Zinc in PDB 7ucu: Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K
Enzymatic activity of Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K
All present enzymatic activity of Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K:
1.1.1.1;
Protein crystallography data
The structure of Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K, PDB code: 7ucu
was solved by
B.V.Plapp,
L.Gakhar,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
19.94 /
1.10
|
Space group
|
P 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
44.19,
51.14,
92.49,
91.9,
103.03,
109.83
|
R / Rfree (%)
|
12.4 /
14.2
|
Other elements in 7ucu:
The structure of Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K also contains other interesting chemical elements:
Zinc Binding Sites:
The binding sites of Zinc atom in the Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K
(pdb code 7ucu). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 4 binding sites of Zinc where determined in the
Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K, PDB code: 7ucu:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 7ucu
Go back to
Zinc Binding Sites List in 7ucu
Zinc binding site 1 out
of 4 in the Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn401
b:8.8
occ:1.00
|
O
|
A:ETF404
|
2.0
|
9.2
|
1.0
|
NE2
|
A:HIS67
|
2.1
|
9.1
|
1.0
|
SG
|
A:CYS174
|
2.3
|
8.8
|
1.0
|
SG
|
A:CYS46
|
2.3
|
8.5
|
1.0
|
C2
|
A:ETF404
|
2.9
|
9.6
|
1.0
|
CE1
|
A:HIS67
|
3.0
|
8.2
|
1.0
|
CD2
|
A:HIS67
|
3.1
|
8.6
|
1.0
|
CB
|
A:CYS46
|
3.3
|
8.5
|
1.0
|
C5N
|
A:NAJ403
|
3.3
|
7.5
|
1.0
|
CB
|
A:CYS174
|
3.4
|
8.3
|
1.0
|
OG
|
A:SER48
|
3.8
|
8.6
|
1.0
|
C4N
|
A:NAJ403
|
3.9
|
8.5
|
1.0
|
C6N
|
A:NAJ403
|
4.0
|
7.5
|
1.0
|
CB
|
A:SER48
|
4.0
|
8.1
|
1.0
|
ND1
|
A:HIS67
|
4.2
|
8.5
|
1.0
|
C1
|
A:ETF404
|
4.2
|
11.5
|
1.0
|
CG
|
A:HIS67
|
4.2
|
7.9
|
1.0
|
F3
|
A:ETF404
|
4.6
|
13.8
|
1.0
|
NH2
|
A:ARG369
|
4.6
|
8.8
|
1.0
|
CA
|
A:CYS174
|
4.7
|
7.7
|
1.0
|
CA
|
A:CYS46
|
4.8
|
9.1
|
1.0
|
F1
|
A:ETF404
|
4.8
|
13.9
|
1.0
|
N
|
A:SER48
|
4.8
|
8.1
|
1.0
|
OE2
|
A:GLU68
|
4.9
|
10.1
|
1.0
|
CE2
|
A:PHE93
|
4.9
|
8.4
|
1.0
|
N1N
|
A:NAJ403
|
4.9
|
7.1
|
1.0
|
C3N
|
A:NAJ403
|
5.0
|
7.4
|
1.0
|
|
Zinc binding site 2 out
of 4 in 7ucu
Go back to
Zinc Binding Sites List in 7ucu
Zinc binding site 2 out
of 4 in the Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn402
b:10.3
occ:1.00
|
SG
|
A:CYS111
|
2.3
|
10.0
|
1.0
|
SG
|
A:CYS100
|
2.3
|
10.7
|
1.0
|
SG
|
A:CYS97
|
2.3
|
11.8
|
1.0
|
SG
|
A:CYS103
|
2.4
|
10.0
|
1.0
|
CB
|
A:CYS111
|
3.3
|
9.5
|
1.0
|
CB
|
A:CYS103
|
3.4
|
10.6
|
1.0
|
CB
|
A:CYS100
|
3.4
|
12.2
|
1.0
|
CB
|
A:CYS97
|
3.4
|
12.3
|
1.0
|
N
|
A:CYS97
|
3.5
|
10.2
|
1.0
|
CA
|
A:CYS111
|
3.7
|
9.4
|
1.0
|
N
|
A:CYS100
|
3.9
|
12.7
|
1.0
|
CA
|
A:CYS97
|
3.9
|
10.9
|
1.0
|
N
|
A:GLY98
|
4.0
|
11.6
|
1.0
|
N
|
A:LEU112
|
4.0
|
9.4
|
1.0
|
CA
|
A:CYS100
|
4.2
|
12.6
|
1.0
|
N
|
A:CYS103
|
4.2
|
10.0
|
1.0
|
C
|
A:CYS97
|
4.3
|
11.7
|
1.0
|
C
|
A:CYS111
|
4.3
|
9.2
|
1.0
|
CA
|
A:CYS103
|
4.4
|
10.1
|
1.0
|
N
|
A:LYS99
|
4.5
|
13.2
|
1.0
|
C
|
A:GLN96
|
4.6
|
9.8
|
1.0
|
C
|
A:CYS100
|
4.9
|
12.2
|
1.0
|
N
|
A:LYS113
|
4.9
|
10.1
|
1.0
|
CG
|
A:LYS113
|
4.9
|
14.2
|
1.0
|
O
|
A:CYS100
|
4.9
|
11.7
|
1.0
|
CA
|
A:GLN96
|
4.9
|
9.2
|
1.0
|
|
Zinc binding site 3 out
of 4 in 7ucu
Go back to
Zinc Binding Sites List in 7ucu
Zinc binding site 3 out
of 4 in the Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn401
b:11.8
occ:1.00
|
O
|
B:ETF404
|
1.9
|
12.0
|
1.0
|
NE2
|
B:HIS67
|
2.0
|
12.2
|
1.0
|
SG
|
B:CYS174
|
2.3
|
11.6
|
1.0
|
SG
|
B:CYS46
|
2.4
|
11.5
|
1.0
|
C2
|
B:ETF404
|
2.9
|
12.4
|
1.0
|
CE1
|
B:HIS67
|
3.0
|
10.8
|
1.0
|
CD2
|
B:HIS67
|
3.1
|
12.4
|
1.0
|
CB
|
B:CYS46
|
3.3
|
12.1
|
1.0
|
C5N
|
B:NAJ403
|
3.3
|
9.8
|
1.0
|
CB
|
B:CYS174
|
3.4
|
10.5
|
1.0
|
OG
|
B:SER48
|
3.8
|
11.1
|
1.0
|
C4N
|
B:NAJ403
|
3.9
|
10.3
|
1.0
|
C6N
|
B:NAJ403
|
4.0
|
9.3
|
1.0
|
CB
|
B:SER48
|
4.0
|
10.7
|
1.0
|
ND1
|
B:HIS67
|
4.2
|
11.2
|
1.0
|
CG
|
B:HIS67
|
4.2
|
10.9
|
1.0
|
C1
|
B:ETF404
|
4.3
|
14.2
|
1.0
|
F3
|
B:ETF404
|
4.6
|
16.2
|
1.0
|
NH2
|
B:ARG369
|
4.6
|
12.1
|
1.0
|
CA
|
B:CYS174
|
4.7
|
10.4
|
1.0
|
CA
|
B:CYS46
|
4.8
|
11.7
|
1.0
|
F1
|
B:ETF404
|
4.8
|
17.4
|
1.0
|
N
|
B:SER48
|
4.9
|
10.9
|
1.0
|
OE2
|
B:GLU68
|
4.9
|
12.7
|
1.0
|
CE2
|
B:PHE93
|
4.9
|
10.9
|
1.0
|
N1N
|
B:NAJ403
|
5.0
|
9.7
|
1.0
|
C3N
|
B:NAJ403
|
5.0
|
9.4
|
1.0
|
|
Zinc binding site 4 out
of 4 in 7ucu
Go back to
Zinc Binding Sites List in 7ucu
Zinc binding site 4 out
of 4 in the Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K
Mono view
Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 4 of Horse Liver Alcohol Dehydrogenase with Nad and Trifluoroethanol at 85K within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn402
b:13.4
occ:1.00
|
SG
|
B:CYS111
|
2.3
|
13.0
|
1.0
|
SG
|
B:CYS100
|
2.3
|
14.0
|
1.0
|
SG
|
B:CYS103
|
2.4
|
12.2
|
1.0
|
SG
|
B:CYS97
|
2.4
|
15.9
|
1.0
|
CB
|
B:CYS111
|
3.3
|
12.3
|
1.0
|
CB
|
B:CYS100
|
3.4
|
16.3
|
1.0
|
CB
|
B:CYS103
|
3.4
|
12.9
|
1.0
|
CB
|
B:CYS97
|
3.4
|
16.1
|
1.0
|
N
|
B:CYS97
|
3.5
|
13.6
|
1.0
|
CA
|
B:CYS111
|
3.7
|
11.4
|
1.0
|
N
|
B:CYS100
|
3.9
|
15.9
|
1.0
|
CA
|
B:CYS97
|
3.9
|
15.6
|
1.0
|
N
|
B:LEU112
|
4.0
|
12.5
|
1.0
|
N
|
B:GLY98
|
4.0
|
15.6
|
1.0
|
CA
|
B:CYS100
|
4.2
|
16.1
|
1.0
|
N
|
B:CYS103
|
4.2
|
11.9
|
1.0
|
C
|
B:CYS111
|
4.3
|
11.9
|
1.0
|
C
|
B:CYS97
|
4.3
|
16.2
|
1.0
|
CA
|
B:CYS103
|
4.4
|
12.1
|
1.0
|
N
|
B:LYS99
|
4.5
|
16.7
|
1.0
|
C
|
B:GLN96
|
4.6
|
12.7
|
1.0
|
C
|
B:CYS100
|
4.8
|
14.4
|
1.0
|
N
|
B:LYS113
|
4.9
|
12.5
|
1.0
|
CG
|
B:LYS113
|
4.9
|
18.8
|
1.0
|
CA
|
B:GLN96
|
4.9
|
11.8
|
1.0
|
O
|
B:CYS100
|
4.9
|
14.9
|
1.0
|
O
|
B:HOH823
|
5.0
|
29.8
|
1.0
|
|
Reference:
B.V.Plapp,
L.Gakhar,
R.Subramanian.
Dependence of Crystallographic Atomic Displacement Factors on Temperature (25-150 K) For Complexes of Horse Liver Alcohol Dehydrogenases Acta Crystallogr.,Sect.D V. D78 1221 2022.
ISSN: ESSN 1399-0047
DOI: 10.1107/S2059798322008361
Page generated: Wed Oct 30 12:01:12 2024
|