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Crystal structure of Argininosuccinate synthase from Mycobacterium thermoresistibile in complex with AMPPNP and Arginine

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

PDB
4XFJ
Type
protein
Length
792 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.55
Source
Mycobacterium thermoresistibile ATCC 19527
Molecule
Argininosuccinate synthase
EC
6.3.4.5
UniProt
G7CBN9
Ligands
ANP, ARG, MG
Pockets
6 · best druggability 0.86

Structure

x-ray diffraction · resolution 1.55 · 2 distinct chains · 45% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AArgininosuccinate synthase (EC 6.3.4.5)protein39545% helix, 22% strandG7CBN9
BArgininosuccinate synthase (EC 6.3.4.5)protein39746% helix, 21% strandG7CBN9

Ligands and binding sites

  • ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · 2 copies · chains A, B
  • ARG · Arginine · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 3 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 6 copies · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111670.860.87103MG
28230.750.7971ANP, MG, ARG
37200.740.8058ANP, MG, ARG
41180.450.7817empty
51170.440.7818empty

Interfaces

1 interface between chains.

  • A–B · 4478 Ų buried · 60 hydrogen bonds · protein-protein

Compared structures

  • 4XFJ · Crystal structure of argininosuccinate synthase from mycobacterium thermoresistibile in… · the same entry in another collection · chain A against A, TM-score 1.00

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