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MolNFT v1 · #141029 · protein

Structural basis for recognition of L-lysine, L-ornithine, and L-2,4- diamino butyric acid by lysine cyclodeaminase

5YU4: “Structural basis for recognition of L-lysine, L-ornithine, and L-2,4- diamino butyric acid by lysine…”. X-ray diffraction, 3 ligands (NAD, DAB, NA), 8 pockets (best druggability 0.78). MolNFT v1 #141029 on GenesisL1: 3D structure…

PDB
5YU4
Type
protein
Length
1,376 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lysine cyclodeaminase
EC
4.3.1.12
UniProt
D9UBW0
Ligands
NAD, DAB, NA
Pockets
8 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DLysine cyclodeaminase (EC 4.3.1.12)protein34440% helix, 22% strandD9UBW0

Ligands and binding sites

  • NAD · Nicotinamide-adenine-dinucleotide · ligand · 4 copies · chains A, B, C, D
  • DAB · 2,4-diaminobutyric acid · ligand · 4 copies · chains A, B, C, D
  • NA · Sodium ion · metal · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13180.780.8952NAD, DAB
23300.780.8853NAD, DAB
33560.770.8854NAD, DAB
43010.770.8846NAD, DAB
53220.670.8237empty

Interfaces

4 interfaces between chains.

  • A–B · 3228 Ų buried · 33 hydrogen bonds · protein-protein
  • C–D · 3187 Ų buried · 26 hydrogen bonds · protein-protein
  • A–C · 806 Ų buried · 18 hydrogen bonds · protein-protein
  • A–D · 38 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 5YU4 · Structural basis for recognition of L-lysine, L-ornithine, and L-2,4-diamino butyric acid… · the same entry in another collection · chain A against A, TM-score 1.00

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