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Chlorine in PDB 4fsd: Arsm Arsenic(III) S-Adenosylmethionine Methyltransferase with As(III)

Protein crystallography data

The structure of Arsm Arsenic(III) S-Adenosylmethionine Methyltransferase with As(III), PDB code: 4fsd was solved by A.A.Ajees, K.Marapakala, C.Packianathan, B.Sankaran, B.P.Rosen, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 50.00 / 1.75
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 85.246, 46.762, 100.528, 90.00, 114.33, 90.00
R / Rfree (%) 19.9 / 23.9

Other elements in 4fsd:

The structure of Arsm Arsenic(III) S-Adenosylmethionine Methyltransferase with As(III) also contains other interesting chemical elements:

Arsenic (As) 1 atom
Calcium (Ca) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Arsm Arsenic(III) S-Adenosylmethionine Methyltransferase with As(III) (pdb code 4fsd). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the Arsm Arsenic(III) S-Adenosylmethionine Methyltransferase with As(III), PDB code: 4fsd:

Chlorine binding site 1 out of 1 in 4fsd

Go back to Chlorine Binding Sites List in 4fsd
Chlorine binding site 1 out of 1 in the Arsm Arsenic(III) S-Adenosylmethionine Methyltransferase with As(III)


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Arsm Arsenic(III) S-Adenosylmethionine Methyltransferase with As(III) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl402

b:45.8
occ:1.00
AS A:ARS401 2.3 38.2 1.0
SG A:CYS174 3.3 34.0 1.0
SG A:CYS224 3.4 32.0 1.0
O A:GLU223 3.6 27.6 1.0
CB A:CYS224 3.6 31.3 1.0
C A:GLU223 4.0 27.1 1.0
O A:HOH637 4.2 49.5 1.0
CB A:CYS174 4.5 30.8 1.0
N A:CYS224 4.5 24.4 1.0
CA A:CYS224 4.7 27.7 1.0
CA A:GLU223 4.7 28.4 1.0
O A:GLY222 4.9 29.0 1.0

Reference:

A.A.Ajees, K.Marapakala, C.Packianathan, B.Sankaran, B.P.Rosen. Structure of An As(III) S-Adenosylmethionine Methyltransferase: Insights Into the Mechanism of Arsenic Biotransformation. Biochemistry V. 51 5476 2012.
ISSN: ISSN 0006-2960
PubMed: 22712827
DOI: 10.1021/BI3004632
Page generated: Sat Dec 12 10:37:56 2020

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