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Crystal structure of streptococcus pneumoniae nanc, covalent complex with a fluorinated NEU5AC derivative

Analyse Crystal structure of streptococcus pneumoniae nanc, covalent complex with a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5F9T
Type
protein
Length
1,318 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Neuraminidase C
EC
3.2.1.18
UniProt
A0A0H2UQE4
Ligands
FSI, SFJ
Pockets
15 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 4% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BNeuraminidase C (EC 3.2.1.18)protein6594% helix, 46% strandA0A0H2UQE4

Ligands and binding sites

  • FSI · 5-acetamido-3,5-dideoxy-3-fluoro-D-erythro-alpha-L-manno-non-2-ulopyranosonic acid · ligand · 2 copies · chains A, B
  • SFJ · (2R,3R,4R,5R,6R)-5-acetamido-2,3-difluoro-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]tetrahydro-2H-pyran-2-carboxylic acid · ligand · 2 copies · chains A, B
  • GOL · Glycerol · additive · chains B

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

Pockets

15 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12380.650.8335FSI
24370.640.7830empty
32940.630.8033FSI
43070.560.7626empty
53070.540.7530empty

Interfaces

1 interface between chains.

  • A–B · 265 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 5F9T · Crystal Structure of Streptococcus pneumoniae NanC, covalent complex with a fluorinated… · the same entry in another collection · chain B against B, TM-score 1.00

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