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MolNFT v1 · #177917 · protein

Crystal structure of tau and acetylated tau peptide antigen

7EYC · Antibody, light chain: “Crystal structure of tau and acetylated tau peptide antigen”. X-ray diffraction, 11 pockets (best druggability 0.80). MolNFT v1 #177917 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
7EYC
Type
protein
Length
876 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antibody, light chain; Antibody, heavy chain; Acetylated tau peptide
Pockets
11 · best druggability 0.80

Structure

x-ray diffraction · 5 distinct chains · 8% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
L, BAntibody, light chainprotein2176% helix, 51% strand—
HAntibody, heavy chainprotein2138% helix, 51% strand—
AAntibody, heavy chainprotein21411% helix, 51% strand—
PAcetylated tau peptideprotein70% helix, 0% strand—
QAcetylated tau peptideprotein80% helix, 0% strand—

Pockets

11 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19100.800.8275empty
2850.570.8719empty
33680.550.7434empty
41550.530.8030empty
5690.450.8220empty

Interfaces

11 interfaces between chains.

  • B–A · 1667 Ų buried · 15 hydrogen bonds · protein-protein
  • L–H · 1644 Ų buried · 14 hydrogen bonds · protein-protein
  • H–A · 655 Ų buried · 13 hydrogen bonds · protein-protein
  • L–P · 457 Ų buried · 8 hydrogen bonds · protein-protein
  • B–Q · 449 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 2 modified (disulfide, acetylation).

Compared structures

  • 7EYC · Crystal structure of Tau and acetylated tau peptide antigen · the same entry in another collection · chain L against L, TM-score 1.00

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