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Chlorine in PDB 8p5c: Crystal Structure of the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S.

Enzymatic activity of Crystal Structure of the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S.

All present enzymatic activity of Crystal Structure of the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S.:
3.4.22.69;

Protein crystallography data

The structure of Crystal Structure of the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S., PDB code: 8p5c was solved by E.Costanzi, N.Demitri, P.Storici, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.54 / 1.51
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 68.296, 99.864, 103.777, 90, 90, 90
R / Rfree (%) 15.9 / 17.8

Other elements in 8p5c:

The structure of Crystal Structure of the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S. also contains other interesting chemical elements:

Sodium (Na) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S. (pdb code 8p5c). 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 the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S., PDB code: 8p5c:

Chlorine binding site 1 out of 1 in 8p5c

Go back to Chlorine Binding Sites List in 8p5c
Chlorine binding site 1 out of 1 in the Crystal Structure of the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S.


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 the Main Protease (3CLPRO/Mpro) of Sars-Cov-2 Obtained in Presence of 5 Millimolar X77 Enantiomer S. within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl404

b:16.9
occ:1.00
 H B:THR224 2.5 26.5 1.0
HA B:PHE223 3.0 25.9 1.0
HD1 B:PHE223 3.0 28.3 1.0
HG22 B:THR224 3.2 32.4 1.0
N B:THR224 3.3 22.1 1.0
HB3 B:PHE223 3.5 26.0 1.0
CA B:PHE223 3.8 21.6 1.0
O B:THR224 3.8 26.7 1.0
CD1 B:PHE223 3.9 23.6 1.0
CB B:PHE223 4.0 21.7 1.0
CG2 B:THR224 4.1 26.9 1.0
C B:PHE223 4.1 21.2 1.0
HG23 B:THR224 4.2 32.4 1.0
CA B:THR224 4.3 21.9 1.0
C B:THR224 4.4 25.5 1.0
CG B:PHE223 4.5 22.3 1.0
HG21 B:THR224 4.7 32.4 1.0
CB B:THR224 4.7 22.6 1.0
O B:ARG222 4.7 22.1 1.0
O B:HOH709 4.8 52.6 1.0
O B:HOH680 4.9 39.2 1.0
HB B:THR224 4.9 27.1 1.0
HB2 B:PHE223 4.9 26.0 1.0
CE1 B:PHE223 5.0 24.3 1.0
N B:PHE223 5.0 20.9 1.0
HE1 B:PHE223 5.0 29.1 1.0

Reference:

S.Albani, E.Costanzi, G.L.Hoang, M.Kuzikov, M.Frings, N.Ansari, N.Demitri, T.T.Nguyen, V.Rizzi, J.B.Schulz, C.Bolm, A.Zaliani, P.Carloni, P.Storici, G.Rossetti. Unexpected Single-Ligand Occupancy and Negative Cooperativity in the Sars-Cov-2 Main Protease. J.Chem.Inf.Model. V. 64 892 2024.
ISSN: ESSN 1549-960X
PubMed: 38051605
DOI: 10.1021/ACS.JCIM.3C01497
Page generated: Sun Jul 13 13:03:42 2025

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