Chlorine in PDB 5kgl: 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form)

All present enzymatic activity of 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form):
5.4.2.12;

The structure of 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form), PDB code: 5kgl was solved by S.Lovell, N.Mehzabeen, K.P.Battaile, H.Yu, P.Dranchak, R.Macarthur, Z.Li, T.Carlow, H.Suga, J.Inglese, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	40.44 / 2.45
Space group	P 21 21 21
Cell size a, b, c (Å), α, β, γ (°)	70.321, 98.852, 173.144, 90.00, 90.00, 90.00
R / Rfree (%)	18.5 / 26

The structure of 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form) also contains other interesting chemical elements:

Manganese	(Mn)	2 atoms
Zinc	(Zn)	2 atoms

The binding sites of Chlorine atom in the 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form) (pdb code 5kgl). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form), PDB code: 5kgl:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in the 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form)


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form) within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl601 b:37.0 occ:1.00 OH A:TYR212 3.6 22.7 1.0 O A:HOH775 4.0 19.1 1.0 CE1 A:TYR212 4.2 19.8 1.0 CZ A:TYR212 4.4 11.8 1.0 NZ A:LYS261 4.6 32.4 1.0 CE A:LYS261 4.7 12.3 1.0

Chlorine binding site 2 out of 2 in the 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form)


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of 2.45A Resolution Structure of Apo Independent Phosphoglycerate Mutase From C. Elegans (Orthorhombic Form) within 5.0Å range: probe atom residue distance (Å) B Occ B:Cl601 b:27.5 occ:1.00 OH B:TYR212 3.4 22.5 1.0 CE1 B:TYR212 4.1 23.6 1.0 CZ B:TYR212 4.3 26.8 1.0 NZ B:LYS261 4.5 24.7 1.0 CE B:LYS261 4.6 14.0 1.0

H.Yu, P.Dranchak, Z.Li, R.Macarthur, M.S.Munson, N.Mehzabeen, N.J.Baird, K.P.Battalie, D.Ross, S.Lovell, C.K.Carlow, H.Suga, J.Inglese. Macrocycle Peptides Delineate Locked-Open Inhibition Mechanism For Microorganism Phosphoglycerate Mutases. Nat Commun V. 8 14932 2017.
ISSN: ESSN 2041-1723
PubMed: 28368002
DOI: 10.1038/NCOMMS14932