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Paramagnetic shifts in solid-state NMR of proteins to elicit structural information

Analyse Paramagnetic shifts in solid-state NMR of proteins to elicit structural… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2K9C
Type
protein
Length
152 residues
Chains
1
Method
solution nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Macrophage metalloelastase
EC
3.4.24.65
UniProt
P39900
Ligands
CO
Pockets
3 · best druggability 0.64

Structure

solution nmr · 1 distinct chain · 24% helix, 4% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMacrophage metalloelastase (EC 3.4.24.65)protein15224% helix, 4% strandP39900

Ligands and binding sites

  • CO · Cobalt (II) ion · metal · chains 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
11960.640.8433empty
21040.610.8721CO
3890.420.7817empty

Compared structures

  • 2K9C · Paramagnetic shifts in solid-state NMR of Proteins to elicit structural information · the same entry in another collection · chain A against A, TM-score 1.00

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