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MolNFT v1 · #94444 · protein

Trypanosoma brucei procathepsin B solved from 40 fs free-electron laser pulse data by serial femtosecond X-ray crystallography

4HWY · Cysteine peptidase C (cpc): “Trypanosoma brucei procathepsin B solved from 40 fs free-electron laser pulse data by serial femtosecond…”. X-ray diffraction, 2 ligands (NAG, BMA), 4 pockets (best druggability 0.53). MolNFT v1 #94444…

PDB
4HWY
Type
protein
Length
308 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cysteine peptidase C (cpc)
EC
3.4.22.-
UniProt
D6XHE1
Ligands
NAG, BMA
Pockets
4 · best druggability 0.53

Structure

x-ray diffraction · 1 distinct chain · 28% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACysteine peptidase C (cpc) (EC 3.4.22.-)protein30828% helix, 24% strandD6XHE1

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A
  • BMA · beta-D-mannopyranose · sugar

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1590.530.8819empty
21430.530.8122empty
3670.400.8020empty
4790.310.7422empty

Modifications

Observed in the structure: 6 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 4HWY · Trypanosoma brucei procathepsin B solved from 40 fs free-electron laser pulse data by… · the same entry in another collection · chain A against A, TM-score 1.00

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