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Crystal structure of the homospermidine synthase (hss) from blastochloris viridis in complex with NAD and 1,3-diaminopropane.

Analyse Crystal structure of the homospermidine synthase (hss) from blastochloris… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4XQC
Type
protein
Length
950 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Homospermidine synthase
EC
2.5.1.44
UniProt
O32323
Ligands
NAD, 13D, 1PS
Pockets
8 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 36% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHomospermidine synthase (EC 2.5.1.44)protein47536% helix, 24% strandO32323

Ligands and binding sites

  • NAD · Nicotinamide-adenine-dinucleotide · ligand · 2 copies · chains A, B
  • 13D · 1,3-diaminopropane · ligand · 2 copies · chains A
  • 1PS · 3-pyridinium-1-ylpropane-1-sulfonate · ligand · 2 copies · chains A, B
  • ACT · Acetate ion · additive · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14720.790.8774NAD, 13D
24990.780.8570NAD
3830.750.9818empty
44260.740.84581PS, ACT
56550.730.807413D, 1PS, ACT

Interfaces

1 interface between chains.

  • A–B · 1777 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 4XQC · Crystal Structure of the Homospermidine Synthase (HSS) from Blastochloris viridis in… · the same entry in another collection · chain A against A, TM-score 1.00
  • O32323 · AlphaFold monomer V2.0 prediction for homospermidine synthase (O32323) · a predicted model of the same protein · chain A against A, TM-score 1.00

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