Atomistry » Iron » PDB 7vp8-7w1p » 7vzy
Atomistry »
  Iron »
    PDB 7vp8-7w1p »
      7vzy »

Iron in PDB 7vzy: The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin

Protein crystallography data

The structure of The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin, PDB code: 7vzy was solved by J.Wei, J.Zheng, J.Zhou, Q.Kang, L.Bai, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 31.88 / 2.81
Space group P 31 2 1
Cell size a, b, c (Å), α, β, γ (°) 111.483, 111.483, 231.355, 90, 90, 120
R / Rfree (%) 17.1 / 22

Other elements in 7vzy:

The structure of The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin also contains other interesting chemical elements:

Chlorine (Cl) 2 atoms

Iron Binding Sites:

The binding sites of Iron atom in the The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin (pdb code 7vzy). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin, PDB code: 7vzy:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 7vzy

Go back to Iron Binding Sites List in 7vzy
Iron binding site 1 out of 2 in the The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe702

b:31.2
occ:1.00
NE2 A:HIS133 2.3 27.2 1.0
OD1 A:ASP333 2.3 27.6 1.0
OD2 A:ASP156 2.3 33.9 1.0
O3P A:AMP703 2.4 31.4 1.0
NE2 A:HIS137 2.4 27.1 1.0
O2P A:AMP703 2.7 39.7 1.0
P A:AMP703 3.0 33.2 1.0
CE1 A:HIS133 3.1 30.1 1.0
CG A:ASP156 3.3 33.2 1.0
CE1 A:HIS137 3.3 26.3 1.0
CD2 A:HIS137 3.3 28.7 1.0
CD2 A:HIS133 3.4 29.3 1.0
CG A:ASP333 3.4 29.7 1.0
CB A:ASP156 3.5 24.9 1.0
OD2 A:ASP333 3.9 35.8 1.0
O1P A:AMP703 4.0 34.3 1.0
O5' A:AMP703 4.2 31.6 1.0
ND1 A:HIS133 4.3 24.3 1.0
ND1 A:HIS137 4.4 31.3 1.0
OD1 A:ASP156 4.4 35.2 1.0
CG A:HIS133 4.5 32.9 1.0
CG A:HIS137 4.5 30.0 1.0
CB A:ASP333 4.6 28.3 1.0
CA A:ASP333 4.6 27.0 1.0
N A:ASP333 4.7 25.6 1.0
N A:GLY305 4.8 26.0 1.0

Iron binding site 2 out of 2 in 7vzy

Go back to Iron Binding Sites List in 7vzy
Iron binding site 2 out of 2 in the The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of The Structure of Gdmn Complex with Amp and 20-O-Methyl-19- Chloroproansamitocin within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe702

b:30.2
occ:1.00
OD1 B:ASP333 2.3 38.0 1.0
NE2 B:HIS133 2.3 25.6 1.0
NE2 B:HIS137 2.4 35.9 1.0
O2P B:AMP703 2.5 34.9 1.0
OD2 B:ASP156 2.6 36.3 1.0
O3P B:AMP703 2.7 50.6 1.0
P B:AMP703 3.0 39.2 1.0
CE1 B:HIS133 3.1 27.5 1.0
CD2 B:HIS137 3.3 32.8 1.0
CE1 B:HIS137 3.3 31.2 1.0
CG B:ASP156 3.4 37.1 1.0
CG B:ASP333 3.4 33.2 1.0
CD2 B:HIS133 3.5 29.2 1.0
CB B:ASP156 3.6 32.8 1.0
OD2 B:ASP333 4.0 39.5 1.0
O1P B:AMP703 4.1 44.2 1.0
O5' B:AMP703 4.3 37.0 1.0
ND1 B:HIS133 4.3 23.2 1.0
ND1 B:HIS137 4.4 33.4 1.0
CG B:HIS137 4.4 28.4 1.0
CG B:HIS133 4.5 24.6 1.0
OD1 B:ASP156 4.6 36.5 1.0
CA B:ASP333 4.6 29.3 1.0
CB B:ASP333 4.6 33.5 1.0
N B:ASP333 4.7 33.6 1.0
O B:ARG158 4.9 32.8 1.0

Reference:

J.Wei, X.Zhang, Y.Zhou, X.Cheng, Z.Lin, M.Tang, J.Zheng, B.Wang, Q.Kang, L.Bai. Endowing Homodimeric Carbamoyltransferase Gdmn with Iterative Functions Through Structural Characterization and Mechanistic Studies. Nat Commun V. 13 6617 2022.
ISSN: ESSN 2041-1723
PubMed: 36329057
DOI: 10.1038/S41467-022-34387-2
Page generated: Fri Aug 9 06:59:46 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