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Crystal structure of siderocalin (ngal, lipocalin 2) complexed with carboxymycobactin S

Analyse Crystal structure of siderocalin (ngal, lipocalin 2) complexed with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1X89
Type
protein
Length
518 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Neutrophil gelatinase-associated lipocalin
UniProt
P80188
Ligands
CM1
Pockets
6 · best druggability 0.66

Structure

x-ray diffraction · 3 distinct chains · 15% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANeutrophil gelatinase-associated lipocalinprotein17414% helix, 43% strandP80188
BNeutrophil gelatinase-associated lipocalinprotein17115% helix, 44% strandP80188
CNeutrophil gelatinase-associated lipocalinprotein17315% helix, 43% strandP80188

Ligands and binding sites

  • CM1 · Carboxymycobactin S · ligand · 3 copies · chains A, B, C

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

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13770.660.7932CM1
23960.650.7835CM1
32920.610.7933CM1
42120.470.7435empty
51250.390.7426empty

Interfaces

2 interfaces between chains.

  • A–C · 403 Ų buried · 9 hydrogen bonds · protein-protein
  • A–B · 112 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 1X89 · Crystal structure of Siderocalin (NGAL, Lipocalin 2) complexed with Carboxymycobactin S · the same entry in another collection · chain A against A, TM-score 1.00

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