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Iron in PDB 7vzq: The Structure of Gdmn V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate

Protein crystallography data

The structure of The Structure of Gdmn V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate, PDB code: 7vzq 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) 44.43 / 2.10
Space group P 31 2 1
Cell size a, b, c (Å), α, β, γ (°) 111.092, 111.092, 231.802, 90, 90, 120
R / Rfree (%) 19.6 / 23.3

Other elements in 7vzq:

The structure of The Structure of Gdmn V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate also contains other interesting chemical elements:

Chlorine (Cl) 1 atom

Iron Binding Sites:

The binding sites of Iron atom in the The Structure of Gdmn V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate (pdb code 7vzq). 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 V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate, PDB code: 7vzq:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 7vzq

Go back to Iron Binding Sites List in 7vzq
Iron binding site 1 out of 2 in the The Structure of Gdmn V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate


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 V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe702

b:31.4
occ:1.00
OD1 A:ASP333 2.3 28.9 1.0
NE2 A:HIS133 2.3 26.5 1.0
OD2 A:ASP156 2.3 35.8 1.0
O1A A:CA0707 2.4 25.8 0.8
NE2 A:HIS137 2.4 27.3 1.0
O3A A:CA0707 3.0 37.0 0.8
CD2 A:HIS137 3.2 27.2 1.0
PA A:CA0707 3.2 33.8 0.8
CE1 A:HIS133 3.2 28.4 1.0
CG A:ASP156 3.3 36.2 1.0
CB A:CA0707 3.3 31.6 0.8
CD2 A:HIS133 3.3 29.2 1.0
CG A:ASP333 3.4 32.1 1.0
N2B A:CA0707 3.4 37.8 0.8
CE1 A:HIS137 3.5 27.3 1.0
CB A:ASP156 3.6 33.5 1.0
OD2 A:ASP333 3.8 31.1 1.0
O1B A:CA0707 4.0 41.9 0.8
O2A A:CA0707 4.3 33.7 0.8
O5' A:CA0707 4.3 37.9 0.8
ND1 A:HIS133 4.3 30.2 1.0
OD1 A:ASP156 4.3 35.2 1.0
CG A:HIS133 4.4 33.7 1.0
CG A:HIS137 4.4 28.5 1.0
ND1 A:HIS137 4.5 25.0 1.0
CB A:ASP333 4.6 32.2 1.0
CA A:ASP333 4.7 27.9 1.0
N A:ASP333 4.9 26.9 1.0
CB A:ALA336 4.9 23.0 1.0
N A:GLY305 5.0 25.5 1.0

Iron binding site 2 out of 2 in 7vzq

Go back to Iron Binding Sites List in 7vzq
Iron binding site 2 out of 2 in the The Structure of Gdmn V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate


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 V24Y/G157A/R158A/G188R Mutant in Complex with Carbamoyl Adenylate Intermediate within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe701

b:34.1
occ:1.00
OD1 B:ASP333 2.3 30.8 1.0
OD2 B:ASP156 2.3 38.3 1.0
NE2 B:HIS133 2.3 31.2 1.0
NE2 B:HIS137 2.4 35.3 1.0
O1A B:CA0704 2.4 32.2 0.8
N2B B:CA0704 2.5 36.6 0.8
CB B:CA0704 3.2 37.5 0.8
O3A B:CA0704 3.2 43.6 0.8
CD2 B:HIS137 3.2 31.5 1.0
CD2 B:HIS133 3.3 33.2 1.0
CG B:ASP156 3.3 39.8 1.0
CE1 B:HIS133 3.4 30.1 1.0
PA B:CA0704 3.4 38.1 0.8
CE1 B:HIS137 3.4 32.7 1.0
CG B:ASP333 3.4 34.8 1.0
CB B:ASP156 3.5 35.1 1.0
OD2 B:ASP333 3.9 32.4 1.0
O1B B:CA0704 4.3 45.9 0.8
CG B:HIS137 4.4 33.9 1.0
OD1 B:ASP156 4.4 37.8 1.0
O5' B:CA0704 4.4 42.4 0.8
CG B:HIS133 4.4 32.6 1.0
ND1 B:HIS133 4.4 31.1 1.0
O2A B:CA0704 4.4 40.1 0.8
ND1 B:HIS137 4.5 32.3 1.0
CA B:ASP333 4.7 26.9 1.0
CB B:ASP333 4.7 31.7 1.0
N B:ASP333 4.8 26.0 1.0
CB B:ALA336 5.0 29.7 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: Thu Aug 7 08:23:15 2025

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