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Crystal structure of SpaA-SLH in complex with beta-D-GlcNAc-(1->3)-4,6-Pyr-beta-D-ManNAcOMe

Analyse Crystal structure of SpaA-SLH in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6CWL
Type
protein
Length
310 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.15
Source
Paenibacillus alvei
Molecule
Surface (S-) layer glycoprotein
UniProt
C1JZ07
Ligands
FHY
Pockets
3 · best druggability 0.67

Structure

x-ray diffraction · resolution 2.15 · 2 distinct chains · 43% helix, 5% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASurface (S-) layer glycoproteinprotein16441% helix, 5% strandC1JZ07
BSurface (S-) layer glycoproteinprotein14645% helix, 5% strandC1JZ07

Ligands and binding sites

  • FHY · (2S,4aR,6R,7S,8R,8aS)-7-(acetylamino)-6-({2-(acetylamino)-3-O-[2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl]-4,6-O-[(1S)-1-carboxylic acidethylidene]-2-deoxy-beta-D-mannopyranosyl}oxy)-8-{[2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl]oxy}-2-methylhexahydro-2H-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15740.670.7756empty
21170.390.7524FHY
3630.370.7812FHY

Interfaces

1 interface between chains.

  • A–B · 423 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 6CWL · Crystal structure of spaa-slh in complex with beta-D-glcnac-(1->3)-4… · the same entry in another collection · chain A against A, TM-score 1.00

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