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6V7D

Human Arginase1 Complexed with Bicyclic Inhibitor Compound 10

Summary for 6V7D
Entry DOI10.2210/pdb6v7d/pdb
DescriptorArginase-1, MANGANESE (II) ION, {3-[(3aR,4R,5S,6aR)-4-azaniumyl-4-carboxyoctahydrocyclopenta[b]pyrrol-1-ium-5-yl]propyl}(trihydroxy)borate(1-), ... (4 entities in total)
Functional Keywordsagonist, arg (arginase), bicyclic, immunotherapy, metalloenzyme, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains6
Total formula weight210989.31
Authors
Palte, R.L.,Lesburg, C.A. (deposition date: 2019-12-08, release date: 2020-05-06, Last modification date: 2023-10-11)
Primary citationMitcheltree, M.J.,Li, D.,Achab, A.,Beard, A.,Chakravarthy, K.,Cheng, M.,Cho, H.,Eangoor, P.,Fan, P.,Gathiaka, S.,Kim, H.Y.,Lesburg, C.A.,Lyons, T.W.,Martinot, T.A.,Miller, J.R.,McMinn, S.,O'Neil, J.,Palani, A.,Palte, R.L.,Sauri, J.,Sloman, D.L.,Zhang, H.,Cumming, J.N.,Fischer, C.
Discovery and Optimization of Rationally Designed Bicyclic Inhibitors of Human Arginase to Enhance Cancer Immunotherapy.
Acs Med.Chem.Lett., 11:582-588, 2020
Cited by
PubMed: 32292567
DOI: 10.1021/acsmedchemlett.0c00058
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.82 Å)
Structure validation

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