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Crystal structure of native xylanase 10B from thermotoga petrophila rku-1

Analyse Crystal structure of native xylanase 10B from thermotoga petrophila rku-1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3NIY
Type
protein
Length
651 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Endo-1,4-beta-xylanase
EC
3.2.1.8
UniProt
A5IL00
Ligands
SO4
Pockets
3 · best druggability 0.54

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEndo-1,4-beta-xylanase (EC 3.2.1.8)protein32644% helix, 20% strandA5IL00
BEndo-1,4-beta-xylanase (EC 3.2.1.8)protein32544% helix, 20% strandA5IL00

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 5 copies · chains A, B
  • ACT · Acetate ion · 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
13370.540.7540empty
21080.440.7819ACT
3920.380.7619ACT

Interfaces

1 interface between chains.

  • A–B · 508 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 3NIY · Crystal structure of native xylanase 10B from Thermotoga petrophila RKU-1 · the same entry in another collection · chain A against A, TM-score 1.00

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