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3-isopropylmalate dehydrogenase from the moderate facultative thermophile, bacillus coagulans

Analyse 3-isopropylmalate dehydrogenase from the moderate facultative thermophile… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2AYQ
Type
protein
Length
713 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
3-isopropylmalate dehydrogenase
EC
1.1.1.85
UniProt
P12010
Pockets
4 · best druggability 0.62

Structure

x-ray diffraction · 2 distinct chains · 45% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A3-isopropylmalate dehydrogenase (EC 1.1.1.85)protein35644% helix, 22% strandP12010
B3-isopropylmalate dehydrogenase (EC 1.1.1.85)protein35746% helix, 22% strandP12010

Pockets

4 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11180.620.8721empty
21180.570.8420empty
33050.560.7630empty
42470.530.7627empty

Interfaces

1 interface between chains.

  • A–B · 2213 Ų buried · 43 hydrogen bonds · protein-protein

Compared structures

  • 2AYQ · 3-isopropylmalate dehydrogenase from the moderate facultative thermophile, bacillus… · the same entry in another collection · chain A against A, TM-score 1.00
  • P12010 · AlphaFold monomer V2.0 prediction for 3-isopropylmalate dehydrogenase (P12010) · a predicted model of the same protein · chain A against A, TM-score 0.95

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