Å) B Occ B:F1763 b:38.8 occ:1.00 F22 B:38O1763 0.0 38.8 1.0 C21 B:38O1763 1.3 36.1 1.0 C23 B:38O1763 2.4 33.5 1.0 C20 B:38O1763 2.4 35.0 1.0 N19 B:38O1763 2.7 40.4 1.0 C18 B:38O1763 3.0 37.7 1.0 O B:HOH2093 3.1 49.2 1.0 C24 B:38O1763 3.7 35.0 1.0 C26 B:38O1763 3.8 33.6 1.0 CG2 B:VAL492 3.9 41.6 1.0 OD2 B:ASP641 4.0 46.7 1.0 C25 B:38O1763 4.2 32.6 1.0 C17 B:38O1763 4.4 38.0 1.0 CG1 B:VAL492 4.5 42.1 1.0 CB B:VAL492 4.5 41.3 1.0 OD1 B:ASP641 4.6 45.2 1.0 CG B:ASP641 4.7 43.8 1.0 N27 B:38O1763 4.9 34.5 1.0 CD1 B:LEU630 4.9 38.2 1.0

T.Bunney, S.Wan, N.Thiyagarajan, L.Sutto, S.V.Williams, P.Ashford, H.Koss, M.A.Knowles, F.L.Gervasio, P.V.Coveney, M.Katan. The Effect of Mutations on Drug Sensitivity and Kinase Activity of Fibroblast Growth Factor Receptors: A Combined Experimental and Theoretical Study Ebiomedicine 2015.
ISSN: ESSN 2352-3964
DOI: 10.1016/J.EBIOM.2015.02.009