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The crystal structure of encm T139V mutant

Analyse The crystal structure of encm T139V mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6FYD
Type
protein
Length
1,824 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative FAD-dependent oxygenase encm
UniProt
Q9KHK2
Ligands
FAD
Pockets
13 · best druggability 0.89

Structure

x-ray diffraction · 1 distinct chain · 35% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DPutative FAD-dependent oxygenase encmprotein45635% helix, 24% strandQ9KHK2

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 4 copies · chains A, B, C, D

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

Pockets

13 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17080.890.9393FAD
27010.880.9397FAD
36840.880.9399FAD
48020.880.90105FAD
59850.820.8398empty

Interfaces

4 interfaces between chains.

  • A–D · 2212 Ų buried · 26 hydrogen bonds · protein-protein
  • B–C · 2209 Ų buried · 27 hydrogen bonds · protein-protein
  • A–B · 520 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 208 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6FYD · The crystal structure of EncM T139V mutant · the same entry in another collection · chain A against A, TM-score 1.00

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