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Human MMP12 in complex with L-glutamate motif inhibitor

Analyse Human MMP12 in complex with L-glutamate motif inhibitor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4EFS
Type
protein
Length
159 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Macrophage metalloelastase
EC
3.4.24.65
UniProt
P39900
Ligands
E37, CA, ZN
Pockets
2 · best druggability 0.57

Structure

x-ray diffraction · 1 distinct chain · 26% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMacrophage metalloelastase (EC 3.4.24.65)protein15926% helix, 17% strandP39900

Ligands and binding sites

  • E37 · N~2~-[4-(4-phenylthiophen-2-yl)benzoyl]-L-alpha-glutamine · ligand · chains A
  • CA · Calcium ion · metal · 3 copies · chains A
  • ZN · Zinc ion · metal · 2 copies · chains A
  • PGO · S-1,2-propanediol · additive · 3 copies · chains A
  • EDO · 1,2-ethanediol · additive · 2 copies · chains A
  • GOL · Glycerol · additive · chains A
  • PGR · R-1,2-propanediol · additive · chains A
  • IMD · Imidazole · additive · chains A

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
11140.570.8423E37, PGO
2750.340.7519GOL

Compared structures

  • 4EFS · Human MMP12 in complex with L-glutamate motif inhibitor · the same entry in another collection · chain A against A, TM-score 1.00

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