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Kutzneria sp. 744 ornithine N-hydroxylase, ktzi-fadox-br

Analyse Kutzneria sp. 744 ornithine N-hydroxylase, ktzi-fadox-br in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4TM3
Type
protein
Length
1,656 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ktzi
UniProt
A8CF85
Ligands
FAD, BR
Pockets
19 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 32% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DKtziprotein41432% helix, 24% strandA8CF85

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 4 copies · chains A, B, C, D
  • BR · Bromide ion · ion · 46 copies · chains A, B, D, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16060.820.8796FAD, BR
28330.820.84107FAD, BR
38150.810.8498FAD, BR
45560.800.8681FAD, BR
56960.770.8277empty

Interfaces

6 interfaces between chains.

  • A–D · 1780 Ų buried · 16 hydrogen bonds · protein-protein
  • B–C · 1658 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 1310 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 1296 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 1026 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 4TM3 · Kutzneria sp. 744 ornithine N-hydroxylase, KtzI-FADox-Br · the same entry in another collection · chain A against A, TM-score 1.00

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