Cobalt in PDB 5n78: Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Protein crystallography data
The structure of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine, PDB code: 5n78
was solved by
M.Lerche,
H.Sandhu,
L.Flockner,
M.Hogbom,
M.Rapp,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
29.44 /
2.85
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
73.721,
117.316,
91.858,
90.00,
103.14,
90.00
|
R / Rfree (%)
|
17.8 /
21.8
|
Other elements in 5n78:
The structure of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine also contains other interesting chemical elements:
Cobalt Binding Sites:
Pages:
>>> Page 1 <<<
Page 2, Binding sites: 11 -
14;
Binding sites:
The binding sites of Cobalt atom in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
(pdb code 5n78). This binding sites where shown within
5.0 Angstroms radius around Cobalt atom.
In total 14 binding sites of Cobalt where determined in the
Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine, PDB code: 5n78:
Jump to Cobalt binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
9;
10;
Cobalt binding site 1 out
of 14 in 5n78
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Cobalt Binding Sites List in 5n78
Cobalt binding site 1 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 1 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co303
b:0.9
occ:1.00
|
CO
|
A:NCO303
|
0.0
|
0.9
|
1.0
|
N5
|
A:NCO303
|
2.0
|
0.5
|
1.0
|
N2
|
A:NCO303
|
2.0
|
0.6
|
1.0
|
N4
|
A:NCO303
|
2.0
|
0.3
|
1.0
|
N6
|
A:NCO303
|
2.0
|
0.1
|
1.0
|
N1
|
A:NCO303
|
2.0
|
0.4
|
1.0
|
N3
|
A:NCO303
|
2.0
|
0.5
|
1.0
|
OD1
|
A:ASN150
|
4.0
|
59.5
|
1.0
|
OE1
|
A:GLU149
|
4.5
|
72.3
|
1.0
|
OD2
|
A:ASP146
|
4.9
|
94.7
|
1.0
|
OD1
|
A:ASP146
|
4.9
|
84.3
|
1.0
|
|
Cobalt binding site 2 out
of 14 in 5n78
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Cobalt Binding Sites List in 5n78
Cobalt binding site 2 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 2 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co304
b:0.4
occ:1.00
|
CO
|
A:NCO304
|
0.0
|
0.4
|
1.0
|
N4
|
A:NCO304
|
2.0
|
0.1
|
1.0
|
N6
|
A:NCO304
|
2.0
|
0.3
|
1.0
|
N2
|
A:NCO304
|
2.0
|
0.9
|
1.0
|
N3
|
A:NCO304
|
2.0
|
0.5
|
1.0
|
N1
|
A:NCO304
|
2.0
|
0.2
|
1.0
|
N5
|
A:NCO304
|
2.0
|
0.2
|
1.0
|
OE1
|
A:GLU147
|
4.3
|
98.7
|
1.0
|
OE1
|
A:GLU81
|
4.5
|
0.8
|
1.0
|
OE2
|
A:GLU81
|
4.6
|
0.2
|
1.0
|
OE2
|
A:GLU147
|
4.7
|
91.8
|
1.0
|
CD
|
A:GLU81
|
4.7
|
0.5
|
1.0
|
CD
|
A:GLU147
|
4.9
|
83.8
|
1.0
|
|
Cobalt binding site 3 out
of 14 in 5n78
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Cobalt Binding Sites List in 5n78
Cobalt binding site 3 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 3 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co305
b:0.2
occ:1.00
|
CO
|
A:NCO305
|
0.0
|
0.2
|
1.0
|
N3
|
A:NCO305
|
2.0
|
0.2
|
1.0
|
N6
|
A:NCO305
|
2.0
|
0.7
|
1.0
|
N5
|
A:NCO305
|
2.0
|
0.4
|
1.0
|
N1
|
A:NCO305
|
2.0
|
0.6
|
1.0
|
N4
|
A:NCO305
|
2.0
|
0.2
|
1.0
|
N2
|
A:NCO305
|
2.0
|
0.8
|
1.0
|
OE1
|
A:GLU55
|
3.9
|
0.7
|
1.0
|
OE2
|
A:GLU55
|
4.5
|
84.5
|
1.0
|
CD
|
A:GLU55
|
4.6
|
88.7
|
1.0
|
|
Cobalt binding site 4 out
of 14 in 5n78
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Cobalt Binding Sites List in 5n78
Cobalt binding site 4 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 4 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Co303
b:91.8
occ:1.00
|
CO
|
B:NCO303
|
0.0
|
91.8
|
1.0
|
N4
|
B:NCO303
|
2.0
|
88.0
|
1.0
|
N5
|
B:NCO303
|
2.0
|
87.3
|
1.0
|
N2
|
B:NCO303
|
2.0
|
90.2
|
1.0
|
N1
|
B:NCO303
|
2.0
|
82.0
|
1.0
|
N6
|
B:NCO303
|
2.0
|
90.2
|
1.0
|
N3
|
B:NCO303
|
2.0
|
88.2
|
1.0
|
O
|
B:HOH403
|
3.7
|
82.5
|
1.0
|
OE1
|
B:GLN252
|
4.0
|
92.8
|
1.0
|
OE1
|
A:GLN252
|
4.1
|
83.7
|
1.0
|
OE1
|
E:GLN252
|
4.2
|
78.2
|
1.0
|
OE1
|
C:GLN252
|
4.2
|
84.8
|
1.0
|
OE1
|
D:GLN252
|
4.3
|
73.3
|
1.0
|
ND2
|
B:ASN249
|
4.4
|
81.7
|
1.0
|
ND2
|
A:ASN249
|
4.4
|
73.9
|
1.0
|
ND2
|
C:ASN249
|
4.7
|
85.2
|
1.0
|
ND2
|
E:ASN249
|
4.8
|
81.1
|
1.0
|
OD1
|
B:ASN249
|
4.8
|
91.4
|
1.0
|
CD
|
B:GLN252
|
4.8
|
78.0
|
1.0
|
CG
|
B:ASN249
|
4.9
|
79.1
|
1.0
|
OD1
|
A:ASN249
|
4.9
|
83.5
|
1.0
|
CD
|
A:GLN252
|
4.9
|
83.1
|
1.0
|
CG
|
A:ASN249
|
4.9
|
73.1
|
1.0
|
NE2
|
A:GLN252
|
4.9
|
87.9
|
1.0
|
NE2
|
B:GLN252
|
4.9
|
78.8
|
1.0
|
OD1
|
E:ASN249
|
5.0
|
93.1
|
1.0
|
|
Cobalt binding site 5 out
of 14 in 5n78
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Cobalt Binding Sites List in 5n78
Cobalt binding site 5 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 5 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Co304
b:0.3
occ:1.00
|
CO
|
B:NCO304
|
0.0
|
0.3
|
1.0
|
N3
|
B:NCO304
|
2.0
|
0.9
|
1.0
|
N5
|
B:NCO304
|
2.0
|
0.1
|
1.0
|
N2
|
B:NCO304
|
2.0
|
0.9
|
1.0
|
N1
|
B:NCO304
|
2.0
|
0.0
|
1.0
|
N4
|
B:NCO304
|
2.0
|
0.3
|
1.0
|
N6
|
B:NCO304
|
2.0
|
0.4
|
1.0
|
OE1
|
B:GLU55
|
4.6
|
93.3
|
1.0
|
OD2
|
B:ASP70
|
4.6
|
91.3
|
1.0
|
OE2
|
B:GLU55
|
4.8
|
95.1
|
1.0
|
|
Cobalt binding site 6 out
of 14 in 5n78
Go back to
Cobalt Binding Sites List in 5n78
Cobalt binding site 6 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 6 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Co305
b:0.8
occ:1.00
|
CO
|
B:NCO305
|
0.0
|
0.8
|
1.0
|
N2
|
B:NCO305
|
2.0
|
0.8
|
1.0
|
N4
|
B:NCO305
|
2.0
|
0.6
|
1.0
|
N1
|
B:NCO305
|
2.0
|
0.5
|
1.0
|
N5
|
B:NCO305
|
2.0
|
0.9
|
1.0
|
N6
|
B:NCO305
|
2.0
|
0.7
|
1.0
|
N3
|
B:NCO305
|
2.0
|
0.4
|
1.0
|
OE1
|
B:GLU149
|
3.8
|
73.1
|
1.0
|
ND2
|
B:ASN150
|
4.3
|
60.9
|
1.0
|
CB
|
B:GLU149
|
4.5
|
50.7
|
1.0
|
CB
|
A:GLU57
|
4.5
|
81.2
|
1.0
|
CD
|
B:GLU149
|
4.9
|
61.6
|
1.0
|
CG
|
A:GLU57
|
4.9
|
91.7
|
1.0
|
OD2
|
B:ASP146
|
4.9
|
82.2
|
1.0
|
|
Cobalt binding site 7 out
of 14 in 5n78
Go back to
Cobalt Binding Sites List in 5n78
Cobalt binding site 7 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 7 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Co303
b:1.0
occ:1.00
|
CO
|
C:NCO303
|
0.0
|
1.0
|
1.0
|
N6
|
C:NCO303
|
2.0
|
0.5
|
1.0
|
N4
|
C:NCO303
|
2.0
|
0.9
|
1.0
|
N1
|
C:NCO303
|
2.0
|
0.8
|
1.0
|
N3
|
C:NCO303
|
2.0
|
0.4
|
1.0
|
N5
|
C:NCO303
|
2.0
|
0.2
|
1.0
|
N2
|
C:NCO303
|
2.0
|
1.0
|
1.0
|
OE1
|
C:GLU55
|
3.9
|
93.5
|
1.0
|
OE2
|
C:GLU55
|
4.3
|
79.8
|
1.0
|
CD
|
C:GLU55
|
4.6
|
85.0
|
1.0
|
O
|
C:LEU50
|
4.7
|
75.4
|
1.0
|
|
Cobalt binding site 8 out
of 14 in 5n78
Go back to
Cobalt Binding Sites List in 5n78
Cobalt binding site 8 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 8 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Co304
b:0.7
occ:1.00
|
CO
|
C:NCO304
|
0.0
|
0.7
|
1.0
|
N1
|
C:NCO304
|
2.0
|
0.1
|
1.0
|
N4
|
C:NCO304
|
2.0
|
0.2
|
1.0
|
N3
|
C:NCO304
|
2.0
|
0.9
|
1.0
|
N6
|
C:NCO304
|
2.0
|
0.0
|
1.0
|
N5
|
C:NCO304
|
2.0
|
0.9
|
1.0
|
N2
|
C:NCO304
|
2.0
|
0.8
|
1.0
|
OD1
|
C:ASP85
|
3.8
|
99.4
|
1.0
|
OE1
|
C:GLU81
|
4.1
|
0.1
|
1.0
|
O
|
C:HOH416
|
4.6
|
78.2
|
1.0
|
CD
|
C:GLU81
|
4.9
|
0.8
|
1.0
|
CG
|
C:ASP85
|
4.9
|
92.5
|
1.0
|
|
Cobalt binding site 9 out
of 14 in 5n78
Go back to
Cobalt Binding Sites List in 5n78
Cobalt binding site 9 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 9 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Co302
b:0.0
occ:1.00
|
CO
|
D:NCO302
|
0.0
|
0.0
|
1.0
|
N2
|
D:NCO302
|
2.0
|
0.1
|
1.0
|
N1
|
D:NCO302
|
2.0
|
0.4
|
1.0
|
N6
|
D:NCO302
|
2.0
|
0.7
|
1.0
|
N4
|
D:NCO302
|
2.0
|
0.9
|
1.0
|
N3
|
D:NCO302
|
2.0
|
0.1
|
1.0
|
N5
|
D:NCO302
|
2.0
|
0.2
|
1.0
|
OE1
|
D:GLU81
|
4.0
|
0.7
|
1.0
|
CD
|
D:GLU81
|
4.4
|
99.5
|
1.0
|
OE2
|
D:GLU81
|
4.5
|
99.0
|
1.0
|
OE1
|
D:GLU147
|
4.9
|
92.0
|
1.0
|
|
Cobalt binding site 10 out
of 14 in 5n78
Go back to
Cobalt Binding Sites List in 5n78
Cobalt binding site 10 out
of 14 in the Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 10 of Crystal Structure of the Cytosolic Domain of the Cora MG2+ Channel From Escherichia Coli in Complex with Magnesium and Cobalt Hexammine within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Co303
b:0.5
occ:1.00
|
CO
|
D:NCO303
|
0.0
|
0.5
|
1.0
|
N2
|
D:NCO303
|
2.0
|
0.9
|
1.0
|
N4
|
D:NCO303
|
2.0
|
0.4
|
1.0
|
N5
|
D:NCO303
|
2.0
|
0.5
|
1.0
|
N1
|
D:NCO303
|
2.0
|
0.9
|
1.0
|
N3
|
D:NCO303
|
2.0
|
0.3
|
1.0
|
N6
|
D:NCO303
|
2.0
|
0.1
|
1.0
|
OE1
|
D:GLU149
|
4.0
|
67.9
|
1.0
|
OD2
|
D:ASP146
|
4.2
|
0.7
|
1.0
|
CB
|
E:GLU57
|
4.7
|
88.1
|
1.0
|
OD1
|
D:ASP146
|
4.8
|
0.2
|
1.0
|
CG
|
D:ASP146
|
4.8
|
94.7
|
1.0
|
OD1
|
D:ASN150
|
4.9
|
67.8
|
1.0
|
O
|
E:HOH404
|
4.9
|
47.8
|
1.0
|
CG
|
E:GLU57
|
4.9
|
0.7
|
1.0
|
|
Reference:
M.Lerche,
H.Sandhu,
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Structure and Cooperativity of the Cytosolic Domain of the Cora Mg(2+) Channel From Escherichia Coli. Structure V. 25 1175 2017.
ISSN: ISSN 1878-4186
PubMed: 28669631
DOI: 10.1016/J.STR.2017.05.024
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