Atomistry » Arsenic » PDB 3sr6-4cx0 » 3ujp
Atomistry »
  Arsenic »
    PDB 3sr6-4cx0 »
      3ujp »

Arsenic in PDB 3ujp: Structure of Mntc Protein at 2.7A

Protein crystallography data

The structure of Structure of Mntc Protein at 2.7A, PDB code: 3ujp was solved by M.Kanteev, N.Adir, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 36.80 / 2.70
Space group P 31 2 1
Cell size a, b, c (Å), α, β, γ (°) 127.520, 127.520, 89.730, 90.00, 90.00, 120.00
R / Rfree (%) 23.1 / 28.4

Other elements in 3ujp:

The structure of Structure of Mntc Protein at 2.7A also contains other interesting chemical elements:

Manganese (Mn) 3 atoms
Zinc (Zn) 6 atoms

Arsenic Binding Sites:

The binding sites of Arsenic atom in the Structure of Mntc Protein at 2.7A (pdb code 3ujp). This binding sites where shown within 5.0 Angstroms radius around Arsenic atom.
In total 4 binding sites of Arsenic where determined in the Structure of Mntc Protein at 2.7A, PDB code: 3ujp:
Jump to Arsenic binding site number: 1; 2; 3; 4;

Arsenic binding site 1 out of 4 in 3ujp

Go back to Arsenic Binding Sites List in 3ujp
Arsenic binding site 1 out of 4 in the Structure of Mntc Protein at 2.7A


Mono view


Stereo pair view

A full contact list of Arsenic with other atoms in the As binding site number 1 of Structure of Mntc Protein at 2.7A within 5.0Å range:
probe atom residue distance (Å) B Occ
A:As2327

b:0.0
occ:1.00
AS A:CAC2327 0.0 0.0 1.0
C2 A:CAC2327 1.5 0.7 1.0
O2 A:CAC2327 1.5 0.8 1.0
C1 A:CAC2327 1.6 0.3 1.0
O1 A:CAC2327 1.6 0.1 1.0
OD1 A:ASP179 3.6 0.9 1.0
OD2 A:ASP179 4.0 0.3 1.0
CG A:ASP179 4.2 0.3 1.0

Arsenic binding site 2 out of 4 in 3ujp

Go back to Arsenic Binding Sites List in 3ujp
Arsenic binding site 2 out of 4 in the Structure of Mntc Protein at 2.7A


Mono view


Stereo pair view

A full contact list of Arsenic with other atoms in the As binding site number 2 of Structure of Mntc Protein at 2.7A within 5.0Å range:
probe atom residue distance (Å) B Occ
A:As332

b:0.7
occ:0.60
AS A:CAC332 0.0 0.7 0.6
O1 A:CAC332 1.6 83.6 1.0
O2 A:CAC332 1.6 89.5 1.0
C1 A:CAC332 1.6 68.1 1.0
C2 A:CAC332 1.6 91.8 1.0
OE2 A:GLU312 2.9 97.1 1.0
OE2 B:GLU135 3.3 87.3 1.0
CD A:GLU312 3.4 97.1 1.0
OE1 B:GLU135 3.4 83.6 1.0
OE1 A:GLU312 3.5 0.5 1.0
OE1 B:GLN171 3.5 94.5 1.0
OD2 A:ASP309 3.6 79.8 1.0
CD B:GLU135 3.7 83.4 1.0
CG A:GLU312 4.5 78.2 1.0
OE2 B:GLU175 4.7 97.5 1.0
CD B:GLN171 4.7 88.1 1.0
CG A:ASP309 4.8 76.9 1.0

Arsenic binding site 3 out of 4 in 3ujp

Go back to Arsenic Binding Sites List in 3ujp
Arsenic binding site 3 out of 4 in the Structure of Mntc Protein at 2.7A


Mono view


Stereo pair view

A full contact list of Arsenic with other atoms in the As binding site number 3 of Structure of Mntc Protein at 2.7A within 5.0Å range:
probe atom residue distance (Å) B Occ
C:As2327

b:0.9
occ:0.60
AS C:CAC2327 0.0 0.9 0.6
O2 C:CAC2327 1.5 0.7 1.0
O1 C:CAC2327 1.6 0.5 1.0
C2 C:CAC2327 1.6 0.9 1.0
C1 C:CAC2327 1.6 98.5 1.0
OE2 C:GLU193 3.5 0.6 1.0
CD C:GLU193 4.2 0.9 1.0
CG C:GLU193 4.5 0.2 1.0

Arsenic binding site 4 out of 4 in 3ujp

Go back to Arsenic Binding Sites List in 3ujp
Arsenic binding site 4 out of 4 in the Structure of Mntc Protein at 2.7A


Mono view


Stereo pair view

A full contact list of Arsenic with other atoms in the As binding site number 4 of Structure of Mntc Protein at 2.7A within 5.0Å range:
probe atom residue distance (Å) B Occ
C:As332

b:0.5
occ:0.60
AS C:CAC332 0.0 0.5 0.6
C2 C:CAC332 1.5 0.6 1.0
O1 C:CAC332 1.6 0.8 1.0
O2 C:CAC332 1.6 0.4 1.0
C1 C:CAC332 1.6 0.9 1.0
OE1 C:GLU207 3.8 0.4 1.0
CD C:GLU207 4.9 0.7 1.0

Reference:

M.Kanteev, N.Adir. Arginine 116 Stabilizes the Entrance to the Metal Ion-Binding Site of the Mntc Protein. Acta Crystallogr.,Sect.F V. 69 237 2013.
ISSN: ESSN 1744-3091
PubMed: 23519795
DOI: 10.1107/S174430911300153X
Page generated: Wed Jul 10 11:56:09 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy