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Crystal structure of caib, a type III CoA transferase in carnitine metabolism

Analyse Crystal structure of caib, a type III CoA transferase in carnitine metabolism in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1XA3
Type
protein
Length
800 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Crotonobetainyl-COA:CARNITINE CoA-transferase
EC
2.8.3.-
UniProt
P31572
Ligands
SO4
Pockets
8 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 39% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BCrotonobetainyl-COA:CARNITINE CoA-transferase (EC 2.8.3.-)protein40039% helix, 18% strandP31572

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 2 copies · chains A, B
  • BTB · 2-[bis-(2-hydroxy-ethyl)-amino]-2-hydroxymethyl-propane-1,3-diol · additive · 2 copies · chains A, B

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

Pockets

8 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16680.740.8050BTB
26610.740.8067SO4, BTB
31190.480.7919empty
4780.420.7917empty
51040.400.7624empty

Interfaces

1 interface between chains.

  • A–B · 6377 Ų buried · 78 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 32 modified (engineered).

Compared structures

  • 1XA3 · Crystal structure of CaiB, a type III CoA transferase in carnitine metabolism · the same entry in another collection · chain A against A, TM-score 1.00
  • P31572 · AlphaFold monomer V2.0 prediction for L-carnitine CoA-transferase (P31572) · a predicted model of the same protein · chain B against A, TM-score 0.99

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