Chlorine in PDB 5br4: E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant
Enzymatic activity of E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant
All present enzymatic activity of E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant:
1.1.1.77;
Protein crystallography data
The structure of E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant, PDB code: 5br4
was solved by
J.K.B.Cahn,
S.Brinkmann-Chen,
F.H.Arnold,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
85.50 /
0.91
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
69.697,
63.769,
91.674,
90.00,
111.15,
90.00
|
R / Rfree (%)
|
12.9 /
14.7
|
Other elements in 5br4:
The structure of E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant also contains other interesting chemical elements:
Chlorine Binding Sites:
The binding sites of Chlorine atom in the E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant
(pdb code 5br4). This binding sites where shown within
5.0 Angstroms radius around Chlorine atom.
In total 4 binding sites of Chlorine where determined in the
E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant, PDB code: 5br4:
Jump to Chlorine binding site number:
1;
2;
3;
4;
Chlorine binding site 1 out
of 4 in 5br4
Go back to
Chlorine Binding Sites List in 5br4
Chlorine binding site 1 out
of 4 in the E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 1 of E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl405
b:10.9
occ:1.00
|
NE2
|
A:HIS267
|
3.0
|
8.6
|
1.0
|
O3
|
A:GOL403
|
3.1
|
25.2
|
1.0
|
O2D
|
A:NAD402
|
3.1
|
9.2
|
1.0
|
CE1
|
A:HIS277
|
3.3
|
8.2
|
1.0
|
C6N
|
A:NAD402
|
3.5
|
7.9
|
1.0
|
C3
|
A:GOL403
|
3.5
|
30.8
|
1.0
|
N1N
|
A:NAD402
|
3.6
|
7.3
|
1.0
|
CG2
|
A:VAL153
|
3.7
|
8.7
|
1.0
|
C2D
|
A:NAD402
|
3.7
|
8.0
|
1.0
|
C5N
|
A:NAD402
|
3.7
|
8.2
|
1.0
|
ND1
|
A:HIS277
|
3.8
|
8.1
|
1.0
|
CD2
|
A:HIS267
|
3.9
|
8.3
|
1.0
|
CE1
|
A:HIS267
|
4.0
|
9.2
|
1.0
|
C2N
|
A:NAD402
|
4.1
|
7.4
|
1.0
|
O
|
A:HOH845
|
4.1
|
9.5
|
1.0
|
NE2
|
A:HIS277
|
4.1
|
7.6
|
1.0
|
C1D
|
A:NAD402
|
4.1
|
7.7
|
1.0
|
CD2
|
A:HIS263
|
4.1
|
7.7
|
1.0
|
C4N
|
A:NAD402
|
4.2
|
8.4
|
1.0
|
C2
|
A:GOL403
|
4.3
|
21.6
|
1.0
|
C3N
|
A:NAD402
|
4.4
|
7.5
|
1.0
|
CB
|
A:VAL153
|
4.4
|
7.4
|
1.0
|
CG1
|
A:VAL153
|
4.4
|
9.1
|
1.0
|
CG
|
A:HIS277
|
4.9
|
7.5
|
1.0
|
NE2
|
A:HIS263
|
4.9
|
7.3
|
1.0
|
|
Chlorine binding site 2 out
of 4 in 5br4
Go back to
Chlorine Binding Sites List in 5br4
Chlorine binding site 2 out
of 4 in the E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 2 of E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Cl406
b:9.4
occ:1.00
|
ND1
|
A:HIS277
|
3.1
|
8.1
|
1.0
|
O
|
A:HOH774
|
3.3
|
12.7
|
1.0
|
NZ
|
A:LYS162
|
3.3
|
8.7
|
1.0
|
O
|
A:HOH845
|
3.3
|
9.5
|
1.0
|
CD2
|
A:HIS267
|
3.5
|
8.3
|
1.0
|
O
|
A:ALA266
|
3.7
|
7.5
|
1.0
|
CA
|
A:HIS267
|
3.7
|
7.4
|
1.0
|
CD
|
A:LYS162
|
3.9
|
10.4
|
1.0
|
C
|
A:ALA266
|
3.9
|
7.3
|
1.0
|
CE
|
A:LYS162
|
3.9
|
11.1
|
1.0
|
N
|
A:HIS267
|
4.0
|
7.1
|
1.0
|
CG
|
A:HIS277
|
4.0
|
7.5
|
1.0
|
CB
|
A:HIS277
|
4.0
|
8.2
|
1.0
|
CE1
|
A:HIS277
|
4.1
|
8.2
|
1.0
|
CA
|
A:HIS277
|
4.1
|
7.7
|
1.0
|
O2D
|
A:NAD402
|
4.3
|
9.2
|
1.0
|
CG
|
A:HIS267
|
4.4
|
7.6
|
1.0
|
CB
|
A:ALA266
|
4.4
|
8.0
|
1.0
|
NE2
|
A:HIS267
|
4.5
|
8.6
|
1.0
|
O
|
A:HIS267
|
4.5
|
7.7
|
1.0
|
OD1
|
A:ASN71
|
4.5
|
9.8
|
1.0
|
CA
|
A:GLY270
|
4.6
|
7.7
|
1.0
|
C
|
A:HIS267
|
4.6
|
7.1
|
1.0
|
N
|
A:GLY270
|
4.7
|
7.4
|
1.0
|
CB
|
A:HIS267
|
4.7
|
7.7
|
1.0
|
CA
|
A:ALA266
|
4.8
|
7.2
|
1.0
|
ND2
|
A:ASN281
|
4.9
|
7.9
|
1.0
|
C2D
|
A:NAD402
|
4.9
|
8.0
|
1.0
|
N
|
A:HIS277
|
4.9
|
8.0
|
1.0
|
|
Chlorine binding site 3 out
of 4 in 5br4
Go back to
Chlorine Binding Sites List in 5br4
Chlorine binding site 3 out
of 4 in the E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 3 of E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl404
b:12.7
occ:1.00
|
O
|
B:HOH515
|
3.0
|
29.7
|
1.0
|
ND1
|
B:HIS277
|
3.1
|
9.8
|
1.0
|
O
|
B:HOH754
|
3.3
|
16.9
|
1.0
|
O
|
B:HOH835
|
3.3
|
11.3
|
1.0
|
NZ
|
B:LYS162
|
3.5
|
14.0
|
1.0
|
CD2
|
B:HIS267
|
3.5
|
10.0
|
1.0
|
O
|
B:ALA266
|
3.7
|
9.1
|
1.0
|
CA
|
B:HIS267
|
3.7
|
9.1
|
1.0
|
C
|
B:ALA266
|
3.9
|
8.3
|
1.0
|
CD
|
B:LYS162
|
3.9
|
15.6
|
1.0
|
N
|
B:HIS267
|
3.9
|
8.7
|
1.0
|
CG
|
B:HIS277
|
4.0
|
8.9
|
1.0
|
CB
|
B:HIS277
|
4.0
|
8.9
|
1.0
|
CE
|
B:LYS162
|
4.0
|
18.4
|
1.0
|
CE1
|
B:HIS277
|
4.1
|
9.5
|
1.0
|
CA
|
B:HIS277
|
4.1
|
8.9
|
1.0
|
O2D
|
B:NAD402
|
4.3
|
11.5
|
1.0
|
CG
|
B:HIS267
|
4.4
|
10.1
|
1.0
|
CB
|
B:ALA266
|
4.4
|
8.9
|
1.0
|
NE2
|
B:HIS267
|
4.5
|
11.4
|
1.0
|
O
|
B:HIS267
|
4.5
|
9.9
|
1.0
|
CA
|
B:GLY270
|
4.6
|
9.6
|
1.0
|
OD1
|
B:ASN71
|
4.6
|
13.2
|
1.0
|
C
|
B:HIS267
|
4.6
|
9.6
|
1.0
|
CB
|
B:HIS267
|
4.7
|
10.2
|
1.0
|
N
|
B:GLY270
|
4.7
|
9.0
|
1.0
|
CA
|
B:ALA266
|
4.8
|
8.6
|
1.0
|
ND2
|
B:ASN281
|
4.8
|
8.8
|
1.0
|
N
|
B:HIS277
|
4.9
|
9.3
|
1.0
|
C2D
|
B:NAD402
|
4.9
|
9.6
|
1.0
|
|
Chlorine binding site 4 out
of 4 in 5br4
Go back to
Chlorine Binding Sites List in 5br4
Chlorine binding site 4 out
of 4 in the E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant
Mono view
Stereo pair view
|
A full contact list of Chlorine with other atoms in the Cl binding
site number 4 of E. Coli Lactaldehyde Reductase (Fuco) M185C Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Cl405
b:13.5
occ:1.00
|
NE2
|
B:HIS267
|
3.0
|
11.4
|
1.0
|
O2D
|
B:NAD402
|
3.1
|
11.5
|
1.0
|
O3
|
B:GOL403
|
3.1
|
26.5
|
1.0
|
CE1
|
B:HIS277
|
3.3
|
9.5
|
1.0
|
C3
|
B:GOL403
|
3.5
|
39.3
|
1.0
|
C6N
|
B:NAD402
|
3.5
|
9.6
|
1.0
|
N1N
|
B:NAD402
|
3.6
|
8.9
|
1.0
|
CG2
|
B:VAL153
|
3.7
|
10.9
|
1.0
|
C5N
|
B:NAD402
|
3.8
|
9.6
|
1.0
|
C2D
|
B:NAD402
|
3.8
|
9.6
|
1.0
|
ND1
|
B:HIS277
|
3.8
|
9.8
|
1.0
|
CD2
|
B:HIS267
|
3.9
|
10.0
|
1.0
|
CE1
|
B:HIS267
|
4.0
|
12.2
|
1.0
|
NE2
|
B:HIS277
|
4.1
|
8.0
|
1.0
|
C2N
|
B:NAD402
|
4.1
|
8.6
|
1.0
|
O
|
B:HOH835
|
4.1
|
11.3
|
1.0
|
CD2
|
B:HIS263
|
4.1
|
7.9
|
1.0
|
C1D
|
B:NAD402
|
4.2
|
9.0
|
1.0
|
C4N
|
B:NAD402
|
4.2
|
9.8
|
1.0
|
CB
|
B:VAL153
|
4.4
|
9.9
|
1.0
|
C3N
|
B:NAD402
|
4.4
|
8.9
|
1.0
|
C2
|
B:GOL403
|
4.4
|
27.3
|
1.0
|
CG1
|
B:VAL153
|
4.4
|
12.0
|
1.0
|
CG
|
B:HIS277
|
4.9
|
8.9
|
1.0
|
NE2
|
B:HIS263
|
4.9
|
8.7
|
1.0
|
CD2
|
B:HIS277
|
5.0
|
8.1
|
1.0
|
|
Reference:
J.K.Cahn,
A.Baumschlager,
S.Brinkmann-Chen,
F.H.Arnold.
Mutations in Adenine-Binding Pockets Enhance Catalytic Properties of Nad(P)H-Dependent Enzymes. Protein Eng.Des.Sel. V. 29 31 2016.
ISSN: ESSN 1741-0134
PubMed: 26512129
DOI: 10.1093/PROTEIN/GZV057
Page generated: Fri Jul 26 05:39:10 2024
|