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Crystal structure of a cupin protein (TM1459) in osmium (os)- substituted form II

Analyse Crystal structure of a cupin protein (TM1459) in osmium (os)- substituted form… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5WSF
Type
protein
Length
445 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Uncharacterized protein TM1459
UniProt
Q9X1H0
Ligands
OS
Pockets
5 · best druggability 0.74

Structure

x-ray diffraction · 3 distinct chains · 5% helix, 59% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BUncharacterized protein TM1459protein1145% helix, 61% strandQ9X1H0
CUncharacterized protein TM1459protein1086% helix, 56% strandQ9X1H0
DUncharacterized protein TM1459protein1096% helix, 60% strandQ9X1H0

Ligands and binding sites

  • OS · Osmium ion · metal · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19750.740.7788empty
21250.460.7824empty
31070.430.7721empty
41160.380.7424empty
5660.320.7519empty

Interfaces

4 interfaces between chains.

  • B–C · 1867 Ų buried · 26 hydrogen bonds · protein-protein
  • A–D · 1840 Ų buried · 18 hydrogen bonds · protein-protein
  • A–C · 290 Ų buried · 5 hydrogen bonds · protein-protein
  • A–B · 88 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 4 modified (oxidation).

Compared structures

  • 5WSF · Crystal structure of a cupin protein (tm1459) in osmium (Os)-substituted form II · the same entry in another collection · chain A against A, TM-score 1.00

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