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Crystal structure of the hlyiir mutant protein with residues 169-186 substituted by a linker containing two thrombin sites

Analyse Crystal structure of the hlyiir mutant protein with residues 169-186… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2WV1
Type
protein
Length
366 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemolysin II regulatory protein
UniProt
Q7X506
Ligands
NO3
Pockets
4 · best druggability 0.68

Structure

x-ray diffraction · 2 distinct chains · 75% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemolysin II regulatory proteinprotein18375% helix, 0% strandQ7X506
BHemolysin II regulatory proteinprotein18375% helix, 0% strandQ7X506

Ligands and binding sites

  • NO3 · Nitrate ion · ion · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12270.680.8535empty
21440.620.8520empty
31050.440.7825empty
4740.370.7719empty

Interfaces

1 interface between chains.

  • A–B · 2026 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 2WV1 · Crystal structure of the hlyiir mutant protein with residues 169-186 substituted by a… · the same entry in another collection · chain A against A, TM-score 1.00

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