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Crystal structure of aspartate-semialdehyde dehydrogenase from haemophilus influenzae

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

PDB
1NWC
Type
protein
Length
712 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aspartate-semialdehyde dehydrogenase
EC
1.2.1.11
UniProt
P44801
Pockets
7 · best druggability 0.61

Structure

x-ray diffraction · 1 distinct chain · 42% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BAspartate-semialdehyde dehydrogenase (EC 1.2.1.11)protein35642% helix, 24% strandP44801

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13640.610.7748empty
23480.600.7743empty
3800.350.7515empty
4520.320.7711empty
5690.320.7515empty

Interfaces

1 interface between chains.

  • A–B · 3477 Ų buried · 46 hydrogen bonds · protein-protein

Compared structures

  • 1NWC · Crystal Structure of Aspartate-Semialdehyde Dehydrogenase from Haemophilus influenzae · the same entry in another collection · chain A against A, TM-score 1.00
  • P44801 · AlphaFold monomer V2.0 prediction for aspartate-semialdehyde dehydrogenase (P44801) · a predicted model of the same protein · chain A against A, TM-score 1.00

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