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Short PCSK9 delta-P' complex with peptide PEP1

Analyse Short PCSK9 delta-P' complex with peptide PEP1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5VLH
Type
protein
Length
382 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proprotein convertase SUBTILISIN/KEXIN type 9…
EC
3.4.21.-
UniProt
Q8NBP7
Ligands
ACE, CA, NH2
Pockets
3 · best druggability 0.27

Structure

x-ray diffraction · 3 distinct chains · 30% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProprotein convertase SUBTILISIN/KEXIN type 9 (EC 3.4.21.-)protein35529% helix, 29% strandQ8NBP7
YCys-arg-leu-pro-TRP-asn-leu-gln-arg-ile-gly-leu-pro-cysprotein1436% helix, 0% strand—
ZACE-thr-val-phe-thr-ser-TRP-glu-glu-tyr-leu-asp-TRP-val- NH2protein1354% helix, 8% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · chains A, Z
  • CA · Calcium ion · metal · chains A
  • NH2 · Amino group · ion · chains Z

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1600.270.7318empty
2500.260.7314empty
3520.230.7216empty

Interfaces

3 interfaces between chains.

  • A–Y · 540 Ų buried · 7 hydrogen bonds · protein-protein
  • A–Z · 358 Ų buried · 4 hydrogen bonds · protein-protein
  • Y–Z · 126 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 1 covalent (disulfide, covalent ligand).

Compared structures

  • 5VLH · Short PCSK9 delta-P' complex with peptide Pep1 · the same entry in another collection · chain Y against Y, TM-score 1.00

Analyse

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