Atomistry » Fluorine » PDB 6qy8-6rkn » 6rkn
Atomistry »
  Fluorine »
    PDB 6qy8-6rkn »
      6rkn »

Fluorine in PDB 6rkn: Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.

Enzymatic activity of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.

All present enzymatic activity of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.:
4.2.1.1;

Protein crystallography data

The structure of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide., PDB code: 6rkn was solved by S.Gloeckner, A.Heine, G.Klebe, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 40.98 / 0.96
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 42.339, 41.555, 72.163, 90.00, 104.57, 90.00
R / Rfree (%) 10.8 / 12.4

Other elements in 6rkn:

The structure of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide. also contains other interesting chemical elements:

Mercury (Hg) 2 atoms
Zinc (Zn) 1 atom

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide. (pdb code 6rkn). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 2 binding sites of Fluorine where determined in the Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide., PDB code: 6rkn:
Jump to Fluorine binding site number: 1; 2;

Fluorine binding site 1 out of 2 in 6rkn

Go back to Fluorine Binding Sites List in 6rkn
Fluorine binding site 1 out of 2 in the Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 1 of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F304

b:14.1
occ:1.00
F11 A:FBS304 0.0 14.1 1.0
C01 A:FBS304 1.4 10.8 1.0
C02 A:FBS304 2.3 9.6 1.0
C06 A:FBS304 2.3 9.6 1.0
HZ A:PHE131 3.0 13.4 1.0
HD13 A:LEU198 3.5 9.9 1.0
C03 A:FBS304 3.6 8.4 1.0
C05 A:FBS304 3.6 7.8 1.0
HD22 A:LEU198 3.7 9.9 1.0
O A:HOH609 3.8 34.2 1.0
CZ A:PHE131 3.8 11.2 1.0
O A:HOH405 4.1 22.5 1.0
C04 A:FBS304 4.1 6.6 1.0
HE21 A:GLN92 4.2 10.3 1.0
HD11 A:LEU198 4.2 9.9 1.0
HE2 A:PHE131 4.2 13.9 1.0
HD21 A:LEU198 4.2 9.9 1.0
O A:HOH586 4.2 11.2 1.0
CD1 A:LEU198 4.2 8.3 1.0
CD2 A:LEU198 4.4 8.2 1.0
CE2 A:PHE131 4.5 11.6 1.0
HE22 A:GLN92 4.6 10.3 1.0
NE2 A:GLN92 4.7 8.6 1.0
HE1 A:PHE131 4.8 12.1 1.0
CE1 A:PHE131 4.8 10.1 1.0
HG11 A:VAL121 4.8 7.3 1.0
HD2 A:PRO202 4.8 11.1 1.0
CG A:LEU198 4.9 7.1 1.0
HB3 A:LEU198 5.0 6.5 1.0
HD12 A:LEU198 5.0 9.9 1.0

Fluorine binding site 2 out of 2 in 6rkn

Go back to Fluorine Binding Sites List in 6rkn
Fluorine binding site 2 out of 2 in the Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide.


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Human Carbonic Anhydrase II in Complex with A Fluorinated Benzenesulfonamide. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F305

b:14.3
occ:0.90
F11 A:FBS305 0.0 14.3 0.9
C01 A:FBS305 1.4 11.7 0.9
C02 A:FBS305 2.3 12.4 0.9
C06 A:FBS305 2.3 11.4 0.9
C03 A:FBS305 3.6 12.1 0.9
C05 A:FBS305 3.6 10.2 0.9
O A:HOH616 3.9 34.1 1.0
C04 A:FBS305 4.1 9.1 0.9
O A:HOH433 4.3 14.1 1.0
O A:HOH595 4.6 9.9 1.0
O A:HOH504 4.7 15.7 1.0
O A:HIS10 4.9 11.9 1.0
HB3 A:ASN11 4.9 14.7 1.0

Reference:

S.Glockner, K.Ngo, B.Wagner, A.Heine, G.Klebe. The Influence of Varying Fluorination Patterns on the Thermodynamics and Kinetics of Benzenesulfonamide Binding to Human Carbonic Anhydrase II. Biomolecules V. 10 2020.
ISSN: ESSN 2218-273X
PubMed: 32230853
DOI: 10.3390/BIOM10040509
Page generated: Fri Aug 2 01:15:20 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