This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
2cr3
From Proteopedia
Solution structure of the first Ig-like domain of human fibroblast growth factor receptor 1
Disease
Known disease associated with this structure: Antley-Bixler syndrome OMIM:[136350], Hypogonadotropic hypogonadism OMIM:[136350], Jackson-Weiss syndrome OMIM:[136350], Kallmann syndrome 2 OMIM:[136350], Osteoglophonic dysplasia OMIM:[136350], Pfeiffer syndrome OMIM:[136350], Trigonocephaly OMIM:[136350]
About this Structure
2CR3 is a 1 chain structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Page seeded by OCA on Tue Feb 17 21:53:01 2009
Categories: Homo sapiens | Transferase | Hatta, R. | Hayashi, F. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Yokoyama, S. | Yoshida, M. | Bfgf-r | Fgfr1 | Ig fold | National project on protein structural and functional analyse | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomic
