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Domain closure in mitochondrial aspartate aminotransferase

Analyse Domain closure in mitochondrial aspartate aminotransferase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1AMA
Type
protein
Length
401 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aspartate aminotransferase
EC
2.6.1.1
UniProt
P00508
Ligands
PLA
Pockets
5 · best druggability 0.62

Structure

x-ray diffraction · 1 distinct chain · 47% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAspartate aminotransferase (EC 2.6.1.1)protein40147% helix, 14% strandP00508

Ligands and binding sites

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

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

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11980.620.8232PLA
22370.530.7626empty
31080.450.7814empty
4530.320.7713empty
5560.270.7416empty

Compared structures

  • 1AMA · Domain closure in mitochondrial aspartate aminotransferase · the same entry in another collection · chain A against A, TM-score 1.00
  • P00508 · AlphaFold monomer V2.0 prediction for aspartate aminotransferase, mitochondrial (P00508) · a predicted model of the same protein · chain A against A, TM-score 0.98

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