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Crystal structure of kni-10006 bound histo-aspartic protease (hap) from plasmodium falciparum

Analyse Crystal structure of kni-10006 bound histo-aspartic protease (hap) from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3FNU
Type
protein
Length
1,304 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hap protein
UniProt
Q8IM15
Ligands
006
Pockets
10 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 12% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DHap proteinprotein32612% helix, 47% strandQ8IM15

Ligands and binding sites

  • 006 · (4R)-3-[(2S,3S)-3-{[(2,6-dimethylphenoxy)acetyl]amino}-2-hydroxy-4-phenylbutanoyl]-N-[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]-5,5-dimethyl-1,3-thiazolidine-4-carboxamide · ligand · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110980.780.80105empty
210010.780.79103006
36090.710.7867006
41950.580.8023006
51680.500.7826empty

Interfaces

5 interfaces between chains.

  • A–B · 1464 Ų buried · 3 hydrogen bonds · protein-protein
  • C–D · 1427 Ų buried · 2 hydrogen bonds · protein-protein
  • B–C · 323 Ų buried · 2 hydrogen bonds · protein-protein
  • B–D · 296 Ų buried · 1 hydrogen bond · protein-protein
  • A–D · 68 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 3FNU · Crystal structure of KNI-10006 bound histo-aspartic protease (HAP) from Plasmodium… · the same entry in another collection · chain A against A, TM-score 1.00

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