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Crystal structure of mycobacterium tuberculosis S-adenosyl-L- homocysteine hydrolase in ternary complex with NAD and 3- deazaadenosine

Analyse Crystal structure of mycobacterium tuberculosis S-adenosyl-L- homocysteine… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2ZIZ
Type
protein
Length
1,940 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Adenosylhomocysteinase
EC
3.3.1.1
UniProt
P60176
Ligands
AD3, NAD
Pockets
19 · best druggability 0.88

Structure

x-ray diffraction · 1 distinct chain · 46% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DAdenosylhomocysteinase (EC 3.3.1.1)protein48546% helix, 14% strandP60176

Ligands and binding sites

  • AD3 · 3-deaza-adenosine · ligand · 4 copies · chains A, B, C, D
  • NAD · Nicotinamide-adenine-dinucleotide · ligand · 4 copies · chains A, B, C, D

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

Pockets

19 pockets found on a 1 Å grid, 15 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16640.880.9367empty
25770.840.9071NAD, AD3
35410.840.9071AD3, NAD
45680.840.9074NAD, AD3
55300.840.9071AD3, NAD

Interfaces

6 interfaces between chains.

  • A–B · 3354 Ų buried · 39 hydrogen bonds · protein-protein
  • C–D · 3324 Ų buried · 36 hydrogen bonds · protein-protein
  • B–D · 1861 Ų buried · 28 hydrogen bonds · protein-protein
  • A–C · 1816 Ų buried · 24 hydrogen bonds · protein-protein
  • A–D · 528 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 2ZIZ · Crystal structure of Mycobacterium tuberculosis S-adenosyl-L-homocysteine hydrolase in… · the same entry in another collection · chain A against A, TM-score 1.00

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