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Structure and activity of human mitochondrial peptide deformylase, a novel cancer target

Analyse Structure and activity of human mitochondrial peptide deformylase, a novel… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3G5K
Type
protein
Length
732 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peptide deformylase, mitochondrial
EC
3.5.1.88
UniProt
Q9HBH1
Ligands
BB2, CO
Pockets
8 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 32% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DPeptide deformylase, mitochondrial (EC 3.5.1.88)protein18332% helix, 32% strandQ9HBH1

Ligands and binding sites

  • BB2 · Actinonin · ligand · 4 copies · chains A, B, C, D
  • CO · Cobalt (II) ion · metal · 4 copies · chains A, B, C, D

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

Pockets

8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14780.670.7847BB2
23670.650.7932BB2
33340.630.7932BB2
43310.620.7831BB2, CO
5740.340.7513empty

Interfaces

2 interfaces between chains.

  • C–D · 859 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 853 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 3G5K · Structure and activity of human mitochondrial peptide deformylase, a novel cancer target · the same entry in another collection · chain D against D, TM-score 1.00
  • Q9HBH1 · AlphaFold monomer V2.0 prediction for peptide deformylase, mitochondrial (Q9HBH1) · a predicted model of the same protein · chain A against A, TM-score 0.95

Analyse

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