Atomistry » Chlorine » PDB 4oak-4ogt » 4odn
Atomistry »
  Chlorine »
    PDB 4oak-4ogt »
      4odn »

Chlorine in PDB 4odn: Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide

Enzymatic activity of Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide

All present enzymatic activity of Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide:
5.2.1.8;

Protein crystallography data

The structure of Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide, PDB code: 4odn was solved by E.M.Quistgaard, C.Low, P.Nordlund, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 28.41 / 1.60
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 39.830, 40.550, 53.220, 90.00, 91.24, 90.00
R / Rfree (%) 17.6 / 19.8

Other elements in 4odn:

The structure of Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide also contains other interesting chemical elements:

Sodium (Na) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide (pdb code 4odn). 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 Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide, PDB code: 4odn:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 4odn

Go back to Chlorine Binding Sites List in 4odn
Chlorine binding site 1 out of 2 in the Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl205

b:34.2
occ:1.00
N A:ILE37 3.1 10.0 1.0
O3 A:GOL204 3.1 53.6 1.0
C3 A:GOL204 3.1 53.5 1.0
CA A:LEU36 3.4 7.8 1.0
O1 A:GOL204 3.5 53.1 1.0
CB A:LEU36 3.6 10.8 1.0
C1 A:GOL204 3.6 52.7 1.0
C A:LEU36 3.7 10.3 1.0
CG1 A:ILE37 3.8 10.4 1.0
CG2 A:ILE37 3.9 11.1 1.0
C2 A:GOL204 3.9 53.3 1.0
CD2 A:LEU36 3.9 14.8 1.0
CB A:ILE37 4.1 9.8 1.0
CA A:ILE37 4.1 8.9 1.0
O2 A:GOL204 4.3 54.8 1.0
CG A:LEU36 4.3 13.2 1.0
CD2 A:LEU40 4.7 10.0 1.0
CD1 A:ILE37 4.7 11.4 1.0
O A:ASN35 4.7 14.6 1.0
N A:LEU36 4.8 8.6 1.0
O A:LEU36 4.9 10.8 1.0
OH A:TYR63 5.0 33.5 1.0

Chlorine binding site 2 out of 2 in 4odn

Go back to Chlorine Binding Sites List in 4odn
Chlorine binding site 2 out of 2 in the Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl206

b:38.2
occ:1.00
OG1 A:THR114 2.8 14.6 1.0
O A:HOH355 2.9 35.6 1.0
O A:GLU112 3.2 21.3 1.0
N A:THR114 3.5 10.2 1.0
CG A:GLU109 3.6 49.1 1.0
N A:GLU109 3.6 25.6 1.0
O A:ALA107 3.7 18.0 1.0
CB A:GLU109 3.7 38.3 1.0
CB A:THR114 3.8 11.9 1.0
CD A:GLU109 3.9 59.1 1.0
OE1 A:GLU109 3.9 63.8 1.0
O A:HOH406 3.9 30.1 1.0
C A:GLU112 3.9 19.1 1.0
C A:ALA107 4.1 18.3 1.0
C A:VAL113 4.1 11.0 1.0
C A:VAL108 4.2 25.7 1.0
CA A:THR114 4.2 10.7 1.0
CA A:VAL113 4.2 11.2 1.0
CA A:GLU109 4.3 28.4 1.0
CA A:VAL108 4.3 22.2 1.0
N A:VAL113 4.4 13.1 1.0
CB A:GLU112 4.4 26.6 1.0
N A:VAL108 4.4 19.2 1.0
CB A:ALA107 4.5 21.2 1.0
OE2 A:GLU109 4.6 61.3 1.0
CA A:GLU112 4.9 20.1 1.0
CA A:ALA107 4.9 18.5 1.0
O A:GLU109 4.9 22.0 1.0
O A:VAL108 5.0 24.9 1.0

Reference:

E.M.Quistgaard, C.Low, P.Nordlund. Structure of Slyd From Thermus Thermophilus in Complex with S2-Plus Peptide To Be Published.
Page generated: Fri Jul 11 20:00:32 2025

Last articles

Fe in 2YXO
Fe in 2YRS
Fe in 2YXC
Fe in 2YNM
Fe in 2YVJ
Fe in 2YP1
Fe in 2YU2
Fe in 2YU1
Fe in 2YQB
Fe in 2YOO
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy