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3EPM

Crystal structure of Caulobacter crescentus ThiC

Summary for 3EPM
Entry DOI10.2210/pdb3epm/pdb
Related3EPN 3EPO
DescriptorThiamine biosynthesis protein thiC, ZINC ION, 4-AMINO-5-HYDROXYMETHYL-2-METHYLPYRIMIDINE, ... (5 entities in total)
Functional Keywordsalpha-beta barrel, sam superfamily, thiamine biosynthesis, biosynthetic protein
Biological sourceCaulobacter crescentus
Total number of polymer chains2
Total formula weight138072.79
Authors
Li, S.,Chatterjee, A.,Zhang, Y.,Grove, T.L.,Lee, M.,Krebs, C.,Booker, S.J.,Begley, T.P.,Ealick, S.E. (deposition date: 2008-09-29, release date: 2008-10-28, Last modification date: 2024-10-30)
Primary citationChatterjee, A.,Li, Y.,Zhang, Y.,Grove, T.L.,Lee, M.,Krebs, C.,Booker, S.J.,Begley, T.P.,Ealick, S.E.
Reconstitution of ThiC in thiamine pyrimidine biosynthesis expands the radical SAM superfamily
Nat.Chem.Biol., 4:758-765, 2008
Cited by
PubMed Abstract: 4-Amino-5-hydroxymethyl-2-methylpyrimidine phosphate (HMP-P) synthase catalyzes a complex rearrangement of 5-aminoimidazole ribonucleotide (AIR) to form HMP-P, the pyrimidine moiety of thiamine phosphate. We determined the three-dimensional structures of HMP-P synthase and its complexes with the product HMP-P and a substrate analog imidazole ribotide. The structure of HMP-P synthase reveals a homodimer in which each protomer comprises three domains: an N-terminal domain with a novel fold, a central (betaalpha)(8) barrel and a disordered C-terminal domain that contains a conserved CX(2)CX(4)C motif, which is suggestive of a [4Fe-4S] cluster. Biochemical studies have confirmed that HMP-P synthase is iron sulfur cluster-dependent, that it is a new member of the radical SAM superfamily and that HMP-P and 5'-deoxyadenosine are products of the reaction. Mössbauer and EPR spectroscopy confirm the presence of one [4Fe-4S] cluster. Structural comparisons reveal that HMP-P synthase is homologous to a group of adenosylcobalamin radical enzymes. This similarity supports an evolutionary relationship between these two superfamilies.
PubMed: 18953358
DOI: 10.1038/nchembio.121
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.793 Å)
Structure validation

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数据于2025-06-25公开中

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