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PCSK9 J16 Fab complex

Analyse PCSK9 J16 Fab complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3SQO
Type
protein
Length
1,007 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proprotein convertase SUBTILISIN/KEXIN type 9; J16 heavy chain; J16 light chain; PCSK9…
EC
3.4.21.-
UniProt
Q8NBP7
Pockets
8 · best druggability 0.72

Structure

x-ray diffraction · 4 distinct chains · 14% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProprotein convertase SUBTILISIN/KEXIN type 9 (EC 3.4.21.-)protein49118% helix, 37% strandQ8NBP7
HJ16 heavy chainprotein2114% helix, 51% strand—
LJ16 light chainprotein2137% helix, 51% strand—
PPCSK9 prodomain (EC 3.4.21.-)protein9228% helix, 39% strandQ8NBP7

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15590.720.8176empty
23820.720.8355empty
35680.610.7359empty
43470.570.7543empty
51070.400.7624empty

Interfaces

4 interfaces between chains.

  • H–L · 1849 Ų buried · 21 hydrogen bonds · protein-protein
  • A–P · 1367 Ų buried · 31 hydrogen bonds · protein-protein
  • A–H · 469 Ų buried · 8 hydrogen bonds · protein-protein
  • A–L · 423 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 disulfide (disulfide).

Compared structures

  • 3SQO · PCSK9 J16 Fab complex · the same entry in another collection · chain A against A, TM-score 1.00

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