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Native structure of endo-1,5-alpha-L-arabinanases from bacillus subtilis

Analyse Native structure of endo-1,5-alpha-L-arabinanases from bacillus subtilis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2X8F
Type
protein
Length
886 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Endo-alpha-1,5-L-arabinanase
EC
3.2.1.99
UniProt
B3FRL6
Ligands
NA, CA, PO4
Pockets
11 · best druggability 0.63

Structure

x-ray diffraction · 1 distinct chain · 5% helix, 44% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BEndo-alpha-1,5-L-arabinanase (EC 3.2.1.99)protein4435% helix, 44% strandB3FRL6

Ligands and binding sites

  • NA · Sodium ion · metal · 4 copies · chains A, B
  • CA · Calcium ion · metal · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 2 copies · chains A, B
  • GOL · Glycerol · additive · 10 copies · chains A, B
  • MPD · (4S)-2-methyl-2,4-pentanediol · additive · chains A
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains B
  • MRD · (4R)-2-methylpentane-2,4-diol · additive · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13410.630.7926NA
23080.610.7925NA
32230.550.7828empty
42750.550.7641empty
52100.500.7627empty

Interfaces

1 interface between chains.

  • A–B · 644 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 2X8F · Native structure of Endo-1,5-alpha-L-arabinanases from Bacillus subtilis · the same entry in another collection · chain A against A, TM-score 1.00

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