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Structure of T255E, E376G mutant of human medium chain acyl- CoA dehydrogenase

Analyse Structure of T255E, E376G mutant of human medium chain acyl- CoA dehydrogenase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1EGE
Type
protein
Length
1,548 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Medium chain acyl-CoA dehydrogenase
EC
1.3.99.3
UniProt
P11310
Ligands
FAD
Pockets
13 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 57% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DMedium chain acyl-CoA dehydrogenase (EC 1.3.99.3)protein38757% helix, 16% strandP11310

Ligands and binding sites

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

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

Pockets

13 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17560.840.8789FAD
27400.820.8680FAD
36700.820.8681FAD
47300.810.8479FAD
510490.790.8088empty

Interfaces

6 interfaces between chains.

  • B–C · 2460 Ų buried · 27 hydrogen bonds · protein-protein
  • A–D · 2431 Ų buried · 22 hydrogen bonds · protein-protein
  • C–D · 1755 Ų buried · 23 hydrogen bonds · protein-protein
  • A–B · 1711 Ų buried · 22 hydrogen bonds · protein-protein
  • B–D · 188 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 1EGE · Structure of T255E, E376G mutant of human medium chain acyl-CoA dehydrogenase · the same entry in another collection · chain D against D, TM-score 1.00
  • P11310 · AlphaFold monomer V2.0 prediction for medium-chain specific acyl-CoA dehydrogenase… · a predicted model of the same protein · chain C against A, TM-score 1.00

Analyse

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