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Crystal structure of HA2-del-L2SEM, central coiled-coil from influenza hemagglutinin HA2 without heptad repeat stutter

Analyse Crystal structure of HA2-del-L2SEM, central coiled-coil from influenza… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4S1X
Type
protein
Length
194 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Truncated hemagglutinin
UniProt
A8TXJ0
Pockets
2 · best druggability 0.48

Structure

x-ray diffraction · 3 distinct chains · 94% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DTruncated hemagglutininprotein3895% helix, 0% strandA8TXJ0
B, ETruncated hemagglutininprotein3795% helix, 0% strandA8TXJ0
C, FTruncated hemagglutininprotein2291% helix, 0% strandA8TXJ0

Ligands and binding sites

  • GOL · Glycerol · additive · chains E

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11920.480.7521empty
2590.310.7512empty

Interfaces

8 interfaces between chains.

  • D–E · 777 Ų buried · 1 hydrogen bond · protein-protein
  • A–B · 767 Ų buried · 2 hydrogen bonds · protein-protein
  • A–C · 625 Ų buried · 2 hydrogen bonds · protein-protein
  • D–F · 601 Ų buried · 3 hydrogen bonds · protein-protein
  • E–F · 346 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 modified (engineered).

Compared structures

  • 4S1X · Crystal structure of HA2-Del-L2seM, Central Coiled-Coil from Influenza Hemagglutinin HA2… · the same entry in another collection · chain A against A, TM-score 1.00

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