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1C3S

CRYSTAL STRUCTURE OF AN HDAC HOMOLOG COMPLEXED WITH SAHA

Summary for 1C3S
Entry DOI10.2210/pdb1c3s/pdb
Related1C3R 1C3S
DescriptorHDLP (HISTONE DEACETYLASE-LIKE PROTEIN), ZINC ION, OCTANEDIOIC ACID HYDROXYAMIDE PHENYLAMIDE, ... (4 entities in total)
Functional Keywordsalpha/beta fold, hydroxamic acid, penta-coordinated zinc, charge-relay system, lyase
Biological sourceAquifex aeolicus
Total number of polymer chains1
Total formula weight43031.37
Authors
Finnin, M.S.,Donigian, J.R.,Pavletich, N.P. (deposition date: 1999-07-28, release date: 1999-09-15, Last modification date: 2024-02-07)
Primary citationFinnin, M.S.,Donigian, J.R.,Cohen, A.,Richon, V.M.,Rifkind, R.A.,Marks, P.A.,Breslow, R.,Pavletich, N.P.
Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors.
Nature, 401:188-193, 1999
Cited by
PubMed: 10490031
DOI: 10.1038/43710
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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