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Chlorine in PDB 2q96: E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18

Enzymatic activity of E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18

All present enzymatic activity of E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18:
3.4.11.18;

Protein crystallography data

The structure of E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18, PDB code: 2q96 was solved by Q.-Z.Ye, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.94 / 1.60
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 39.285, 62.028, 52.426, 90.00, 108.76, 90.00
R / Rfree (%) 21.1 / 23.5

Other elements in 2q96:

The structure of E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18 also contains other interesting chemical elements:

Manganese (Mn) 2 atoms
Sodium (Na) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18 (pdb code 2q96). 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 E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18, PDB code: 2q96:

Chlorine binding site 1 out of 1 in 2q96

Go back to Chlorine Binding Sites List in 2q96
Chlorine binding site 1 out of 1 in the E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of E. Coli Methionine Aminopeptidase Mn-Form with Inhibitor A18 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl400

b:1.0
occ:1.00
CLAP A:A18400 0.0 1.0 1.0
CAJ A:A18400 1.7 12.3 1.0
CAK A:A18400 2.7 12.8 1.0
CAI A:A18400 2.7 13.5 1.0
CAL A:A18400 3.1 13.1 1.0
CAD A:A18400 3.4 14.2 1.0
SG A:CYS59 3.5 12.1 1.0
CB A:CYS59 3.5 8.0 1.0
CAC A:A18400 3.6 14.3 1.0
CA A:CYS59 3.7 10.5 1.0
CD2 A:TYR62 3.8 11.3 1.0
CAF A:A18400 4.0 14.4 1.0
CAH A:A18400 4.0 15.8 1.0
CE2 A:PHE177 4.0 9.2 1.0
CB A:TYR62 4.2 11.9 1.0
CG A:TYR62 4.3 10.8 1.0
SG A:CYS70 4.3 8.2 1.0
O A:CYS59 4.3 10.1 1.0
CZ A:PHE177 4.4 7.8 1.0
OAM A:A18400 4.5 11.3 1.0
CAG A:A18400 4.5 16.0 1.0
C A:CYS59 4.5 10.2 1.0
CE2 A:TYR62 4.5 11.5 1.0
O A:HOH519 4.6 11.2 1.0
CD2 A:TYR65 4.6 9.8 1.0
CAB A:A18400 4.6 13.6 1.0
N A:CYS59 4.7 9.0 1.0
O A:ALA58 4.9 11.4 1.0
CG A:TYR65 4.9 9.6 1.0
CE2 A:TYR65 5.0 10.9 1.0

Reference:

Z.Q.Ma, S.X.Xie, Q.Q.Huang, F.J.Nan, T.D.Hurley, Q.Z.Ye. Structural Analysis of Inhibition of E. Coli Methionine Aminopeptidase: Implication of Loop Flexibility in Selective Inhibition of Bacterial Enzymes. Bmc Struct.Biol. V. 7 84 2007.
ISSN: ESSN 1472-6807
PubMed: 18093325
DOI: 10.1186/1472-6807-7-84
Page generated: Sat Jul 20 10:33:10 2024

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