Mercury in PDB 6sas: Human Carbonic Anhydrase II in Complex with Fragment.
Enzymatic activity of Human Carbonic Anhydrase II in Complex with Fragment.
All present enzymatic activity of Human Carbonic Anhydrase II in Complex with Fragment.:
4.2.1.1;
Protein crystallography data
The structure of Human Carbonic Anhydrase II in Complex with Fragment., PDB code: 6sas
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)
|
41.06 /
1.10
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
42.383,
41.543,
72.121,
90.00,
104.33,
90.00
|
R / Rfree (%)
|
13.2 /
14.9
|
Other elements in 6sas:
The structure of Human Carbonic Anhydrase II in Complex with Fragment. also contains other interesting chemical elements:
Mercury Binding Sites:
The binding sites of Mercury atom in the Human Carbonic Anhydrase II in Complex with Fragment.
(pdb code 6sas). This binding sites where shown within
5.0 Angstroms radius around Mercury atom.
In total 2 binding sites of Mercury where determined in the
Human Carbonic Anhydrase II in Complex with Fragment., PDB code: 6sas:
Jump to Mercury binding site number:
1;
2;
Mercury binding site 1 out
of 2 in 6sas
Go back to
Mercury Binding Sites List in 6sas
Mercury binding site 1 out
of 2 in the Human Carbonic Anhydrase II in Complex with Fragment.
Mono view
Stereo pair view
|
A full contact list of Mercury with other atoms in the Hg binding
site number 1 of Human Carbonic Anhydrase II in Complex with Fragment. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Hg303
b:9.3
occ:0.27
|
HG
|
A:BE7304
|
1.1
|
10.4
|
0.7
|
SG
|
A:CYS206
|
1.5
|
8.1
|
0.7
|
HB3
|
A:CYS206
|
2.1
|
11.2
|
0.3
|
SG
|
A:CYS206
|
2.4
|
8.5
|
0.3
|
O
|
A:HOH459
|
2.6
|
18.5
|
1.0
|
CB
|
A:CYS206
|
2.6
|
9.3
|
0.3
|
CB
|
A:CYS206
|
2.9
|
6.9
|
0.7
|
O
|
A:VAL135
|
3.1
|
11.0
|
1.0
|
HB3
|
A:CYS206
|
3.2
|
8.3
|
0.7
|
C5
|
A:BE7304
|
3.2
|
10.7
|
0.7
|
O
|
A:GLN137
|
3.2
|
8.4
|
1.0
|
HB3
|
A:LEU204
|
3.3
|
13.2
|
1.0
|
H
|
A:GLN137
|
3.3
|
11.1
|
1.0
|
HA
|
A:CYS206
|
3.3
|
8.1
|
0.7
|
HB2
|
A:CYS206
|
3.4
|
11.2
|
0.3
|
CA
|
A:CYS206
|
3.5
|
6.7
|
0.7
|
CA
|
A:CYS206
|
3.5
|
8.7
|
0.3
|
HA
|
A:CYS206
|
3.6
|
10.4
|
0.3
|
C
|
A:VAL135
|
3.6
|
9.3
|
1.0
|
HA
|
A:VAL135
|
3.6
|
10.0
|
1.0
|
N
|
A:CYS206
|
3.6
|
8.4
|
0.3
|
N
|
A:GLN137
|
3.6
|
9.3
|
1.0
|
HB2
|
A:CYS206
|
3.7
|
8.3
|
0.7
|
N
|
A:CYS206
|
3.7
|
6.6
|
0.7
|
C
|
A:GLU205
|
3.7
|
7.8
|
1.0
|
O
|
A:GLU205
|
3.8
|
9.1
|
1.0
|
C
|
A:GLN137
|
3.8
|
8.0
|
1.0
|
O
|
A:HOH527
|
3.9
|
15.8
|
1.0
|
H
|
A:GLU205
|
3.9
|
9.8
|
1.0
|
HA
|
A:GLN136
|
3.9
|
12.2
|
1.0
|
C6
|
A:BE7304
|
4.0
|
13.7
|
0.7
|
H
|
A:CYS206
|
4.0
|
10.1
|
0.3
|
N
|
A:GLU205
|
4.1
|
8.1
|
1.0
|
CA
|
A:VAL135
|
4.1
|
8.3
|
1.0
|
C
|
A:GLN136
|
4.1
|
9.3
|
1.0
|
C4
|
A:BE7304
|
4.1
|
11.9
|
0.7
|
H
|
A:CYS206
|
4.2
|
8.0
|
0.7
|
CB
|
A:LEU204
|
4.2
|
11.0
|
1.0
|
N
|
A:GLN136
|
4.2
|
9.7
|
1.0
|
HA
|
A:PRO138
|
4.2
|
11.5
|
1.0
|
CA
|
A:GLN136
|
4.3
|
10.2
|
1.0
|
CA
|
A:GLN137
|
4.3
|
8.9
|
1.0
|
HB
|
A:VAL135
|
4.4
|
11.9
|
1.0
|
HB2
|
A:LEU204
|
4.4
|
13.2
|
1.0
|
HD13
|
A:LEU204
|
4.5
|
17.9
|
1.0
|
C
|
A:LEU204
|
4.5
|
7.7
|
1.0
|
CA
|
A:GLU205
|
4.5
|
7.8
|
1.0
|
HD22
|
A:LEU204
|
4.6
|
18.7
|
1.0
|
O
|
A:ALA134
|
4.6
|
8.7
|
1.0
|
N
|
A:PRO138
|
4.7
|
8.8
|
1.0
|
HA
|
A:GLN137
|
4.8
|
10.6
|
1.0
|
CA
|
A:LEU204
|
4.8
|
8.9
|
1.0
|
H
|
A:GLN136
|
4.8
|
11.6
|
1.0
|
CB
|
A:VAL135
|
4.9
|
9.9
|
1.0
|
CA
|
A:PRO138
|
4.9
|
9.6
|
1.0
|
HA
|
A:LEU204
|
4.9
|
10.6
|
1.0
|
C
|
A:CYS206
|
4.9
|
7.7
|
0.3
|
O
|
A:GLN136
|
4.9
|
10.7
|
1.0
|
C
|
A:CYS206
|
4.9
|
6.8
|
0.7
|
|
Mercury binding site 2 out
of 2 in 6sas
Go back to
Mercury Binding Sites List in 6sas
Mercury binding site 2 out
of 2 in the Human Carbonic Anhydrase II in Complex with Fragment.
Mono view
Stereo pair view
|
A full contact list of Mercury with other atoms in the Hg binding
site number 2 of Human Carbonic Anhydrase II in Complex with Fragment. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Hg304
b:10.4
occ:0.73
|
HG
|
A:BE7304
|
0.0
|
10.4
|
0.7
|
HG
|
A:HG303
|
1.1
|
9.3
|
0.3
|
C5
|
A:BE7304
|
2.2
|
10.7
|
0.7
|
HB3
|
A:CYS206
|
2.3
|
11.2
|
0.3
|
SG
|
A:CYS206
|
2.4
|
8.1
|
0.7
|
O
|
A:HOH459
|
2.9
|
18.5
|
1.0
|
O
|
A:GLN137
|
3.0
|
8.4
|
1.0
|
CB
|
A:CYS206
|
3.0
|
9.3
|
0.3
|
HA
|
A:CYS206
|
3.1
|
8.1
|
0.7
|
C4
|
A:BE7304
|
3.1
|
11.9
|
0.7
|
O
|
A:GLU205
|
3.1
|
9.1
|
1.0
|
C6
|
A:BE7304
|
3.2
|
13.7
|
0.7
|
SG
|
A:CYS206
|
3.2
|
8.5
|
0.3
|
HA
|
A:CYS206
|
3.3
|
10.4
|
0.3
|
C
|
A:GLN137
|
3.4
|
8.0
|
1.0
|
CB
|
A:CYS206
|
3.4
|
6.9
|
0.7
|
HA
|
A:PRO138
|
3.4
|
11.5
|
1.0
|
C
|
A:GLU205
|
3.4
|
7.8
|
1.0
|
H
|
A:GLN137
|
3.5
|
11.1
|
1.0
|
CA
|
A:CYS206
|
3.5
|
8.7
|
0.3
|
CA
|
A:CYS206
|
3.5
|
6.7
|
0.7
|
HB3
|
A:CYS206
|
3.6
|
8.3
|
0.7
|
N
|
A:CYS206
|
3.6
|
8.4
|
0.3
|
N
|
A:GLN137
|
3.7
|
9.3
|
1.0
|
N
|
A:CYS206
|
3.7
|
6.6
|
0.7
|
O
|
A:HOH527
|
3.8
|
15.8
|
1.0
|
HB2
|
A:CYS206
|
3.8
|
11.2
|
0.3
|
H
|
A:GLU205
|
3.9
|
9.8
|
1.0
|
N
|
A:PRO138
|
4.0
|
8.8
|
1.0
|
O
|
A:VAL135
|
4.0
|
11.0
|
1.0
|
HB3
|
A:LEU204
|
4.0
|
13.2
|
1.0
|
CA
|
A:GLN137
|
4.1
|
8.9
|
1.0
|
CA
|
A:PRO138
|
4.1
|
9.6
|
1.0
|
N
|
A:GLU205
|
4.1
|
8.1
|
1.0
|
C
|
A:GLN136
|
4.2
|
9.3
|
1.0
|
H
|
A:CYS206
|
4.2
|
10.1
|
0.3
|
HB2
|
A:CYS206
|
4.2
|
8.3
|
0.7
|
HA
|
A:GLN136
|
4.3
|
12.2
|
1.0
|
H
|
A:CYS206
|
4.3
|
8.0
|
0.7
|
CA
|
A:GLU205
|
4.3
|
7.8
|
1.0
|
HA
|
A:GLN137
|
4.4
|
10.6
|
1.0
|
C
|
A:VAL135
|
4.4
|
9.3
|
1.0
|
C3
|
A:BE7304
|
4.4
|
13.1
|
0.7
|
HA
|
A:VAL135
|
4.5
|
10.0
|
1.0
|
C7
|
A:BE7304
|
4.5
|
14.5
|
0.7
|
HB2
|
A:GLU205
|
4.5
|
9.5
|
1.0
|
CA
|
A:GLN136
|
4.6
|
10.2
|
1.0
|
O
|
A:GLN136
|
4.7
|
10.7
|
1.0
|
HD3
|
A:PRO138
|
4.7
|
12.4
|
1.0
|
N
|
A:GLN136
|
4.8
|
9.7
|
1.0
|
C
|
A:LEU204
|
4.8
|
7.7
|
1.0
|
CB
|
A:LEU204
|
4.9
|
11.0
|
1.0
|
O
|
A:HOH572
|
4.9
|
35.8
|
1.0
|
HB3
|
A:PRO138
|
4.9
|
13.9
|
1.0
|
CB
|
A:GLU205
|
4.9
|
8.0
|
1.0
|
CD
|
A:PRO138
|
5.0
|
10.3
|
1.0
|
C
|
A:CYS206
|
5.0
|
6.8
|
0.7
|
C
|
A:CYS206
|
5.0
|
7.7
|
0.3
|
C2
|
A:BE7304
|
5.0
|
14.9
|
0.7
|
|
Reference:
S.Glockner,
A.Heine,
G.Klebe.
A Proof-of-Concept Fragment Screening of A Hit-Validated 96-Compounds Library Against Human Carbonic Anhydrase II. Biomolecules V. 10 2020.
ISSN: ESSN 2218-273X
PubMed: 32235320
DOI: 10.3390/BIOM10040518
Page generated: Sun Aug 11 08:09:55 2024
|