Magnesium in PDB 4qn0: Crystal Structure of the Cps-6 Mutant Q130K
Protein crystallography data
The structure of Crystal Structure of the Cps-6 Mutant Q130K, PDB code: 4qn0
was solved by
J.L.J.Lin,
H.S.Yuan,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
26.48 /
2.74
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
67.550,
122.442,
73.522,
90.00,
96.02,
90.00
|
R / Rfree (%)
|
18.5 /
23.5
|
Magnesium Binding Sites:
The binding sites of Magnesium atom in the Crystal Structure of the Cps-6 Mutant Q130K
(pdb code 4qn0). This binding sites where shown within
5.0 Angstroms radius around Magnesium atom.
In total 4 binding sites of Magnesium where determined in the
Crystal Structure of the Cps-6 Mutant Q130K, PDB code: 4qn0:
Jump to Magnesium binding site number:
1;
2;
3;
4;
Magnesium binding site 1 out
of 4 in 4qn0
Go back to
Magnesium Binding Sites List in 4qn0
Magnesium binding site 1 out
of 4 in the Crystal Structure of the Cps-6 Mutant Q130K
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 1 of Crystal Structure of the Cps-6 Mutant Q130K within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mg401
b:19.6
occ:1.00
|
O
|
A:HOH546
|
1.7
|
30.0
|
1.0
|
O
|
A:HOH532
|
2.0
|
70.5
|
1.0
|
O
|
A:HOH541
|
2.3
|
57.1
|
1.0
|
O
|
A:HOH542
|
2.4
|
67.0
|
1.0
|
OD1
|
A:ASN180
|
2.4
|
25.9
|
1.0
|
CG
|
A:ASN180
|
3.5
|
26.4
|
1.0
|
N
|
A:HIS148
|
3.6
|
13.7
|
1.0
|
ND2
|
A:ASN180
|
3.9
|
25.8
|
1.0
|
OE2
|
A:GLU188
|
3.9
|
23.6
|
1.0
|
O
|
A:HIS148
|
4.0
|
17.5
|
1.0
|
OE1
|
A:GLU188
|
4.2
|
21.3
|
1.0
|
CA
|
A:GLY147
|
4.3
|
13.6
|
1.0
|
C
|
A:GLY147
|
4.4
|
14.1
|
1.0
|
OE1
|
A:GLN174
|
4.4
|
15.2
|
1.0
|
CA
|
A:HIS148
|
4.4
|
13.5
|
1.0
|
CB
|
A:HIS148
|
4.4
|
12.4
|
1.0
|
CD
|
A:GLU188
|
4.5
|
21.5
|
1.0
|
CD1
|
A:TRP184
|
4.5
|
19.8
|
1.0
|
O
|
A:ASN180
|
4.6
|
26.5
|
1.0
|
C
|
A:HIS148
|
4.6
|
15.7
|
1.0
|
CB
|
A:ASN180
|
4.8
|
26.7
|
1.0
|
NE1
|
A:TRP184
|
5.0
|
22.0
|
1.0
|
|
Magnesium binding site 2 out
of 4 in 4qn0
Go back to
Magnesium Binding Sites List in 4qn0
Magnesium binding site 2 out
of 4 in the Crystal Structure of the Cps-6 Mutant Q130K
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 2 of Crystal Structure of the Cps-6 Mutant Q130K within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mg401
b:34.8
occ:1.00
|
OD1
|
B:ASN180
|
2.1
|
11.6
|
1.0
|
O
|
B:HOH559
|
2.4
|
37.8
|
1.0
|
O
|
B:HOH555
|
2.5
|
76.8
|
1.0
|
O
|
B:HOH540
|
2.6
|
2.0
|
1.0
|
O
|
B:HOH560
|
2.8
|
81.9
|
1.0
|
CG
|
B:ASN180
|
3.2
|
12.9
|
1.0
|
ND2
|
B:ASN180
|
3.7
|
11.4
|
1.0
|
N
|
B:HIS148
|
3.9
|
12.2
|
1.0
|
O
|
B:HOH557
|
4.0
|
20.9
|
1.0
|
OE2
|
B:GLU188
|
4.0
|
17.1
|
1.0
|
O
|
B:HIS148
|
4.1
|
9.6
|
1.0
|
O
|
B:ASN180
|
4.1
|
14.5
|
1.0
|
OE1
|
B:GLN174
|
4.1
|
9.6
|
1.0
|
CA
|
B:GLY147
|
4.1
|
12.2
|
1.0
|
OE1
|
B:GLU188
|
4.2
|
19.7
|
1.0
|
CD1
|
B:TRP184
|
4.3
|
14.2
|
1.0
|
C
|
B:GLY147
|
4.4
|
11.8
|
1.0
|
CB
|
B:ASN180
|
4.4
|
12.2
|
1.0
|
CD
|
B:GLU188
|
4.5
|
19.2
|
1.0
|
C
|
B:ASN180
|
4.7
|
13.4
|
1.0
|
CA
|
B:ASN180
|
4.7
|
12.5
|
1.0
|
O
|
B:HOH558
|
4.7
|
64.4
|
1.0
|
NE1
|
B:TRP184
|
4.8
|
15.1
|
1.0
|
CA
|
B:HIS148
|
4.8
|
11.1
|
1.0
|
C
|
B:HIS148
|
4.9
|
11.2
|
1.0
|
CB
|
B:HIS148
|
5.0
|
8.8
|
1.0
|
|
Magnesium binding site 3 out
of 4 in 4qn0
Go back to
Magnesium Binding Sites List in 4qn0
Magnesium binding site 3 out
of 4 in the Crystal Structure of the Cps-6 Mutant Q130K
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 3 of Crystal Structure of the Cps-6 Mutant Q130K within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Mg401
b:24.9
occ:1.00
|
O
|
C:HOH541
|
1.9
|
87.2
|
1.0
|
O
|
C:HOH536
|
2.0
|
90.0
|
1.0
|
OD1
|
C:ASN180
|
2.3
|
17.0
|
1.0
|
O
|
C:HOH535
|
2.6
|
77.6
|
1.0
|
O
|
C:HOH539
|
2.8
|
70.2
|
1.0
|
CG
|
C:ASN180
|
3.4
|
19.7
|
1.0
|
N
|
C:HIS148
|
3.8
|
13.6
|
1.0
|
ND2
|
C:ASN180
|
3.9
|
22.2
|
1.0
|
OE2
|
C:GLU188
|
3.9
|
25.9
|
1.0
|
O
|
C:HIS148
|
4.1
|
12.8
|
1.0
|
O
|
C:ASN180
|
4.2
|
20.6
|
1.0
|
OE1
|
C:GLU188
|
4.3
|
27.0
|
1.0
|
CA
|
C:GLY147
|
4.3
|
14.2
|
1.0
|
OE1
|
C:GLN174
|
4.4
|
19.4
|
1.0
|
O
|
C:HOH542
|
4.4
|
76.4
|
1.0
|
C
|
C:GLY147
|
4.5
|
13.2
|
1.0
|
O
|
C:HOH518
|
4.5
|
18.2
|
1.0
|
CD
|
C:GLU188
|
4.6
|
26.6
|
1.0
|
CA
|
C:HIS148
|
4.6
|
13.3
|
1.0
|
CB
|
C:HIS148
|
4.6
|
12.4
|
1.0
|
CD1
|
C:TRP184
|
4.7
|
22.3
|
1.0
|
CB
|
C:ASN180
|
4.7
|
21.5
|
1.0
|
C
|
C:HIS148
|
4.8
|
12.8
|
1.0
|
C
|
C:ASN180
|
4.8
|
22.8
|
1.0
|
CA
|
C:ASN180
|
4.9
|
23.2
|
1.0
|
|
Magnesium binding site 4 out
of 4 in 4qn0
Go back to
Magnesium Binding Sites List in 4qn0
Magnesium binding site 4 out
of 4 in the Crystal Structure of the Cps-6 Mutant Q130K
Mono view
Stereo pair view
|
A full contact list of Magnesium with other atoms in the Mg binding
site number 4 of Crystal Structure of the Cps-6 Mutant Q130K within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Mg401
b:29.7
occ:1.00
|
O
|
D:HOH530
|
1.2
|
30.0
|
1.0
|
OD1
|
D:ASN180
|
2.3
|
30.5
|
1.0
|
O
|
D:HOH525
|
2.6
|
86.8
|
1.0
|
O
|
D:HOH524
|
2.7
|
83.8
|
1.0
|
O
|
D:HOH523
|
2.8
|
84.8
|
1.0
|
CG
|
D:ASN180
|
3.4
|
30.1
|
1.0
|
O
|
D:ASN180
|
3.7
|
33.2
|
1.0
|
ND2
|
D:ASN180
|
3.9
|
22.2
|
1.0
|
OE2
|
D:GLU188
|
4.0
|
30.4
|
1.0
|
OE1
|
D:GLU188
|
4.1
|
34.9
|
1.0
|
N
|
D:HIS148
|
4.4
|
22.4
|
1.0
|
O
|
D:HOH509
|
4.4
|
11.1
|
1.0
|
CD
|
D:GLU188
|
4.5
|
34.9
|
1.0
|
CD1
|
D:TRP184
|
4.5
|
29.0
|
1.0
|
O
|
D:HIS148
|
4.6
|
26.6
|
1.0
|
C
|
D:ASN180
|
4.6
|
34.2
|
1.0
|
OE1
|
D:GLN174
|
4.7
|
27.3
|
1.0
|
CB
|
D:ASN180
|
4.7
|
32.9
|
1.0
|
CA
|
D:GLY147
|
4.8
|
23.0
|
1.0
|
CA
|
D:ASN180
|
4.9
|
32.8
|
1.0
|
NE1
|
D:TRP184
|
4.9
|
29.1
|
1.0
|
|
Reference:
J.L.J.Lin,
A.Nakagawa,
R.Skeen-Gaar,
W.Z.Yang,
P.Zhao,
Z.Zhang,
X.Ge,
S.Mitani,
D.Xue,
H.S.Yuan.
Oxidative Stress Impairs Cell Death By Repressing the Nuclease Activity of Mitochondrial Endonuclease G Cell Rep V. 16 279 2016.
ISSN: ESSN 2211-1247
PubMed: 27346342
DOI: 10.1016/J.CELREP.2016.05.090
Page generated: Tue Aug 20 02:06:55 2024
|