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The structure of mono-acetylated sahh

Analyse The structure of mono-acetylated sahh in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PGF
Type
protein
Length
858 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Adenosylhomocysteinase
EC
3.3.1.1
UniProt
P23526
Ligands
NAD, ADN
Pockets
7 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 43% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAdenosylhomocysteinase (EC 3.3.1.1)protein43044% helix, 17% strandP23526
BAdenosylhomocysteinase (EC 3.3.1.1)protein42842% helix, 17% strandP23526

Ligands and binding sites

  • NAD · Nicotinamide-adenine-dinucleotide · ligand · 2 copies · chains A, B
  • ADN · Adenosine · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18210.780.8195empty
24840.740.8364NAD, ADN
34220.720.8266NAD, ADN
42740.560.7733empty
52800.530.7532empty

Interfaces

1 interface between chains.

  • A–B · 1839 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (acetylation).

Compared structures

  • 4PGF · The structure of mono-acetylated SAHH · the same entry in another collection · chain A against A, TM-score 1.00
  • P23526 · AlphaFold monomer V2.0 prediction for adenosylhomocysteinase (P23526) · a predicted model of the same protein · chain A against A, TM-score 1.00

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