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Crystal complex of sys-1/POP-1 at 2.5A resolution

Analyse Crystal complex of sys-1/POP-1 at 2.5A resolution in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3C2G
Type
protein
Length
1,249 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sys-1 protein; Pop-1 8-residue peptide
UniProt
Q9XVI2, Q10666
Pockets
10 · best druggability 0.40

Structure

x-ray diffraction · 3 distinct chains · 70% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASys-1 proteinprotein61870% helix, 0% strandQ9XVI2
BSys-1 proteinprotein61570% helix, 0% strandQ9XVI2
C, DPop-1 8-residue peptideprotein80% helix, 0% strandQ10666

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11540.400.7324empty
2710.390.7917empty
3760.390.7824empty
4720.360.7613empty
5830.350.7517empty

Interfaces

3 interfaces between chains.

  • A–B · 842 Ų buried · 14 hydrogen bonds · protein-protein
  • B–D · 655 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 616 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 30 modified (engineered).

Compared structures

  • 3C2G · Crystal complex of SYS-1/POP-1 at 2.5A resolution · the same entry in another collection · chain A against A, TM-score 1.00
  • Q10666 · AlphaFold monomer V2.0 prediction for protein pop-1 (Q10666) · a predicted model of the same protein · chain C against A, TM-score 0.63

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