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MolNFT v1 · #88844 · protein

An unprecedented NADPH domain conformation in lysine monooxygenase nbtg from nocardia farcinica

4D7E · L-lys monooxygenase: “An unprecedented NADPH domain conformation in lysine monooxygenase nbtg from nocardia farcinica”. X-ray diffraction, 1 ligand (FAD), 20 pockets (best druggability 0.82). MolNFT v1 #88844 on GenesisL1: 3D…

PDB
4D7E
Type
protein
Length
1,465 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
L-lys monooxygenase
UniProt
Q5Z1T5
Ligands
FAD
Pockets
20 · best druggability 0.82

Structure

x-ray diffraction · 4 distinct chains · 38% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AL-lys monooxygenaseprotein39637% helix, 23% strandQ5Z1T5
BL-lys monooxygenaseprotein39237% helix, 21% strandQ5Z1T5
CL-lys monooxygenaseprotein37738% helix, 22% strandQ5Z1T5
DL-lys monooxygenaseprotein30041% helix, 14% strandQ5Z1T5

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110260.820.8390FAD
211300.820.8386FAD
39970.780.8092empty
49760.770.7986FAD
57980.770.8170FAD

Interfaces

5 interfaces between chains.

  • B–D · 1391 Ų buried · 18 hydrogen bonds · protein-protein
  • A–C · 1338 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 924 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 451 Ų buried · 4 hydrogen bonds · protein-protein
  • B–C · 138 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4D7E · An unprecedented NADPH domain conformation in Lysine Monooxygenase NbtG from Nocardia… · the same entry in another collection · chain A against A, TM-score 1.00

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