GL1X · GenesisL1 explorer

Research workbench

Crystal structure of mutant E159A of beta-alanine synthase from saccharomyces kluyveri

Analyse Crystal structure of mutant E159A of beta-alanine synthase from saccharomyces… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2V8D
Type
protein
Length
866 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-alanine synthase
EC
3.5.1.6
UniProt
Q96W94
Ligands
ZN
Pockets
6 · best druggability 0.68

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-alanine synthase (EC 3.5.1.6)protein43735% helix, 22% strandQ96W94
BBeta-alanine synthase (EC 3.5.1.6)protein42934% helix, 23% strandQ96W94

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14810.680.7954empty
24210.640.7851ZN
3650.460.8317empty
41230.450.7721empty
51120.400.7618empty

Interfaces

1 interface between chains.

  • A–B · 2363 Ų buried · 20 hydrogen bonds · protein-protein

Compared structures

  • 2V8D · Crystal structure of mutant E159A of beta-alanine synthase from Saccharomyces kluyveri · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.