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MolNFT v1 · #71133 · protein

Structure of the 14-3-3/PMA2 complex stabilized by epibestatin

3M50 · 14-3-3-like protein C: “Structure of the 14-3-3/PMA2 complex stabilized by epibestatin”. X-ray diffraction, 1 ligand (EBT), 2 pockets (best druggability 0.66). MolNFT v1 #71133 on GenesisL1: 3D structure, binding sites and pockets…

PDB
3M50
Type
protein
Length
249 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
14-3-3-like protein C; N.PLUMBAGINIFOLIA H+-translocating ATPase mRNA
UniProt
P93343, Q42932
Ligands
EBT
Pockets
2 · best druggability 0.66

Structure

x-ray diffraction · 2 distinct chains · 81% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A14-3-3-like protein Cprotein21885% helix, 0% strandP93343
PN.PLUMBAGINIFOLIA H+-translocating ATPase mRNAprotein3148% helix, 0% strandQ42932

Ligands and binding sites

  • EBT · N-[(2R,3R)-3-amino-2-hydroxy-4-phenylbutanoyl]-L-leucine · ligand · chains A, P

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13390.660.8036EBT
21240.430.7620empty

Interfaces

1 interface between chains.

  • A–P · 1010 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 3M50 · Structure of the 14-3-3/PMA2 complex stabilized by Epibestatin · the same entry in another collection · chain A against A, TM-score 1.00
  • P93343 · AlphaFold monomer V2.0 prediction for 14-3-3-like protein C (P93343) · a predicted model of the same protein · chain A against A, TM-score 0.99

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