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Ligands
Code Name Style Show Link
994 4-(2-anilinopyridin-3-yl)-N-(3,4,5-trimethoxyphenyl)-1,3,5-triazin-2-amine
Non-standard Residues
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PTR O-phosphotyrosine
Glycosylation
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Modification
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Code : 2P2H   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE
Title : Crystal structure of the VEGFR2 kinase domain in complex with a pyridinyl-triazine inhibitor
Release Data : 2007-03-20
Compound :
mol_id molecule chains synonym
1 Vascular endothelial growth factor receptor 2 A VEGFR-2, Kinase insert domain receptor, Protein-tyrosine kinase receptor Flk-1, CD309 antigen
ec: 2.7.10.1
fragment: kinase domain
mutation: C817A, V916T, E990V, (delete 940-989)
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Trichoplusia ni  (taxid:7111)
gene: KDR, FLK1
expression_system_common: Cabbage looper
expression_system_vector_type: baculovirus
Authors : Whittington, D.A., Kim, J.L., Long, A.M., Rose, P., Gu, Y., Zhao, H.
Keywords : receptor tyrosine kinase, KDR, Transferase
Exp. method : X-RAY DIFFRACTION ( 1.950 Å )
Citation :

Evolution of a Highly Selective and Potent 2-(Pyridin-2-yl)-1,3,5-triazine Tie-2 Kinase Inhibitor

Hodous, B.L.,Geuns-Meyer, S.D.,Hughes, P.E.  et al.
(2007)  J.Med.Chem.  50 : 611 - 626

PubMed: 17253678
DOI: 10.1021/jm061107l

Chain : A
UniProt : P35968 (VGFR2_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-tyrosyl-[protein] = ADP + H(+) + O-phospho-L-tyrosyl- [protein] 2.7.10.1 PROSITE-ProRule:PRU10028, PubMed:10037737, PubMed:10102632
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