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2.15 Angstrom Resolution Crystal Structure of Argininosuccinate Synthase from Bordetella pertussis

Analyse 2.15 Angstrom Resolution Crystal Structure of Argininosuccinate Synthase from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5US8
Type
protein
Length
890 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.15
Source
Bordetella pertussis (strain Tohama I / ATCC BAA-589 / NCTC 13251)
Molecule
Argininosuccinate synthase
EC
6.3.4.5
UniProt
Q7VTJ9
Ligands
ADN, SO4
Pockets
9 · best druggability 0.83

Structure

x-ray diffraction · resolution 2.15 · 1 distinct chain · 42% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BArgininosuccinate synthase (EC 6.3.4.5)protein44542% helix, 19% strandQ7VTJ9

Ligands and binding sites

  • ADN · Adenosine · ligand · chains A, B
  • SO4 · Sulfate ion · ion
  • EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · 3 copies · chains A, B
  • PGE · Triethylene glycol · additive · chains A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

9 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13370.830.9352ADN
21240.780.9627empty
311180.750.7889empty
411880.750.7885EPE
54100.590.7528empty

Interfaces

1 interface between chains.

  • A–B · 4782 Ų buried · 64 hydrogen bonds · protein-protein

Compared structures

  • 5US8 · 2.15 ångström resolution crystal structure of argininosuccinate synthase from bordetella… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q7VTJ9 · AlphaFold monomer V2.0 prediction for argininosuccinate synthase (Q7VTJ9) · a predicted model of the same protein · chain A against A, TM-score 0.95

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