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Structure of the GREM2-GDF5 inhibitory complex

Analyse Structure of the GREM2-GDF5 inhibitory complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5HK5
Type
protein
Length
925 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Gremlin-2; GROWTH/DIFFERENTIATION factor 5
UniProt
O88273, P43026
Pockets
13 · best druggability 0.77

Structure

x-ray diffraction · 4 distinct chains · 7% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
EGremlin-2protein1285% helix, 55% strandO88273
F, GGremlin-2protein1295% helix, 51% strandO88273
HGremlin-2protein1193% helix, 50% strandO88273
A, B, C, DGROWTH/DIFFERENTIATION factor 5protein10518% helix, 46% strandP43026

Pockets

13 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111570.770.7989empty
23630.580.7641empty
33960.580.7547empty
41920.560.8026empty
52490.510.7539empty

Interfaces

15 interfaces between chains.

  • G–H · 1831 Ų buried · 37 hydrogen bonds · protein-protein
  • E–F · 1753 Ų buried · 36 hydrogen bonds · protein-protein
  • E–A · 1587 Ų buried · 19 hydrogen bonds · protein-protein
  • G–B · 1542 Ų buried · 21 hydrogen bonds · protein-protein
  • A–C · 1285 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 30 disulfide (disulfide).

Compared structures

  • 5HK5 · Structure of the Grem2-GDF5 Inhibitory Complex · the same entry in another collection · chain D against D, TM-score 1.00
  • P43026 · AlphaFold monomer V2.0 prediction for GROWTH/DIFFERENTIATION factor 5 (P43026) · a predicted model of the same protein · chain B against A, TM-score 0.95

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