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Probing the role of aromatic residues at the secondary saccharide binding sites of human salivary alpha-amylase in substrate hydrolysis and bacterial binding

Analyse Probing the role of aromatic residues at the secondary saccharide binding sites… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3DHP
Type
protein
Length
496 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-amylase 1
EC
3.2.1.1
UniProt
P04745
Ligands
AGL, HMC, GLC, CA, CL
Pockets
5 · best druggability 0.58

Structure

x-ray diffraction · 1 distinct chain · 27% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAlpha-amylase 1 (EC 3.2.1.1)protein49627% helix, 24% strandP04745

Ligands and binding sites

  • AGL · 4-amino-4,6-dideoxy-alpha-D-glucopyranose · ligand · chains A
  • HMC · 5-hydroxymethyl-chonduritol · ligand · chains A
  • GLC · alpha-D-glucopyranose · sugar · 2 copies · chains A
  • CA · Calcium ion · metal · chains A
  • CL · Chloride ion · ion · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12640.580.7827GLC, AGL, HMC
2810.370.7617empty
3710.330.7518empty
4710.330.7623empty
5640.320.7614empty

Modifications

Observed in the structure: 5 disulfide, 1 modified (disulfide, cyclization).

Compared structures

  • 3DHP · Probing the role of aromatic residues at the secondary saccharide binding sites of human… · the same entry in another collection · chain A against A, TM-score 1.00

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