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Zinc in PDB 2o4z: Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor

Enzymatic activity of Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor

All present enzymatic activity of Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor:
4.2.1.1;

Protein crystallography data

The structure of Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor, PDB code: 2o4z was solved by C.Temperini, J.Y.Winum, J.L.Montero, A.Scozzafava, C.T.Supuran, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 2.10
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 42.100, 41.390, 72.300, 90.00, 104.38, 90.00
R / Rfree (%) 20.8 / 26.6

Other elements in 2o4z:

The structure of Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor also contains other interesting chemical elements:

Mercury (Hg) 1 atom

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor (pdb code 2o4z). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total only one binding site of Zinc was determined in the Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor, PDB code: 2o4z:

Zinc binding site 1 out of 1 in 2o4z

Go back to Zinc Binding Sites List in 2o4z
Zinc binding site 1 out of 1 in the Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Crystal Structure of the Carbonic Anhydrase II Complexed with Hydroxysulfamide Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn262

b:12.1
occ:1.00
N1 A:HSW300 1.9 17.9 1.0
NE2 A:HIS94 1.9 3.8 1.0
NE2 A:HIS96 2.0 6.9 1.0
ND1 A:HIS119 2.1 9.8 1.0
CD2 A:HIS94 2.8 4.5 1.0
CE1 A:HIS119 3.0 8.8 1.0
CE1 A:HIS96 3.0 6.7 1.0
CE1 A:HIS94 3.0 6.9 1.0
CD2 A:HIS96 3.0 7.7 1.0
S1 A:HSW300 3.1 16.6 1.0
CG A:HIS119 3.1 8.5 1.0
O2 A:HSW300 3.2 18.8 1.0
CB A:HIS119 3.5 7.8 1.0
OG1 A:THR199 3.9 9.8 1.0
O3 A:HSW300 3.9 23.9 1.0
CG A:HIS94 4.0 6.9 1.0
O1 A:HSW300 4.0 17.5 1.0
ND1 A:HIS94 4.0 5.2 1.0
ND1 A:HIS96 4.1 7.2 1.0
NE2 A:HIS119 4.1 9.9 1.0
OE1 A:GLU106 4.1 6.2 1.0
CG A:HIS96 4.2 8.2 1.0
N2 A:HSW300 4.2 19.8 1.0
CD2 A:HIS119 4.2 9.3 1.0
O A:HOH441 4.6 27.1 1.0
CD A:GLU106 5.0 7.0 1.0
CA A:HIS119 5.0 7.8 1.0

Reference:

C.Temperini, J.Y.Winum, J.L.Montero, A.Scozzafava, C.T.Supuran. Carbonic Anhydrase Inhibitors: the X-Ray Crystal Structure of the Adduct of N-Hydroxysulfamide with Isozyme II Explains Why This New Zinc Binding Function Is Effective in the Design of Potent Inhibitors. Bioorg.Med.Chem.Lett. V. 17 2795 2007.
ISSN: ISSN 0960-894X
PubMed: 17346964
DOI: 10.1016/J.BMCL.2007.02.068
Page generated: Wed Dec 16 03:45:19 2020

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