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Homoserine dehydrogenase K195A mutant from thermus thermophilus HB8 complexed with hse and NADP+

Analyse Homoserine dehydrogenase K195A mutant from thermus thermophilus HB8 complexed… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6A0U
Type
protein
Length
662 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Homoserine dehydrogenase
EC
1.1.1.3
UniProt
Q5SL04
Ligands
NAP, HSE, UNL, NA
Pockets
6 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 39% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
B, AHomoserine dehydrogenase (EC 1.1.1.3)protein33139% helix, 24% strandQ5SL04

Ligands and binding sites

  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains B, A
  • HSE · L-homoserine · ligand · 2 copies · chains B, A
  • UNL · Unknown ligand · ligand · chains B
  • NA · Sodium ion · metal · 2 copies · chains B, A
  • FMT · Formic acid · additive · 15 copies · chains B, A
  • GOL · Glycerol · additive · 2 copies · chains B, A
  • CXS · 3-cyclohexyl-1-propylsulfonic acid · additive · chains 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, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12420.750.8947FMT
23370.660.8147NAP, HSE
33310.630.7947NAP, HSE
4510.590.9219GOL
51590.500.7825GOL

Interfaces

1 interface between chains.

  • B–A · 1994 Ų buried · 31 hydrogen bonds · protein-protein

Compared structures

  • 6A0U · Homoserine dehydrogenase K195A mutant from Thermus thermophilus HB8 complexed with HSE… · the same entry in another collection · chain B against B, TM-score 1.00

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