Chlorine in PDB 2xno: Structure of NEK2 Bound to CCT243779

All present enzymatic activity of Structure of NEK2 Bound to CCT243779:
2.7.11.1;

The structure of Structure of NEK2 Bound to CCT243779, PDB code: 2xno was solved by C.Mas-Droux, R.Bayliss, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	36.674 / 1.98
Space group	C 1 2 1
Cell size a, b, c (Å), α, β, γ (°)	101.050, 56.880, 81.340, 90.00, 133.46, 90.00
R / Rfree (%)	17.03 / 21.41

The structure of Structure of NEK2 Bound to CCT243779 also contains other interesting chemical elements:

Fluorine

(F)

3 atoms

The binding sites of Chlorine atom in the Structure of NEK2 Bound to CCT243779 (pdb code 2xno). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Structure of NEK2 Bound to CCT243779, PDB code: 2xno:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in the Structure of NEK2 Bound to CCT243779


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of NEK2 Bound to CCT243779 within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl1281 b:71.2 occ:1.00 CZ A:TYR107 3.8 23.4 1.0 CG A:ARG105 3.9 57.7 1.0 CA A:ARG105 3.9 37.7 1.0 C A:ARG105 4.0 35.4 1.0 CE2 A:TYR107 4.0 17.6 1.0 CE1 A:TYR107 4.1 29.0 1.0 O A:ARG105 4.1 33.0 1.0 OH A:TYR107 4.1 19.6 1.0 CB A:ARG105 4.2 47.1 1.0 N A:GLN106 4.4 32.7 1.0 CD2 A:TYR107 4.5 23.0 1.0 CD1 A:TYR107 4.5 24.1 1.0 CD1 A:LEU212 4.5 18.1 1.0 CG A:TYR107 4.7 26.5 1.0 O A:HOH2088 4.8 34.8 1.0 CD A:ARG105 4.9 65.8 1.0

Chlorine binding site 2 out of 2 in the Structure of NEK2 Bound to CCT243779


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Structure of NEK2 Bound to CCT243779 within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl1282 b:42.7 occ:1.00 O A:HOH2064 2.7 66.9 1.0 N A:GLU110 2.9 11.7 1.0 O A:HOH2149 3.3 26.4 1.0 NH2 A:ARG239 3.4 47.9 1.0 O A:HOH2097 3.4 25.1 1.0 CB A:GLU110 3.6 13.6 1.0 C A:ASP109 3.8 15.3 1.0 CA A:GLU110 3.8 16.4 1.0 CA A:ASP109 3.8 20.6 1.0 CZ A:ARG239 4.2 51.6 1.0 O A:HOH2045 4.4 21.2 1.0 O A:ARG239 4.5 17.9 1.0 NH1 A:ARG239 4.5 52.5 1.0 O A:LEU108 4.5 16.7 1.0 CB A:ASP109 4.6 23.7 1.0 OD1 A:ASP109 4.7 37.5 1.0 O A:HOH2094 4.7 48.9 1.0 CE2 A:TYR240 4.8 13.2 1.0 O A:HOH2152 4.8 42.0 1.0 N A:ASP109 4.9 12.8 1.0 CD2 A:TYR240 4.9 12.8 1.0 O A:ASP109 5.0 16.0 1.0 C A:GLU110 5.0 13.5 1.0 N A:GLU111 5.0 11.7 1.0

S.Solanki, P.Innocenti, C.Mas-Droux, K.Boxall, C.Barillari, R.L.Van Montfort, G.W.Aherne, R.Bayliss, S.Hoelder. Benzimidazole Inhibitors Induce A Dfg-Out Conformation of Never in Mitosis Gene A-Related Kinase 2 (NEK2) Without Binding to the Back Pocket and Reveal A Nonlinear Structure-Activity Relationship. J.Med.Chem. V. 54 1626 2011.
ISSN: ISSN 0022-2623
PubMed: 21366329
DOI: 10.1021/JM1011726