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Chlorine in PDB 2fzv: Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri

Protein crystallography data

The structure of Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri, PDB code: 2fzv was solved by I.I.Vorontsov, G.Minasov, J.S.Brunzelle, L.Shuvalova, F.R.Collart, A.Joachimiak, W.F.Anderson, Midwest Center For Structural Genomics(Mcsg), with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.81 / 1.70
Space group P 43 21 2
Cell size a, b, c (Å), α, β, γ (°) 117.821, 117.821, 154.080, 90.00, 90.00, 90.00
R / Rfree (%) 19.9 / 24.6

Other elements in 2fzv:

The structure of Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri also contains other interesting chemical elements:

Calcium (Ca) 1 atom

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri (pdb code 2fzv). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri, PDB code: 2fzv:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 2fzv

Go back to Chlorine Binding Sites List in 2fzv
Chlorine binding site 1 out of 2 in the Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl257

b:13.8
occ:1.00
O A:HOH367 2.9 28.1 1.0
O A:HOH353 2.9 26.0 1.0
O A:HOH265 3.1 5.7 1.0
N A:SER175 3.3 17.0 1.0
O A:SER175 3.5 18.5 1.0
CG A:ARG197 3.5 19.0 0.5
OE1 A:GLN150 3.5 27.7 1.0
CG A:ARG197 3.6 22.2 0.5
NH2 A:ARG197 3.8 17.3 0.5
CD2 A:TYR194 3.9 19.6 1.0
CB A:ARG197 3.9 18.1 0.5
C A:SER175 4.0 18.1 1.0
CB A:ARG197 4.0 19.1 0.5
CZ A:ARG197 4.0 17.7 0.5
CA A:SER174 4.0 17.4 1.0
CA A:SER175 4.1 18.4 1.0
C A:SER174 4.2 18.4 1.0
NE A:ARG197 4.2 19.3 0.5
CE2 A:TYR194 4.4 18.0 1.0
CD A:ARG197 4.4 19.4 0.5
O A:GLN173 4.5 19.9 1.0
NH1 A:ARG197 4.5 15.8 0.5
OG A:SER174 4.6 19.3 1.0
CB A:SER175 4.6 17.4 1.0
CD A:ARG197 4.7 21.8 0.5
CB A:SER174 4.7 17.7 1.0
CA A:TYR194 4.8 18.7 1.0
CD A:GLN150 4.8 21.1 1.0
O A:HOH430 4.8 29.3 1.0
N A:ILE176 4.9 18.7 1.0
NE A:ARG197 4.9 27.1 0.5
CG A:TYR194 4.9 19.6 1.0

Chlorine binding site 2 out of 2 in 2fzv

Go back to Chlorine Binding Sites List in 2fzv
Chlorine binding site 2 out of 2 in the Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Crystal Structure of An Apo Form of A Flavin-Binding Protein From Shigella Flexneri within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl258

b:11.2
occ:1.00
O A:HOH315 2.9 15.0 1.0
O A:HOH279 3.1 7.5 1.0
O C:HOH461 3.1 30.1 1.0
NH1 C:ARG159 3.3 17.9 1.0
NH1 A:ARG159 3.3 19.0 1.0
CG A:ARG159 3.5 19.5 1.0
CD A:ARG159 3.5 17.8 1.0
CD C:ARG159 3.6 18.0 1.0
CG C:ARG159 3.7 16.3 1.0
O C:HOH258 3.8 8.2 1.0
O C:THR169 3.9 20.6 1.0
CB A:THR169 4.1 21.6 1.0
O A:HOH286 4.1 8.3 1.0
O A:THR169 4.1 18.3 1.0
O C:HOH285 4.3 12.5 1.0
CZ C:ARG159 4.3 20.2 1.0
CB C:THR169 4.3 19.0 1.0
CZ A:ARG159 4.3 17.6 1.0
NE A:ARG159 4.4 17.8 1.0
NE C:ARG159 4.4 18.5 1.0
CG2 A:THR169 4.7 18.6 1.0
OG1 A:THR169 4.7 23.1 1.0
C C:THR169 4.8 19.6 1.0
OG1 C:THR169 4.9 21.5 1.0
C A:THR169 4.9 19.4 1.0
CB A:ARG159 5.0 17.9 1.0
CA C:THR169 5.0 18.7 1.0
CA A:THR169 5.0 18.8 1.0

Reference:

I.I.Vorontsov, G.Minasov, J.S.Brunzelle, L.Shuvalova, O.Kiryukhina, F.R.Collart, W.F.Anderson. Crystal Structure of An Apo Form of Shigella Flexneri Arsh Protein with An Nadph-Dependent Fmn Reductase Activity Protein Sci. V. 16 2483 2007.
ISSN: ISSN 0961-8368
PubMed: 17962405
DOI: 10.1110/PS.073029607
Page generated: Sat Jul 20 07:15:20 2024

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