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Structure of malonyl-coenzyme a reductase from crenarchaeota

Analyse Structure of malonyl-coenzyme a reductase from crenarchaeota in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4DPK
Type
protein
Length
1,416 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Malonyl-COA/SUCCINYL-CoA reductase
EC
1.2.1.75, 1.2.1.76
UniProt
Q96YK1
Ligands
PO4
Pockets
17 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 33% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DMalonyl-COA/SUCCINYL-CoA reductase (EC 1.2.1.75, 1.2.1.76)protein35433% helix, 23% strandQ96YK1

Ligands and binding sites

  • PO4 · Phosphate ion · ion · 12 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11620.820.9830empty
21290.740.9325empty
36090.700.7875empty
45550.660.7764PO4
53570.620.7846PO4

Interfaces

6 interfaces between chains.

  • A–B · 1754 Ų buried · 37 hydrogen bonds · protein-protein
  • C–D · 1753 Ų buried · 39 hydrogen bonds · protein-protein
  • B–C · 767 Ų buried · 13 hydrogen bonds · protein-protein
  • A–D · 764 Ų buried · 15 hydrogen bonds · protein-protein
  • B–D · 649 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 4DPK · Structure of malonyl-coenzyme A reductase from crenarchaeota · the same entry in another collection · chain A against A, TM-score 1.00
  • Q96YK1 · AlphaFold monomer V2.0 prediction for malonyl-CoA reductase (Q96YK1) · a predicted model of the same protein · chain A against A, TM-score 1.00

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