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ARG475GLN mutant of mitochondrial aldehyde dehydrogenase, apo form, pseudo-merohedrally twinned

Analyse ARG475GLN mutant of mitochondrial aldehyde dehydrogenase, apo form… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2ONO
Type
protein
Length
3,952 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aldehyde dehydrogenase
EC
1.2.1.3
UniProt
P05091
Pockets
20 · best druggability 0.90

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, HAldehyde dehydrogenase (EC 1.2.1.3)protein49440% helix, 21% strandP05091

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18010.900.9488empty
28010.890.9272empty
39770.840.85130empty
42000.830.9737empty
52360.830.9642empty

Interfaces

14 interfaces between chains.

  • E–F · 2825 Ų buried · 37 hydrogen bonds · protein-protein
  • G–H · 2773 Ų buried · 32 hydrogen bonds · protein-protein
  • A–B · 2756 Ų buried · 33 hydrogen bonds · protein-protein
  • C–D · 2745 Ų buried · 33 hydrogen bonds · protein-protein
  • A–D · 1612 Ų buried · 35 hydrogen bonds · protein-protein

Compared structures

  • 2ONO · Arg475Gln Mutant of Mitochondrial Aldehyde Dehydrogenase, apo form, pseudo-merohedrally… · the same entry in another collection · chain E against E, TM-score 1.00
  • P05091 · AlphaFold monomer V2.0 prediction for aldehyde dehydrogenase, mitochondrial (P05091) · a predicted model of the same protein · chain C against A, TM-score 1.00

Analyse

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