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MolNFT v1 · #155262 · protein

Cryo-EM structure of phosphorylated TYR39 a-synuclein amyloid fibril

6L1T · Alpha-synuclein: “Cryo-EM structure of phosphorylated TYR39 a-synuclein amyloid fibril”. Electron microscopy, 7 pockets (best druggability 0.76). MolNFT v1 #155262 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6L1T
Type
protein
Length
1,000 residues
Chains
10
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-synuclein
UniProt
P37840
Pockets
7 · best druggability 0.76

Structure

electron microscopy · 1 distinct chain · 0% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, JAlpha-synucleinprotein1000% helix, 50% strandP37840

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14710.760.8543empty
24780.730.8343empty
32590.710.8635empty
42430.710.8635empty
5990.600.8840empty

Interfaces

19 interfaces between chains.

  • D–E · 4029 Ų buried · 143 hydrogen bonds · protein-protein
  • C–D · 3914 Ų buried · 114 hydrogen bonds · protein-protein
  • G–H · 3907 Ų buried · 110 hydrogen bonds · protein-protein
  • I–J · 3898 Ų buried · 103 hydrogen bonds · protein-protein
  • B–C · 3890 Ų buried · 111 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 modified (phosphorylation).

Compared structures

  • 6L1T · Cryo-EM structure of phosphorylated Tyr39 a-synuclein amyloid fibril · the same entry in another collection · chain A against A, TM-score 1.00

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