Cobalt in PDB 5d6s: Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus.
Protein crystallography data
The structure of Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus., PDB code: 5d6s
was solved by
K.A.P.Payne,
K.Fisher,
M.S.Dunstan,
H.Sjuts,
D.Leys,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
88.58 /
2.65
|
Space group
|
P 31 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
106.120,
106.120,
332.280,
90.00,
90.00,
120.00
|
R / Rfree (%)
|
21.4 /
25.3
|
Other elements in 5d6s:
The structure of Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus. also contains other interesting chemical elements:
Cobalt Binding Sites:
The binding sites of Cobalt atom in the Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus.
(pdb code 5d6s). This binding sites where shown within
5.0 Angstroms radius around Cobalt atom.
In total 5 binding sites of Cobalt where determined in the
Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus., PDB code: 5d6s:
Jump to Cobalt binding site number:
1;
2;
3;
4;
5;
Cobalt binding site 1 out
of 5 in 5d6s
Go back to
Cobalt Binding Sites List in 5d6s
Cobalt binding site 1 out
of 5 in the Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 1 of Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co403
b:51.0
occ:1.00
|
CO
|
A:B12403
|
0.0
|
51.0
|
1.0
|
N21
|
A:B12403
|
1.9
|
52.9
|
1.0
|
N24
|
A:B12403
|
1.9
|
44.0
|
1.0
|
N22
|
A:B12403
|
1.9
|
48.4
|
1.0
|
N23
|
A:B12403
|
1.9
|
50.2
|
1.0
|
O
|
A:HOH518
|
2.6
|
61.3
|
1.0
|
C9
|
A:B12403
|
2.8
|
48.8
|
1.0
|
C19
|
A:B12403
|
2.8
|
49.0
|
1.0
|
C4
|
A:B12403
|
2.8
|
58.0
|
1.0
|
C11
|
A:B12403
|
2.9
|
47.2
|
1.0
|
C1
|
A:B12403
|
2.9
|
49.5
|
1.0
|
C14
|
A:B12403
|
2.9
|
51.7
|
1.0
|
C6
|
A:B12403
|
2.9
|
47.4
|
1.0
|
C16
|
A:B12403
|
3.0
|
51.2
|
1.0
|
C10
|
A:B12403
|
3.2
|
45.6
|
1.0
|
C5
|
A:B12403
|
3.3
|
52.1
|
1.0
|
C15
|
A:B12403
|
3.4
|
52.0
|
1.0
|
C20
|
A:B12403
|
3.5
|
49.1
|
1.0
|
C18
|
A:B12403
|
4.1
|
48.2
|
1.0
|
C3
|
A:B12403
|
4.1
|
59.4
|
1.0
|
C2
|
A:B12403
|
4.2
|
54.0
|
1.0
|
C8
|
A:B12403
|
4.2
|
48.1
|
1.0
|
C12
|
A:B12403
|
4.2
|
53.3
|
1.0
|
C7
|
A:B12403
|
4.2
|
47.0
|
1.0
|
C13
|
A:B12403
|
4.2
|
56.4
|
1.0
|
C17
|
A:B12403
|
4.2
|
48.6
|
1.0
|
C49
|
A:B12403
|
4.4
|
66.4
|
1.0
|
C26
|
A:B12403
|
4.7
|
55.2
|
1.0
|
C35
|
A:B12403
|
4.7
|
49.8
|
1.0
|
C37
|
A:B12403
|
4.8
|
47.5
|
1.0
|
C46
|
A:B12403
|
4.9
|
58.5
|
1.0
|
C53
|
A:B12403
|
4.9
|
49.8
|
1.0
|
C48
|
A:B12403
|
4.9
|
58.2
|
1.0
|
C30
|
A:B12403
|
4.9
|
61.2
|
1.0
|
C41
|
A:B12403
|
5.0
|
49.0
|
1.0
|
|
Cobalt binding site 2 out
of 5 in 5d6s
Go back to
Cobalt Binding Sites List in 5d6s
Cobalt binding site 2 out
of 5 in the Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 2 of Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Co403
b:47.4
occ:1.00
|
CO
|
B:B12403
|
0.0
|
47.4
|
1.0
|
N21
|
B:B12403
|
1.9
|
42.7
|
1.0
|
N24
|
B:B12403
|
1.9
|
39.4
|
1.0
|
N22
|
B:B12403
|
1.9
|
40.2
|
1.0
|
N23
|
B:B12403
|
1.9
|
38.9
|
1.0
|
C9
|
B:B12403
|
2.8
|
40.9
|
1.0
|
C19
|
B:B12403
|
2.8
|
43.6
|
1.0
|
C1
|
B:B12403
|
2.8
|
46.8
|
1.0
|
C11
|
B:B12403
|
2.9
|
39.4
|
1.0
|
C4
|
B:B12403
|
2.9
|
43.9
|
1.0
|
C14
|
B:B12403
|
2.9
|
41.4
|
1.0
|
C6
|
B:B12403
|
2.9
|
39.8
|
1.0
|
C16
|
B:B12403
|
3.0
|
39.0
|
1.0
|
C10
|
B:B12403
|
3.2
|
37.8
|
1.0
|
C5
|
B:B12403
|
3.3
|
39.5
|
1.0
|
C15
|
B:B12403
|
3.3
|
41.0
|
1.0
|
C20
|
B:B12403
|
3.3
|
43.0
|
1.0
|
C18
|
B:B12403
|
4.1
|
44.8
|
1.0
|
C2
|
B:B12403
|
4.1
|
47.9
|
1.0
|
C8
|
B:B12403
|
4.1
|
43.9
|
1.0
|
C7
|
B:B12403
|
4.1
|
44.5
|
1.0
|
C3
|
B:B12403
|
4.2
|
47.8
|
1.0
|
C12
|
B:B12403
|
4.2
|
43.6
|
1.0
|
C13
|
B:B12403
|
4.2
|
45.5
|
1.0
|
C17
|
B:B12403
|
4.2
|
42.5
|
1.0
|
C49
|
B:B12403
|
4.5
|
60.0
|
1.0
|
C26
|
B:B12403
|
4.6
|
51.0
|
1.0
|
C37
|
B:B12403
|
4.7
|
40.2
|
1.0
|
C35
|
B:B12403
|
4.8
|
45.0
|
1.0
|
C53
|
B:B12403
|
4.8
|
41.4
|
1.0
|
C41
|
B:B12403
|
4.9
|
44.3
|
1.0
|
C46
|
B:B12403
|
4.9
|
43.9
|
1.0
|
C48
|
B:B12403
|
4.9
|
52.1
|
1.0
|
C30
|
B:B12403
|
5.0
|
52.8
|
1.0
|
|
Cobalt binding site 3 out
of 5 in 5d6s
Go back to
Cobalt Binding Sites List in 5d6s
Cobalt binding site 3 out
of 5 in the Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 3 of Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Co403
b:65.4
occ:1.00
|
CO
|
C:B12403
|
0.0
|
65.4
|
1.0
|
N21
|
C:B12403
|
1.9
|
65.7
|
1.0
|
N24
|
C:B12403
|
1.9
|
64.8
|
1.0
|
N23
|
C:B12403
|
1.9
|
53.5
|
1.0
|
N22
|
C:B12403
|
1.9
|
67.4
|
1.0
|
C1
|
C:B12403
|
2.8
|
64.2
|
1.0
|
C11
|
C:B12403
|
2.8
|
57.9
|
1.0
|
C9
|
C:B12403
|
2.8
|
64.4
|
1.0
|
C19
|
C:B12403
|
2.8
|
66.8
|
1.0
|
C4
|
C:B12403
|
2.9
|
71.5
|
1.0
|
C14
|
C:B12403
|
2.9
|
55.2
|
1.0
|
C6
|
C:B12403
|
2.9
|
69.7
|
1.0
|
C16
|
C:B12403
|
2.9
|
67.2
|
1.0
|
C10
|
C:B12403
|
3.2
|
62.8
|
1.0
|
C20
|
C:B12403
|
3.2
|
58.4
|
1.0
|
C5
|
C:B12403
|
3.3
|
65.0
|
1.0
|
C15
|
C:B12403
|
3.4
|
57.0
|
1.0
|
C18
|
C:B12403
|
4.1
|
67.7
|
1.0
|
C12
|
C:B12403
|
4.1
|
54.4
|
1.0
|
C2
|
C:B12403
|
4.1
|
66.5
|
1.0
|
C8
|
C:B12403
|
4.2
|
70.6
|
1.0
|
C3
|
C:B12403
|
4.2
|
71.7
|
1.0
|
C7
|
C:B12403
|
4.2
|
75.2
|
1.0
|
C13
|
C:B12403
|
4.2
|
55.4
|
1.0
|
C17
|
C:B12403
|
4.2
|
63.0
|
1.0
|
C49
|
C:B12403
|
4.7
|
71.3
|
1.0
|
C46
|
C:B12403
|
4.7
|
56.6
|
1.0
|
C26
|
C:B12403
|
4.7
|
64.8
|
1.0
|
C37
|
C:B12403
|
4.8
|
73.8
|
1.0
|
C41
|
C:B12403
|
4.8
|
66.0
|
1.0
|
C35
|
C:B12403
|
4.8
|
60.4
|
1.0
|
C53
|
C:B12403
|
4.8
|
54.6
|
1.0
|
|
Cobalt binding site 4 out
of 5 in 5d6s
Go back to
Cobalt Binding Sites List in 5d6s
Cobalt binding site 4 out
of 5 in the Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 4 of Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Co403
b:55.9
occ:1.00
|
CO
|
D:B12403
|
0.0
|
55.9
|
1.0
|
N21
|
D:B12403
|
1.9
|
57.5
|
1.0
|
N24
|
D:B12403
|
1.9
|
48.5
|
1.0
|
N23
|
D:B12403
|
1.9
|
51.5
|
1.0
|
N22
|
D:B12403
|
1.9
|
55.5
|
1.0
|
C9
|
D:B12403
|
2.8
|
59.6
|
1.0
|
C19
|
D:B12403
|
2.8
|
54.1
|
1.0
|
C4
|
D:B12403
|
2.9
|
59.9
|
1.0
|
C1
|
D:B12403
|
2.9
|
54.9
|
1.0
|
C11
|
D:B12403
|
2.9
|
50.8
|
1.0
|
C14
|
D:B12403
|
2.9
|
50.9
|
1.0
|
C6
|
D:B12403
|
2.9
|
57.2
|
1.0
|
C16
|
D:B12403
|
2.9
|
55.6
|
1.0
|
C10
|
D:B12403
|
3.2
|
57.0
|
1.0
|
C5
|
D:B12403
|
3.3
|
58.8
|
1.0
|
C15
|
D:B12403
|
3.3
|
53.0
|
1.0
|
C20
|
D:B12403
|
3.5
|
53.2
|
1.0
|
C2
|
D:B12403
|
4.1
|
57.4
|
1.0
|
C18
|
D:B12403
|
4.1
|
54.0
|
1.0
|
C3
|
D:B12403
|
4.2
|
61.9
|
1.0
|
C8
|
D:B12403
|
4.2
|
56.5
|
1.0
|
C12
|
D:B12403
|
4.2
|
53.7
|
1.0
|
C7
|
D:B12403
|
4.2
|
57.3
|
1.0
|
C13
|
D:B12403
|
4.2
|
49.6
|
1.0
|
C17
|
D:B12403
|
4.2
|
54.2
|
1.0
|
O
|
D:HOH514
|
4.5
|
55.5
|
1.0
|
C26
|
D:B12403
|
4.5
|
51.6
|
1.0
|
C49
|
D:B12403
|
4.6
|
59.1
|
1.0
|
C35
|
D:B12403
|
4.7
|
58.0
|
1.0
|
C37
|
D:B12403
|
4.8
|
61.5
|
1.0
|
C53
|
D:B12403
|
4.8
|
52.1
|
1.0
|
C46
|
D:B12403
|
4.9
|
59.9
|
1.0
|
C41
|
D:B12403
|
4.9
|
61.5
|
1.0
|
C48
|
D:B12403
|
5.0
|
53.6
|
1.0
|
|
Cobalt binding site 5 out
of 5 in 5d6s
Go back to
Cobalt Binding Sites List in 5d6s
Cobalt binding site 5 out
of 5 in the Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 5 of Structure of Epoxyqueuosine Reductase From Streptococcus Thermophilus. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Co403
b:72.7
occ:1.00
|
CO
|
E:B12403
|
0.0
|
72.7
|
1.0
|
O
|
E:HOH507
|
1.8
|
54.5
|
1.0
|
N21
|
E:B12403
|
1.9
|
82.6
|
1.0
|
N24
|
E:B12403
|
1.9
|
71.3
|
1.0
|
N23
|
E:B12403
|
1.9
|
69.8
|
1.0
|
N22
|
E:B12403
|
1.9
|
73.8
|
1.0
|
C9
|
E:B12403
|
2.8
|
78.3
|
1.0
|
C11
|
E:B12403
|
2.8
|
68.8
|
1.0
|
C1
|
E:B12403
|
2.9
|
75.6
|
1.0
|
C19
|
E:B12403
|
2.9
|
74.6
|
1.0
|
C4
|
E:B12403
|
2.9
|
80.2
|
1.0
|
C6
|
E:B12403
|
2.9
|
76.4
|
1.0
|
C14
|
E:B12403
|
2.9
|
63.3
|
1.0
|
C16
|
E:B12403
|
3.0
|
68.6
|
1.0
|
C10
|
E:B12403
|
3.2
|
75.1
|
1.0
|
C5
|
E:B12403
|
3.3
|
79.5
|
1.0
|
C20
|
E:B12403
|
3.3
|
71.5
|
1.0
|
C15
|
E:B12403
|
3.4
|
64.9
|
1.0
|
C12
|
E:B12403
|
4.1
|
61.8
|
1.0
|
C18
|
E:B12403
|
4.1
|
68.5
|
1.0
|
C8
|
E:B12403
|
4.1
|
72.5
|
1.0
|
C2
|
E:B12403
|
4.2
|
77.7
|
1.0
|
C3
|
E:B12403
|
4.2
|
81.8
|
1.0
|
C7
|
E:B12403
|
4.2
|
71.1
|
1.0
|
C13
|
E:B12403
|
4.2
|
60.4
|
1.0
|
C17
|
E:B12403
|
4.3
|
65.2
|
1.0
|
C49
|
E:B12403
|
4.5
|
66.6
|
1.0
|
C46
|
E:B12403
|
4.7
|
62.8
|
1.0
|
C26
|
E:B12403
|
4.7
|
73.9
|
1.0
|
C35
|
E:B12403
|
4.7
|
81.2
|
1.0
|
C37
|
E:B12403
|
4.8
|
73.7
|
1.0
|
C41
|
E:B12403
|
4.8
|
68.0
|
1.0
|
C53
|
E:B12403
|
4.9
|
63.5
|
1.0
|
C48
|
E:B12403
|
4.9
|
59.5
|
1.0
|
|
Reference:
K.A.Payne,
K.Fisher,
H.Sjuts,
M.S.Dunstan,
B.Bellina,
L.Johannissen,
P.Barran,
S.Hay,
S.E.Rigby,
D.Leys.
Epoxyqueuosine Reductase Structure Suggests A Mechanism For Cobalamin-Dependent Trna Modification. J.Biol.Chem. V. 290 27572 2015.
ISSN: ESSN 1083-351X
PubMed: 26378237
DOI: 10.1074/JBC.M115.685693
Page generated: Tue Jul 30 17:49:48 2024
|