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Crystal structure of ZN1.7-E16V human ubiquitin (hub) mutant adduct, from a solution 70 mm zinc ACETATE/1.3 mm E16V hub

Analyse Crystal structure of ZN1.7-E16V human ubiquitin (hub) mutant adduct, from a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5NL5
Type
protein
Length
216 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Polyubiquitin-B
UniProt
P0CG47
Ligands
ZN
Pockets
1 · best druggability 0.35

Structure

x-ray diffraction · 1 distinct chain · 25% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CPolyubiquitin-Bprotein7225% helix, 29% strandP0CG47

Ligands and binding sites

  • ZN · Zinc ion · metal · 5 copies · chains A, C, B
  • EDO · 1,2-ethanediol · additive · 4 copies · chains A, B, C
  • ACT · Acetate ion · additive · 3 copies · chains A, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1780.350.7614empty

Interfaces

2 interfaces between chains.

  • A–B · 348 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 307 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 5NL5 · Crystal structure of Zn1.7-E16V human ubiquitin (hUb) mutant adduct, from a solution 70… · the same entry in another collection · chain A against A, TM-score 1.00

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