Chlorine in PDB 8w0c: Crystal Structure of Acetyl-Coa Synthetase 2 From Candida Albicans in Complex with A Cyclopentyl Ester Amp Inhibitor

The structure of Crystal Structure of Acetyl-Coa Synthetase 2 From Candida Albicans in Complex with A Cyclopentyl Ester Amp Inhibitor, PDB code: 8w0c was solved by Seattle Structural Genomics Center For Infectious Disease, Seattlestructural Genomics Center For Infectious Disease (Ssgcid), with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	49.58 / 2.35
Space group	P 61 2 2
Cell size a, b, c (Å), α, β, γ (°)	139.409, 139.409, 543.793, 90, 90, 120
R / Rfree (%)	18.1 / 21

The structure of Crystal Structure of Acetyl-Coa Synthetase 2 From Candida Albicans in Complex with A Cyclopentyl Ester Amp Inhibitor also contains other interesting chemical elements:

Sodium

(Na)

2 atoms

The binding sites of Chlorine atom in the Crystal Structure of Acetyl-Coa Synthetase 2 From Candida Albicans in Complex with A Cyclopentyl Ester Amp Inhibitor (pdb code 8w0c). 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 Acetyl-Coa Synthetase 2 From Candida Albicans in Complex with A Cyclopentyl Ester Amp Inhibitor, PDB code: 8w0c:

Chlorine binding site 1 out of 1 in the Crystal Structure of Acetyl-Coa Synthetase 2 From Candida Albicans in Complex with A Cyclopentyl Ester Amp Inhibitor


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 Acetyl-Coa Synthetase 2 From Candida Albicans in Complex with A Cyclopentyl Ester Amp Inhibitor within 5.0Å range: probe atom residue distance (Å) B Occ B:Cl703 b:81.0 occ:1.00 O B:HOH839 3.5 63.7 1.0 NH1 B:ARG618 3.7 58.4 1.0 NH2 B:ARG618 3.9 59.4 1.0 CZ B:ARG618 4.2 48.8 1.0 CG1 B:VAL614 4.7 55.8 1.0

L.Liu, S.Lovell, K.P.Battaile. Crystal Structure of Acetyl-Coa Synthetase 2 From Candida Albicans in Complex with A Cyclopentyl Ester Amp Inhibitor To Be Published.