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Sodium in PDB 4ouc: Structure of Human Haspin in Complex with Histone H3 Substrate

Enzymatic activity of Structure of Human Haspin in Complex with Histone H3 Substrate

All present enzymatic activity of Structure of Human Haspin in Complex with Histone H3 Substrate:
2.7.11.1;

Protein crystallography data

The structure of Structure of Human Haspin in Complex with Histone H3 Substrate, PDB code: 4ouc was solved by A.Chaikuad, F.Von Delft, C.H.Arrowsmith, A.M.Edwards, C.Bountra, S.Knapp, Structural Genomics Consortium (Sgc), with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 31.15 / 1.90
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 50.540, 79.130, 100.760, 90.00, 90.00, 90.00
R / Rfree (%) 16.4 / 21.1

Other elements in 4ouc:

The structure of Structure of Human Haspin in Complex with Histone H3 Substrate also contains other interesting chemical elements:

Iodine (I) 3 atoms

Sodium Binding Sites:

The binding sites of Sodium atom in the Structure of Human Haspin in Complex with Histone H3 Substrate (pdb code 4ouc). 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 Structure of Human Haspin in Complex with Histone H3 Substrate, PDB code: 4ouc:

Sodium binding site 1 out of 1 in 4ouc

Go back to Sodium Binding Sites List in 4ouc
Sodium binding site 1 out of 1 in the Structure of Human Haspin in Complex with Histone H3 Substrate


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 1 of Structure of Human Haspin in Complex with Histone H3 Substrate within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Na801

b:17.1
occ:1.00
O A:GLU554 2.4 19.3 1.0
O A:PHE556 2.4 21.1 1.0
OG A:SER684 2.5 19.7 1.0
O A:HOH1108 2.6 26.2 1.0
O A:HOH1107 2.7 33.5 1.0
CB A:SER684 3.5 17.4 1.0
C A:PHE556 3.6 16.7 1.0
C A:GLU554 3.6 19.5 1.0
OE2 A:GLU606 3.9 22.0 1.0
O A:VAL683 4.0 18.1 1.0
CA A:SER684 4.0 16.7 1.0
C A:GLY555 4.1 16.7 1.0
N A:PHE556 4.1 16.2 1.0
O A:HOH1111 4.2 45.7 1.0
O A:HOH1109 4.2 27.4 1.0
CA A:GLY555 4.3 16.8 1.0
O A:HOH1284 4.3 42.3 1.0
CA A:ILE557 4.4 17.4 1.0
N A:ILE557 4.4 18.3 1.0
N A:GLY555 4.4 17.5 1.0
OE1 A:GLU606 4.4 28.0 1.0
OE1 A:GLN682 4.4 25.6 1.0
CD1 A:ILE557 4.4 18.1 1.0
CD A:GLU606 4.5 26.5 1.0
CA A:PHE556 4.5 16.7 1.0
CG A:GLN682 4.5 22.2 1.0
O A:HOH911 4.6 17.9 1.0
N A:SER684 4.6 15.8 1.0
C A:VAL683 4.6 16.6 1.0
O A:GLY555 4.7 16.8 1.0
CD A:GLN682 4.7 23.4 1.0
CA A:GLU554 4.7 20.9 1.0
CB A:GLU554 4.8 23.0 1.0

Reference:

A.Maiolica, M.De Medina-Redondo, E.M.Schoof, A.Chaikuad, F.Villa, M.Gatti, S.Jeganathan, H.J.Lou, K.Novy, S.Hauri, U.H.Toprak, F.Herzog, P.Meraldi, L.Penengo, B.E.Turk, S.Knapp, R.Linding, R.Aebersold. Modulation of the Chromatin Phosphoproteome By the Haspin Protein Kinase. Mol Cell Proteomics V. 13 1724 2014.
PubMed: 24732914
DOI: 10.1074/MCP.M113.034819
Page generated: Tue Dec 15 06:57:18 2020

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