Atomistry » Zinc » PDB 4hk7-4hwp » 4ht2
Atomistry »
  Zinc »
    PDB 4hk7-4hwp »
      4ht2 »

Zinc in PDB 4ht2: Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor.

Enzymatic activity of Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor.

All present enzymatic activity of Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor.:
4.2.1.1;

Protein crystallography data

The structure of Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor., PDB code: 4ht2 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) 26.50 / 1.45
Space group P 1
Cell size a, b, c (Å), α, β, γ (°) 46.709, 67.261, 80.689, 81.78, 84.01, 86.48
R / Rfree (%) 15 / 18.8

Other elements in 4ht2:

The structure of Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor. also contains other interesting chemical elements:

Fluorine (F) 20 atoms

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor. (pdb code 4ht2). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 4 binding sites of Zinc where determined in the Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor., PDB code: 4ht2:
Jump to Zinc binding site number: 1; 2; 3; 4;

Zinc binding site 1 out of 4 in 4ht2

Go back to Zinc Binding Sites List in 4ht2
Zinc binding site 1 out of 4 in the Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the 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 Human Carbonic Anhydrase Isozyme XII with the Inhibitor. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn301

b:5.0
occ:1.00
NE2 A:HIS91 2.0 4.0 1.0
ND1 A:HIS117 2.0 5.2 1.0
N23 A:V50302 2.1 9.6 0.5
NE2 A:HIS93 2.1 5.0 1.0
N23 A:V50302 2.1 3.4 0.5
CE1 A:HIS117 3.0 5.1 1.0
O9 A:V50302 3.0 6.4 0.5
S7 A:V50302 3.0 8.6 0.5
CD2 A:HIS91 3.0 6.0 1.0
O9 A:V50302 3.0 6.0 0.5
CD2 A:HIS93 3.0 4.1 1.0
CE1 A:HIS91 3.0 4.1 1.0
CE1 A:HIS93 3.1 5.6 1.0
CG A:HIS117 3.1 5.0 1.0
S7 A:V50302 3.1 5.2 0.5
CB A:HIS117 3.6 6.0 1.0
F13 A:V50302 3.7 8.5 0.5
OE1 A:GLU104 3.9 6.0 1.0
OG1 A:THR198 4.0 5.0 1.0
O8 A:V50302 4.0 8.7 0.5
NE2 A:HIS117 4.1 5.2 1.0
C5 A:V50302 4.1 3.7 0.5
ND1 A:HIS91 4.2 5.3 1.0
CG A:HIS93 4.2 4.0 1.0
ND1 A:HIS93 4.2 6.0 1.0
CG A:HIS91 4.2 4.8 1.0
CD2 A:HIS117 4.2 5.1 1.0
C5 A:V50302 4.2 7.7 0.5
C4 A:V50302 4.3 6.4 0.5
O8 A:V50302 4.3 3.6 0.5
O2 A:EDO304 4.4 22.5 0.5
F13 A:V50302 4.9 11.0 0.5
CD A:GLU104 4.9 5.6 1.0
C4 A:V50302 5.0 8.4 0.5

Zinc binding site 2 out of 4 in 4ht2

Go back to Zinc Binding Sites List in 4ht2
Zinc binding site 2 out of 4 in the Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor.


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor. within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Zn301

b:5.8
occ:1.00
N23 B:V50302 2.0 7.9 1.0
NE2 B:HIS91 2.0 5.0 1.0
NE2 B:HIS93 2.1 4.0 1.0
ND1 B:HIS117 2.1 6.5 1.0
CE1 B:HIS117 2.9 5.7 1.0
CD2 B:HIS91 3.0 9.1 1.0
CE1 B:HIS93 3.0 5.4 1.0
O9 B:V50302 3.0 8.0 1.0
S7 B:V50302 3.1 7.9 1.0
CE1 B:HIS91 3.1 5.7 1.0
CD2 B:HIS93 3.1 5.2 1.0
CG B:HIS117 3.1 5.5 1.0
CB B:HIS117 3.6 6.1 1.0
OE1 B:GLU104 3.9 5.5 1.0
OG1 B:THR198 4.0 5.1 1.0
NE2 B:HIS117 4.1 5.6 1.0
O8 B:V50302 4.2 7.8 1.0
ND1 B:HIS93 4.2 5.5 1.0
CG B:HIS91 4.2 5.9 1.0
ND1 B:HIS91 4.2 5.8 1.0
CG B:HIS93 4.2 5.0 1.0
CD2 B:HIS117 4.2 5.0 1.0
C5 B:V50302 4.3 7.2 1.0
C1 B:EDO304 4.5 19.6 1.0
F11 B:V50302 4.8 11.0 1.0
C2 B:EDO304 4.8 15.7 1.0
CD B:GLU104 4.9 4.9 1.0
C6 B:V50302 5.0 8.0 1.0

Zinc binding site 3 out of 4 in 4ht2

Go back to Zinc Binding Sites List in 4ht2
Zinc binding site 3 out of 4 in the Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor.


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 3 of Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor. within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Zn301

b:5.2
occ:1.00
ND1 C:HIS117 2.0 4.8 1.0
NE2 C:HIS91 2.0 5.8 1.0
N23 C:V50302 2.0 7.0 1.0
NE2 C:HIS93 2.0 5.2 1.0
CE1 C:HIS117 2.9 3.8 1.0
CD2 C:HIS91 3.0 6.3 1.0
CD2 C:HIS93 3.0 4.5 1.0
CE1 C:HIS91 3.0 6.5 1.0
CE1 C:HIS93 3.0 5.2 1.0
S7 C:V50302 3.0 7.7 1.0
O9 C:V50302 3.0 7.9 1.0
CG C:HIS117 3.2 5.2 1.0
CB C:HIS117 3.6 5.7 1.0
OE1 C:GLU104 3.9 5.3 1.0
OG1 C:THR198 3.9 5.5 1.0
NE2 C:HIS117 4.1 5.3 1.0
CG C:HIS91 4.1 5.1 1.0
O8 C:V50302 4.2 6.9 1.0
ND1 C:HIS91 4.2 6.2 1.0
ND1 C:HIS93 4.2 5.5 1.0
CG C:HIS93 4.2 5.0 1.0
C5 C:V50302 4.2 10.3 1.0
CD2 C:HIS117 4.2 6.2 1.0
C1 C:EDO303 4.7 24.1 1.0
F11 C:V50302 4.8 12.5 1.0
C6 C:V50302 5.0 11.9 1.0
C2 C:EDO303 5.0 22.6 1.0
CD C:GLU104 5.0 4.0 1.0

Zinc binding site 4 out of 4 in 4ht2

Go back to Zinc Binding Sites List in 4ht2
Zinc binding site 4 out of 4 in the Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor.


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 4 of Crystal Structure of Human Carbonic Anhydrase Isozyme XII with the Inhibitor. within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Zn301

b:4.6
occ:1.00
N23 D:V50302 2.0 6.2 1.0
NE2 D:HIS91 2.1 4.2 1.0
NE2 D:HIS93 2.1 4.6 1.0
ND1 D:HIS117 2.1 4.7 1.0
CE1 D:HIS117 2.9 5.9 1.0
CE1 D:HIS91 3.0 3.4 1.0
CD2 D:HIS91 3.0 4.5 1.0
O9 D:V50302 3.0 7.8 1.0
CE1 D:HIS93 3.0 4.8 1.0
S7 D:V50302 3.1 7.2 1.0
CD2 D:HIS93 3.1 4.3 1.0
CG D:HIS117 3.2 3.5 1.0
CB D:HIS117 3.6 3.5 1.0
OE1 D:GLU104 3.9 5.0 1.0
OG1 D:THR198 4.0 4.4 1.0
NE2 D:HIS117 4.1 3.8 1.0
ND1 D:HIS91 4.2 4.2 1.0
O8 D:V50302 4.2 5.7 1.0
CG D:HIS91 4.2 3.0 1.0
ND1 D:HIS93 4.2 4.8 1.0
CG D:HIS93 4.2 4.2 1.0
C5 D:V50302 4.2 6.6 1.0
CD2 D:HIS117 4.2 4.1 1.0
C2 D:EDO304 4.6 19.6 1.0
C1 D:EDO304 4.7 20.5 1.0
F13 D:V50302 4.8 10.0 1.0
CD D:GLU104 4.9 5.4 1.0
C4 D:V50302 4.9 7.4 1.0

Reference:

V.Dudutiene, A.Zubriene, A.Smirnov, J.Gylyte, D.Timm, E.Manakova, S.Grazulis, D.Matulis. 4-Substituted-2,3,5,6-Tetrafluorobenzenesulfonamides As Inhibitors of Carbonic Anhydrases I, II, VII, XII, and XIII. Bioorg.Med.Chem. V. 21 2093 2013.
ISSN: ISSN 0968-0896
PubMed: 23394791
DOI: 10.1016/J.BMC.2013.01.008
Page generated: Wed Dec 16 05:22:44 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