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A thermophilic hydrolase

Analyse A thermophilic hydrolase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3X2E
Type
protein
Length
1,604 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Adenosylhomocysteinase
EC
3.3.1.1
UniProt
O51933
Ligands
NAI
Pockets
11 · best druggability 0.87

Structure

x-ray diffraction · 1 distinct chain · 45% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DAdenosylhomocysteinase (EC 3.3.1.1)protein40145% helix, 16% strandO51933

Ligands and binding sites

  • NAI · 1,4-dihydronicotinamide adenine dinucleotide · ligand · 4 copies · chains A, B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110770.870.8884empty
29340.780.8088NAI
38990.770.8088NAI
48000.760.8076NAI
511340.750.7899NAI

Interfaces

6 interfaces between chains.

  • C–D · 2239 Ų buried · 23 hydrogen bonds · protein-protein
  • A–B · 2223 Ų buried · 22 hydrogen bonds · protein-protein
  • A–C · 1787 Ų buried · 27 hydrogen bonds · protein-protein
  • B–D · 1722 Ų buried · 27 hydrogen bonds · protein-protein
  • B–C · 401 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 3X2E · A thermophilic hydrolase · the same entry in another collection · chain A against A, TM-score 1.00
  • O51933 · AlphaFold monomer V2.0 prediction for adenosylhomocysteinase (O51933) · a predicted model of the same protein · chain A against A, TM-score 0.95

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