Chlorine in PDB 4wf0: Crystal Structure of Ilid - An Improved Light-Inducible Dimer

The structure of Crystal Structure of Ilid - An Improved Light-Inducible Dimer, PDB code: 4wf0 was solved by R.Hallett, T.Williams, B.Kuhlman, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	31.08 / 1.95
Space group	P 21 21 21
Cell size a, b, c (Å), α, β, γ (°)	62.156, 70.339, 80.378, 90.00, 90.00, 90.00
R / Rfree (%)	23.1 / 24.4

The binding sites of Chlorine atom in the Crystal Structure of Ilid - An Improved Light-Inducible Dimer (pdb code 4wf0). 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 Crystal Structure of Ilid - An Improved Light-Inducible Dimer, PDB code: 4wf0:

Chlorine binding site 1 out of 1 in the Crystal Structure of Ilid - An Improved Light-Inducible Dimer


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of Ilid - An Improved Light-Inducible Dimer within 5.0Å range: probe atom residue distance (Å) B Occ B:Cl602 b:29.8 occ:1.00 H B:ARG442 2.6 27.5 1.0 HB2 B:ARG442 2.7 34.0 1.0 O B:HOH710 3.0 35.1 1.0 HG3 B:ARG442 3.2 35.2 1.0 N B:ARG442 3.4 22.9 1.0 HB2 B:SER441 3.5 32.7 1.0 CB B:ARG442 3.5 28.3 1.0 HH11 B:ARG442 3.6 35.4 1.0 CG B:ARG442 3.8 29.4 1.0 HD13 B:LEU435 4.0 33.6 1.0 CA B:ARG442 4.1 23.2 1.0 HA B:SER441 4.1 26.8 1.0 HD2 B:ARG442 4.1 43.1 1.0 OE1 B:GLU443 4.2 24.3 1.0 HB3 B:ARG442 4.3 34.0 1.0 H B:GLU443 4.3 27.8 1.0 CB B:SER441 4.3 27.2 1.0 NH1 B:ARG442 4.3 29.5 1.0 C B:SER441 4.4 23.0 1.0 CA B:SER441 4.5 22.3 1.0 CD B:ARG442 4.6 35.9 1.0 HG2 B:ARG442 4.6 35.2 1.0 HH12 B:ARG442 4.6 35.4 1.0 HB3 B:SER441 4.7 32.7 1.0 HD11 B:LEU435 4.8 33.6 1.0 CD1 B:LEU435 4.8 28.0 1.0 HA B:ARG442 4.8 27.8 1.0 N B:GLU443 4.9 23.2 1.0

R.A.Hallett, G.Guntas, T.Williams, S.P.Zimmerman, H.Yumerefendi, B.Kuhlman, J.E.Bear. Engineering An Improved Light-Induced Dimer (Ilid) For Controlling the Localization and Activity of Signaling Proteins To Be Published.