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The three-dimensional structure of N-succinyldiaminopimelate aminotransferase from mycobacterium tuberculosis

Analyse The three-dimensional structure of N-succinyldiaminopimelate aminotransferase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2O0R
Type
protein
Length
769 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
RV0858C (N-succinyldiaminopimelate aminotransferase)
EC
2.6.1.-
UniProt
O53870
Ligands
NA, CL
Pockets
9 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 47% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARV0858C (N-succinyldiaminopimelate aminotransferase) (EC 2.6.1.-)protein38547% helix, 17% strandO53870
BRV0858C (N-succinyldiaminopimelate aminotransferase) (EC 2.6.1.-)protein38447% helix, 17% strandO53870

Ligands and binding sites

  • NA · Sodium ion · metal · chains B
  • CL · Chloride ion · ion · 2 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A, B

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

Pockets

9 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13140.700.8350GOL
22660.690.8543GOL
3940.420.7823empty
4860.410.7816empty
51040.400.7619empty

Interfaces

1 interface between chains.

  • A–B · 2552 Ų buried · 46 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (cofactor).

Compared structures

  • 2O0R · The three-dimensional structure of N-Succinyldiaminopimelate aminotransferase from… · the same entry in another collection · chain A against A, TM-score 1.00

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