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Crystal structure of M1 zinc metallopeptidase E323A mutant bound to Tyr-ser-ala substrate from Deinococcus radiodurans

Analyse Crystal structure of M1 zinc metallopeptidase E323A mutant bound to Tyr-ser-ala… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6IFG
Type
protein
Length
868 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.9
Source
Deinococcus radiodurans (strain ATCC 13939 / DSM 20539 / JCM 16871 / LMG 4051 /…
Molecule
Zinc metalloprotease; Tripeptides (TYR-SER-ALA)
UniProt
Q9RVZ5
Ligands
ZN
Pockets
9 · best druggability 0.45

Structure

x-ray diffraction · resolution 1.9 · 3 distinct chains · 29% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AZinc metalloproteaseprotein43029% helix, 34% strandQ9RVZ5
BZinc metalloproteaseprotein43229% helix, 34% strandQ9RVZ5
E, FTripeptides (TYR-SER-ALA)protein30% helix, 33% strand—

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, E, B, F
  • FMT · Formic acid · additive · 13 copies · chains A, E, B

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

Pockets

9 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11120.450.7929FMT
21300.430.7620empty
31160.400.7530FMT
4660.380.7915empty
51070.370.7420empty

Interfaces

3 interfaces between chains.

  • A–B · 488 Ų buried · 6 hydrogen bonds · protein-protein
  • A–E · 382 Ų buried · 13 hydrogen bonds · protein-protein
  • B–F · 376 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 6IFG · Crystal structure of M1 zinc metallopeptidase E323A mutant bound to tyr-ser-ala substrate… · the same entry in another collection · chain A against A, TM-score 1.00

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