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Chlorine in PDB 7sf3: Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M

Enzymatic activity of Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M

All present enzymatic activity of Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M:
3.4.22.69;

Protein crystallography data

The structure of Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M, PDB code: 7sf3 was solved by M.Westberg, D.Fernandez, M.Z.Lin, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 37.30 / 1.75
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 45.684, 64.44, 105.449, 90, 90, 90
R / Rfree (%) 16.9 / 19.5

Other elements in 7sf3:

The structure of Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M also contains other interesting chemical elements:

Fluorine (F) 3 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M (pdb code 7sf3). 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 Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M, PDB code: 7sf3:

Chlorine binding site 1 out of 1 in 7sf3

Go back to Chlorine Binding Sites List in 7sf3
Chlorine binding site 1 out of 1 in the Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Sars-Cov-2 Main Protease (Mpro) in Complex with ML1006M within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl402

b:54.9
occ:0.50
N A:ALA285 3.6 26.9 1.0
OG A:SER284 3.7 37.4 1.0
N A:LEU286 4.2 25.4 1.0
CG A:LEU286 4.3 34.1 1.0
CB A:ALA285 4.3 30.7 1.0
CA A:SER284 4.3 27.9 1.0
CA A:ALA285 4.4 29.2 1.0
CD1 A:LEU286 4.4 38.1 1.0
CB A:SER284 4.5 29.7 1.0
C A:SER284 4.5 26.6 1.0
C A:ALA285 4.7 27.5 1.0
CB A:LEU286 4.7 27.9 1.0

Reference:

M.Westberg, Y.Su, X.Zou, A.Rustagi, A.Beck, L.Ning, D.Fernandez, C.Blish, M.Z.Lin. Rational Design of A New Class of Protease Inhibitors For the Potential Treatment of Coronavirus Diseases To Be Published.
Page generated: Sun Jul 13 07:05:13 2025

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