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Structure the ananain protease from ananas comosus covalently bound to the tlck inhibitor

Analyse Structure the ananain protease from ananas comosus covalently bound to the tlck… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6YCD
Type
protein
Length
430 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ananain
EC
3.4.22.31
UniProt
P80884
Ligands
TCK, SO4
Pockets
3 · best druggability 0.57

Structure

x-ray diffraction · 1 distinct chain · 24% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BAnanain (EC 3.4.22.31)protein21524% helix, 22% strandP80884

Ligands and binding sites

  • TCK · N-[(1S)-5-amino-1-(chloroacetyl)pentyl]-4-methylbenzenesulfonamide · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 3 copies · chains A, B
  • GOL · Glycerol · additive · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12460.570.7835empty
2890.390.7719empty
3550.360.7915empty

Interfaces

1 interface between chains.

  • A–B · 440 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 2 covalent (disulfide, covalent ligand).

Compared structures

  • 6YCD · Structure the ananain protease from Ananas comosus covalently bound to the TLCK inhibitor · the same entry in another collection · chain A against A, TM-score 1.00
  • P80884 · AlphaFold monomer V2.0 prediction for ananain (P80884) · a predicted model of the same protein · chain A against A, TM-score 0.99

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