Zinc in PDB 7nub: Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp

Enzymatic activity of Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp

All present enzymatic activity of Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp:
6.1.1.4;

Protein crystallography data

The structure of Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp, PDB code: 7nub was solved by L.Pang, S.V.Strelkov, S.D.Weeks, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 65.39 / 3.02
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 49.309, 81.748, 217.95, 90, 90, 90
R / Rfree (%) 22.1 / 28.7

Other elements in 7nub:

The structure of Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp also contains other interesting chemical elements:

Magnesium (Mg) 1 atom

Zinc Binding Sites:

The binding sites of Zinc atom in the Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp (pdb code 7nub). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total only one binding site of Zinc was determined in the Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp, PDB code: 7nub:

Zinc binding site 1 out of 1 in 7nub

Go back to Zinc Binding Sites List in 7nub
Zinc binding site 1 out of 1 in the Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Crystal Structure of Neisseria Gonorrhoeae Leurs L550G Mutant in Complex with the Reaction Intermediate Leu-Amp within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Zn902

b:82.7
occ:1.00
 SG A:CYS493 2.4 64.6 1.0
SG A:CYS490 2.4 61.3 1.0
SG A:CYS452 2.5 68.5 1.0
SG A:CYS449 2.5 64.5 1.0
CB A:CYS493 2.9 72.2 1.0
CB A:CYS452 3.0 61.5 1.0
CB A:CYS490 3.3 52.0 1.0
CB A:CYS449 3.5 58.7 1.0
N A:CYS493 3.5 79.5 1.0
N A:CYS452 3.7 62.3 1.0
CA A:CYS493 3.8 79.4 1.0
CA A:CYS452 4.0 61.6 1.0
CB A:CYS492 4.5 62.6 1.0
CB A:LYS451 4.5 66.6 1.0
C A:CYS492 4.5 72.7 1.0
N A:GLY494 4.6 80.6 1.0
C A:CYS493 4.6 83.5 1.0
C A:LYS451 4.7 75.4 1.0
CA A:CYS490 4.7 49.8 1.0
CA A:CYS492 4.9 69.3 1.0
CA A:CYS449 4.9 57.3 1.0
N A:CYS492 4.9 71.7 1.0

Reference:

L.Pang, V.Zanki, S.V.Strelkov, A.Van Aerschot, I.Gruic-Sovulj, S.D.Weeks. Partitioning of the Initial Catalytic Steps of Leucyl-Trna Synthetase Is Driven By An Active Site Peptide-Plane Flip. Commun Biol V. 5 883 2022.
ISSN: ESSN 2399-3642
PubMed: 36038645
DOI: 10.1038/S42003-022-03825-8
Page generated: Wed Oct 30 07:56:50 2024

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