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MolNFT v2 · #1571 · protein

A 30 ångström U-shaped catalytic tunnel in the crystal structure of polyamine oxidase

1B5Q · Protein (polyamine oxidase): “A 30 ångström U-shaped catalytic tunnel in the crystal structure of polyamine oxidase”. X-ray diffraction at 1.9, 5 ligands (FAD, MD2, NAG), 15 pockets (best druggability 0.84). MolNFT v2 #1571 on…

PDB
1B5Q
Type
protein
Length
1,383 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.9
Source
Zea mays
Molecule
Protein (polyamine oxidase)
Ligands
FAD, MD2, NAG, MAN, FCA
Pockets
15 · best druggability 0.84

Structure

x-ray diffraction · resolution 1.9 · 2 distinct chains · 34% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein (polyamine oxidase)protein45933% helix, 22% strand—
B, CProtein (polyamine oxidase)protein46234% helix, 22% strand—

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 3 copies · chains A, B, C
  • MD2 · N,N'-bis(2,3-butadienyl)-1,4-butane-diamine · ligand · 3 copies · chains A, B, C
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A, B, C
  • MAN · alpha-D-mannopyranose · sugar · 2 copies
  • FCA · alpha-D-fucopyranose · sugar

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

Pockets

15 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19210.840.85108FAD, MD2
27770.840.8795empty
38070.840.86100FAD, MD2
47560.830.8683FAD, MD2
51520.560.8228empty

Interfaces

1 interface between chains.

  • A–B · 1903 Ų buried · 26 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide, 3 glycan (disulfide, N-glycosylation).

Compared structures

  • 1B5Q · A 30 ångström U-shaped catalytic tunnel in the crystal structure of polyamine oxidase · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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