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Structure of dihydrodipicolinate synthase from streptococcus PNEUMONIAE,BOUND to pyruvate and lysine

Analyse Structure of dihydrodipicolinate synthase from streptococcus PNEUMONIAE,BOUND… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4FHA
Type
protein
Length
614 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydrodipicolinate synthase
EC
4.2.1.52
UniProt
A5LD17
Ligands
LYS, NA
Pockets
5 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 49% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BDihydrodipicolinate synthase (EC 4.2.1.52)protein30749% helix, 13% strandA5LD17

Ligands and binding sites

  • LYS · Lysine · ligand · 2 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14000.730.8451LYS
21400.480.7824empty
31120.420.7622empty
4790.380.7720empty
5700.350.7716empty

Interfaces

1 interface between chains.

  • A–B · 1953 Ų buried · 21 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (nonstandard).

Compared structures

  • 4FHA · Structure of Dihydrodipicolinate Synthase from Streptococcus pneumoniae,bound to pyruvate… · the same entry in another collection · chain B against B, TM-score 1.00

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