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4Q3S

Crystal structure of Schistosoma mansoni arginase in complex with inhibitor ABHPE

Summary for 4Q3S
Entry DOI10.2210/pdb4q3s/pdb
Related4Q3P 4Q3Q 4Q3R 4Q3T 4Q3U 4Q3V 4Q40 4Q41 4Q42
DescriptorArginase, MANGANESE (II) ION, [(5R)-5-amino-5-carboxy-7-(piperidin-1-yl)heptyl](trihydroxy)borate(1-), ... (5 entities in total)
Functional Keywordsarginase-deacetylase fold, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceSchistosoma mansoni (Blood fluke)
Total number of polymer chains4
Total formula weight171458.16
Authors
Hai, Y.,Edwards, J.E.,Van Zandt, M.C.,Hoffmann, K.F.,Christianson, D.W. (deposition date: 2014-04-12, release date: 2014-07-16, Last modification date: 2023-09-20)
Primary citationHai, Y.,Edwards, J.E.,Van Zandt, M.C.,Hoffmann, K.F.,Christianson, D.W.
Crystal Structure of Schistosoma mansoni Arginase, a Potential Drug Target for the Treatment of Schistosomiasis.
Biochemistry, 53:4671-4684, 2014
Cited by
PubMed: 25007099
DOI: 10.1021/bi5004519
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.11 Å)
Structure validation

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