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Human adometdc with no putrescine bound

Analyse Human adometdc with no putrescine bound in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3EP9
Type
protein
Length
300 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
S-adenosylmethionine decarboxylase beta chain; S-adenosylmethionine decarboxylase alpha…
EC
4.1.1.50
UniProt
P17707
Ligands
PYR
Pockets
3 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 25% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BS-adenosylmethionine decarboxylase beta chain (EC 4.1.1.50)protein5623% helix, 38% strandP17707
AS-adenosylmethionine decarboxylase alpha chain (EC 4.1.1.50)protein24425% helix, 39% strandP17707

Ligands and binding sites

  • PYR · Pyruvic acid · ligand · chains B, A
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains B, A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1580.700.9718empty
21880.660.8626PYR, TRS
31870.470.7529empty

Interfaces

1 interface between chains.

  • B–A · 3065 Ų buried · 46 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 3EP9 · Human AdoMetDC with no putrescine bound · the same entry in another collection · chain B against B, TM-score 1.00
  • P17707 · AlphaFold monomer V2.0 prediction for S-adenosylmethionine decarboxylase proenzyme… · a predicted model of the same protein · chain A against A, TM-score 0.99

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