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Crystal structure of aspartate-semialdehyde dehydrogenase from acinetobacter baumannii

Analyse Crystal structure of aspartate-semialdehyde dehydrogenase from acinetobacter… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7SKB
Type
protein
Length
1,492 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aspartate-semialdehyde dehydrogenase
EC
1.2.1.11
UniProt
V5VGT0
Pockets
12 · best druggability 0.66

Structure

x-ray diffraction · 3 distinct chains · 41% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DAspartate-semialdehyde dehydrogenase (EC 1.2.1.11)protein37341% helix, 22% strandV5VGT0
BAspartate-semialdehyde dehydrogenase (EC 1.2.1.11)protein37442% helix, 22% strandV5VGT0
CAspartate-semialdehyde dehydrogenase (EC 1.2.1.11)protein37241% helix, 22% strandV5VGT0

Ligands and binding sites

  • TLA · L(+)-tartaric acid · additive · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15090.660.7846empty
24030.610.7756TLA
33440.590.7746empty
43110.580.7748empty
53260.580.7746empty

Interfaces

4 interfaces between chains.

  • C–D · 3783 Ų buried · 56 hydrogen bonds · protein-protein
  • A–B · 3777 Ų buried · 59 hydrogen bonds · protein-protein
  • A–C · 541 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 10 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 7SKB · Crystal Structure of aspartate-semialdehyde dehydrogenase from Acinetobacter baumannii · the same entry in another collection · chain A against A, TM-score 1.00

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