8OHQ

Crystal structure of human heparanase in complex with competitive inhibitor derrived from siastatin B

This is a non-PDB format compatible entry.

Summary for 8OHQ

• Entry DOI: 10.2210/pdb8ohq/pdb
• Descriptor: Heparanase 50 kDa subunit, Heparanase 8 kDa subunit, alpha-L-fucopyranose-(1-6)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (8 entities in total)
• Functional Keywords: inhibitor, complex, hydrolase
• Biological source: Homo sapiens (human); More
• Total number of polymer chains: 2
• Total formula weight: 53330.31

Authors

Wu, L.,Davies, G.J.,Overkleeft, H.S.,Armstrong, Z.,Yurong, C. (deposition date: 2023-03-21, release date: 2024-01-10, Last modification date: 2024-01-24)

• Primary citation: Chen, Y.,van den Nieuwendijk, A.M.C.H.,Wu, L.,Moran, E.,Skoulikopoulou, F.,van Riet, V.,Overkleeft, H.S.,Davies, G.J.,Armstrong, Z.; Molecular Basis for Inhibition of Heparanases and beta-Glucuronidases by Siastatin B.; J.Am.Chem.Soc., 146:125-133, 2024; PubMed: 38118176; DOI: 10.1021/jacs.3c04162

Experimental method

X-RAY DIFFRACTION (1.7 Å)