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Summary Structural Experimental Function Sequence Neighbor Download Link


<Asymmetric unit>
= <Biological unit>

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PDB ID2osc  sequence information (FASTA format)   
RELATED PDB ID2oo8
DescriptorTie-2
TitleSynthesis, Structural Analysis, and SAR Studies of Triazine Derivatives as Potent, Selective Tie-2 Inhibitors
Functional KeywordsKinase domain Tie-2, Transferase
Biological sourceHomo sapiens (human)
Cellular location [UNP - Q02763] Membrane; Single-pass type I membrane protein
Organ source [UNP - Q02763] Placenta
Total number of polymer chains1
Total molecular weight36703 (the details in Structural Details Page)
AuthorsBellon, S.F. , Kim, J. (deposition date : 2007-02-05, release date : 2007-03-20)
Primary citationHodous, B.L. , Geuns-Meyer, S.D. , Hughes, P.E. , Albrecht, B.K. , Bellon, S. , Caenepeel, S. , Cee, V.J. , Chaffee, S.C. , Emery, M. , Fretland, J. , Gallant, P. , Gu, Y. , Johnson, R.E. , Kim, J.L. , Long, A.M. , Morrison, M. , Olivieri, P.R. , Patel, V.F. , Polverino, A. , Rose, P. , Wang, L. , Zhao, H.
Synthesis, structural analysis, and SAR studies of triazine derivatives as potent, selective Tie-2 inhibitors.
Bioorg.Med.Chem.Lett., 17:2886 - 2889, 2007.(PubMed : 17350837)  (DOI: 10.1016/j.bmcl.2007.02.067)
Experimental methodX-RAY DIFFRACTION ( 2.8[Å] )
Other Database Information
Yorodumi , CATH , CE , FSSP , SCOP , VAST , UniProt ( Q02763 ) , eF-site , KEGG ( EC 2.7.10.1 ) , PISA