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7D73

Cryo-EM structure of GMPPA/GMPPB complex bound to GTP (State I)

Summary for 7D73
Entry DOI10.2210/pdb7d73/pdb
EMDB information30600
DescriptorMannose-1-phosphate guanyltransferase alpha, Mannose-1-phosphate guanyltransferase beta, GUANOSINE-5'-DIPHOSPHATE-ALPHA-D-MANNOSE, ... (4 entities in total)
Functional Keywordsgmppa, gmppb, gdp-mannose homeostasis, cell cycle, transferase
Biological sourceHomo sapiens (Human)
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Total number of polymer chains12
Total formula weight510836.85
Authors
Zheng, L.,Liu, Z.,Wang, Y.,Yang, F.,Wang, J.,Qing, J.,Cai, X.,Mo, X.,Gao, N.,Jia, D. (deposition date: 2020-10-02, release date: 2021-05-05, Last modification date: 2021-12-01)
Primary citationZheng, L.,Liu, Z.,Wang, Y.,Yang, F.,Wang, J.,Huang, W.,Qin, J.,Tian, M.,Cai, X.,Liu, X.,Mo, X.,Gao, N.,Jia, D.
Cryo-EM structures of human GMPPA-GMPPB complex reveal how cells maintain GDP-mannose homeostasis.
Nat.Struct.Mol.Biol., 28:1-12, 2021
Cited by
PubMed Abstract: GDP-mannose (GDP-Man) is a key metabolite essential for protein glycosylation and glycophosphatidylinositol anchor synthesis, and aberrant cellular GDP-Man levels have been associated with multiple human diseases. How cells maintain homeostasis of GDP-Man is unknown. Here, we report the cryo-EM structures of human GMPPA-GMPPB complex, the protein machinery responsible for GDP-Man synthesis, in complex with GDP-Man or GTP. Unexpectedly, we find that the catalytically inactive subunit GMPPA displays a much higher affinity to GDP-Man than the active subunit GMPPB and, subsequently, inhibits the catalytic activity of GMPPB through a unique C-terminal loop of GMPPA. Importantly, disruption of the interactions between GMPPA and GMPPB or the binding of GDP-Man to GMPPA in zebrafish leads to abnormal brain development and muscle abnormality, analogous to phenotypes observed in individuals carrying GMPPA or GMPPB mutations. We conclude that GMPPA acts as a cellular sensor to maintain mannose homeostasis through allosterically regulating GMPPB.
PubMed: 33986552
DOI: 10.1038/s41594-021-00591-9
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3 Å)
Structure validation

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