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Chlorine in PDB 3rmm: Human Thrombin in Complex with MI332

Enzymatic activity of Human Thrombin in Complex with MI332

All present enzymatic activity of Human Thrombin in Complex with MI332:
3.4.21.5;

Protein crystallography data

The structure of Human Thrombin in Complex with MI332, PDB code: 3rmm was solved by A.Biela, A.Heine, G.Klebe, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.50 / 1.58
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 70.100, 71.100, 72.700, 90.00, 100.40, 90.00
R / Rfree (%) 15.5 / 17.9

Other elements in 3rmm:

The structure of Human Thrombin in Complex with MI332 also contains other interesting chemical elements:

Sodium (Na) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Human Thrombin in Complex with MI332 (pdb code 3rmm). 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 Human Thrombin in Complex with MI332, PDB code: 3rmm:

Chlorine binding site 1 out of 1 in 3rmm

Go back to Chlorine Binding Sites List in 3rmm
Chlorine binding site 1 out of 1 in the Human Thrombin in Complex with MI332


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Human Thrombin in Complex with MI332 within 5.0Å range:
probe atom residue distance (Å) B Occ
H:Cl1

b:11.8
occ:1.00
CL3 H:M321 0.0 11.8 1.0
C29 H:M321 1.8 11.5 1.0
C31 H:M321 2.7 11.5 1.0
C28 H:M321 2.8 14.7 1.0
O H:TRP215 3.4 11.8 1.0
O H:PHE227 3.4 11.3 1.0
N H:PHE227 3.6 10.1 1.0
CA H:GLY226 3.7 12.2 1.0
CG1 H:VAL213 3.8 10.1 1.0
CB H:ALA190 3.9 14.8 1.0
N H:TRP215 3.9 12.0 1.0
C H:TRP215 3.9 10.4 1.0
CZ H:TYR228 4.0 9.6 1.0
C H:GLY226 4.0 11.4 1.0
C24 H:M321 4.0 10.7 1.0
N H:SER214 4.0 10.3 1.0
C27 H:M321 4.0 14.7 1.0
OH H:TYR228 4.1 11.6 1.0
CE2 H:TYR228 4.2 11.3 1.0
C H:PHE227 4.2 10.8 1.0
CE1 H:TYR228 4.3 11.8 1.0
CA H:TRP215 4.3 11.5 1.0
OD1 H:ASP189 4.4 12.9 1.0
CA H:PHE227 4.5 9.3 1.0
C H:SER214 4.5 10.7 1.0
C25 H:M321 4.5 14.5 1.0
CA H:VAL213 4.6 8.2 1.0
C H:VAL213 4.7 10.1 1.0
N H:GLY216 4.7 13.5 1.0
CD2 H:TYR228 4.7 10.4 1.0
CB H:VAL213 4.7 8.2 1.0
CD1 H:TYR228 4.8 12.1 1.0
O H:HOH1064 4.8 14.0 1.0
CA H:SER214 4.9 9.8 1.0
CA H:ALA190 5.0 14.6 1.0
O H:GLY226 5.0 12.6 1.0

Reference:

A.Biela, F.Sielaff, F.Terwesten, A.Heine, T.Steinmetzer, G.Klebe. Ligand Binding Stepwise Disrupts Water Network in Thrombin: Enthalpic and Entropic Changes Reveal Classical Hydrophobic Effect J.Med.Chem. V. 55 6094 2012.
ISSN: ISSN 0022-2623
PubMed: 22612268
DOI: 10.1021/JM300337Q
Page generated: Fri Jul 11 09:54:01 2025

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