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LYS27-linked triubiquitin

Analyse LYS27-linked triubiquitin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5JBY
Type
protein
Length
418 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquitin; D-ubiquitin
UniProt
P0CG47
Pockets
5 · best druggability 0.82

Structure

x-ray diffraction · 4 distinct chains · 28% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, EUbiquitinprotein7326% helix, 34% strandP0CG47
B, DD-ubiquitinprotein6727% helix, 31% strand—
CUbiquitinprotein7231% helix, 33% strandP0CG47
FD-ubiquitinprotein6627% helix, 30% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12870.820.9439empty
26480.760.8287empty
3790.410.7914empty
4940.390.7716empty
5850.380.7719empty

Interfaces

12 interfaces between chains.

  • A–D · 442 Ų buried · 5 hydrogen bonds · protein-protein
  • B–E · 437 Ų buried · 6 hydrogen bonds · protein-protein
  • A–E · 413 Ų buried · 16 hydrogen bonds · protein-protein
  • C–D · 384 Ų buried · 8 hydrogen bonds · protein-protein
  • C–F · 383 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 188 d-amino, 3 modified (D-amino acid, nonstandard).

Compared structures

  • 5JBY · Lys27-linked triubiquitin · the same entry in another collection · chain F against F, TM-score 1.00
  • P0CG47 · AlphaFold monomer V2.0 prediction for polyubiquitin-B (P0CG47) · a predicted model of the same protein · chain C against A, TM-score 0.95

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