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8U7E

Structure of Sts-1 HP domain with rebamipide derivative

Summary for 8U7E
Entry DOI10.2210/pdb8u7e/pdb
Related8U5M
DescriptorUbiquitin-associated and SH3 domain-containing protein B, N-(4-ethylbenzoyl)-3-(2-oxo-1,2-dihydroquinolin-4-yl)-L-alanine (3 entities in total)
Functional Keywordssts-1, histidine phosphatase, inhibitor, ubash3b, tula-2, hydrolase-hydrolase inhibitor complex, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains6
Total formula weight193679.68
Authors
Aziz, F.,Dey, R.,French, J.B. (deposition date: 2023-09-15, release date: 2024-02-07, Last modification date: 2024-02-21)
Primary citationAziz, F.,Reddy, K.,Fernandez Vega, V.,Dey, R.,Hicks, K.A.,Rao, S.,Jordan, L.O.,Smith, E.,Shumate, J.,Scampavia, L.,Carpino, N.,Spicer, T.P.,French, J.B.
Rebamipide and Derivatives are Potent, Selective Inhibitors of Histidine Phosphatase Activity of the Suppressor of T Cell Receptor Signaling Proteins.
J.Med.Chem., 67:1949-1960, 2024
Cited by
PubMed: 38252624
DOI: 10.1021/acs.jmedchem.3c01763
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.63 Å)
Structure validation

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