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Crystal structure of unbranched mixed tri-ubiquitin chain containing K48 and K63 linkages.

Analyse Crystal structure of unbranched mixed tri-ubiquitin chain containing K48 and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5O44
Type
protein
Length
452 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ubiquitin; Polyubiquitin-B
UniProt
Q45TR8, P0CG47
Ligands
MG, SO4
Pockets
2 · best druggability 0.38

Structure

x-ray diffraction · 3 distinct chains · 25% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, EUbiquitinprotein7625% helix, 28% strandQ45TR8
C, BPolyubiquitin-Bprotein7426% helix, 35% strandP0CG47
D, FPolyubiquitin-Bprotein7625% helix, 34% strandP0CG47

Ligands and binding sites

  • MG · Magnesium ion · metal · 3 copies · chains A, D, E
  • SO4 · Sulfate ion · ion · 9 copies · chains A, C, D, F, B, E

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1740.380.7817empty
2540.310.7615empty

Interfaces

8 interfaces between chains.

  • C–D · 720 Ų buried · 7 hydrogen bonds · protein-protein
  • B–F · 656 Ų buried · 6 hydrogen bonds · protein-protein
  • D–E · 492 Ų buried · 17 hydrogen bonds · protein-protein
  • D–F · 491 Ų buried · 5 hydrogen bonds · protein-protein
  • C–B · 413 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 isopeptide (isopeptide).

Compared structures

  • 5O44 · Crystal structure of unbranched mixed tri-Ubiquitin chain containing K48 and K63 linkages. · the same entry in another collection · chain B against B, TM-score 1.00

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