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Crystal structure of human beta-crystallin B3

Analyse Crystal structure of human beta-crystallin B3 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3QK3
Type
protein
Length
527 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-crystallin B3
UniProt
P26998
Ligands
SO4
Pockets
3 · best druggability 0.88

Structure

x-ray diffraction · 2 distinct chains · 9% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-crystallin B3protein17510% helix, 42% strandP26998
B, CBeta-crystallin B3protein1769% helix, 44% strandP26998

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 5 copies · chains A, B, C
  • EDO · 1,2-ethanediol · additive · 5 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111450.880.89114SO4
21090.450.7922empty
31010.420.7718empty

Interfaces

3 interfaces between chains.

  • A–B · 763 Ų buried · 19 hydrogen bonds · protein-protein
  • A–C · 697 Ų buried · 16 hydrogen bonds · protein-protein
  • B–C · 515 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 3QK3 · Crystal structure of human beta-crystallin B3 · the same entry in another collection · chain A against A, TM-score 1.00
  • P26998 · AlphaFold monomer V2.0 prediction for beta-crystallin B3 (P26998) · a predicted model of the same protein · chain B against A, TM-score 0.99

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