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5ZMA

Structural basis for an allosteric Eya2 phosphatase inhibitor

Summary for 5ZMA
Entry DOI10.2210/pdb5zma/pdb
DescriptorEyes absent homolog 2, 3-fluoro-N'-[(E)-{5-[(pyrimidin-2-yl)sulfanyl]furan-2-yl}methylidene]benzohydrazide (2 entities in total)
Functional Keywordseya2, eyes absent protein, phosphatase, transcription coactivator, transcription
Biological sourceHomo sapiens (Human)
Total number of polymer chains3
Total formula weight100106.09
Authors
Anantharajan, J.,Jansson, A.E.,Kang, C. (deposition date: 2018-04-02, release date: 2019-06-05, Last modification date: 2023-11-22)
Primary citationAnantharajan, J.,Zhou, H.,Zhang, L.,Hotz, T.,Vincent, M.Y.,Blevins, M.A.,Jansson, A.E.,Kuan, J.W.L.,Ng, E.Y.,Yeo, Y.K.,Baburajendran, N.,Lin, G.,Hung, A.W.,Joy, J.,Patnaik, S.,Marugan, J.,Rudra, P.,Ghosh, D.,Hill, J.,Keller, T.H.,Zhao, R.,Ford, H.L.,Kang, C.
Structural and Functional Analyses of an Allosteric EYA2 Phosphatase Inhibitor That Has On-Target Effects in Human Lung Cancer Cells.
Mol.Cancer Ther., 18:1484-1496, 2019
Cited by
PubMed: 31285279
DOI: 10.1158/1535-7163.MCT-18-1239
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.175 Å)
Structure validation

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