4J95
Crystal Structure of FGF Receptor 2 (FGFR2) Kinase Domain Harboring the Pathogenic K659N Mutation Responsible for an Unclassified Craniosynostosis Syndrome in Space Group C2.
Summary for 4J95
Entry DOI | 10.2210/pdb4j95/pdb |
Related | 2PSQ 2PVF 2PVY 4J96 4J97 4J98 4J99 |
Descriptor | Fibroblast growth factor receptor 2, PHOSPHOMETHYLPHOSPHONIC ACID ADENYLATE ESTER, SULFATE ION, ... (4 entities in total) |
Functional Keywords | kinase domain fold consisting of n- and c-lobes, receptor tyrosine kinase, atp binding, transferase |
Biological source | Homo sapiens (human) |
Cellular location | Cell membrane; Single-pass type I membrane protein. Isoform 1: Cell membrane; Single-pass type I membrane protein. Isoform 3: Cell membrane; Single-pass type I membrane protein. Isoform 14: Secreted. Isoform 19: Secreted: P21802 |
Total number of polymer chains | 4 |
Total formula weight | 151075.29 |
Authors | Chen, H.,Mohammadi, M. (deposition date: 2013-02-15, release date: 2013-08-07, Last modification date: 2023-09-20) |
Primary citation | Chen, H.,Huang, Z.,Dutta, K.,Blais, S.,Neubert, T.A.,Li, X.,Cowburn, D.,Traaseth, N.J.,Mohammadi, M. Cracking the Molecular Origin of Intrinsic Tyrosine Kinase Activity through Analysis of Pathogenic Gain-of-Function Mutations. Cell Rep, 4:376-384, 2013 Cited by PubMed: 23871672DOI: 10.1016/j.celrep.2013.06.025 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3767 Å) |
Structure validation
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