Atomistry » Fluorine » PDB 4pb2-4q0d » 4q08
Atomistry »
  Fluorine »
    PDB 4pb2-4q0d »
      4q08 »

Fluorine in PDB 4q08: 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: 4q08 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) 40.65 / 1.07
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 41.821, 41.058, 71.468, 90.00, 103.56, 90.00
R / Rfree (%) 12.8 / 15.6

Other elements in 4q08:

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

Zinc (Zn) 1 atom

Fluorine Binding Sites:

The binding sites of Fluorine atom in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor (pdb code 4q08). This binding sites where shown within 5.0 Angstroms radius around Fluorine atom.
In total 6 binding sites of Fluorine where determined in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor, PDB code: 4q08:
Jump to Fluorine binding site number: 1; 2; 3; 4; 5; 6;

Fluorine binding site 1 out of 6 in 4q08

Go back to Fluorine Binding Sites List in 4q08
Fluorine binding site 1 out of 6 in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F 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:F305

b:10.6
occ:0.50
 F18 A:V90305 0.0 10.6 0.5
C5 A:V90305 1.3 8.4 0.5
C5 A:V90305 1.8 12.5 0.5
C4 A:V90305 1.9 11.4 0.5
F18 A:V90305 2.1 17.9 0.5
C6 A:V90305 2.3 7.3 0.5
C4 A:V90305 2.3 6.5 0.5
N7 A:V90305 2.4 12.2 0.5
C20 A:V90305 2.5 15.5 0.5
N7 A:V90305 2.7 6.9 0.5
C6 A:V90305 2.7 14.8 0.5
C21 A:V90305 2.7 9.0 0.5
C19 A:V90305 2.8 7.6 0.5
C3 A:V90305 2.9 9.2 0.5
C19 A:V90305 2.9 21.2 0.5
S12 A:V90305 2.9 15.6 0.5
C20 A:V90305 3.0 7.8 0.5
O A:HOH663 3.1 22.5 1.0
C14 A:V90305 3.3 20.9 0.5
C14 A:V90305 3.3 24.4 0.5
C21 A:V90305 3.3 10.6 0.5
OG1 A:THR199 3.3 10.7 1.0
C1 A:V90305 3.4 14.0 0.5
C2 A:V90305 3.5 10.4 0.5
C1 A:V90305 3.6 7.8 0.5
C3 A:V90305 3.6 6.1 0.5
C13 A:V90305 3.7 24.9 0.5
S12 A:V90305 3.8 21.5 0.5
O15 A:V90305 4.0 39.2 0.5
O15 A:V90305 4.0 15.0 0.5
C2 A:V90305 4.0 7.1 0.5
C13 A:V90305 4.1 18.9 0.5
O A:HOH716 4.1 31.6 1.0
C22 A:V90305 4.1 23.1 0.5
S8 A:V90305 4.2 9.4 0.5
C26 A:V90305 4.3 22.0 0.5
C26 A:V90305 4.3 8.8 0.5
O9 A:V90305 4.3 10.1 0.5
C23 A:V90305 4.5 10.5 0.5
C22 A:V90305 4.5 11.5 0.5
C25 A:V90305 4.6 17.8 0.5
F17 A:V90305 4.6 28.6 0.5
CB A:THR199 4.6 9.4 1.0
NE2 A:GLN92 4.7 12.3 0.5
F17 A:V90305 4.7 9.9 0.5
O10 A:V90305 4.7 10.7 0.5
F16 A:V90305 4.7 14.3 0.5
C25 A:V90305 4.8 14.6 0.5
NZ A:LYS67 4.8 23.6 0.5

Fluorine binding site 2 out of 6 in 4q08

Go back to Fluorine Binding Sites List in 4q08
Fluorine binding site 2 out of 6 in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 2 of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F305

b:17.9
occ:0.50
 F18 A:V90305 0.0 17.9 0.5
C5 A:V90305 1.4 12.5 0.5
C21 A:V90305 1.9 10.6 0.5
F18 A:V90305 2.1 10.6 0.5
C20 A:V90305 2.3 7.8 0.5
C6 A:V90305 2.4 14.8 0.5
C4 A:V90305 2.4 11.4 0.5
C20 A:V90305 2.6 15.5 0.5
C5 A:V90305 2.7 8.4 0.5
C19 A:V90305 2.7 21.2 0.5
N7 A:V90305 2.9 12.2 0.5
S12 A:V90305 3.0 21.5 0.5
NZ A:LYS67 3.0 23.6 0.5
C19 A:V90305 3.1 7.6 0.5
C6 A:V90305 3.2 7.3 0.5
CE A:LYS67 3.2 19.5 0.5
O A:HOH716 3.2 31.6 1.0
NE2 A:GLN92 3.3 12.3 0.5
C22 A:V90305 3.4 11.5 0.5
S12 A:V90305 3.4 15.6 0.5
OE1 A:GLN92 3.4 10.2 0.5
C4 A:V90305 3.5 6.5 0.5
NE2 A:GLN92 3.6 11.2 0.5
C1 A:V90305 3.7 14.0 0.5
C3 A:V90305 3.7 9.2 0.5
N7 A:V90305 3.7 6.9 0.5
C14 A:V90305 3.8 20.9 0.5
C21 A:V90305 3.8 9.0 0.5
CD A:GLN92 3.9 8.7 0.5
C23 A:V90305 4.0 10.5 0.5
C13 A:V90305 4.1 18.9 0.5
C2 A:V90305 4.2 10.4 0.5
C26 A:V90305 4.2 22.0 0.5
O15 A:V90305 4.2 15.0 0.5
O A:HOH717 4.2 28.3 1.0
CD A:GLN92 4.4 7.7 0.5
C1 A:V90305 4.4 7.8 0.5
CD A:LYS67 4.5 13.9 0.5
C26 A:V90305 4.6 8.8 0.5
O A:HOH663 4.6 22.5 1.0
C3 A:V90305 4.6 6.1 0.5
CD A:LYS67 4.7 11.7 0.5
C14 A:V90305 4.7 24.4 0.5
ND1 A:HIS94 4.7 7.1 1.0
F17 A:V90305 4.8 28.6 0.5
C13 A:V90305 4.8 24.9 0.5
OE1 A:GLN92 4.9 8.8 0.5
C2 A:V90305 4.9 7.1 0.5
CE1 A:HIS94 4.9 7.0 1.0
C22 A:V90305 5.0 23.1 0.5

Fluorine binding site 3 out of 6 in 4q08

Go back to Fluorine Binding Sites List in 4q08
Fluorine binding site 3 out of 6 in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 3 of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F305

b:9.9
occ:0.50
 F17 A:V90305 0.0 9.9 0.5
C25 A:V90305 0.5 17.8 0.5
C1 A:V90305 1.3 7.8 0.5
C26 A:V90305 1.8 22.0 0.5
C24 A:V90305 1.9 22.2 0.5
C2 A:V90305 2.3 7.1 0.5
C6 A:V90305 2.4 7.3 0.5
F16 A:V90305 2.6 7.6 0.5
C19 A:V90305 2.8 21.2 0.5
C23 A:V90305 2.8 24.8 0.5
C21 A:V90305 2.9 9.0 0.5
N7 A:V90305 3.0 12.2 0.5
S12 A:V90305 3.1 15.6 0.5
C20 A:V90305 3.3 15.5 0.5
CD1 A:LEU140 3.4 11.3 1.0
CG1 A:VAL121 3.4 9.4 1.0
CD2 A:LEU197 3.4 12.7 1.0
C22 A:V90305 3.4 23.1 0.5
C3 A:V90305 3.6 6.1 0.5
C5 A:V90305 3.6 8.4 0.5
C13 A:V90305 3.7 24.9 0.5
O10 A:V90305 3.7 10.7 0.5
C4 A:V90305 4.1 6.5 0.5
C4 A:V90305 4.4 11.4 0.5
CG2 A:VAL121 4.4 7.7 1.0
CB A:VAL121 4.5 7.4 1.0
O9 A:V90305 4.6 10.1 0.5
NE2 A:GLN92 4.6 12.3 0.5
O A:HOH680 4.6 27.0 1.0
S8 A:V90305 4.7 9.4 0.5
CG A:LEU197 4.7 11.3 1.0
F18 A:V90305 4.7 10.6 0.5
CD1 A:LEU197 4.8 12.5 1.0
CG A:LEU140 4.8 10.7 1.0
O A:HOH717 4.8 28.3 1.0
C14 A:V90305 4.8 24.4 0.5
S8 A:V90305 5.0 5.5 0.5

Fluorine binding site 4 out of 6 in 4q08

Go back to Fluorine Binding Sites List in 4q08
Fluorine binding site 4 out of 6 in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 4 of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F305

b:28.6
occ:0.50
 F17 A:V90305 0.0 28.6 0.5
C25 A:V90305 0.6 14.6 0.5
C26 A:V90305 1.1 8.8 0.5
C1 A:V90305 1.4 14.0 0.5
C24 A:V90305 1.5 10.4 0.5
C19 A:V90305 2.1 7.6 0.5
C2 A:V90305 2.4 10.4 0.5
C6 A:V90305 2.4 14.8 0.5
C23 A:V90305 2.4 10.5 0.5
F16 A:V90305 2.7 14.3 0.5
C13 A:V90305 2.9 18.9 0.5
S12 A:V90305 3.0 21.5 0.5
C20 A:V90305 3.0 7.8 0.5
C22 A:V90305 3.1 11.5 0.5
N7 A:V90305 3.2 6.9 0.5
CG2 A:THR199 3.4 11.2 1.0
C21 A:V90305 3.5 10.6 0.5
C3 A:V90305 3.7 9.2 0.5
C5 A:V90305 3.7 12.5 0.5
OH A:TYR7 3.9 12.2 1.0
CE1 A:HIS96 3.9 6.9 1.0
C14 A:V90305 3.9 20.9 0.5
C4 A:V90305 4.2 11.4 0.5
OG1 A:THR199 4.2 10.7 1.0
CB A:SER65 4.4 11.1 1.0
CB A:THR199 4.4 9.4 1.0
CD2 A:HIS94 4.4 7.0 1.0
C4 A:V90305 4.5 6.5 0.5
NE2 A:HIS96 4.5 6.2 1.0
F18 A:V90305 4.6 10.6 0.5
NE2 A:HIS94 4.6 6.0 1.0
CB A:HIS64 4.7 10.6 1.0
ND1 A:HIS96 4.7 7.0 1.0
F18 A:V90305 4.8 17.9 0.5
N11 A:V90305 4.8 4.0 0.5
ZN A:ZN301 4.9 6.2 1.0
CG A:HIS94 5.0 6.8 1.0
O A:HOH424 5.0 9.7 1.0

Fluorine binding site 5 out of 6 in 4q08

Go back to Fluorine Binding Sites List in 4q08
Fluorine binding site 5 out of 6 in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 5 of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F305

b:7.6
occ:0.50
 F16 A:V90305 0.0 7.6 0.5
C2 A:V90305 1.3 7.1 0.5
O10 A:V90305 1.8 10.7 0.5
C1 A:V90305 2.3 7.8 0.5
C3 A:V90305 2.4 6.1 0.5
F17 A:V90305 2.6 9.9 0.5
O10 A:V90305 2.9 5.9 0.5
S8 A:V90305 2.9 5.5 0.5
O9 A:V90305 3.0 6.3 0.5
C25 A:V90305 3.1 17.8 0.5
S8 A:V90305 3.1 9.4 0.5
O9 A:V90305 3.2 10.1 0.5
N7 A:V90305 3.3 12.2 0.5
CD2 A:LEU197 3.4 12.7 1.0
C26 A:V90305 3.5 22.0 0.5
CG2 A:VAL142 3.5 8.2 1.0
C4 A:V90305 3.6 6.5 0.5
C6 A:V90305 3.6 7.3 0.5
CG2 A:VAL121 3.7 7.7 1.0
CG1 A:VAL121 3.8 9.4 1.0
C19 A:V90305 4.0 21.2 0.5
C5 A:V90305 4.1 8.4 0.5
N11 A:V90305 4.1 9.0 0.5
C3 A:V90305 4.3 9.2 0.5
CD1 A:LEU140 4.3 11.3 1.0
C4 A:V90305 4.3 11.4 0.5
CB A:VAL121 4.3 7.4 1.0
N11 A:V90305 4.4 4.0 0.5
C24 A:V90305 4.5 22.2 0.5
CG A:LEU197 4.7 11.3 1.0
CG2 A:VAL206 4.7 8.1 1.0
C21 A:V90305 4.7 9.0 0.5
CB A:VAL142 4.7 6.8 1.0
CA A:LEU197 4.8 6.9 1.0
N7 A:V90305 4.9 6.9 0.5
CG1 A:VAL142 4.9 7.8 1.0
CB A:LEU197 4.9 8.1 1.0
CE1 A:HIS94 5.0 7.0 1.0

Fluorine binding site 6 out of 6 in 4q08

Go back to Fluorine Binding Sites List in 4q08
Fluorine binding site 6 out of 6 in the Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor


Mono view


Stereo pair view

A full contact list of Fluorine with other atoms in the F binding site number 6 of Crystal Structure of Chimeric Carbonic Anhydrase XII with Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:F305

b:14.3
occ:0.50
 F16 A:V90305 0.0 14.3 0.5
C2 A:V90305 1.4 10.4 0.5
C26 A:V90305 1.8 8.8 0.5
N7 A:V90305 2.1 6.9 0.5
N11 A:V90305 2.2 4.0 0.5
C1 A:V90305 2.4 14.0 0.5
C3 A:V90305 2.4 9.2 0.5
C19 A:V90305 2.5 7.6 0.5
F17 A:V90305 2.7 28.6 0.5
CE1 A:HIS96 2.7 6.9 1.0
C25 A:V90305 2.8 14.6 0.5
ZN A:ZN301 2.9 6.2 1.0
N11 A:V90305 2.9 9.0 0.5
S8 A:V90305 3.0 9.4 0.5
NE2 A:HIS96 3.0 6.2 1.0
OG1 A:THR198 3.2 6.9 1.0
CG2 A:THR199 3.3 11.2 1.0
C4 A:V90305 3.3 6.5 0.5
NE2 A:HIS94 3.5 6.0 1.0
S8 A:V90305 3.6 5.5 0.5
C6 A:V90305 3.7 14.8 0.5
C20 A:V90305 3.7 7.8 0.5
C4 A:V90305 3.7 11.4 0.5
O9 A:V90305 3.8 10.1 0.5
OG1 A:THR199 3.8 10.7 1.0
C3 A:V90305 3.9 6.1 0.5
O A:HOH424 4.0 9.7 1.0
ND1 A:HIS96 4.0 7.0 1.0
CB A:THR199 4.1 9.4 1.0
CD2 A:HIS94 4.2 7.0 1.0
C5 A:V90305 4.2 12.5 0.5
C24 A:V90305 4.2 10.4 0.5
N A:THR199 4.3 8.1 1.0
CE1 A:HIS94 4.3 7.0 1.0
CD2 A:HIS96 4.4 6.8 1.0
O9 A:V90305 4.4 6.3 0.5
O10 A:V90305 4.4 10.7 0.5
C A:THR198 4.5 7.0 1.0
C5 A:V90305 4.5 8.4 0.5
OH A:TYR7 4.5 12.2 1.0
O10 A:V90305 4.5 5.9 0.5
OE1 A:GLU106 4.6 7.0 1.0
CB A:THR198 4.6 6.7 1.0
F18 A:V90305 4.7 10.6 0.5
CA A:THR199 4.8 8.3 1.0
O A:THR198 4.8 7.8 1.0
ND1 A:HIS119 4.8 5.8 1.0
N7 A:V90305 4.8 12.2 0.5
CA A:THR198 4.8 7.4 1.0
CG A:HIS96 4.9 6.4 1.0
N A:THR198 4.9 7.0 1.0
C23 A:V90305 4.9 10.5 0.5
OE2 A:GLU106 4.9 8.2 1.0
C21 A:V90305 4.9 10.6 0.5

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 Dec 13 12:11:08 2020

Last articles

Zn in 7VD8
Zn in 7V1R
Zn in 7V1Q
Zn in 7VPF
Zn in 7T85
Zn in 7T5F
Zn in 7NF9
Zn in 7M4M
Zn in 7M4O
Zn in 7M4N
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy