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HRV14 3C in complex with single chain antibody YDF

Analyse HRV14 3C in complex with single chain antibody YDF in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6KYZ
Type
protein
Length
824 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.845
Source
Homo sapiens; Human rhinovirus 14
Molecule
Genome polyprotein; YDF H chain; YDF L chain
EC
3.4.22.29, 3.6.1.15, 3.4.22.28, 2.7.7.48
UniProt
P03303
Pockets
8 · best druggability 0.64

Structure

x-ray diffraction · resolution 1.845 · 4 distinct chains · 9% helix, 57% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGenome polyprotein (EC 3.4.22.29, 3.6.1.15, 3.4.22.28, 2.7.7.48)protein18012% helix, 58% strandP03303
B, EYDF H chainprotein1275% helix, 54% strand—
C, FYDF L chainprotein1076% helix, 52% strand—
DGenome polyprotein (EC 3.4.22.29, 3.6.1.15, 3.4.22.28, 2.7.7.48)protein17611% helix, 60% strandP03303

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14640.640.7748empty
24420.630.7849empty
3580.520.8718empty
4920.470.8118empty
51090.440.7721empty

Interfaces

9 interfaces between chains.

  • E–F · 805 Ų buried · 13 hydrogen bonds · protein-protein
  • B–C · 765 Ų buried · 13 hydrogen bonds · protein-protein
  • A–C · 513 Ų buried · 16 hydrogen bonds · protein-protein
  • D–F · 500 Ų buried · 15 hydrogen bonds · protein-protein
  • A–B · 490 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 6KYZ · HRV14 3C in complex with single chain antibody ydf · the same entry in another collection · chain A against A, TM-score 1.00

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