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MHC with 9-mer peptide

Analyse MHC with 9-mer peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5F1I
Type
protein
Length
3,030 residues
Chains
24
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MHC class I dla-88; BETA2M; 9-mer peptide
UniProt
J9UGS3
Pockets
20 · best druggability 0.82

Structure

x-ray diffraction · 4 distinct chains · 22% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, JMHC class I dla-88protein27026% helix, 39% strandJ9UGS3
B, E, H, K, N, Q, T, WBETA2Mprotein990% helix, 53% strand—
C, F, I, L, O, R, U, X9-mer peptideprotein90% helix, 0% strand—
D, G, M, P, S, VMHC class I dla-88protein27127% helix, 39% strandJ9UGS3

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11570.820.9727empty
28650.780.8188empty
311490.770.7993empty
411990.770.79107empty
58900.770.8087empty

Interfaces

46 interfaces between chains.

  • V–W · 1326 Ų buried · 21 hydrogen bonds · protein-protein
  • M–N · 1312 Ų buried · 20 hydrogen bonds · protein-protein
  • D–E · 1297 Ų buried · 21 hydrogen bonds · protein-protein
  • G–H · 1290 Ų buried · 17 hydrogen bonds · protein-protein
  • P–Q · 1270 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 24 disulfide (disulfide).

Compared structures

  • 5F1I · MHC with 9-mer peptide · the same entry in another collection · chain A against A, TM-score 1.00

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