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Crystal structure of conserved protein of unknown function with hot dog fold from alicyclobacillus acidocaldarius

Analyse Crystal structure of conserved protein of unknown function with hot dog fold… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3RQB
Type
protein
Length
529 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Uncharacterized protein
UniProt
C8WTQ0
Ligands
CL
Pockets
4 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 18% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUncharacterized proteinprotein26419% helix, 40% strandC8WTQ0
BUncharacterized proteinprotein26517% helix, 40% strandC8WTQ0

Ligands and binding sites

  • CL · Chloride ion · ion · 3 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15750.790.8569empty
25450.760.8372CL
31710.420.7330empty
4600.270.7315CL

Interfaces

1 interface between chains.

  • A–B · 2923 Ų buried · 43 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 18 modified (engineered).

Compared structures

  • 3RQB · Crystal Structure of Conserved Protein of Unknown Function with Hot dog Fold from… · the same entry in another collection · chain A against A, TM-score 1.00

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