5T19
Structure of PTP1B complexed with N-(3'-(1,1-dioxido-4-oxo-1,2,5-thiadiazolidin-2-yl)-4'-methyl-[1,1'-biphenyl]-4-yl)acetamide
Summary for 5T19
Entry DOI | 10.2210/pdb5t19/pdb |
Descriptor | Tyrosine-protein phosphatase non-receptor type 1, MAGNESIUM ION, 5-[4-methyl-4'-(methylamino)[1,1'-biphenyl]-3-yl]-1lambda~6~,2,5-thiadiazolidine-1,1,3-trione, ... (5 entities in total) |
Functional Keywords | hydrolase, protein tyrosine phosphatase, 5-(aryl)-1, 2, 5-thiadiazolidin-3-one-1, 1-dioxide unit |
Biological source | Homo sapiens (Human) |
Cellular location | Endoplasmic reticulum membrane ; Peripheral membrane protein ; Cytoplasmic side : P18031 |
Total number of polymer chains | 1 |
Total formula weight | 38022.89 |
Authors | Laciak, A.R.,Tanner, J.J. (deposition date: 2016-08-18, release date: 2017-04-12, Last modification date: 2023-10-04) |
Primary citation | Punthasee, P.,Laciak, A.R.,Cummings, A.H.,Ruddraraju, K.V.,Lewis, S.M.,Hillebrand, R.,Singh, H.,Tanner, J.J.,Gates, K.S. Covalent Allosteric Inactivation of Protein Tyrosine Phosphatase 1B (PTP1B) by an Inhibitor-Electrophile Conjugate. Biochemistry, 56:2051-2060, 2017 Cited by PubMed: 28345882DOI: 10.1021/acs.biochem.7b00151 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.1001 Å) |
Structure validation
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