Atomistry » Mercury » PDB 7ca2-7tfw » 7ntb
Atomistry »
  Mercury »
    PDB 7ca2-7tfw »
      7ntb »

Mercury in PDB 7ntb: Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative

Enzymatic activity of Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative

All present enzymatic activity of Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative:
4.2.1.1;

Protein crystallography data

The structure of Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative, PDB code: 7ntb was solved by A.Di Fiore, G.De Simone, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 1.70
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 42.14, 41.31, 72.1, 90, 104.39, 90
R / Rfree (%) 17.3 / 21.7

Other elements in 7ntb:

The structure of Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative also contains other interesting chemical elements:

Zinc (Zn) 1 atom

Mercury Binding Sites:

The binding sites of Mercury atom in the Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative (pdb code 7ntb). 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 Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative, PDB code: 7ntb:

Mercury binding site 1 out of 1 in 7ntb

Go back to Mercury Binding Sites List in 7ntb
Mercury binding site 1 out of 1 in the Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative


Mono view


Stereo pair view

A full contact list of Mercury with other atoms in the Hg binding site number 1 of Crystal Structure of Human Carbonic Anhydrase with A Benzophenone- Derivative within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Hg303

b:13.7
occ:1.00
 HG A:MBO303 0.0 13.7 1.0
CE1 A:MBO303 2.0 13.2 1.0
SG A:CYS206 2.2 11.5 1.0
O A:HOH655 2.9 25.6 1.0
O A:GLU205 3.0 7.3 1.0
CE6 A:MBO303 3.0 14.4 1.0
CE2 A:MBO303 3.0 13.2 1.0
O A:GLN137 3.1 7.2 1.0
CB A:CYS206 3.1 10.0 1.0
C A:GLU205 3.3 7.6 1.0
CA A:CYS206 3.5 7.0 1.0
C A:GLN137 3.5 8.9 1.0
N A:CYS206 3.6 6.3 1.0
N A:GLN137 3.9 12.2 1.0
O A:HOH605 4.0 18.1 1.0
N A:PRO138 4.0 9.0 1.0
C A:GLN136 4.1 15.4 1.0
CA A:PRO138 4.1 9.3 1.0
N A:GLU205 4.2 5.4 1.0
CA A:GLN137 4.2 9.4 1.0
CA A:GLU205 4.3 5.5 1.0
CE5 A:MBO303 4.3 13.9 1.0
CE3 A:MBO303 4.4 13.9 1.0
O A:VAL135 4.4 17.1 1.0
O A:GLN136 4.5 14.3 1.0
CA A:GLN136 4.5 17.0 1.0
C A:VAL135 4.7 15.4 1.0
N A:GLN136 4.8 15.5 1.0
CB A:GLU205 4.9 5.9 1.0
CE4 A:MBO303 4.9 13.2 1.0
C A:CYS206 4.9 6.7 1.0
C A:LEU204 5.0 6.7 1.0

Reference:

D.Pagnozzi, N.Pala, G.Biosa, R.Dallocchio, A.Dessi, P.K.Singh, D.Rogolino, A.Di Fiore, G.De Simone, C.T.Supuran, M.Sechi. Interaction Studies Between Carbonic Anhydrase and A Sulfonamide Inhibitor By Experimental and Theoretical Approaches Acs Med.Chem.Lett. V. 13 271 2022.
ISSN: ISSN 1948-5875
DOI: 10.1021/ACSMEDCHEMLETT.1C00644
Page generated: Sun Aug 11 08:39:51 2024

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy