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Structure paper

TitlePotent, Selective Inhibitors of Protein Tyrosine Phosphatase 1B
Journal, issue, pagesBIOORG. MED. CHEM. LETT., Vol. 13, Page 1887-1890, Year 2003
Publish dateFeb 16, 2003 (structure data deposition date)
AuthorsXin, Z. / Oost, T.K. / Abad-Zapatero, C. / Hajduk, P.J. / Pei, Z. / Szczepankiewicz, B.G. / Hutchins, C.W. / Ballaron, S.J. / Stashko, M.A. / Lubben, T. ...Xin, Z. / Oost, T.K. / Abad-Zapatero, C. / Hajduk, P.J. / Pei, Z. / Szczepankiewicz, B.G. / Hutchins, C.W. / Ballaron, S.J. / Stashko, M.A. / Lubben, T. / Trevillyan, J.M. / Jirousek, M.R. / Liu, G.
External linksBIOORG. MED. CHEM. LETT. / PubMed:12749891
MethodsX-ray diffraction
Resolution2.4 Å
Structure data

PDB-1nz7:
POTENT, SELECTIVE INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B USING A SECOND PHOSPHOTYROSINE BINDING SITE, complexed with compound 19.
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

ChemComp-901:
2-[(4-{2-ACETYLAMINO-2-[4-(1-CARBOXY-3-METHYLSULFANYL-PROPYLCARBAMOYL)-BUTYLCARBAMOYL]-ETHYL}-2-ETHYL-PHENYL)-OXALYL-AM

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE / PROTEIN TYROSINE PHOSPHATASE FOLD / OXAMIC ACID INHIBITOR BOUND TO P-LOOP

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