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1g1b

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{{STRUCTURE_1g1b| PDB=1g1b | SCENE= }}
{{STRUCTURE_1g1b| PDB=1g1b | SCENE= }}
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'''CHORISMATE LYASE (WILD-TYPE) WITH BOUND PRODUCT'''
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===CHORISMATE LYASE (WILD-TYPE) WITH BOUND PRODUCT===
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==Overview==
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The enzyme chorismate lyase (CL) catalyzes the removal of pyruvate from chorismate to produce 4-hydroxy benzoate (4HB) for the ubiquinone pathway. In Escherichia coli, CL is monomeric, with 164 residues. We have determined the structure of the CL product complex by crystallographic heavy-atom methods and report the structure at 1.4-A resolution for a fully active double Cys-to-Ser mutant and at 2.0-A resolution for the wild-type. The fold involves a 6-stranded antiparallel beta-sheet with no spanning helices and novel connectivity. The product is bound internally, adjacent to the sheet, with its polar groups coordinated by two main-chain amides and by the buried side-chains of Arg 76 and Glu 155. The 4HB is completely sequestered from solvent in a largely hydrophobic environment behind two helix-turn-helix loops. The extensive product binding that is observed is consistent with biochemical measurements of slow product release and 10-fold stronger binding of product than substrate. Substrate binding and kinetically rate-limiting product release apparently require the rearrangement of these active-site-covering loops. Implications for the biological function of the high product binding are considered in light of the unique cellular role of 4HB, which is produced by cytoplasmic CL but is used by the membrane-bound enzyme 4HB octaprenyltransferase.
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(as it appears on PubMed at http://www.pubmed.gov), where 11455603 is the PubMed ID number.
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{{ABSTRACT_PUBMED_11455603}}
==About this Structure==
==About this Structure==
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[[Category: Mayhew, M.]]
[[Category: Mayhew, M.]]
[[Category: Vilker, V L.]]
[[Category: Vilker, V L.]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 17:00:30 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 1 04:15:20 2008''

Revision as of 01:15, 1 July 2008

Image:1g1b.png

Template:STRUCTURE 1g1b

CHORISMATE LYASE (WILD-TYPE) WITH BOUND PRODUCT

Template:ABSTRACT PUBMED 11455603

About this Structure

1G1B is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.

Reference

The crystal structure of chorismate lyase shows a new fold and a tightly retained product., Gallagher DT, Mayhew M, Holden MJ, Howard A, Kim KJ, Vilker VL, Proteins. 2001 Aug 15;44(3):304-11. PMID:11455603

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