Zinc in PDB 5th4: Crystal Structure of 1-Hydroxypyridine-2(1H)-Thione Bound to Human Carbonic Anhydrase 2 L198G

Enzymatic activity of Crystal Structure of 1-Hydroxypyridine-2(1H)-Thione Bound to Human Carbonic Anhydrase 2 L198G

All present enzymatic activity of Crystal Structure of 1-Hydroxypyridine-2(1H)-Thione Bound to Human Carbonic Anhydrase 2 L198G:
4.2.1.1;

Protein crystallography data

The structure of Crystal Structure of 1-Hydroxypyridine-2(1H)-Thione Bound to Human Carbonic Anhydrase 2 L198G, PDB code: 5th4 was solved by B.Dick, S.Cohen, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 40.00 / 1.47
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 42.200, 41.333, 72.159, 90.00, 104.65, 90.00
R / Rfree (%) 18.1 / 21.2

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of 1-Hydroxypyridine-2(1H)-Thione Bound to Human Carbonic Anhydrase 2 L198G (pdb code 5th4). 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 1-Hydroxypyridine-2(1H)-Thione Bound to Human Carbonic Anhydrase 2 L198G, PDB code: 5th4:

Zinc binding site 1 out of 1 in 5th4

Go back to Zinc Binding Sites List in 5th4
Zinc binding site 1 out of 1 in the Crystal Structure of 1-Hydroxypyridine-2(1H)-Thione Bound to Human Carbonic Anhydrase 2 L198G


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 1-Hydroxypyridine-2(1H)-Thione Bound to Human Carbonic Anhydrase 2 L198G within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn301

b:10.6
occ:1.00
 NE2 A:HIS96 2.0 8.6 1.0
NE2 A:HIS94 2.0 8.1 1.0
ND1 A:HIS119 2.1 7.6 1.0
O8 A:BEW302 2.4 30.9 1.0
S7 A:BEW302 2.6 21.9 1.0
CE1 A:HIS119 3.0 7.0 1.0
CD2 A:HIS96 3.0 8.3 1.0
CD2 A:HIS94 3.0 8.7 1.0
CE1 A:HIS94 3.1 7.4 1.0
N2 A:BEW302 3.1 33.8 1.0
CE1 A:HIS96 3.1 8.4 1.0
C1 A:BEW302 3.1 26.6 1.0
CG A:HIS119 3.2 6.8 1.0
CB A:HIS119 3.6 6.5 1.0
OG1 A:THR199 3.6 10.8 1.0
OE1 A:GLU106 4.0 9.6 1.0
NE2 A:HIS119 4.2 6.9 1.0
ND1 A:HIS96 4.2 8.1 1.0
CG A:HIS94 4.2 7.8 1.0
ND1 A:HIS94 4.2 7.8 1.0
CG A:HIS96 4.2 7.8 1.0
O A:HOH544 4.2 18.6 1.0
C3 A:BEW302 4.2 33.7 1.0
CD2 A:HIS119 4.3 7.4 1.0
C6 A:BEW302 4.4 33.7 1.0
O A:HOH503 4.4 33.5 1.0
CB A:THR199 5.0 8.7 1.0

Reference:

B.L.Dick, A.Patel, J.A.Mccammon, S.M.Cohen. Effect of Donor Atom Identity on Metal-Binding Pharmacophore Coordination. J. Biol. Inorg. Chem. V. 22 605 2017.
ISSN: ESSN 1432-1327
PubMed: 28389830
DOI: 10.1007/S00775-017-1454-3
Page generated: Wed Dec 16 10:55:44 2020

Last articles

Zn in 8WB0
Zn in 8WAX
Zn in 8WAU
Zn in 8WAZ
Zn in 8WAY
Zn in 8WAV
Zn in 8WAW
Zn in 8WAT
Zn in 8W7M
Zn in 8WD3
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy