GL1X · GenesisL1 explorer

MolNFT v1 · #43758 · protein

Structural model for a 40-residue beta-amyloid fibril with three-fold symmetry, negative stagger

2LMQ · Beta-amyloid protein 40: “Structural model for a 40-residue beta-amyloid fibril with three-fold symmetry, negative stagger”. Solid-state nmr, 13 pockets (best druggability 0.78). MolNFT v1 #43758 on GenesisL1: 3D structure, binding…

PDB
2LMQ
Type
protein
Length
576 residues
Chains
18
Method
solid-state nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-amyloid protein 40
UniProt
P05067
Pockets
13 · best druggability 0.78

Structure

solid-state nmr · 1 distinct chain · 0% helix, 38% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, RBeta-amyloid protein 40protein320% helix, 38% strandP05067

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12840.780.9060empty
22580.740.8745empty
32220.720.8852empty
46660.720.7955empty
55640.700.7958empty

Interfaces

88 interfaces between chains.

  • K–L · 1413 Ų buried · 36 hydrogen bonds · protein-protein
  • O–P · 1397 Ų buried · 28 hydrogen bonds · protein-protein
  • I–J · 1395 Ų buried · 35 hydrogen bonds · protein-protein
  • C–D · 1385 Ų buried · 38 hydrogen bonds · protein-protein
  • B–C · 1377 Ų buried · 47 hydrogen bonds · protein-protein

Compared structures

  • 2LMQ · Structural Model for a 40-residue Beta-Amyloid Fibril with Three-Fold Symmetry, Negative… · the same entry in another collection · chain K against K, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.