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Zinc in PDB 4q09: Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor

Enzymatic activity of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor

All present enzymatic activity of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor:
4.2.1.1;

Protein crystallography data

The structure of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor, PDB code: 4q09 was solved by A.Smirnov, E.Manakova, S.Grazulis, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 69.03 / 1.20
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 41.835, 41.011, 71.006, 90.00, 103.56, 90.00
R / Rfree (%) 13.9 / 17.8

Other elements in 4q09:

The structure of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor also contains other interesting chemical elements:

Fluorine (F) 3 atoms

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor (pdb code 4q09). 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 Chimeric Carbonic Anhydrase XII with Inhibitor, PDB code: 4q09:

Zinc binding site 1 out of 1 in 4q09

Go back to Zinc Binding Sites List in 4q09
Zinc binding site 1 out of 1 in the Crystal Structure of Chimeric Carbonic Anhydrase XII with 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 Chimeric Carbonic Anhydrase XII with Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn301

b:7.6
occ:1.00
N10 A:V14302 1.9 10.4 1.0
NE2 A:HIS96 2.0 8.8 1.0
ND1 A:HIS119 2.0 8.0 1.0
NE2 A:HIS94 2.0 8.4 1.0
CE1 A:HIS119 2.9 8.3 1.0
CD2 A:HIS96 3.0 8.6 1.0
CD2 A:HIS94 3.0 7.8 1.0
CE1 A:HIS96 3.0 8.7 1.0
CE1 A:HIS94 3.1 8.1 1.0
S7 A:V14302 3.1 8.7 1.0
F12 A:V14302 3.1 12.4 1.0
CG A:HIS119 3.1 7.5 1.0
O9 A:V14302 3.3 8.9 1.0
CB A:HIS119 3.5 8.6 1.0
C3 A:V14302 3.7 10.7 1.0
C4 A:V14302 3.7 10.1 1.0
OE1 A:GLU106 3.8 8.9 1.0
OG1 A:THR198 3.9 7.5 1.0
NE2 A:HIS119 4.1 8.2 1.0
ND1 A:HIS94 4.2 7.7 1.0
CG A:HIS94 4.2 8.2 1.0
ND1 A:HIS96 4.2 9.3 1.0
CG A:HIS96 4.2 8.4 1.0
CD2 A:HIS119 4.2 8.4 1.0
O8 A:V14302 4.3 9.4 1.0
C2 A:V14302 4.8 13.7 1.0
CD A:GLU106 4.8 8.2 1.0
C5 A:V14302 4.9 11.2 1.0
CH2 A:TRP208 4.9 9.4 1.0

Reference:

V.Dudutiene, J.Matuliene, A.Smirnov, D.D.Timm, A.Zubriene, L.Baranauskiene, V.Morkunaite, J.Smirnoviene, V.Michailoviene, V.Juozapaitiene, A.Mickeviciute, J.Kazokaite, S.Baksyte, A.Kasiliauskaite, J.Jachno, J.Revuckiene, M.Kisonaite, V.Pilipuityte, E.Ivanauskaite, G.Milinaviciute, V.Smirnovas, V.Petrikaite, V.Kairys, V.Petrauskas, P.Norvaisas, D.Linge, P.Gibieza, E.Capkauskaite, A.Zaksauskas, E.Kazlauskas, E.Manakova, S.Grazulis, J.E.Ladbury, D.Matulis. Discovery and Characterization of Novel Selective Inhibitors of Carbonic Anhydrase IX. J.Med.Chem. V. 57 9435 2014.
ISSN: ISSN 0022-2623
PubMed: 25358084
DOI: 10.1021/JM501003K
Page generated: Sun Oct 27 06:13:04 2024

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