Zinc in PDB 4qiy: Crystal Structure of Human Carbonic Anhydrase Isozyme II with Inhibitor
Enzymatic activity of Crystal Structure of Human Carbonic Anhydrase Isozyme II with Inhibitor
All present enzymatic activity of Crystal Structure of Human Carbonic Anhydrase Isozyme II with Inhibitor:
4.2.1.1;
Protein crystallography data
The structure of Crystal Structure of Human Carbonic Anhydrase Isozyme II with Inhibitor, PDB code: 4qiy
was solved by
E.Manakova,
A.Smirnov,
S.Grazulis,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
69.46 /
1.30
|
Space group
|
P 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
73.594,
41.206,
84.047,
90.00,
109.30,
90.00
|
R / Rfree (%)
|
15.1 /
19.2
|
Other elements in 4qiy:
The structure of Crystal Structure of Human Carbonic Anhydrase Isozyme II with Inhibitor also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Crystal Structure of Human Carbonic Anhydrase Isozyme II with Inhibitor
(pdb code 4qiy). 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 II with Inhibitor, PDB code: 4qiy:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 4qiy
Go back to
Zinc Binding Sites List in 4qiy
Zinc binding site 1 out
of 4 in the Crystal Structure of Human Carbonic Anhydrase Isozyme II 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 Human Carbonic Anhydrase Isozyme II with Inhibitor within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn301
b:8.2
occ:1.00
|
N4
|
A:WWX302
|
1.9
|
9.5
|
1.0
|
NE2
|
A:HIS96
|
2.0
|
7.3
|
1.0
|
NE2
|
A:HIS94
|
2.0
|
8.2
|
1.0
|
ND1
|
A:HIS119
|
2.1
|
7.6
|
1.0
|
F11
|
A:WWX302
|
2.8
|
17.0
|
1.0
|
CE1
|
A:HIS119
|
2.9
|
8.7
|
1.0
|
CD2
|
A:HIS94
|
3.0
|
8.1
|
1.0
|
CD2
|
A:HIS96
|
3.0
|
8.8
|
1.0
|
CE1
|
A:HIS94
|
3.1
|
9.1
|
1.0
|
CE1
|
A:HIS96
|
3.1
|
9.7
|
1.0
|
S1
|
A:WWX302
|
3.1
|
13.2
|
1.0
|
CG
|
A:HIS119
|
3.2
|
6.5
|
1.0
|
O2
|
A:WWX302
|
3.2
|
12.7
|
1.0
|
C6
|
A:WWX302
|
3.4
|
15.3
|
1.0
|
CB
|
A:HIS119
|
3.5
|
7.9
|
1.0
|
C5
|
A:WWX302
|
3.6
|
15.4
|
1.0
|
OE1
|
A:GLU106
|
3.9
|
9.2
|
1.0
|
OG1
|
A:THR199
|
3.9
|
8.7
|
1.0
|
NE2
|
A:HIS119
|
4.1
|
8.3
|
1.0
|
CG
|
A:HIS94
|
4.1
|
7.9
|
1.0
|
ND1
|
A:HIS94
|
4.2
|
9.1
|
1.0
|
CG
|
A:HIS96
|
4.2
|
8.2
|
1.0
|
ND1
|
A:HIS96
|
4.2
|
9.0
|
1.0
|
CD2
|
A:HIS119
|
4.2
|
7.7
|
1.0
|
O3
|
A:WWX302
|
4.3
|
17.5
|
1.0
|
C7
|
A:WWX302
|
4.4
|
17.2
|
1.0
|
C10
|
A:WWX302
|
4.8
|
17.4
|
1.0
|
CD
|
A:GLU106
|
4.8
|
9.1
|
1.0
|
F12
|
A:WWX302
|
4.9
|
21.2
|
1.0
|
|
Zinc binding site 2 out
of 4 in 4qiy
Go back to
Zinc Binding Sites List in 4qiy
Zinc binding site 2 out
of 4 in the Crystal Structure of Human Carbonic Anhydrase Isozyme II with 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 II with Inhibitor within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn301
b:7.6
occ:1.00
|
N4
|
B:WWX302
|
1.9
|
10.4
|
1.0
|
NE2
|
B:HIS94
|
2.0
|
6.9
|
1.0
|
NE2
|
B:HIS96
|
2.0
|
6.8
|
1.0
|
ND1
|
B:HIS119
|
2.1
|
7.2
|
1.0
|
F11
|
B:WWX302
|
2.8
|
15.0
|
1.0
|
CE1
|
B:HIS119
|
2.9
|
8.0
|
1.0
|
CD2
|
B:HIS96
|
3.0
|
8.2
|
1.0
|
CD2
|
B:HIS94
|
3.0
|
6.8
|
1.0
|
CE1
|
B:HIS96
|
3.0
|
8.4
|
1.0
|
CE1
|
B:HIS94
|
3.1
|
7.8
|
1.0
|
S1
|
B:WWX302
|
3.1
|
10.9
|
1.0
|
CG
|
B:HIS119
|
3.1
|
6.8
|
1.0
|
O2
|
B:WWX302
|
3.2
|
12.9
|
1.0
|
C6
|
B:WWX302
|
3.4
|
13.4
|
1.0
|
CB
|
B:HIS119
|
3.6
|
6.2
|
1.0
|
C5
|
B:WWX302
|
3.6
|
12.8
|
1.0
|
OE1
|
B:GLU106
|
3.9
|
8.5
|
1.0
|
OG1
|
B:THR199
|
3.9
|
7.3
|
1.0
|
NE2
|
B:HIS119
|
4.1
|
8.6
|
1.0
|
CG
|
B:HIS94
|
4.2
|
7.9
|
1.0
|
CG
|
B:HIS96
|
4.2
|
7.2
|
1.0
|
ND1
|
B:HIS94
|
4.2
|
8.1
|
1.0
|
ND1
|
B:HIS96
|
4.2
|
7.3
|
1.0
|
CD2
|
B:HIS119
|
4.2
|
8.1
|
1.0
|
O3
|
B:WWX302
|
4.3
|
14.9
|
1.0
|
C7
|
B:WWX302
|
4.4
|
16.0
|
1.0
|
C10
|
B:WWX302
|
4.8
|
14.9
|
1.0
|
F12
|
B:WWX302
|
4.8
|
21.5
|
1.0
|
CD
|
B:GLU106
|
4.9
|
8.8
|
1.0
|
CH2
|
B:TRP209
|
4.9
|
8.3
|
1.0
|
|
Zinc binding site 3 out
of 4 in 4qiy
Go back to
Zinc Binding Sites List in 4qiy
Zinc binding site 3 out
of 4 in the Crystal Structure of Human Carbonic Anhydrase Isozyme II with 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 II with Inhibitor within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Zn301
b:7.6
occ:1.00
|
N4
|
C:WWX302
|
2.0
|
11.4
|
1.0
|
NE2
|
C:HIS94
|
2.0
|
7.3
|
1.0
|
NE2
|
C:HIS96
|
2.0
|
7.2
|
1.0
|
ND1
|
C:HIS119
|
2.1
|
7.4
|
1.0
|
F11
|
C:WWX302
|
2.8
|
15.0
|
1.0
|
CE1
|
C:HIS119
|
2.9
|
7.2
|
1.0
|
CD2
|
C:HIS94
|
3.0
|
7.0
|
1.0
|
CD2
|
C:HIS96
|
3.0
|
7.7
|
1.0
|
CE1
|
C:HIS94
|
3.0
|
8.2
|
1.0
|
CE1
|
C:HIS96
|
3.0
|
8.2
|
1.0
|
S1
|
C:WWX302
|
3.1
|
11.1
|
1.0
|
CG
|
C:HIS119
|
3.2
|
6.5
|
1.0
|
O2
|
C:WWX302
|
3.2
|
12.8
|
1.0
|
C6
|
C:WWX302
|
3.4
|
13.0
|
1.0
|
CB
|
C:HIS119
|
3.6
|
7.1
|
1.0
|
C5
|
C:WWX302
|
3.6
|
13.9
|
1.0
|
OE1
|
C:GLU106
|
3.9
|
9.3
|
1.0
|
OG1
|
C:THR199
|
3.9
|
8.3
|
1.0
|
NE2
|
C:HIS119
|
4.1
|
8.0
|
1.0
|
ND1
|
C:HIS94
|
4.2
|
7.5
|
1.0
|
CG
|
C:HIS94
|
4.2
|
6.8
|
1.0
|
ND1
|
C:HIS96
|
4.2
|
8.2
|
1.0
|
CG
|
C:HIS96
|
4.2
|
7.6
|
1.0
|
CD2
|
C:HIS119
|
4.2
|
7.6
|
1.0
|
O3
|
C:WWX302
|
4.3
|
14.5
|
1.0
|
C7
|
C:WWX302
|
4.4
|
14.6
|
1.0
|
F12
|
C:WWX302
|
4.8
|
21.0
|
1.0
|
C10
|
C:WWX302
|
4.8
|
17.4
|
1.0
|
CD
|
C:GLU106
|
4.8
|
9.2
|
1.0
|
CH2
|
C:TRP209
|
4.9
|
8.5
|
1.0
|
|
Zinc binding site 4 out
of 4 in 4qiy
Go back to
Zinc Binding Sites List in 4qiy
Zinc binding site 4 out
of 4 in the Crystal Structure of Human Carbonic Anhydrase Isozyme II with 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 II with Inhibitor within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Zn301
b:8.4
occ:1.00
|
N4
|
D:WWX302
|
1.9
|
10.4
|
1.0
|
NE2
|
D:HIS94
|
2.0
|
8.4
|
1.0
|
NE2
|
D:HIS96
|
2.0
|
7.8
|
1.0
|
ND1
|
D:HIS119
|
2.1
|
7.2
|
1.0
|
F11
|
D:WWX302
|
2.8
|
17.1
|
1.0
|
CE1
|
D:HIS119
|
2.9
|
8.0
|
1.0
|
CD2
|
D:HIS94
|
2.9
|
8.0
|
1.0
|
CD2
|
D:HIS96
|
3.0
|
9.1
|
1.0
|
CE1
|
D:HIS94
|
3.0
|
8.7
|
1.0
|
CE1
|
D:HIS96
|
3.1
|
9.2
|
1.0
|
S1
|
D:WWX302
|
3.1
|
13.3
|
1.0
|
CG
|
D:HIS119
|
3.1
|
6.3
|
1.0
|
O2
|
D:WWX302
|
3.3
|
14.5
|
1.0
|
C6
|
D:WWX302
|
3.4
|
15.0
|
1.0
|
CB
|
D:HIS119
|
3.5
|
8.2
|
1.0
|
C5
|
D:WWX302
|
3.6
|
15.2
|
1.0
|
OE1
|
D:GLU106
|
3.9
|
9.3
|
1.0
|
OG1
|
D:THR199
|
3.9
|
9.2
|
1.0
|
NE2
|
D:HIS119
|
4.1
|
8.7
|
1.0
|
CG
|
D:HIS94
|
4.1
|
7.5
|
1.0
|
ND1
|
D:HIS94
|
4.2
|
8.7
|
1.0
|
ND1
|
D:HIS96
|
4.2
|
8.6
|
1.0
|
CG
|
D:HIS96
|
4.2
|
7.7
|
1.0
|
CD2
|
D:HIS119
|
4.2
|
8.0
|
1.0
|
O3
|
D:WWX302
|
4.3
|
18.0
|
1.0
|
C7
|
D:WWX302
|
4.4
|
18.6
|
1.0
|
CD
|
D:GLU106
|
4.8
|
8.7
|
1.0
|
F12
|
D:WWX302
|
4.8
|
22.2
|
1.0
|
C10
|
D:WWX302
|
4.9
|
17.6
|
1.0
|
|
Reference:
V.Dudutiene,
A.Zubriene,
A.Smirnov,
D.D.Timm,
J.Smirnoviene,
J.Kazokaite,
V.Michailoviene,
A.Zaksauskas,
E.Manakova,
S.Grazulis,
D.Matulis.
Functionalization of Fluorinated Benzenesulfonamides and Their Inhibitory Properties Toward Carbonic Anhydrases Chemmedchem V. 10 662 2015.
ISSN: ISSN 1860-7179
PubMed: 25758852
DOI: 10.1002/CMDC.201402490
Page generated: Sun Oct 27 06:35:26 2024
|