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Human serum albumin complexed with octanoate and N-acetyl-L-methionine

Analyse Human serum albumin complexed with octanoate and N-acetyl-L-methionine in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5X52
Type
protein
Length
1,136 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Serum albumin
UniProt
P02768
Ligands
OCA, AME, PO4
Pockets
20 · best druggability 0.86

Structure

x-ray diffraction · 2 distinct chains · 71% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASerum albuminprotein57171% helix, 0% strandP02768
BSerum albuminprotein56571% helix, 0% strandP02768

Ligands and binding sites

  • OCA · Octanoic acid (caprylic acid) · ligand · 3 copies · chains A, B
  • AME · N-acetylmethionine · ligand · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 2 copies · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18870.860.8799AME, OCA, PO4
211550.820.8398AME, OCA, PO4
31240.750.9422empty
4820.720.9520OCA
51130.700.9123empty

Interfaces

1 interface between chains.

  • A–B · 648 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 33 disulfide (disulfide).

Compared structures

  • 5X52 · Human serum albumin complexed with octanoate and N-acetyl-L-methionine · the same entry in another collection · chain A against A, TM-score 1.00
  • P02768 · AlphaFold monomer V2.0 prediction for albumin (P02768) · a predicted model of the same protein · chain B against A, TM-score 0.98

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