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Crystallographic refinement and atomic models of two different forms of citrate synthase at 2.7 and 1.7 ångströms resolution

Analyse Crystallographic refinement and atomic models of two different forms of citrate… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2CTS
Type
protein
Length
437 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Citrate synthase
EC
4.1.3.7
UniProt
P00889
Ligands
COA
Pockets
4 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 62% helix, 3% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACitrate synthase (EC 4.1.3.7)protein43762% helix, 3% strandP00889

Ligands and binding sites

  • COA · Coenzyme A · ligand · chains A
  • CIT · Citric acid · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15520.670.7760COA, CIT
21420.430.7524empty
3860.380.7717empty
4610.310.7517empty

Compared structures

  • 2CTS · Crystallographic refinement and atomic models of two different forms of citrate synthase… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00889 · AlphaFold monomer V2.0 prediction for citrate synthase, mitochondrial (P00889) · a predicted model of the same protein · chain A against A, TM-score 0.95

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