Atomistry » Chlorine » PDB 3ruu-3s8l » 3s2y
Atomistry »
  Chlorine »
    PDB 3ruu-3s8l »
      3s2y »

Chlorine in PDB 3s2y: Crystal Structure of A Chromate/Uranium Reductase From Gluconacetobacter Hansenii

Protein crystallography data

The structure of Crystal Structure of A Chromate/Uranium Reductase From Gluconacetobacter Hansenii, PDB code: 3s2y was solved by H.Jin, Y.Zhang, G.W.Buchko, P.Li, T.C.Squier, H.Robinson, S.M.Varnum, P.E.Long, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 45.82 / 2.24
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 119.677, 90.051, 95.234, 90.00, 119.61, 90.00
R / Rfree (%) 19.3 / 23.8

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of A Chromate/Uranium Reductase From Gluconacetobacter Hansenii (pdb code 3s2y). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 3 binding sites of Chlorine where determined in the Crystal Structure of A Chromate/Uranium Reductase From Gluconacetobacter Hansenii, PDB code: 3s2y:
Jump to Chlorine binding site number: 1; 2; 3;

Chlorine binding site 1 out of 3 in 3s2y

Go back to Chlorine Binding Sites List in 3s2y
Chlorine binding site 1 out of 3 in the Crystal Structure of A Chromate/Uranium Reductase From Gluconacetobacter Hansenii


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 A Chromate/Uranium Reductase From Gluconacetobacter Hansenii within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl201

b:52.8
occ:1.00
N10 A:FMN200 3.9 32.2 1.0
C1' A:FMN200 4.0 33.9 1.0
C10 A:FMN200 4.2 31.5 1.0
C9A A:FMN200 4.3 31.4 1.0
O A:HOH326 4.4 39.1 1.0
N1 A:FMN200 4.5 30.0 1.0
C9 A:FMN200 4.6 30.8 1.0
C4A A:FMN200 4.8 28.9 1.0
C5A A:FMN200 4.8 32.1 1.0
O A:HOH275 4.9 42.6 1.0

Chlorine binding site 2 out of 3 in 3s2y

Go back to Chlorine Binding Sites List in 3s2y
Chlorine binding site 2 out of 3 in the Crystal Structure of A Chromate/Uranium Reductase From Gluconacetobacter Hansenii


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 A Chromate/Uranium Reductase From Gluconacetobacter Hansenii within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl200

b:50.3
occ:1.00
N10 C:FMN200 3.7 33.8 1.0
C1' C:FMN200 3.9 31.8 1.0
C9A C:FMN200 4.0 31.3 1.0
C10 C:FMN200 4.0 32.8 1.0
CZ B:PHE137 4.2 40.1 1.0
C9 C:FMN200 4.4 28.6 1.0
N1 C:FMN200 4.5 33.3 1.0
C5A C:FMN200 4.5 34.2 1.0
C4A C:FMN200 4.6 33.3 1.0
NH1 B:ARG101 4.6 44.4 1.0
O B:HOH240 4.7 45.6 1.0
CE2 B:PHE137 4.7 32.5 1.0
O B:HOH263 4.7 45.3 1.0
N5 C:FMN200 4.8 31.1 1.0

Chlorine binding site 3 out of 3 in 3s2y

Go back to Chlorine Binding Sites List in 3s2y
Chlorine binding site 3 out of 3 in the Crystal Structure of A Chromate/Uranium Reductase From Gluconacetobacter Hansenii


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Crystal Structure of A Chromate/Uranium Reductase From Gluconacetobacter Hansenii within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Cl201

b:54.1
occ:1.00
N10 B:FMN201 3.8 30.8 1.0
C1' B:FMN201 3.8 34.2 1.0
C9A B:FMN201 4.0 30.9 1.0
C10 B:FMN201 4.2 32.6 1.0
NH1 C:ARG101 4.2 45.7 1.0
C9 B:FMN201 4.3 27.6 1.0
CZ C:PHE137 4.6 36.9 1.0
N1 B:FMN201 4.6 33.7 1.0
C5A B:FMN201 4.6 35.1 1.0
C4A B:FMN201 4.7 29.5 1.0
CE2 C:PHE137 4.9 38.9 1.0
N5 B:FMN201 4.9 30.5 1.0

Reference:

H.Jin, Y.Zhang, G.W.Buchko, S.M.Varnum, H.Robinson, T.C.Squier, P.E.Long. Structure Determination and Functional Analysis of A Chromate Reductase From Gluconacetobacter Hansenii. Plos One V. 7 42432 2012.
ISSN: ESSN 1932-6203
PubMed: 22879982
DOI: 10.1371/JOURNAL.PONE.0042432
Page generated: Sat Dec 12 10:08:25 2020

Last articles

Zn in 8WB0
Zn in 8WAX
Zn in 8WAU
Zn in 8WAZ
Zn in 8WAY
Zn in 8WAV
Zn in 8WAW
Zn in 8WAT
Zn in 8W7M
Zn in 8WD3
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy