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The crystal structure of TNF family member eda-A2

Analyse The crystal structure of TNF family member eda-A2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1RJ8
Type
protein
Length
840 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ectodysplasin-a isoform eda-A2
UniProt
Q92838
Pockets
8 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 5% helix, 59% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, D, E, F, GEctodysplasin-a isoform eda-A2protein1405% helix, 59% strandQ92838

Pockets

8 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13320.740.8658empty
22800.680.8439empty
31030.400.7617empty
4850.360.7512empty
5840.350.7514empty

Interfaces

9 interfaces between chains.

  • F–G · 1084 Ų buried · 21 hydrogen bonds · protein-protein
  • B–D · 1019 Ų buried · 20 hydrogen bonds · protein-protein
  • A–D · 1018 Ų buried · 15 hydrogen bonds · protein-protein
  • A–B · 1010 Ų buried · 15 hydrogen bonds · protein-protein
  • E–G · 976 Ų buried · 14 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 1RJ8 · The crystal structure of TNF family member EDA-A2 · the same entry in another collection · chain G against G, TM-score 1.00
  • Q92838 · AlphaFold monomer V2.0 prediction for ectodysplasin-a (Q92838) · a predicted model of the same protein · chain E against A, TM-score 0.97

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