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6MC1

Structure of MAP kinase phosphatase 5 in complex with 3,3-dimethyl-1-((9-(methylthio)-5,6-dihydrothieno[3,4-h]quinazolin-2-yl)thio)butan-2-one, an allosteric inhibitor

Summary for 6MC1
Entry DOI10.2210/pdb6mc1/pdb
DescriptorDual specificity protein phosphatase 10, 3,3-dimethyl-1-{[9-(methylsulfanyl)-5,6-dihydrothieno[3,4-h]quinazolin-2-yl]sulfanyl}butan-2-one, 2,3-DIHYDROXY-1,4-DITHIOBUTANE, ... (4 entities in total)
Functional Keywordsphosphatase, protein-tyrosine phosphatase, dual specificity phosphatase, phosphatase-inhibitor complex, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains6
Total formula weight107717.36
Authors
Gannam, Z.T.K.,Anderson, K.S.,Bennett, A.M.,Lolis, E. (deposition date: 2018-08-30, release date: 2020-08-19, Last modification date: 2023-10-11)
Primary citationGannam, Z.T.K.,Min, K.,Shillingford, S.R.,Zhang, L.,Herrington, J.,Abriola, L.,Gareiss, P.C.,Pantouris, G.,Tzouvelekis, A.,Kaminski, N.,Zhang, X.,Yu, J.,Jamali, H.,Ellman, J.A.,Lolis, E.,Anderson, K.S.,Bennett, A.M.
An allosteric site on MKP5 reveals a strategy for small-molecule inhibition.
Sci.Signal., 13:-, 2020
Cited by
PubMed: 32843541
DOI: 10.1126/scisignal.aba3043
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

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