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The structure of human MAT2A in complex with SAM, adenosine, methionine and ppnp.

Analyse The structure of human MAT2A in complex with SAM, adenosine, methionine and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5A1I
Type
protein
Length
381 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
S-adenosylmethionine synthase isoform type-2
EC
2.5.1.6
UniProt
P31153
Ligands
MET, PPK, SAM, ADN, MG, K
Pockets
1 · best druggability 0.30

Structure

x-ray diffraction · 1 distinct chain · 33% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AS-adenosylmethionine synthase isoform type-2 (EC 2.5.1.6)protein38133% helix, 26% strandP31153

Ligands and binding sites

  • MET · Methionine · ligand · chains A
  • PPK · (diphosphono)aminophosphonic acid · ligand · chains A
  • SAM · S-adenosylmethionine · ligand · chains A
  • ADN · Adenosine · ligand · chains A
  • MG · Magnesium ion · metal · 2 copies · chains A
  • K · Potassium ion · metal · 2 copies · chains A
  • PEG · Di(hydroxyethyl)ether · additive · chains A
  • EDO · 1,2-ethanediol · additive
  • PG4 · Tetraethylene glycol · additive · chains A

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

Pockets

1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1520.300.7615empty

Compared structures

  • 5A1I · The structure of Human MAT2A in complex with SAM, Adenosine, Methionine and PPNP. · the same entry in another collection · chain A against A, TM-score 1.00
  • P31153 · AlphaFold monomer V2.0 prediction for S-adenosylmethionine synthase isoform type-2… · a predicted model of the same protein · chain A against A, TM-score 0.99

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