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Ligand · PKH

PKH · ~{N}-[(1~{R},2~{R},4~{S},7~{E})-7-[azanyl(sulfanyl)methylidene]-7$l^{4}-azabicyclo[2.2.1]heptan-2-yl]-2-chloranyl-4-(6-cyclopropylpyrazin-2-yl)benzamide

PKH, ~{N}-[(1~{R},2~{R},4~{S},7~{E})-7-[azanyl(sulfanyl)methylidene]-7$l^{4}-azabicyclo[2.2.1]heptan-2-yl]-2-chloranyl-4-(6-cyclopropylpyrazin-2-yl)benzamide (C21 H23 Cl N5 O S +1, 429.0 g/mol), in the MolNFT structures on GenesisL1: bound…

Component
PKH
Formula
C21 H23 Cl N5 O S +1
Class
ligand
Structures
1
PDB entries
1

Binding sites

PKH in 1 structure; the first of them:

  • 8D0A · Crystal structure of human USP30 in complex with a covalent inhibitor 829 and a Fab · PKH A601 · binds GLY74, ASN75, CYS77, PHE78, PHE157, GLU158, GLN160, GLU164 and 10 more

Residues it binds most

PHE 1, GLU 1, GLY 1, HIS 1, ASN 1, ASP 1, CYS 1, GLN 1, LEU 1, MET 1 (residue and the binding sites it lines).

Found with

  • ZN · Zinc ion

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