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Chlorine in PDB 5q0o: Ligand Binding to Farnesoid-X-Receptor

Protein crystallography data

The structure of Ligand Binding to Farnesoid-X-Receptor, PDB code: 5q0o was solved by M.G.Rudolph, J.Benz, D.Burger, R.Thoma, A.Ruf, C.Joseph, B.Kuhn, C.Shao, H.Yang, S.K.Burley, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 27.82 / 1.90
Space group C 2 2 21
Cell size a, b, c (Å), α, β, γ (°) 72.012, 83.684, 188.652, 90.00, 90.00, 90.00
R / Rfree (%) 19.1 / 22.2

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Ligand Binding to Farnesoid-X-Receptor (pdb code 5q0o). 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 Ligand Binding to Farnesoid-X-Receptor, PDB code: 5q0o:

Chlorine binding site 1 out of 1 in 5q0o

Go back to Chlorine Binding Sites List in 5q0o
Chlorine binding site 1 out of 1 in the Ligand Binding to Farnesoid-X-Receptor


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Ligand Binding to Farnesoid-X-Receptor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl501

b:28.5
occ:1.00
O A:HOH715 3.0 41.6 1.0
NE2 A:GLN420 3.2 29.3 1.0
O A:HOH681 3.4 22.7 1.0
CB A:PHE434 3.7 21.1 1.0
CG A:GLN420 3.8 27.9 1.0
CE A:LYS424 4.0 51.4 1.0
CD A:GLN420 4.0 40.7 1.0
O A:HOH607 4.1 35.0 1.0
CD2 A:PHE434 4.1 23.4 1.0
O A:PRO431 4.3 28.1 1.0
CG A:PHE434 4.3 21.9 1.0
NZ A:LYS424 4.5 56.6 1.0
CG A:LYS424 4.5 40.5 1.0
CD A:LYS424 4.8 45.9 1.0
O A:HOH771 4.9 43.8 1.0
CA A:PHE434 4.9 19.4 1.0
N A:PHE434 5.0 19.9 1.0
O A:GLN420 5.0 22.2 1.0

Reference:

Z.Gaieb, S.Liu, S.Gathiaka, M.Chiu, H.Yang, C.Shao, V.A.Feher, W.P.Walters, B.Kuhn, M.G.Rudolph, S.K.Burley, M.K.Gilson, R.E.Amaro. D3R Grand Challenge 2: Blind Prediction of Protein-Ligand Poses, Affinity Rankings, and Relative Binding Free Energies. J. Comput. Aided Mol. Des. V. 32 1 2018.
ISSN: ISSN 1573-4951
PubMed: 29204945
DOI: 10.1007/S10822-017-0088-4
Page generated: Sat Jul 12 07:19:19 2025

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