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Crystal structure of M-crystallin in the presence of nickel

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

PDB
5HT9
Type
protein
Length
168 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.869
Source
Methanosarcina acetivorans C2A
Molecule
Beta/gama crystallin family protein
UniProt
Q8TMX3
Ligands
MG, NI
Pockets
1 · best druggability 0.39

Structure

x-ray diffraction · resolution 1.869 · 1 distinct chain · 11% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BBeta/gama crystallin family proteinprotein8411% helix, 49% strandQ8TMX3

Ligands and binding sites

  • MG · Magnesium ion · metal · 4 copies · chains A, B
  • NI · Nickel (II) ion · metal · 2 copies · chains A, B
  • BTB · 2-[bis-(2-hydroxy-ethyl)-amino]-2-hydroxymethyl-propane-1,3-diol · additive · 2 copies · chains A, B

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
1630.390.7912empty

Interfaces

1 interface between chains.

  • A–B · 335 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 5HT9 · Crystal structure of M-crystallin in the presence of nickel · the same entry in another collection · chain A against A, TM-score 1.00

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