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Crystal structure of a lysin

Analyse Crystal structure of a lysin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2NW0
Type
protein
Length
378 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Plyb
EC
3.2.1.17
Pockets
3 · best druggability 0.63

Structure

x-ray diffraction · 1 distinct chain · 30% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPlyb (EC 3.2.1.17)protein18930% helix, 29% strand—

Ligands and binding sites

  • ACT · Acetate ion · additive · 6 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
14980.630.7657ACT
21150.410.7619ACT
31300.400.7432empty

Interfaces

1 interface between chains.

  • A–B · 424 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 2NW0 · Crystal structure of a lysin · the same entry in another collection · chain A against A, TM-score 1.00

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