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Crystal structure of efga from methylobacterium extorquens in complex with formaldehyde

Analyse Crystal structure of efga from methylobacterium extorquens in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6C0Z
Type
protein
Length
548 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Efga
UniProt
H1KGY6
Ligands
21H
Pockets
3 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 39% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
B, A, C, DEfgaprotein13739% helix, 19% strandH1KGY6

Ligands and binding sites

  • 21H · oxydimethanol · ligand · 3 copies · chains A, D, C
  • FMT · Formic acid · additive · chains B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18980.750.7855empty
22380.540.7730empty
31890.540.7927empty

Interfaces

5 interfaces between chains.

  • B–A · 835 Ų buried · 20 hydrogen bonds · protein-protein
  • B–C · 689 Ų buried · 5 hydrogen bonds · protein-protein
  • A–D · 683 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 198 Ų buried · 3 hydrogen bonds · protein-protein
  • B–D · 188 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 6C0Z · Crystal structure of Efga from Methylobacterium extorquens in complex with formaldehyde · the same entry in another collection · chain B against B, TM-score 1.00

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