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Sodium in PDB 5hy1: High Resolution Structure of Barbiturase

Enzymatic activity of High Resolution Structure of Barbiturase

All present enzymatic activity of High Resolution Structure of Barbiturase:
3.5.2.1;

Protein crystallography data

The structure of High Resolution Structure of Barbiturase, PDB code: 5hy1 was solved by T.S.Peat, C.Scott, S.Balotra, M.Wilding, J.Newman, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 41.20 / 2.01
Space group I 2 2 2
Cell size a, b, c (Å), α, β, γ (°) 69.403, 82.356, 114.552, 90.00, 90.00, 90.00
R / Rfree (%) 18.6 / 22.3

Other elements in 5hy1:

The structure of High Resolution Structure of Barbiturase also contains other interesting chemical elements:

Chlorine (Cl) 3 atoms

Sodium Binding Sites:

The binding sites of Sodium atom in the High Resolution Structure of Barbiturase (pdb code 5hy1). This binding sites where shown within 5.0 Angstroms radius around Sodium atom.
In total only one binding site of Sodium was determined in the High Resolution Structure of Barbiturase, PDB code: 5hy1:

Sodium binding site 1 out of 1 in 5hy1

Go back to Sodium Binding Sites List in 5hy1
Sodium binding site 1 out of 1 in the High Resolution Structure of Barbiturase


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 1 of High Resolution Structure of Barbiturase within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Na402

b:34.1
occ:1.00
O A:GLN353 2.7 21.9 1.0
O A:ALA350 2.7 18.6 1.0
OE2 A:GLU301 2.8 17.9 1.0
O A:PRO355 2.9 26.4 1.0
O A:GLY358 2.9 20.5 1.0
O A:GLY354 3.1 24.3 1.0
CD A:GLU301 3.2 19.8 1.0
C A:GLN353 3.6 18.8 1.0
C A:GLY354 3.6 25.5 1.0
C A:PRO355 3.6 24.2 1.0
CB A:ALA350 3.6 21.1 1.0
OE1 A:GLU301 3.7 21.5 1.0
O A:HOH503 3.7 28.7 1.0
C A:ALA350 3.8 21.4 1.0
C A:GLY358 3.8 20.1 1.0
O A:HOH556 3.8 29.0 1.0
CG A:GLU301 4.0 20.7 1.0
N A:GLN353 4.2 21.1 1.0
N A:GLU356 4.2 23.1 1.0
CA A:GLY354 4.2 22.4 1.0
CA A:GLU356 4.2 22.8 1.0
N A:GLY358 4.2 18.7 1.0
N A:PRO355 4.2 23.1 1.0
N A:GLY354 4.3 21.5 1.0
CA A:ALA350 4.4 19.0 1.0
CA A:GLN353 4.4 19.2 1.0
N A:GLY359 4.5 19.8 1.0
CA A:PRO355 4.5 22.8 1.0
CA A:GLY359 4.5 19.0 1.0
N A:GLY357 4.5 20.5 1.0
CA A:GLY358 4.6 19.6 1.0
C A:GLU356 4.7 23.2 1.0
N A:ALA351 4.8 21.9 1.0
N A:HIS352 4.8 21.9 1.0
CB A:GLN353 4.9 19.4 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: Tue Dec 15 11:04:01 2020

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