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Crystal structure of aspartate beta-semialdehide dehydrogenase from streptococcus pneumoniae with D-2,3-diaminopropionate

Analyse Crystal structure of aspartate beta-semialdehide dehydrogenase from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3PYL
Type
protein
Length
1,429 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aspartate-semialdehyde dehydrogenase
EC
1.2.1.11
UniProt
A5MTN0
Ligands
2RA
Pockets
9 · best druggability 0.65

Structure

x-ray diffraction · 4 distinct chains · 34% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAspartate-semialdehyde dehydrogenase (EC 1.2.1.11)protein35834% helix, 23% strandA5MTN0
BAspartate-semialdehyde dehydrogenase (EC 1.2.1.11)protein35435% helix, 24% strandA5MTN0
CAspartate-semialdehyde dehydrogenase (EC 1.2.1.11)protein36134% helix, 23% strandA5MTN0
DAspartate-semialdehyde dehydrogenase (EC 1.2.1.11)protein35635% helix, 24% strandA5MTN0

Ligands and binding sites

  • 2RA · 3-amino-D-alanine · ligand · 3 copies · chains A, B, C

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

Pockets

9 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13440.650.80412RA
23720.640.79412RA
33930.640.7940empty
47140.640.7460empty
53580.630.79402RA

Interfaces

3 interfaces between chains.

  • C–D · 2958 Ų buried · 63 hydrogen bonds · protein-protein
  • A–B · 2935 Ų buried · 63 hydrogen bonds · protein-protein
  • A–C · 306 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 3PYL · Crystal structure of aspartate beta-semialdehide dehydrogenase from Streptococcus… · the same entry in another collection · chain C against C, TM-score 1.00

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