Zinc in PDB 9cm6: Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide
Enzymatic activity of Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide
All present enzymatic activity of Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide:
1.1.1.1;
Protein crystallography data
The structure of Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide, PDB code: 9cm6
was solved by
S.Mukherjee,
S.G.Boxer,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
37.87 /
1.47
|
Space group
|
P 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
44.246,
50.393,
92.808,
92.75,
102.92,
109.01
|
R / Rfree (%)
|
15.8 /
18.8
|
Zinc Binding Sites:
The binding sites of Zinc atom in the Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide
(pdb code 9cm6). 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 V203L in Complex with Nadh and N- Cylcohexyl Formamide, PDB code: 9cm6:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 9cm6
Go back to
Zinc Binding Sites List in 9cm6
Zinc binding site 1 out
of 4 in the Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide
 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 V203L in Complex with Nadh and N- Cylcohexyl Formamide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn401
b:15.3
occ:1.00
|
NE2
|
A:HIS67
|
2.1
|
13.9
|
1.0
|
O9
|
A:CXF404
|
2.2
|
15.7
|
1.0
|
SG
|
A:CYS46
|
2.3
|
12.3
|
1.0
|
SG
|
A:CYS174
|
2.3
|
12.8
|
1.0
|
C7
|
A:CXF404
|
2.8
|
16.8
|
1.0
|
CD2
|
A:HIS67
|
3.1
|
14.8
|
1.0
|
CE1
|
A:HIS67
|
3.1
|
13.9
|
1.0
|
CB
|
A:CYS46
|
3.2
|
12.0
|
1.0
|
C5N
|
A:NAI403
|
3.4
|
11.8
|
1.0
|
CB
|
A:CYS174
|
3.4
|
10.6
|
1.0
|
OG
|
A:SER48
|
4.0
|
13.5
|
1.0
|
C6N
|
A:NAI403
|
4.0
|
12.7
|
1.0
|
C4N
|
A:NAI403
|
4.0
|
11.9
|
1.0
|
CB
|
A:SER48
|
4.1
|
12.3
|
1.0
|
N8
|
A:CXF404
|
4.2
|
17.2
|
1.0
|
CG
|
A:HIS67
|
4.2
|
12.1
|
1.0
|
ND1
|
A:HIS67
|
4.2
|
13.2
|
1.0
|
NH2
|
A:ARG369
|
4.4
|
13.9
|
1.0
|
OE2
|
A:GLU68
|
4.7
|
13.9
|
1.0
|
CA
|
A:CYS46
|
4.7
|
11.6
|
1.0
|
CA
|
A:CYS174
|
4.8
|
9.9
|
1.0
|
N
|
A:SER48
|
4.9
|
10.3
|
1.0
|
|
Zinc binding site 2 out
of 4 in 9cm6
Go back to
Zinc Binding Sites List in 9cm6
Zinc binding site 2 out
of 4 in the Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide
 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 V203L in Complex with Nadh and N- Cylcohexyl Formamide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Zn402
b:13.3
occ:1.00
|
SG
|
A:CYS100
|
2.3
|
12.7
|
1.0
|
SG
|
A:CYS111
|
2.3
|
12.9
|
1.0
|
SG
|
A:CYS97
|
2.3
|
14.4
|
1.0
|
SG
|
A:CYS103
|
2.4
|
13.2
|
1.0
|
CB
|
A:CYS97
|
3.4
|
14.0
|
1.0
|
CB
|
A:CYS103
|
3.4
|
13.4
|
1.0
|
CB
|
A:CYS111
|
3.4
|
11.8
|
1.0
|
CB
|
A:CYS100
|
3.4
|
14.2
|
1.0
|
N
|
A:CYS97
|
3.5
|
13.4
|
1.0
|
CA
|
A:CYS111
|
3.8
|
10.6
|
1.0
|
N
|
A:CYS100
|
3.9
|
16.5
|
1.0
|
CA
|
A:CYS97
|
3.9
|
14.7
|
1.0
|
N
|
A:GLY98
|
4.0
|
15.3
|
1.0
|
N
|
A:LEU112
|
4.0
|
12.2
|
1.0
|
N
|
A:CYS103
|
4.2
|
12.0
|
1.0
|
CA
|
A:CYS100
|
4.2
|
15.1
|
1.0
|
C
|
A:CYS97
|
4.3
|
15.8
|
1.0
|
C
|
A:CYS111
|
4.3
|
11.1
|
1.0
|
CA
|
A:CYS103
|
4.4
|
13.5
|
1.0
|
N
|
A:LYS99
|
4.4
|
17.7
|
1.0
|
C
|
A:GLN96
|
4.6
|
13.7
|
1.0
|
CG
|
A:LYS113
|
4.7
|
16.8
|
1.0
|
N
|
A:LYS113
|
4.8
|
14.1
|
1.0
|
C
|
A:CYS100
|
4.9
|
14.7
|
1.0
|
O
|
A:CYS100
|
4.9
|
14.1
|
1.0
|
CA
|
A:GLN96
|
4.9
|
12.5
|
1.0
|
CA
|
A:GLY98
|
5.0
|
17.3
|
1.0
|
C
|
A:LYS99
|
5.0
|
20.2
|
1.0
|
|
Zinc binding site 3 out
of 4 in 9cm6
Go back to
Zinc Binding Sites List in 9cm6
Zinc binding site 3 out
of 4 in the Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide
 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 V203L in Complex with Nadh and N- Cylcohexyl Formamide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn401
b:17.2
occ:1.00
|
O9
|
B:CXF404
|
2.1
|
18.6
|
1.0
|
NE2
|
B:HIS67
|
2.1
|
17.8
|
1.0
|
SG
|
B:CYS174
|
2.3
|
15.8
|
1.0
|
SG
|
B:CYS46
|
2.3
|
14.6
|
1.0
|
C7
|
B:CXF404
|
2.8
|
18.6
|
1.0
|
CD2
|
B:HIS67
|
3.1
|
16.8
|
1.0
|
CE1
|
B:HIS67
|
3.2
|
15.4
|
1.0
|
CB
|
B:CYS46
|
3.3
|
13.9
|
1.0
|
CB
|
B:CYS174
|
3.4
|
14.5
|
1.0
|
C5N
|
B:NAI403
|
3.5
|
14.2
|
1.0
|
OG
|
B:SER48
|
4.0
|
15.7
|
1.0
|
C6N
|
B:NAI403
|
4.1
|
13.4
|
1.0
|
C4N
|
B:NAI403
|
4.1
|
14.8
|
1.0
|
CB
|
B:SER48
|
4.1
|
14.6
|
1.0
|
N8
|
B:CXF404
|
4.2
|
20.0
|
1.0
|
CG
|
B:HIS67
|
4.2
|
14.9
|
1.0
|
ND1
|
B:HIS67
|
4.2
|
14.3
|
1.0
|
NH2
|
B:ARG369
|
4.4
|
15.9
|
1.0
|
OE2
|
B:GLU68
|
4.7
|
16.8
|
1.0
|
CA
|
B:CYS174
|
4.7
|
14.1
|
1.0
|
CA
|
B:CYS46
|
4.7
|
13.5
|
1.0
|
CE2
|
B:PHE93
|
4.9
|
14.0
|
1.0
|
N
|
B:SER48
|
4.9
|
13.9
|
1.0
|
|
Zinc binding site 4 out
of 4 in 9cm6
Go back to
Zinc Binding Sites List in 9cm6
Zinc binding site 4 out
of 4 in the Horse Liver Alcohol Dehydrogenase V203L in Complex with Nadh and N- Cylcohexyl Formamide
 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 V203L in Complex with Nadh and N- Cylcohexyl Formamide within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Zn402
b:18.0
occ:1.00
|
SG
|
B:CYS103
|
2.3
|
16.1
|
1.0
|
SG
|
B:CYS100
|
2.3
|
17.9
|
1.0
|
SG
|
B:CYS111
|
2.3
|
16.6
|
1.0
|
SG
|
B:CYS97
|
2.4
|
19.8
|
1.0
|
CB
|
B:CYS111
|
3.4
|
16.5
|
1.0
|
CB
|
B:CYS100
|
3.4
|
21.6
|
1.0
|
CB
|
B:CYS97
|
3.5
|
18.8
|
1.0
|
CB
|
B:CYS103
|
3.5
|
15.7
|
1.0
|
N
|
B:CYS97
|
3.5
|
17.9
|
1.0
|
CA
|
B:CYS111
|
3.8
|
15.7
|
1.0
|
N
|
B:CYS100
|
3.8
|
25.8
|
1.0
|
CA
|
B:CYS97
|
3.9
|
18.6
|
1.0
|
N
|
B:GLY98
|
3.9
|
20.1
|
1.0
|
N
|
B:LEU112
|
4.0
|
16.4
|
1.0
|
CA
|
B:CYS100
|
4.2
|
24.8
|
1.0
|
N
|
B:CYS103
|
4.2
|
16.3
|
1.0
|
C
|
B:CYS97
|
4.3
|
18.9
|
1.0
|
C
|
B:CYS111
|
4.3
|
15.0
|
1.0
|
CA
|
B:CYS103
|
4.4
|
16.4
|
1.0
|
N
|
B:LYS99
|
4.5
|
25.3
|
1.0
|
C
|
B:GLN96
|
4.6
|
17.7
|
1.0
|
CG
|
B:LYS113
|
4.7
|
22.1
|
1.0
|
N
|
B:LYS113
|
4.8
|
16.7
|
1.0
|
C
|
B:CYS100
|
4.8
|
26.1
|
1.0
|
O
|
B:CYS100
|
4.9
|
29.7
|
1.0
|
CA
|
B:GLN96
|
4.9
|
16.2
|
1.0
|
CA
|
B:GLY98
|
4.9
|
21.2
|
1.0
|
C
|
B:LYS99
|
5.0
|
28.7
|
1.0
|
|
Reference:
S.Mukherjee,
S.D.E.Fried,
Y.Mao,
S.G.Boxer.
Role of Electrostatics in Hydride Transfer By Horse Liver Alcohol Dehydrogenase To Be Published.
Page generated: Fri Aug 22 16:59:46 2025
|