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Chlorine in PDB 7sfi: Sars-Cov-2 Main Protease (Mpro) in Complex with ML104

Enzymatic activity of Sars-Cov-2 Main Protease (Mpro) in Complex with ML104

All present enzymatic activity of Sars-Cov-2 Main Protease (Mpro) in Complex with ML104:
3.4.22.69;

Protein crystallography data

The structure of Sars-Cov-2 Main Protease (Mpro) in Complex with ML104, PDB code: 7sfi 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) 35.24 / 1.95
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 45.49, 63.586, 105.64, 90, 90, 90
R / Rfree (%) 19.5 / 23.9

Other elements in 7sfi:

The structure of Sars-Cov-2 Main Protease (Mpro) in Complex with ML104 also contains other interesting chemical elements:

Fluorine (F) 3 atoms
Calcium (Ca) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Sars-Cov-2 Main Protease (Mpro) in Complex with ML104 (pdb code 7sfi). 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 ML104, PDB code: 7sfi:

Chlorine binding site 1 out of 1 in 7sfi

Go back to Chlorine Binding Sites List in 7sfi
Chlorine binding site 1 out of 1 in the Sars-Cov-2 Main Protease (Mpro) in Complex with ML104


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 ML104 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl402

b:45.4
occ:0.50
N A:ALA285 3.6 27.5 1.0
OG A:SER284 3.7 38.8 1.0
N A:LEU286 4.1 28.1 1.0
CB A:ALA285 4.2 32.1 1.0
CG A:LEU286 4.3 30.3 1.0
CA A:SER284 4.3 29.6 1.0
CA A:ALA285 4.3 29.8 1.0
CD1 A:LEU286 4.4 32.7 1.0
CB A:SER284 4.4 29.2 1.0
C A:SER284 4.5 29.6 1.0
C A:ALA285 4.6 28.7 1.0
CB A:LEU286 4.7 28.3 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: Tue Jul 30 04:11:46 2024

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