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3I3S

Crystal Structure of H-Ras with Thr50 replaced by Isoleucine

Summary for 3I3S
Entry DOI10.2210/pdb3i3s/pdb
DescriptorGTPase HRas, PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER, MAGNESIUM ION, ... (5 entities in total)
Functional Keywordsgtpases, h-ras, noonan syndrome, cell membrane, disease mutation, golgi apparatus, gtp-binding, lipoprotein, membrane, methylation, nucleotide-binding, palmitate, prenylation, proto-oncogene, s-nitrosylation, signaling protein
Biological sourceHomo sapiens (human)
Cellular locationCell membrane; Lipid-anchor; Cytoplasmic side: P01112
Total number of polymer chains1
Total formula weight19522.44
Authors
Gremer, L.,Dvorsky, R.,Merbitz-Zahradnik, T.,Wittinghofer, A.,Ahmadian, M.R. (deposition date: 2009-06-30, release date: 2009-12-22, Last modification date: 2023-09-06)
Primary citationCirstea, I.C.,Kutsche, K.,Dvorsky, R.,Gremer, L.,Carta, C.,Horn, D.,Roberts, A.E.,Lepri, F.,Merbitz-Zahradnik, T.,Konig, R.,Kratz, C.P.,Pantaleoni, F.,Dentici, M.L.,Joshi, V.A.,Kucherlapati, R.S.,Mazzanti, L.,Mundlos, S.,Patton, M.A.,Silengo, M.C.,Rossi, C.,Zampino, G.,Digilio, C.,Stuppia, L.,Seemanova, E.,Pennacchio, L.A.,Gelb, B.D.,Dallapiccola, B.,Wittinghofer, A.,Ahmadian, M.R.,Tartaglia, M.,Zenker, M.
A restricted spectrum of NRAS mutations causes Noonan syndrome.
Nat.Genet., 42:27-29, 2010
Cited by
PubMed: 19966803
DOI: 10.1038/ng.497
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.36 Å)
Structure validation

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