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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: Tue Jul 15 15:20:58 2025

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