A Rich Man, Poor Man Story of S-Adenosylmethionine and Cobalamin Revisited

被引:41
作者
Bridwell-Rabb, Jennifer [1 ,2 ,3 ,4 ]
Grell, Tsehai A. J. [2 ]
Drennan, Catherine L. [1 ,2 ,3 ]
机构
[1] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
[2] MIT, Dept Chem, Cambridge, MA 02139 USA
[3] MIT, Dept Biol, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 87 | 2018年 / 87卷
关键词
S-adenosylmethionine; cobalamin; Fe-S cluster; metalloprotein; radical chemistry; methylation; RADICAL SAM ENZYME; DEPENDENT METHIONINE SYNTHASE; X-RAY-STRUCTURE; LYASE ACTIVATING ENZYME; SPORE-PHOTOPRODUCT-LYASE; ESCHERICHIA-COLI; LYSINE 2,3-AMINOMUTASE; CRYSTAL-STRUCTURE; SULFUR INSERTION; LIPOYL SYNTHASE;
D O I
10.1146/annurev-biochem-062917-012500
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
S-adenosylmethionine (AdoMet) has been referred to as both "a poor man's adenosylcobalamin (AdoCbl)" and "a rich man's AdoCbl," but today, with the ever-increasing number of functions attributed to each cofactor, both appear equally rich and surprising. The recent characterization of an organometallic species in an AdoMet radical enzyme suggests that the line that differentiates them in nature will be constantly challenged. Here, we compare and contrast AdoMet and cobalamin (Cbl) and consider why Cbl-dependent AdoMet radical enzymes require two cofactors that are so similar in their reactivity. We further carry out structural comparisons employing the recently determined crystal structure of oxetanocin-A biosynthetic enzyme OxsB, the first three-dimensional structural data on a Cbl-dependent AdoMet radical enzyme. We find that the structural motifs responsible for housing the AdoMet radical machinery are largely conserved, whereas the motifs responsible for binding additional cofactors are much more varied.
引用
收藏
页码:555 / 584
页数:30
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