6P7K

Structure of HMG-CoA reductase from Burkholderia cenocepacia

Summary for 6P7K

• Entry DOI: 10.2210/pdb6p7k/pdb
• Descriptor: 3-hydroxy-3-methylglutaryl coenzyme A reductase, ADENOSINE-5'-DIPHOSPHATE, COENZYME A, ... (4 entities in total)
• Functional Keywords: hmg-coa, mevalonate, morpheein, reductase, oxidoreductase
• Biological source: Burkholderia cenocepacia
• Total number of polymer chains: 1
• Total formula weight: 48506.67

Authors

Walker, A.M.,Peacock, R.B.,Hicks, C.W.,Dewing, S.M.,Lewis, K.M.,Abboud, J.,Stewart, S.W.A.,Kang, C.,Watson, J.M. (deposition date: 2019-06-05, release date: 2020-04-08, Last modification date: 2023-10-11)

Primary citation

Peacock, R.B.,Hicks, C.W.,Walker, A.M.,Dewing, S.M.,Lewis, K.M.,Abboud, J.C.,Stewart, S.W.A.,Kang, C.,Watson, J.M.
Structural and Functional Characterization of Dynamic Oligomerization in Burkholderia cenocepacia HMG-CoA Reductase.
Biochemistry, 58:3960-3970, 2019

PubMed Abstract: The enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase (HMGR), in most organisms, catalyzes the four-electron reduction of the thioester ()-HMG-CoA to the primary alcohol ()-mevalonate, utilizing NADPH as the hydride donor. In some organisms, including the opportunistic lung pathogen , it catalyzes the reverse reaction, utilizing NAD as a hydride acceptor in the oxidation of mevalonate. HMGR has been previously shown to exist as an ensemble of multiple non-additive oligomeric states, each with different levels of enzymatic activity, suggesting that the enzyme exhibits characteristics of the morpheein model of allostery. We have characterized a number of factors, including pH, substrate concentration, and enzyme concentration, that modulate the structural transitions that influence the interconversion among the multiple oligomers. We have also determined the crystal structure of HMGR in the hexameric state bound to coenzyme A and ADP. This hexameric assembly provides important clues about how the transition among oligomers might occur, and why HMGR, unique among characterized HMGRs, exhibits morpheein-like behavior.

PubMed: 31469273
DOI: 10.1021/acs.biochem.9b00494

Experimental method

X-RAY DIFFRACTION (1.722 Å)