Title of article :
Crystal structure of activated ribulose-1,5-bisphosphate carboxylase/oxygenase from green alga Chlamydomonas reinhardtii complexed with 2-carboxyarabinitol-1,5-bisphosphate
Author/Authors :
Eiichi Mizohata، نويسنده , , Hiroyoshi Matsumura، نويسنده , , Yousuke Okano، نويسنده , , Maki Kumei، نويسنده , , Hiroki Takuma، نويسنده , , Jun Onodera، نويسنده , , Ko Kato، نويسنده , , Naoki Shibata، نويسنده , , Tsuyoshi Inoue، نويسنده , , Akiho Yokota، نويسنده , , Yasushi Kai، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2002
Pages :
13
From page :
679
To page :
691
Abstract :
Ribulose-1,5-bisphosphate carboxylase/oxygenase (rubisco) catalyzes the initial steps of photosynthetic carbon reduction and photorespiratory carbon oxidation cycles by combining CO2 and O2, respectively, with ribulose-1,5-bisphosphate. Many photosynthetic organisms have form I rubiscos comprised of eight large (L) and eight small (S) subunits. The crystal structure of the complex of activated rubisco from the green alga Chlamydomonas reinhardtii and the reaction intermediate analogue 2-carboxyarabinitol-1,5-bisphosphate (2-CABP) has been solved at 1.84 Å resolution (Rcryst of 15.2 % and Rfree of 18.1 %). The subunit arrangement of Chlamydomonas rubisco is the same as those of the previously solved form I rubiscos. Especially, the present structure is very similar to the activated spinach structure complexed with 2-CABP in the L-subunit folding and active-site conformation, but differs in S-subunit folding. The central insertion of the Chlamydomonas S-subunit forms the longer βA-βB loop that protrudes deeper into the solvent channel of rubisco than higher plant, cyanobacterial, and red algal (red-like) βA-βB loops. The C-terminal extension of the Chlamydomonas S-subunit does not protrude into the solvent channel, unlike that of the red algal S-subunit, but lies on the protein surface anchored by interactions with the N-terminal region of the S-subunit. Further, the present high-resolution structure has revealed novel post-translational modifications. Residue 1 of the S-subunit is Nα-methylmethionine, residues 104 and 151 of the L-subunit are 4-hydroxyproline, and residues 256 and 369 of the L-subunit are Sγ-methylcysteine. Furthermore, the unusual electron density of residue 471 of the L-subunit, which has been deduced to be threonine from the genomic DNA sequence, suggests that the residue is isoleucine produced by RNA editing or Oγ-methylthreonine.
Keywords :
Chlamydomonas reinhardtii , post-translational modification , Photosynthesis , RUBISCO , X-ray crystal structure
Journal title :
Journal of Molecular Biology
Serial Year :
2002
Journal title :
Journal of Molecular Biology
Record number :
1241491
Link To Document :
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