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Structure of alas from S. cerevisiae non-covalently bound to plp cofactor

Analyse Structure of alas from S. cerevisiae non-covalently bound to plp cofactor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5TXR
Type
protein
Length
955 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
5-aminolevulinate synthase, mitochondrial
EC
2.3.1.37
UniProt
P09950
Ligands
PLP, K
Pockets
11 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 43% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
B5-aminolevulinate synthase, mitochondrial (EC 2.3.1.37)protein47643% helix, 14% strandP09950
A5-aminolevulinate synthase, mitochondrial (EC 2.3.1.37)protein47943% helix, 14% strandP09950

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains B, A
  • K · Potassium ion · metal · chains A
  • FMT · Formic acid · additive · 10 copies · chains B, A
  • GOL · Glycerol · additive · chains B, A

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

Pockets

11 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16260.790.8490FMT, PLP
25360.760.8383FMT, PLP
31880.530.7931empty
41670.480.7727empty
51350.460.7723empty

Interfaces

1 interface between chains.

  • B–A · 4901 Ų buried · 78 hydrogen bonds · protein-protein

Compared structures

  • 5TXR · Structure of ALAS from S. cerevisiae non-covalently bound to PLP cofactor · the same entry in another collection · chain B against B, TM-score 1.00
  • P09950 · AlphaFold monomer V2.0 prediction for 5-aminolevulinate synthase, mitochondrial (P09950) · a predicted model of the same protein · chain A against A, TM-score 1.00

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