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1H6Q

Translationally Controlled Tumor-associated Protein p23fyp from Schizosaccharomyces pombe

Summary for 1H6Q
Entry DOI10.2210/pdb1h6q/pdb
Related1H7Y
NMR InformationBMRB: 4447
DescriptorTRANSLATIONALLY CONTROLLED TUMOR PROTEIN (1 entity in total)
Functional Keywordstumor-associated protein, function unknown
Biological sourceSCHIZOSACCHAROMYCES POMBE (FISSION YEAST)
Cellular locationCytoplasm : Q10344
Total number of polymer chains1
Total formula weight19066.47
Authors
Thaw, P.,Baxter, N.J.,Sedelnikova, S.E.,Price, C.,Waltho, J.P.,Craven, C.J. (deposition date: 2001-06-20, release date: 2001-08-09, Last modification date: 2024-05-15)
Primary citationThaw, P.,Baxter, N.J.,Hounslow, A.M.,Price, C.,Waltho, J.P.,Craven, C.J.
Structure of TCTP reveals unexpected relationship with guanine nucleotide-free chaperones.
Nat. Struct. Biol., 8:701-704, 2001
Cited by
PubMed Abstract: The translationally controlled tumor-associated proteins (TCTPs) are a highly conserved and abundantly expressed family of eukaryotic proteins that are implicated in both cell growth and the human acute allergic response but whose intracellular biochemical function has remained elusive. We report here the solution structure of the TCTP from Schizosaccharomyces pombe, which, on the basis of sequence homology, defines the fold of the entire family. We show that TCTPs form a structural superfamily with the Mss4/Dss4 family of proteins, which bind to the GDP/GTP free form of Rab proteins (members of the Ras superfamily) and have been termed guanine nucleotide-free chaperones (GFCs). Mss4 also acts as a relatively inefficient guanine nucleotide exchange factor (GEF). We further show that the Rab protein binding site on Mss4 coincides with the region of highest sequence conservation in the TCTP family. This is the first link to any other family of proteins that has been established for the TCTP family and suggests the presence of a GFC/GEF at extremely high abundance in eukaryotic cells.
PubMed: 11473261
DOI: 10.1038/90415
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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