GL1X · GenesisL1 explorer

Research workbench

Crystal structure of a glycoside hydrolase family 105 (GH105) enzyme from thielavia terrestris

Analyse Crystal structure of a glycoside hydrolase family 105 (GH105) enzyme from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4XUV
Type
protein
Length
662 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glycoside hydrolase family 105 protein
UniProt
G2QVG2
Pockets
5 · best druggability 0.64

Structure

x-ray diffraction · 2 distinct chains · 64% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGlycoside hydrolase family 105 proteinprotein33264% helix, 7% strandG2QVG2
BGlycoside hydrolase family 105 proteinprotein33065% helix, 7% strandG2QVG2

Ligands and binding sites

  • GOL · Glycerol · additive · 3 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11470.640.8631empty
21520.560.8221empty
31410.560.8223empty
41530.480.7725empty
5840.350.7517GOL

Interfaces

1 interface between chains.

  • A–B · 1333 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 4XUV · Crystal structure of a glycoside hydrolase family 105 (GH105) enzyme from Thielavia… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.