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 DOI | 10.2210/pdb6mc1/pdb |
Descriptor | Dual 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 Keywords | phosphatase, protein-tyrosine phosphatase, dual specificity phosphatase, phosphatase-inhibitor complex, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 6 |
Total formula weight | 107717.36 |
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 citation | Gannam, 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: 32843541DOI: 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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