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Crystal structure of mycobacterium tuberculosis 7,8-diaminopelargonic acid synthase in complex with substrate analog sinefungin

Analyse Crystal structure of mycobacterium tuberculosis 7,8-diaminopelargonic acid… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3LV2
Type
protein
Length
836 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Adenosylmethionine-8-amino-7-oxononanoate aminotransferase
EC
2.6.1.62
UniProt
P0A4X6
Ligands
PLP, SFG
Pockets
7 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAdenosylmethionine-8-amino-7-oxononanoate aminotransferase (EC 2.6.1.62)protein42142% helix, 20% strandP0A4X6
BAdenosylmethionine-8-amino-7-oxononanoate aminotransferase (EC 2.6.1.62)protein41542% helix, 20% strandP0A4X6

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • SFG · Sinefungin · ligand · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13910.810.8964PLP, SFG
26350.770.8279PLP
3800.500.8318empty
4650.440.8218empty
5750.390.7819empty

Interfaces

1 interface between chains.

  • A–B · 4619 Ų buried · 49 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 3LV2 · Crystal structure of Mycobacterium tuberculosis 7,8-diaminopelargonic acid synthase in… · the same entry in another collection · chain B against B, TM-score 1.00

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