Atomistry » Mercury » PDB 3kbc-3wa8 » 3kne
Atomistry »
  Mercury »
    PDB 3kbc-3wa8 »
      3kne »

Mercury in PDB 3kne: Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole

Enzymatic activity of Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole

All present enzymatic activity of Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole:
4.2.1.1;

Protein crystallography data

The structure of Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole, PDB code: 3kne was solved by J.Schulze-Wischeler, A.Heine, G.Klebe, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 10.00 / 1.35
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 42.400, 41.500, 72.000, 90.00, 104.30, 90.00
R / Rfree (%) 12.8 / 18.3

Other elements in 3kne:

The structure of Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole also contains other interesting chemical elements:

Zinc (Zn) 1 atom

Mercury Binding Sites:

The binding sites of Mercury atom in the Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole (pdb code 3kne). This binding sites where shown within 5.0 Angstroms radius around Mercury atom.
In total only one binding site of Mercury was determined in the Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole, PDB code: 3kne:

Mercury binding site 1 out of 1 in 3kne

Go back to Mercury Binding Sites List in 3kne
Mercury binding site 1 out of 1 in the Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole


Mono view


Stereo pair view

A full contact list of Mercury with other atoms in the Hg binding site number 1 of Carbonic Anhydrase II H64C Mutant in Complex with An in Situ Formed Triazole within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Hg501

b:22.2
occ:1.00
 HG A:BE7501 0.0 22.2 1.0
C5 A:BE7501 2.1 7.5 1.0
SG A:CYS205 2.1 23.5 1.0
C4 A:BE7501 2.9 18.0 1.0
O A:GLN136 3.0 10.9 1.0
C6 A:BE7501 3.1 24.6 1.0
O A:GLU204 3.1 12.2 1.0
CB A:CYS205 3.1 16.9 1.0
C A:GLN136 3.4 8.8 1.0
C A:GLU204 3.4 8.6 1.0
CA A:CYS205 3.4 8.1 1.0
N A:CYS205 3.7 7.3 1.0
N A:GLN136 3.7 10.3 1.0
O A:HOH1171 3.9 21.3 1.0
N A:PRO137 3.9 9.6 1.0
O A:VAL134 4.0 16.8 1.0
CA A:GLN136 4.0 10.4 1.0
C A:GLN135 4.1 13.5 1.0
CA A:PRO137 4.1 11.0 1.0
N A:GLU204 4.2 9.2 1.0
C3 A:BE7501 4.3 23.0 1.0
CA A:GLU204 4.3 8.9 1.0
C7 A:BE7501 4.4 20.4 1.0
C A:VAL134 4.4 11.5 1.0
CA A:GLN135 4.6 13.9 1.0
O A:GLN135 4.6 14.3 1.0
N A:GLN135 4.8 12.8 1.0
C A:LEU203 4.8 7.1 1.0
C A:CYS205 4.9 9.0 1.0
CB A:LEU203 4.9 9.9 1.0
C2 A:BE7501 4.9 18.2 1.0
CD A:PRO137 4.9 11.8 1.0
CB A:GLU204 5.0 10.0 1.0

Reference:

J.Schulze Wischeler, D.Sun, N.U.Sandner, U.Linne, A.Heine, U.Koert, G.Klebe. Stereo- and Regioselective Azide/Alkyne Cycloadditions in Carbonic Anhydrase II Via Tethering, Monitored By Crystallography and Mass Spectrometry. Chemistry V. 17 5842 2011.
ISSN: ISSN 0947-6539
PubMed: 21506176
DOI: 10.1002/CHEM.201002437
Page generated: Sun Aug 11 04:00:31 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy