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The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed by an ASPARTATE/HISTIDINE pair and involves a smooth, methionine-rich surface for binding the fatty acyl moiety

Analyse The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2GD2
Type
protein
Length
1,416 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Probable alpha-methylacyl-CoA racemase mcr
EC
5.1.99.4
Ligands
CAA
Pockets
11 · best druggability 0.71

Structure

x-ray diffraction · 1 distinct chain · 41% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DProbable alpha-methylacyl-CoA racemase mcr (EC 5.1.99.4)protein35441% helix, 15% strand—

Ligands and binding sites

  • CAA · Acetoacetyl-coenzyme A · ligand · 4 copies · chains A, B, C, D
  • GOL · Glycerol · additive · 2 copies · chains A, B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15570.710.7962CAA, GOL
25520.710.7969CAA, GOL
34750.700.8157CAA
45150.700.7958CAA
55240.610.7561empty

Interfaces

3 interfaces between chains.

  • C–D · 6424 Ų buried · 106 hydrogen bonds · protein-protein
  • A–B · 6381 Ų buried · 108 hydrogen bonds · protein-protein
  • A–D · 319 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 2GD2 · The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed… · the same entry in another collection · chain A against A, TM-score 1.00

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