Sodium in PDB 5hxz: Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes
Enzymatic activity of Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes
All present enzymatic activity of Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes:
3.5.2.1;
Protein crystallography data
The structure of Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes, PDB code: 5hxz
was solved by
T.S.Peat,
S.Balotra,
M.Wilding,
J.Newman,
C.Scott,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
45.30 /
2.36
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
81.630,
83.732,
215.102,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
22.4 /
25.5
|
Other elements in 5hxz:
The structure of Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes also contains other interesting chemical elements:
Sodium Binding Sites:
The binding sites of Sodium atom in the Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes
(pdb code 5hxz). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 4 binding sites of Sodium where determined in the
Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes, PDB code: 5hxz:
Jump to Sodium binding site number:
1;
2;
3;
4;
Sodium binding site 1 out
of 4 in 5hxz
Go back to
Sodium Binding Sites List in 5hxz
Sodium binding site 1 out
of 4 in the Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 1 of Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Na404
b:23.5
occ:1.00
|
O
|
A:ALA350
|
2.7
|
24.0
|
1.0
|
OE2
|
A:GLU301
|
2.7
|
25.2
|
1.0
|
O
|
A:GLN353
|
2.8
|
22.2
|
1.0
|
O
|
A:GLY358
|
2.8
|
17.7
|
1.0
|
O
|
A:PRO355
|
3.0
|
26.9
|
1.0
|
CD
|
A:GLU301
|
3.2
|
26.5
|
1.0
|
O
|
A:GLY354
|
3.4
|
25.7
|
1.0
|
CB
|
A:ALA350
|
3.4
|
21.3
|
1.0
|
OE1
|
A:GLU301
|
3.7
|
19.4
|
1.0
|
C
|
A:ALA350
|
3.7
|
21.8
|
1.0
|
C
|
A:PRO355
|
3.7
|
29.0
|
1.0
|
C
|
A:GLN353
|
3.7
|
21.6
|
1.0
|
C
|
A:GLY358
|
3.8
|
16.8
|
1.0
|
C
|
A:GLY354
|
3.9
|
28.6
|
1.0
|
CG
|
A:GLU301
|
4.0
|
25.6
|
1.0
|
CA
|
A:ALA350
|
4.2
|
20.8
|
1.0
|
CA
|
A:GLU356
|
4.2
|
26.7
|
1.0
|
N
|
A:GLU356
|
4.3
|
29.1
|
1.0
|
N
|
A:GLY358
|
4.3
|
27.8
|
1.0
|
N
|
A:GLY357
|
4.3
|
25.7
|
1.0
|
N
|
A:GLN353
|
4.3
|
23.7
|
1.0
|
N
|
A:PRO355
|
4.5
|
26.4
|
1.0
|
CA
|
A:GLY354
|
4.5
|
21.6
|
1.0
|
N
|
A:GLY354
|
4.5
|
26.7
|
1.0
|
CA
|
A:GLY359
|
4.5
|
19.4
|
1.0
|
N
|
A:GLY359
|
4.6
|
17.9
|
1.0
|
CA
|
A:GLN353
|
4.6
|
21.9
|
1.0
|
C
|
A:GLU356
|
4.7
|
30.3
|
1.0
|
CA
|
A:PRO355
|
4.7
|
24.9
|
1.0
|
CA
|
A:GLY358
|
4.7
|
23.0
|
1.0
|
N
|
A:ALA351
|
4.7
|
20.0
|
1.0
|
NH1
|
A:ARG220
|
4.8
|
41.6
|
1.0
|
CB
|
A:GLU301
|
5.0
|
15.7
|
1.0
|
CB
|
A:GLN353
|
5.0
|
22.2
|
1.0
|
|
Sodium binding site 2 out
of 4 in 5hxz
Go back to
Sodium Binding Sites List in 5hxz
Sodium binding site 2 out
of 4 in the Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 2 of Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Na402
b:26.0
occ:1.00
|
O
|
B:GLN353
|
2.7
|
26.4
|
1.0
|
O
|
B:GLY358
|
2.7
|
15.6
|
1.0
|
O
|
B:PRO355
|
2.8
|
20.6
|
1.0
|
O
|
B:ALA350
|
2.8
|
31.5
|
1.0
|
OE2
|
B:GLU301
|
2.9
|
27.4
|
1.0
|
O
|
B:GLY354
|
3.1
|
20.8
|
1.0
|
CD
|
B:GLU301
|
3.5
|
25.7
|
1.0
|
C
|
B:PRO355
|
3.5
|
23.7
|
1.0
|
CB
|
B:ALA350
|
3.6
|
23.8
|
1.0
|
C
|
B:GLY354
|
3.6
|
26.1
|
1.0
|
C
|
B:GLN353
|
3.6
|
28.6
|
1.0
|
C
|
B:GLY358
|
3.7
|
17.2
|
1.0
|
C
|
B:ALA350
|
3.8
|
28.9
|
1.0
|
OE1
|
B:GLU301
|
4.0
|
21.2
|
1.0
|
N
|
B:GLU356
|
4.1
|
20.7
|
1.0
|
CA
|
B:GLU356
|
4.1
|
26.4
|
1.0
|
N
|
B:GLY358
|
4.2
|
23.5
|
1.0
|
N
|
B:PRO355
|
4.2
|
23.8
|
1.0
|
CA
|
B:GLY354
|
4.3
|
23.4
|
1.0
|
CG
|
B:GLU301
|
4.3
|
23.9
|
1.0
|
N
|
B:GLY357
|
4.3
|
19.9
|
1.0
|
N
|
B:GLN353
|
4.3
|
26.6
|
1.0
|
CA
|
B:ALA350
|
4.3
|
28.2
|
1.0
|
N
|
B:GLY354
|
4.3
|
23.2
|
1.0
|
CA
|
B:PRO355
|
4.4
|
21.6
|
1.0
|
N
|
B:GLY359
|
4.5
|
21.0
|
1.0
|
CA
|
B:GLY359
|
4.5
|
23.6
|
1.0
|
CA
|
B:GLN353
|
4.5
|
23.9
|
1.0
|
C
|
B:GLU356
|
4.6
|
27.7
|
1.0
|
CA
|
B:GLY358
|
4.6
|
21.7
|
1.0
|
N
|
B:ALA351
|
4.8
|
24.8
|
1.0
|
NH1
|
B:ARG220
|
4.9
|
41.8
|
1.0
|
CB
|
B:GLN353
|
5.0
|
25.3
|
1.0
|
N
|
B:HIS352
|
5.0
|
22.8
|
1.0
|
|
Sodium binding site 3 out
of 4 in 5hxz
Go back to
Sodium Binding Sites List in 5hxz
Sodium binding site 3 out
of 4 in the Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 3 of Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Na401
b:38.0
occ:1.00
|
OE2
|
C:GLU301
|
2.7
|
30.5
|
1.0
|
O
|
C:PRO355
|
2.7
|
30.4
|
1.0
|
O
|
C:GLY358
|
2.8
|
25.9
|
1.0
|
O
|
C:ALA350
|
2.9
|
23.9
|
1.0
|
O
|
C:GLN353
|
3.0
|
23.1
|
1.0
|
CD
|
C:GLU301
|
3.2
|
24.6
|
1.0
|
O
|
C:GLY354
|
3.3
|
28.5
|
1.0
|
C
|
C:PRO355
|
3.5
|
31.7
|
1.0
|
CB
|
C:ALA350
|
3.6
|
23.6
|
1.0
|
C
|
C:GLY358
|
3.7
|
25.3
|
1.0
|
OE1
|
C:GLU301
|
3.8
|
23.7
|
1.0
|
C
|
C:GLY354
|
3.8
|
29.6
|
1.0
|
C
|
C:ALA350
|
3.8
|
30.1
|
1.0
|
C
|
C:GLN353
|
3.9
|
27.9
|
1.0
|
CA
|
C:GLU356
|
3.9
|
36.1
|
1.0
|
N
|
C:GLU356
|
4.0
|
28.3
|
1.0
|
N
|
C:GLY357
|
4.0
|
30.2
|
1.0
|
CG
|
C:GLU301
|
4.0
|
22.7
|
1.0
|
N
|
C:GLY358
|
4.0
|
31.4
|
1.0
|
C
|
C:GLU356
|
4.3
|
37.6
|
1.0
|
N
|
C:PRO355
|
4.3
|
35.4
|
1.0
|
CA
|
C:ALA350
|
4.3
|
23.6
|
1.0
|
CA
|
C:PRO355
|
4.5
|
31.9
|
1.0
|
N
|
C:GLN353
|
4.5
|
29.4
|
1.0
|
CA
|
C:GLY358
|
4.5
|
27.5
|
1.0
|
CA
|
C:GLY354
|
4.5
|
29.7
|
1.0
|
N
|
C:GLY359
|
4.5
|
21.9
|
1.0
|
N
|
C:GLY354
|
4.6
|
34.6
|
1.0
|
CA
|
C:GLY359
|
4.6
|
21.4
|
1.0
|
CA
|
C:GLN353
|
4.8
|
24.7
|
1.0
|
N
|
C:ALA351
|
4.8
|
29.0
|
1.0
|
C
|
C:GLY357
|
4.9
|
31.9
|
1.0
|
CA
|
C:GLY357
|
5.0
|
29.0
|
1.0
|
|
Sodium binding site 4 out
of 4 in 5hxz
Go back to
Sodium Binding Sites List in 5hxz
Sodium binding site 4 out
of 4 in the Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes
Mono view
Stereo pair view
|
A full contact list of Sodium with other atoms in the Na binding
site number 4 of Structure-Function Analysis of Functionally Diverse Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Na403
b:27.1
occ:1.00
|
O
|
D:ALA350
|
2.4
|
23.4
|
1.0
|
O
|
D:GLN353
|
2.7
|
26.7
|
1.0
|
OE2
|
D:GLU301
|
3.0
|
30.3
|
1.0
|
O
|
D:GLY354
|
3.1
|
23.9
|
1.0
|
O
|
D:GLY358
|
3.2
|
23.5
|
1.0
|
O
|
D:PRO355
|
3.2
|
22.1
|
1.0
|
C
|
D:ALA350
|
3.4
|
24.6
|
1.0
|
CD
|
D:GLU301
|
3.5
|
23.0
|
1.0
|
C
|
D:GLN353
|
3.5
|
28.2
|
1.0
|
CB
|
D:ALA350
|
3.5
|
19.5
|
1.0
|
OE1
|
D:GLU301
|
3.7
|
19.7
|
1.0
|
C
|
D:GLY354
|
3.7
|
25.1
|
1.0
|
C
|
D:PRO355
|
3.7
|
27.2
|
1.0
|
N
|
D:GLN353
|
3.9
|
18.8
|
1.0
|
CA
|
D:ALA350
|
4.1
|
23.0
|
1.0
|
C
|
D:GLY358
|
4.2
|
22.4
|
1.0
|
N
|
D:GLU356
|
4.2
|
26.4
|
1.0
|
CA
|
D:GLU356
|
4.2
|
31.9
|
1.0
|
CA
|
D:GLN353
|
4.2
|
21.1
|
1.0
|
N
|
D:GLY354
|
4.3
|
28.0
|
1.0
|
CA
|
D:GLY354
|
4.4
|
22.6
|
1.0
|
N
|
D:ALA351
|
4.4
|
20.8
|
1.0
|
N
|
D:PRO355
|
4.4
|
30.0
|
1.0
|
CG
|
D:GLU301
|
4.4
|
21.2
|
1.0
|
N
|
D:HIS352
|
4.5
|
21.6
|
1.0
|
CA
|
D:PRO355
|
4.6
|
30.4
|
1.0
|
N
|
D:GLY357
|
4.6
|
29.5
|
1.0
|
CA
|
D:ALA351
|
4.6
|
27.7
|
1.0
|
CB
|
D:GLN353
|
4.7
|
24.3
|
1.0
|
N
|
D:GLY358
|
4.7
|
23.3
|
1.0
|
NH1
|
D:ARG220
|
4.7
|
42.9
|
1.0
|
CA
|
D:GLY359
|
4.8
|
21.5
|
1.0
|
C
|
D:ALA351
|
4.8
|
25.0
|
1.0
|
C
|
D:GLU356
|
4.8
|
26.2
|
1.0
|
N
|
D:GLY359
|
4.9
|
18.2
|
1.0
|
C
|
D:HIS352
|
4.9
|
24.2
|
1.0
|
|
Reference:
T.S.Peat,
S.Balotra,
M.Wilding,
C.J.Hartley,
J.Newman,
C.Scott.
High-Resolution X-Ray Structures of Two Functionally Distinct Members of the Cyclic Amide Hydrolase Family of Toblerone Fold Enzymes. Appl. Environ. Microbiol. V. 83 2017.
ISSN: ESSN 1098-5336
PubMed: 28235873
DOI: 10.1128/AEM.03365-16
Page generated: Mon Oct 7 21:29:54 2024
|