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Joint X-RAY/NEUTRON structure of aspartate aminotransferase with alpha-methyl-aspartate at pH 7.5

Analyse Joint X-RAY/NEUTRON structure of aspartate aminotransferase with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5VJZ
Type
protein
Length
824 residues
Chains
2
Method
neutron diffraction; x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aspartate aminotransferase, cytoplasmic
EC
2.6.1.1, 2.6.1.3
UniProt
P00503
Ligands
PLA
Pockets
11 · best druggability 0.72

Structure

neutron diffraction; x-ray diffraction · 1 distinct chain · 46% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BAspartate aminotransferase, cytoplasmic (EC 2.6.1.1, 2.6.1.3)protein41246% helix, 13% strandP00503

Ligands and binding sites

  • PLA · 2-[(3-hydroxy-2-methyl-5-phosphonooxymethyl-pyridin-4-ylmethyl)-amino]-2-methyl-succinic acid · ligand · chains A, B

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

Pockets

11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17570.720.7865empty
2960.690.9325empty
32960.690.8452PLA
41520.550.8124empty
51700.550.8027empty

Interfaces

1 interface between chains.

  • A–B · 3578 Ų buried · 69 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (cofactor).

Compared structures

  • 5VJZ · Joint X-ray/neutron structure of aspartate aminotransferase with alpha-methyl-aspartate… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00503 · AlphaFold monomer V2.0 prediction for aspartate aminotransferase, cytoplasmic (P00503) · a predicted model of the same protein · chain B against A, TM-score 0.99

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