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Crystal structure analysis of human clybl in complex with free coash

Analyse Crystal structure analysis of human clybl in complex with free coash in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5VXC
Type
protein
Length
301 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Citrate lyase subunit beta-like protein, mitochondrial
UniProt
Q8N0X4
Ligands
COA, MG
Pockets
3 · best druggability 0.44

Structure

x-ray diffraction · 1 distinct chain · 51% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACitrate lyase subunit beta-like protein, mitochondrialprotein30151% helix, 16% strandQ8N0X4

Ligands and binding sites

  • COA · Coenzyme A · ligand · chains A
  • MG · Magnesium ion · metal · chains A

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11340.440.7720MG
21380.400.7420empty
3990.350.7422empty

Compared structures

  • 5VXC · Crystal Structure Analysis of human CLYBL in complex with free CoASH · the same entry in another collection · chain A against A, TM-score 1.00
  • Q8N0X4 · AlphaFold monomer V2.0 prediction for citramalyl-CoA lyase, mitochondrial (Q8N0X4) · a predicted model of the same protein · chain A against A, TM-score 0.99

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