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Crystal structure of hyhel-63 complexed with hel mutant K96A

Analyse Crystal structure of hyhel-63 complexed with hel mutant K96A in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1NBY
Type
protein
Length
553 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antibody kappa light chain; Immunoglobulin gamma 1 chain; Lysozyme C
EC
3.2.1.17
UniProt
P01837, P01865, P00698
Pockets
5 · best druggability 0.65

Structure

x-ray diffraction · 3 distinct chains · 14% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAntibody kappa light chainprotein2146% helix, 50% strandP01837
BImmunoglobulin gamma 1 chainprotein2107% helix, 52% strandP01865
CLysozyme C (EC 3.2.1.17)protein12940% helix, 11% strandP00698

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12240.650.8335empty
23240.550.7544empty
31540.470.7620empty
4920.380.7617empty
5530.260.7317empty

Interfaces

3 interfaces between chains.

  • A–B · 1802 Ų buried · 15 hydrogen bonds · protein-protein
  • B–C · 597 Ų buried · 14 hydrogen bonds · protein-protein
  • A–C · 421 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 1NBY · Crystal Structure of HyHEL-63 complexed with HEL mutant K96A · the same entry in another collection · chain A against A, TM-score 1.00
  • P01837 · AlphaFold monomer V2.0 prediction for immunoglobulin kappa constant (P01837) · a predicted model of the same protein · chain A against A, TM-score 0.49
  • P01865 · AlphaFold monomer V2.0 prediction for ig gamma-2A chain C region, membrane-bound form… · a predicted model of the same protein · chain B against A, TM-score 0.48

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