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Chlorine in PDB 2w5b: Human NEK2 Kinase Atpgammas-Bound

Enzymatic activity of Human NEK2 Kinase Atpgammas-Bound

All present enzymatic activity of Human NEK2 Kinase Atpgammas-Bound:
2.7.11.1;

Protein crystallography data

The structure of Human NEK2 Kinase Atpgammas-Bound, PDB code: 2w5b was solved by R.Bayliss, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.56 / 2.40
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 99.602, 57.064, 80.802, 90.00, 133.45, 90.00
R / Rfree (%) 18.3 / 24.5

Other elements in 2w5b:

The structure of Human NEK2 Kinase Atpgammas-Bound also contains other interesting chemical elements:

Magnesium (Mg) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Human NEK2 Kinase Atpgammas-Bound (pdb code 2w5b). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the Human NEK2 Kinase Atpgammas-Bound, PDB code: 2w5b:

Chlorine binding site 1 out of 1 in 2w5b

Go back to Chlorine Binding Sites List in 2w5b
Chlorine binding site 1 out of 1 in the Human NEK2 Kinase Atpgammas-Bound


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Human NEK2 Kinase Atpgammas-Bound within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1281

b:62.4
occ:1.00
O A:ARG105 3.7 64.2 1.0
C A:ARG105 3.7 63.6 1.0
CA A:ARG105 3.9 62.5 1.0
CZ A:TYR107 4.0 33.6 1.0
CE2 A:TYR107 4.1 26.9 1.0
N A:GLN106 4.3 59.6 1.0
OH A:TYR107 4.3 33.3 1.0
CE1 A:TYR107 4.4 33.6 1.0
CB A:ARG105 4.5 61.7 1.0
CD2 A:TYR107 4.6 31.6 1.0
CD1 A:LEU212 4.6 22.5 1.0
CD1 A:TYR107 4.8 31.0 1.0
CA A:GLN106 4.9 53.7 1.0
CG A:TYR107 4.9 33.1 1.0
C A:GLN106 4.9 42.6 1.0
O A:GLY101 5.0 29.2 1.0

Reference:

I.Westwood, D.M.Cheary, J.E.Baxter, M.W.Richards, R.L.Van Montfort, A.M.Fry, R.Bayliss. Insights Into the Conformational Variability and Regulation of Human NEK2 Kinase. J.Mol.Biol. V. 386 476 2009.
ISSN: ISSN 0022-2836
PubMed: 19124027
DOI: 10.1016/J.JMB.2008.12.033
Page generated: Sat Dec 12 09:22:24 2020

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