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H2-ld complexed with A5 peptide

Analyse H2-ld complexed with A5 peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6L9N
Type
protein
Length
1,544 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MHC; B2M; Ser-pro-ser-tyr-ala-tyr-his-gln-phe
Pockets
19 · best druggability 0.83

Structure

x-ray diffraction · 3 distinct chains · 19% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, D, G, JMHCprotein27827% helix, 40% strand—
B, E, H, KB2Mprotein990% helix, 49% strand—
C, F, I, LSer-pro-ser-tyr-ala-tyr-his-gln-pheprotein90% helix, 0% strand—

Pockets

19 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19340.830.8494empty
210500.810.8384empty
311190.810.8395empty
410850.810.8290empty
51750.570.8130empty

Interfaces

16 interfaces between chains.

  • D–E · 1251 Ų buried · 21 hydrogen bonds · protein-protein
  • J–K · 1250 Ų buried · 22 hydrogen bonds · protein-protein
  • G–H · 1250 Ų buried · 17 hydrogen bonds · protein-protein
  • A–B · 1247 Ų buried · 19 hydrogen bonds · protein-protein
  • G–J · 1105 Ų buried · 25 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 disulfide (disulfide).

Compared structures

  • 6L9N · H2-Ld complexed with A5 peptide · the same entry in another collection · chain J against J, TM-score 1.00

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