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Chlorine in PDB 2xnm: Structure of NEK2 Bound to Cct

Enzymatic activity of Structure of NEK2 Bound to Cct

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

Protein crystallography data

The structure of Structure of NEK2 Bound to Cct, PDB code: 2xnm 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) 36.734 / 1.85
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 100.800, 56.830, 81.300, 90.00, 133.21, 90.00
R / Rfree (%) 16.32 / 19.62

Other elements in 2xnm:

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

Fluorine (F) 3 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Structure of NEK2 Bound to Cct (pdb code 2xnm). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 3 binding sites of Chlorine where determined in the Structure of NEK2 Bound to Cct, PDB code: 2xnm:
Jump to Chlorine binding site number: 1; 2; 3;

Chlorine binding site 1 out of 3 in 2xnm

Go back to Chlorine Binding Sites List in 2xnm
Chlorine binding site 1 out of 3 in the Structure of NEK2 Bound to Cct


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 Cct within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1289

b:74.0
occ:1.00
O A:HOH2112 3.8 62.8 1.0
CA A:ARG105 3.8 33.6 1.0
C A:ARG105 3.8 35.7 1.0
CZ A:TYR107 3.9 26.6 1.0
O A:ARG105 4.0 37.0 1.0
CB A:ARG105 4.1 35.5 1.0
CE1 A:TYR107 4.1 32.9 1.0
CE2 A:TYR107 4.1 21.0 1.0
OH A:TYR107 4.2 21.8 1.0
N A:GLN106 4.3 30.7 1.0
CD1 A:TYR107 4.5 26.9 1.0
CD2 A:TYR107 4.6 26.5 1.0
CD1 A:LEU212 4.6 21.9 1.0
CG A:TYR107 4.7 28.5 1.0

Chlorine binding site 2 out of 3 in 2xnm

Go back to Chlorine Binding Sites List in 2xnm
Chlorine binding site 2 out of 3 in the Structure of NEK2 Bound to Cct


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 Cct within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1290

b:45.5
occ:1.00
N A:GLU110 3.1 10.7 1.0
O A:HOH2196 3.4 28.1 1.0
NH2 A:ARG239 3.5 49.7 1.0
O A:HOH2127 3.6 22.2 1.0
CB A:GLU110 3.7 12.8 1.0
CA A:ASP109 3.9 17.0 1.0
C A:ASP109 3.9 13.9 1.0
CA A:GLU110 4.0 14.6 1.0
O A:HOH2084 4.2 45.7 1.0
O A:ARG239 4.3 18.4 1.0
CZ A:ARG239 4.3 49.9 1.0
O A:HOH2048 4.5 25.6 1.0
O A:LEU108 4.6 17.8 1.0
O A:HOH2121 4.7 51.2 1.0
CB A:ASP109 4.7 20.5 1.0
CG A:ARG239 4.8 32.9 1.0
OD1 A:ASP109 4.8 35.1 1.0
CE2 A:TYR240 4.8 14.5 1.0
NH1 A:ARG239 4.8 46.6 1.0
CD2 A:TYR240 4.9 13.8 1.0
N A:ASP109 5.0 14.9 1.0

Chlorine binding site 3 out of 3 in 2xnm

Go back to Chlorine Binding Sites List in 2xnm
Chlorine binding site 3 out of 3 in the Structure of NEK2 Bound to Cct


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Structure of NEK2 Bound to Cct within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl1292

b:55.7
occ:1.00
O A:HOH2150 2.6 36.5 1.0
ND1 A:HIS277 2.9 21.3 1.0
ND2 A:ASN154 3.5 14.8 1.0
CG A:HIS277 3.6 21.5 1.0
CB A:HIS277 3.7 16.4 1.0
CE1 A:HIS277 3.8 23.1 1.0
CG A:ASN154 3.8 15.3 1.0
ND1 A:HIS279 3.9 36.1 1.0
CB A:PRO65 3.9 18.6 1.0
CE1 A:HIS279 4.0 38.5 1.0
C A:HIS278 4.1 17.6 1.0
O A:HIS278 4.1 18.4 1.0
N A:HIS279 4.3 15.9 1.0
OD1 A:ASN154 4.3 16.2 1.0
N A:HIS278 4.3 10.3 1.0
O A:PRO65 4.3 14.4 1.0
CG A:HIS279 4.4 33.4 1.0
CA A:HIS279 4.5 25.0 1.0
CB A:ASN154 4.5 15.0 1.0
NE2 A:HIS279 4.5 40.6 1.0
NZ A:LYS156 4.5 16.6 1.0
CA A:PRO65 4.6 15.8 1.0
C A:HIS277 4.7 11.7 1.0
CA A:HIS277 4.7 10.3 1.0
CA A:HIS278 4.7 14.2 1.0
CD2 A:HIS277 4.7 21.9 1.0
CD2 A:HIS279 4.8 38.5 1.0
CE A:LYS156 4.8 21.4 1.0
C A:PRO65 4.8 13.2 1.0
NE2 A:HIS277 4.8 27.9 1.0

Reference:

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
Page generated: Fri Jul 11 02:03:37 2025

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