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8BAC

Crystal structure of human heparanase in complex with competitive inhibitor GD05

This is a non-PDB format compatible entry.
Summary for 8BAC
Entry DOI10.2210/pdb8bac/pdb
DescriptorHeparanase 50 kDa subunit, Heparanase 8 kDa subunit, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (6 entities in total)
Functional Keywordsinhibitor complex, hydrolase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight52672.48
Authors
Armstrong, Z.,Davies, G.J. (deposition date: 2022-10-11, release date: 2023-03-01, Last modification date: 2024-02-07)
Primary citationDoherty, G.G.,Ler, G.J.M.,Wimmer, N.,Bernhardt, P.V.,Ashmus, R.A.,Vocadlo, D.J.,Armstrong, Z.,Davies, G.J.,Maccarana, M.,Li, J.P.,Kayal, Y.,Ferro, V.
Synthesis of Uronic Acid 1-Azasugars as Putative Inhibitors of alpha-Iduronidase, beta-Glucuronidase and Heparanase.
Chembiochem, 24:e202200619-e202200619, 2023
Cited by
PubMed: 36453606
DOI: 10.1002/cbic.202200619
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.05 Å)
Structure validation

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