GL1X · GenesisL1 explorer

MolNFT v1 · #57513 · protein

Crystal structure of rat selenocysteine lyase

3A9X: “Crystal structure of rat selenocysteine lyase”. X-ray diffraction, 2 ligands (PLP, PO4), 10 pockets (best druggability 0.81). MolNFT v1 #57513 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
3A9X
Type
protein
Length
788 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Selenocysteine lyase
EC
4.4.1.16
UniProt
Q68FT9
Ligands
PLP, PO4
Pockets
10 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 47% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASelenocysteine lyase (EC 4.4.1.16)protein38846% helix, 16% strandQ68FT9
BSelenocysteine lyase (EC 4.4.1.16)protein40048% helix, 15% strandQ68FT9

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 3 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15870.810.87105PLP, PO4
25240.750.8230empty
32580.600.8042empty
41470.480.7824empty
5530.460.8513empty

Interfaces

1 interface between chains.

  • A–B · 2035 Ų buried · 21 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 3A9X · Crystal structure of rat selenocysteine lyase · the same entry in another collection · chain A against A, TM-score 1.00
  • Q68FT9 · AlphaFold monomer V2.0 prediction for selenocysteine lyase (Q68FT9) · a predicted model of the same protein · chain B against A, TM-score 0.99

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