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Structure of 3,6-anhydro-L-galactose dehydrogenase in complex with nap

Analyse Structure of 3,6-anhydro-L-galactose dehydrogenase in complex with nap in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6J76
Type
protein
Length
954 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aldehyde dehydrogenase a
EC
1.2.1.22
UniProt
A0A090SK43
Ligands
NAP
Pockets
3 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAldehyde dehydrogenase a (EC 1.2.1.22)protein47741% helix, 23% strandA0A090SK43
BAldehyde dehydrogenase a (EC 1.2.1.22)protein47742% helix, 23% strandA0A090SK43

Ligands and binding sites

  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111630.840.85110empty
27180.730.7984NAP
36830.710.7886NAP

Interfaces

1 interface between chains.

  • A–B · 2528 Ų buried · 52 hydrogen bonds · protein-protein

Compared structures

  • 6J76 · Structure of 3,6-anhydro-L-galactose Dehydrogenase in Complex with NAP · the same entry in another collection · chain A against A, TM-score 1.00

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