Manganese in PDB 1en4: Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant
Enzymatic activity of Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant
All present enzymatic activity of Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant:
1.15.1.1;
Protein crystallography data
The structure of Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant, PDB code: 1en4
was solved by
R.A.Edwards,
M.M.Whittaker,
E.N.Baker,
J.W.Whittaker,
G.B.Jameson,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
45.00 /
2.00
|
Space group
|
C 2 2 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
101.766,
109.239,
180.889,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
16.9 /
19.2
|
Manganese Binding Sites:
The binding sites of Manganese atom in the Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant
(pdb code 1en4). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 4 binding sites of Manganese where determined in the
Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant, PDB code: 1en4:
Jump to Manganese binding site number:
1;
2;
3;
4;
Manganese binding site 1 out
of 4 in 1en4
Go back to
Manganese Binding Sites List in 1en4
Manganese binding site 1 out
of 4 in the Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 1 of Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn501
b:11.1
occ:1.00
|
OD2
|
A:ASP167
|
2.0
|
9.4
|
1.0
|
NE2
|
A:HIS171
|
2.2
|
11.7
|
1.0
|
NE2
|
A:HIS81
|
2.2
|
11.8
|
1.0
|
NE2
|
A:HIS26
|
2.3
|
9.5
|
1.0
|
O
|
A:HOH625
|
2.3
|
10.1
|
1.0
|
CG
|
A:ASP167
|
3.1
|
13.8
|
1.0
|
CE1
|
A:HIS81
|
3.2
|
12.4
|
1.0
|
CD2
|
A:HIS171
|
3.2
|
14.0
|
1.0
|
CE1
|
A:HIS26
|
3.2
|
11.0
|
1.0
|
CD2
|
A:HIS81
|
3.2
|
12.5
|
1.0
|
CE1
|
A:HIS171
|
3.2
|
12.8
|
1.0
|
CD2
|
A:HIS26
|
3.3
|
10.3
|
1.0
|
OD1
|
A:ASP167
|
3.6
|
12.9
|
1.0
|
ND1
|
A:HIS81
|
4.3
|
9.8
|
1.0
|
CB
|
A:ASP167
|
4.3
|
11.9
|
1.0
|
ND1
|
A:HIS26
|
4.3
|
10.7
|
1.0
|
CZ3
|
A:TRP128
|
4.3
|
11.2
|
0.5
|
ND1
|
A:HIS171
|
4.3
|
11.4
|
1.0
|
CG
|
A:HIS171
|
4.4
|
12.2
|
1.0
|
CG
|
A:HIS81
|
4.4
|
11.2
|
1.0
|
CZ2
|
A:TRP128
|
4.4
|
14.6
|
0.5
|
CG
|
A:HIS26
|
4.4
|
12.2
|
1.0
|
CH2
|
A:TRP128
|
4.4
|
10.1
|
0.5
|
CB
|
A:TRP169
|
4.6
|
8.7
|
1.0
|
NE2
|
A:HIS146
|
4.7
|
13.2
|
1.0
|
CG
|
A:TRP169
|
4.8
|
9.6
|
1.0
|
OH
|
A:TYR34
|
4.9
|
19.3
|
1.0
|
CB
|
A:ALA172
|
5.0
|
8.2
|
1.0
|
|
Manganese binding site 2 out
of 4 in 1en4
Go back to
Manganese Binding Sites List in 1en4
Manganese binding site 2 out
of 4 in the Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 2 of Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn502
b:13.6
occ:1.00
|
OD2
|
B:ASP167
|
1.9
|
14.0
|
1.0
|
NE2
|
B:HIS81
|
2.2
|
13.2
|
1.0
|
NE2
|
B:HIS26
|
2.2
|
9.5
|
1.0
|
O
|
B:HOH620
|
2.2
|
13.7
|
1.0
|
NE2
|
B:HIS171
|
2.3
|
12.1
|
1.0
|
CG
|
B:ASP167
|
3.0
|
14.9
|
1.0
|
CE1
|
B:HIS81
|
3.1
|
14.7
|
1.0
|
CE1
|
B:HIS26
|
3.1
|
13.0
|
1.0
|
CD2
|
B:HIS171
|
3.2
|
10.0
|
1.0
|
CD2
|
B:HIS81
|
3.2
|
11.9
|
1.0
|
CE1
|
B:HIS171
|
3.2
|
10.9
|
1.0
|
CD2
|
B:HIS26
|
3.2
|
11.3
|
1.0
|
OD1
|
B:ASP167
|
3.5
|
13.9
|
1.0
|
CH2
|
B:TRP128
|
4.2
|
18.2
|
0.5
|
CZ3
|
B:TRP128
|
4.2
|
14.8
|
0.5
|
ND1
|
B:HIS81
|
4.3
|
13.9
|
1.0
|
ND1
|
B:HIS26
|
4.3
|
12.7
|
1.0
|
CB
|
B:ASP167
|
4.3
|
12.7
|
1.0
|
CG
|
B:HIS81
|
4.3
|
13.8
|
1.0
|
ND1
|
B:HIS171
|
4.3
|
8.8
|
1.0
|
CG
|
B:HIS171
|
4.4
|
10.6
|
1.0
|
CG
|
B:HIS26
|
4.4
|
11.0
|
1.0
|
CZ2
|
B:TRP128
|
4.4
|
13.4
|
0.5
|
CB
|
B:TRP169
|
4.6
|
10.6
|
1.0
|
NE2
|
B:HIS146
|
4.7
|
13.8
|
1.0
|
CG
|
B:TRP169
|
4.7
|
10.7
|
1.0
|
CB
|
B:ALA172
|
4.9
|
11.5
|
1.0
|
OH
|
B:TYR34
|
4.9
|
21.5
|
1.0
|
CD1
|
B:TRP169
|
4.9
|
10.1
|
1.0
|
CE2
|
B:TYR34
|
5.0
|
16.9
|
1.0
|
|
Manganese binding site 3 out
of 4 in 1en4
Go back to
Manganese Binding Sites List in 1en4
Manganese binding site 3 out
of 4 in the Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 3 of Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mn503
b:13.8
occ:1.00
|
OD2
|
C:ASP167
|
2.0
|
14.0
|
1.0
|
NE2
|
C:HIS171
|
2.1
|
12.0
|
1.0
|
NE2
|
C:HIS26
|
2.2
|
14.9
|
1.0
|
NE2
|
C:HIS81
|
2.3
|
14.6
|
1.0
|
O
|
C:HOH472
|
2.3
|
8.8
|
1.0
|
CE1
|
C:HIS171
|
3.0
|
14.4
|
1.0
|
CG
|
C:ASP167
|
3.1
|
12.2
|
1.0
|
CE1
|
C:HIS81
|
3.2
|
14.0
|
1.0
|
CE1
|
C:HIS26
|
3.2
|
16.1
|
1.0
|
CD2
|
C:HIS171
|
3.2
|
13.9
|
1.0
|
CD2
|
C:HIS26
|
3.2
|
13.7
|
1.0
|
CD2
|
C:HIS81
|
3.3
|
13.8
|
1.0
|
OD1
|
C:ASP167
|
3.6
|
12.1
|
1.0
|
ND1
|
C:HIS171
|
4.2
|
14.2
|
1.0
|
ND1
|
C:HIS26
|
4.3
|
14.5
|
1.0
|
ND1
|
C:HIS81
|
4.3
|
14.6
|
1.0
|
CG
|
C:HIS171
|
4.3
|
12.5
|
1.0
|
CB
|
C:ASP167
|
4.3
|
12.4
|
1.0
|
CZ2
|
C:TRP128
|
4.3
|
12.1
|
0.5
|
CG
|
C:HIS26
|
4.4
|
13.7
|
1.0
|
CZ3
|
C:TRP128
|
4.4
|
17.8
|
0.5
|
CG
|
C:HIS81
|
4.4
|
17.2
|
1.0
|
CB
|
C:TRP169
|
4.6
|
14.1
|
1.0
|
CH2
|
C:TRP128
|
4.6
|
18.0
|
0.5
|
NE2
|
C:HIS146
|
4.7
|
15.3
|
1.0
|
CG
|
C:TRP169
|
4.7
|
13.4
|
1.0
|
OH
|
C:TYR34
|
4.9
|
22.3
|
1.0
|
CB
|
C:ALA172
|
4.9
|
11.3
|
1.0
|
CD1
|
C:TRP169
|
4.9
|
14.0
|
1.0
|
|
Manganese binding site 4 out
of 4 in 1en4
Go back to
Manganese Binding Sites List in 1en4
Manganese binding site 4 out
of 4 in the Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant
Mono view
Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 4 of Crystal Structure Analysis of the E. Coli Manganese Superoxide Dismutase Q146H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mn504
b:16.6
occ:1.00
|
OD2
|
D:ASP167
|
1.9
|
13.9
|
1.0
|
NE2
|
D:HIS171
|
2.2
|
14.3
|
1.0
|
NE2
|
D:HIS81
|
2.2
|
17.0
|
1.0
|
NE2
|
D:HIS26
|
2.3
|
11.3
|
1.0
|
O
|
D:HOH473
|
2.3
|
15.2
|
1.0
|
CG
|
D:ASP167
|
3.0
|
17.5
|
1.0
|
CE1
|
D:HIS171
|
3.1
|
13.2
|
1.0
|
CE1
|
D:HIS81
|
3.2
|
15.5
|
1.0
|
CD2
|
D:HIS81
|
3.2
|
15.7
|
1.0
|
CE1
|
D:HIS26
|
3.2
|
11.0
|
1.0
|
CD2
|
D:HIS171
|
3.2
|
12.0
|
1.0
|
CD2
|
D:HIS26
|
3.3
|
11.6
|
1.0
|
OD1
|
D:ASP167
|
3.5
|
15.9
|
1.0
|
CZ2
|
D:TRP128
|
4.2
|
14.2
|
0.5
|
ND1
|
D:HIS171
|
4.3
|
11.4
|
1.0
|
ND1
|
D:HIS81
|
4.3
|
12.2
|
1.0
|
CZ3
|
D:TRP128
|
4.3
|
22.4
|
0.5
|
CB
|
D:ASP167
|
4.3
|
13.8
|
1.0
|
CG
|
D:HIS81
|
4.3
|
17.1
|
1.0
|
ND1
|
D:HIS26
|
4.3
|
14.4
|
1.0
|
CG
|
D:HIS171
|
4.4
|
14.4
|
1.0
|
CG
|
D:HIS26
|
4.4
|
13.9
|
1.0
|
CH2
|
D:TRP128
|
4.5
|
21.7
|
0.5
|
CB
|
D:TRP169
|
4.6
|
10.0
|
1.0
|
NE2
|
D:HIS146
|
4.6
|
15.8
|
1.0
|
CG
|
D:TRP169
|
4.7
|
11.6
|
1.0
|
OH
|
D:TYR34
|
4.8
|
24.0
|
1.0
|
CB
|
D:ALA172
|
4.9
|
15.4
|
1.0
|
CH2
|
D:TRP128
|
5.0
|
15.2
|
0.5
|
CD1
|
D:TRP169
|
5.0
|
9.5
|
1.0
|
|
Reference:
R.A.Edwards,
M.M.Whittaker,
J.W.Whittaker,
E.N.Baker,
G.B.Jameson.
Outer Sphere Mutations Perturb Metal Reactivity in Manganese Superoxide Dismutase. Biochemistry V. 40 15 2001.
ISSN: ISSN 0006-2960
PubMed: 11141052
DOI: 10.1021/BI0018943
Page generated: Sat Oct 5 10:11:41 2024
|