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. Author manuscript; available in PMC: 2012 May 1.
Published in final edited form as: FEMS Microbiol Rev. 2011 Jan 19;35(3):475–497. doi: 10.1111/j.1574-6976.2010.00259.x

Fig. 8. Crystal structure of AccD5 from M. tuberculosis.

Fig. 8

(A) The overall hexameric fold of AccD5 is similar to that of PccB. (B) The active site lies at the dimeric, di-domain interface. (C) A comparison of the active sites between PccB and AccD5 shows that AccD5 cannot accommodate a substrate larger than propionyl-CoA (Lin et al., 2006)