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Crystal structure of thermotoga maritima alpha-glucuronidase (TM0752) in complex with NADH and D-glucuronic acid

Analyse Crystal structure of thermotoga maritima alpha-glucuronidase (TM0752) in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7CTM
Type
protein
Length
469 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-glucosidase, putative
UniProt
Q9WZL1
Ligands
NAI, BDP
Pockets
2 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 47% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAlpha-glucosidase, putativeprotein46947% helix, 16% strandQ9WZL1

Ligands and binding sites

  • NAI · 1,4-dihydronicotinamide adenine dinucleotide · ligand · chains A
  • BDP · beta-D-glucopyranuronic acid · sugar · chains A
  • IPA · Isopropyl alcohol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16890.760.8267NAI, BDP
21460.510.7930empty

Modifications

Observed in the structure: 1 disulfide, 1 modified (disulfide, oxidation).

Compared structures

  • 7CTM · Crystal structure of Thermotoga maritima alpha-glucuronidase (TM0752) in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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