Atomistry » Magnesium » PDB 7t21-7tgn » 7tgn
Atomistry »
  Magnesium »
    PDB 7t21-7tgn »
      7tgn »

Magnesium in PDB 7tgn: Crystal Structure of Desd, the Desferrioxamine Synthetase From the Streptomyces Violaceus Salmycin Biosynthetic Pathway

Protein crystallography data

The structure of Crystal Structure of Desd, the Desferrioxamine Synthetase From the Streptomyces Violaceus Salmycin Biosynthetic Pathway, PDB code: 7tgn was solved by K.D.Patel, A.M.Gulick, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 49.47 / 2.30
Space group P 43 21 2
Cell size a, b, c (Å), α, β, γ (°) 108.53, 108.53, 517.75, 90, 90, 90
R / Rfree (%) 19.6 / 23

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Crystal Structure of Desd, the Desferrioxamine Synthetase From the Streptomyces Violaceus Salmycin Biosynthetic Pathway (pdb code 7tgn). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Crystal Structure of Desd, the Desferrioxamine Synthetase From the Streptomyces Violaceus Salmycin Biosynthetic Pathway, PDB code: 7tgn:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 7tgn

Go back to Magnesium Binding Sites List in 7tgn
Magnesium binding site 1 out of 2 in the Crystal Structure of Desd, the Desferrioxamine Synthetase From the Streptomyces Violaceus Salmycin Biosynthetic Pathway


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Crystal Structure of Desd, the Desferrioxamine Synthetase From the Streptomyces Violaceus Salmycin Biosynthetic Pathway within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg605

b:61.8
occ:1.00
O B:HOH727 2.5 51.4 1.0
O B:HOH716 2.6 53.6 1.0
OD1 A:ASN242 2.8 50.8 1.0
OE2 A:GLU166 2.9 57.1 1.0
OD1 B:ASN242 2.9 51.0 1.0
OE2 B:GLU166 3.1 54.5 1.0
OE1 A:GLU166 3.4 53.9 1.0
CG A:ASN242 3.5 51.0 1.0
CD A:GLU166 3.5 55.1 1.0
CG B:ASN242 3.6 53.6 1.0
ND2 A:ASN242 3.7 50.2 1.0
CD B:GLU166 3.8 52.2 1.0
OE1 B:GLU166 3.8 53.3 1.0
ND2 B:ASN242 3.9 52.5 1.0
NE2 B:HIS165 4.6 51.5 1.0
CB A:ASN242 4.7 48.1 1.0
NE1 A:TRP238 4.7 50.6 1.0
CE1 B:HIS165 4.8 52.9 1.0
NE2 A:HIS165 4.8 56.1 1.0
CE1 A:HIS165 4.8 54.2 1.0
CB B:ASN242 4.9 50.5 1.0
CG A:GLU166 4.9 50.8 1.0
NE1 B:TRP238 5.0 51.3 1.0

Magnesium binding site 2 out of 2 in 7tgn

Go back to Magnesium Binding Sites List in 7tgn
Magnesium binding site 2 out of 2 in the Crystal Structure of Desd, the Desferrioxamine Synthetase From the Streptomyces Violaceus Salmycin Biosynthetic Pathway


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Crystal Structure of Desd, the Desferrioxamine Synthetase From the Streptomyces Violaceus Salmycin Biosynthetic Pathway within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Mg605

b:54.2
occ:1.00
O C:HOH737 2.4 49.7 1.0
O D:HOH757 2.5 49.8 1.0
OD1 D:ASN242 2.8 49.4 1.0
OE2 C:GLU166 3.0 54.2 1.0
ND2 C:ASN242 3.1 45.5 1.0
OE2 D:GLU166 3.2 52.7 1.0
CG D:ASN242 3.5 51.0 1.0
OE1 C:GLU166 3.5 52.6 1.0
CD C:GLU166 3.6 54.6 1.0
OE1 D:GLU166 3.7 50.9 1.0
CG C:ASN242 3.7 49.8 1.0
ND2 D:ASN242 3.8 48.4 1.0
CD D:GLU166 3.8 53.7 1.0
OD1 C:ASN242 3.9 50.1 1.0
CB D:ASN242 4.7 47.6 1.0
NE2 C:HIS165 4.8 54.0 1.0
CE1 C:HIS165 4.8 55.1 1.0
O2 D:EDO604 4.8 63.3 1.0
NE1 C:TRP238 4.8 49.8 1.0
NE1 D:TRP238 4.9 48.6 1.0
CB C:ASN242 4.9 45.2 1.0
C2 C:EDO602 5.0 62.5 1.0

Reference:

J.Yang, V.S.Banas, K.D.Patel, G.S.M.Rivera, L.S.Mydy, A.M.Gulick, T.A.Wencewicz. An Acyl-Adenylate Mimic Reveals the Structural Basis For Substrate Recognition By the Iterative Siderophore Synthetase Desd. J.Biol.Chem. V. 298 02166 2022.
ISSN: ESSN 1083-351X
PubMed: 35750210
DOI: 10.1016/J.JBC.2022.102166
Page generated: Thu Oct 3 09:11:18 2024

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy