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3VHA

Hsp90 alpha N-terminal domain in complex with a macrocyclic inhibitor

Summary for 3VHA
Entry DOI10.2210/pdb3vha/pdb
Related3B24 3B25 3B26 3B27 3B28 3VHC 3VHD
DescriptorHeat shock protein HSP 90-alpha, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, 22-methyl-13,18-dioxa-7-thia-3,5-diazatetracyclo[17.3.1.1~2,6~.1~8,12~]pentacosa-1(23),2(25),3,5,8(24),9,11,19,21-nonaen-4-amine, ... (4 entities in total)
Functional Keywordschaperone-chaperone inhibitor complex, chaperone/chaperone inhibitor
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P07900
Total number of polymer chains1
Total formula weight26362.68
Authors
Fukami, T.A.,Ono, N. (deposition date: 2011-08-24, release date: 2012-07-18, Last modification date: 2024-03-20)
Primary citationSuda, A.,Koyano, H.,Hayase, T.,Hada, K.,Kawasaki, K.,Komiyama, S.,Hasegawa, K.,Fukami, T.A.,Sato, S.,Miura, T.,Ono, N.,Yamazaki, T.,Saitoh, R.,Shimma, N.,Shiratori, Y.,Tsukuda, T.
Design and synthesis of novel macrocyclic 2-amino-6-arylpyrimidine Hsp90 inhibitors
Bioorg.Med.Chem.Lett., 22:1136-1141, 2012
Cited by
PubMed: 22192591
DOI: 10.1016/j.bmcl.2011.11.100
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.39 Å)
Structure validation

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