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Crystal structure of abhpai-mn-pyruvate-succinic semialdehyde complex, class II aldolase, hpai from acinetobacter baumannii

Analyse Crystal structure of abhpai-mn-pyruvate-succinic semialdehyde complex, class II… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7ETF
Type
protein
Length
759 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
4-hydroxy-2-oxoheptanedioate aldolase
EC
4.1.2.52
UniProt
A0A5R9HKL3
Ligands
PYR, SSN, MN, CA
Pockets
14 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 44% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C4-hydroxy-2-oxoheptanedioate aldolase (EC 4.1.2.52)protein25344% helix, 16% strandA0A5R9HKL3

Ligands and binding sites

  • PYR · Pyruvic acid · ligand · 3 copies · chains A, B, C
  • SSN · 4-oxobutanoic acid · ligand · 3 copies · chains A, C, B
  • MN · Manganese (II) ion · metal · 3 copies · chains A, B, C
  • CA · Calcium ion · metal · chains A, B, C

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

Pockets

14 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15190.810.8846empty
23290.670.8140PYR, MN, SSN
32940.660.8241SSN, PYR, MN
42980.660.8240PYR, MN, SSN
51060.620.8825empty

Interfaces

3 interfaces between chains.

  • B–C · 1060 Ų buried · 15 hydrogen bonds · protein-protein
  • A–B · 1058 Ų buried · 15 hydrogen bonds · protein-protein
  • A–C · 1057 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 7ETF · Crystal structure of AbHpaI-Mn-pyruvate-succinic semialdehyde complex, Class II aldolase… · the same entry in another collection · chain A against A, TM-score 1.00

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