Fluorine in PDB 4i85: Crystal Structure of Transthyretin in Complex with CHF5074 at Neutral pH

The structure of Crystal Structure of Transthyretin in Complex with CHF5074 at Neutral pH, PDB code: 4i85 was solved by G.Zanotti, L.Cendron, C.Folli, P.Florio, B.P.Imbimbo, R.Berni, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	29.94 / 1.67
Space group	P 21 21 2
Cell size a, b, c (Å), α, β, γ (°)	42.260, 84.860, 63.950, 90.00, 90.00, 90.00
R / Rfree (%)	18.4 / 23

The structure of Crystal Structure of Transthyretin in Complex with CHF5074 at Neutral pH also contains other interesting chemical elements:

Chlorine

(Cl)

4 atoms

The binding sites of Fluorine atom in the Crystal Structure of Transthyretin in Complex with CHF5074 at Neutral pH (pdb code 4i85). 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 Transthyretin in Complex with CHF5074 at Neutral pH, PDB code: 4i85:
Jump to Fluorine binding site number: 1; 2;

Fluorine binding site 1 out of 2 in the Crystal Structure of Transthyretin in Complex with CHF5074 at Neutral pH


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Crystal Structure of Transthyretin in Complex with CHF5074 at Neutral pH within 5.0Å range: probe atom residue distance (Å) B Occ A:F201 b:28.4 occ:0.50 FAC A:H50201 0.0 28.4 0.5 CAO A:H50201 1.3 26.6 0.5 CAJ A:H50201 2.4 30.7 0.5 CAT A:H50201 2.4 24.9 0.5 CAR A:H50201 2.7 21.0 0.5 CAG A:H50201 2.8 16.9 0.5 CAS A:H50201 3.6 28.8 0.5 CAI A:H50201 3.7 24.3 0.5 CAK A:H50201 3.8 17.3 0.5 CAF A:H50201 4.0 15.8 0.5 CAH A:H50201 4.1 31.4 0.5 CAQ A:H50201 4.8 16.6 0.5 CAU A:H50201 4.8 31.0 0.5 CAP A:H50201 4.9 14.8 0.5

Fluorine binding site 2 out of 2 in the Crystal Structure of Transthyretin in Complex with CHF5074 at Neutral pH


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Crystal Structure of Transthyretin in Complex with CHF5074 at Neutral pH within 5.0Å range: probe atom residue distance (Å) B Occ B:F201 b:17.6 occ:0.50 FAC B:H50201 0.0 17.6 0.5 CAO B:H50201 1.4 16.4 0.5 CAT B:H50201 2.4 18.1 0.5 CAJ B:H50201 2.4 17.3 0.5 CAR B:H50201 2.7 15.0 0.5 CAG B:H50201 2.7 16.3 0.5 CAI B:H50201 3.7 18.6 0.5 CAS B:H50201 3.7 17.1 0.5 CAK B:H50201 3.8 14.7 0.5 CAF B:H50201 3.9 13.0 0.5 CAH B:H50201 4.2 20.7 0.5 CAQ B:H50201 4.6 12.3 0.5 CAP B:H50201 4.8 13.6 0.5 CAU B:H50201 4.8 20.6 0.5 CAL B:H50201 5.0 21.1 0.5

G.Zanotti, L.Cendron, C.Folli, P.Florio, B.P.Imbimbo, R.Berni. Structural Evidence For Native State Stabilization of A Conformationally Labile Amyloidogenic Transthyretin Variant By Fibrillogenesis Inhibitors. Febs Lett. V. 587 2325 2013.
ISSN: ISSN 0014-5793
PubMed: 23792159
DOI: 10.1016/J.FEBSLET.2013.06.016