This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


1hjf

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 4: Line 4:
==Overview==
==Overview==
-
Deacetoxycephalosporin C synthase is an iron(II) 2-oxoglutaratedependent, oxygenase that catalyzes the oxidative ring-expansion of penicillin N to, deacetoxycephalosporin C. The wild-type enzyme is only able to efficiently, utilize 2-oxoglutarate and 2-oxoadipate as a 2-oxoacid co-substrate., Mutation of arginine 258, the side chain of which forms an electrostatic, interaction with the 5-carboxylate of the 2-oxoglutarate co-substrate, to, a glutamine residue reduced activity to about 5% of the wild-type enzyme, with 2-oxoglutarate. However, other aliphatic 2-oxoacids, which were not, co-substrates for the wild-type enzyme, were utilized by the R258Q mutant., These 2-oxoacids "rescued" catalytic activity to the level observed for, the wild-type enzyme as judged by penicillin N and G conversion. These, co-substrates underwent oxidative decarboxylation as observed for, 2-oxoglutarate in the normal reaction with the wild-type enzyme. Crystal, structures of the iron(II)- 2-oxo-3-methylbutanoate (1.5 A), and, iron(II)-2-oxo-4-methylpentanoate (1.6 A) enzyme complexes were obtained, which reveal the molecular basis for this "chemical co-substrate rescue", and help to rationalize the co-substrate selectivity of, 2-oxoglutaratedependent oxygenases.
+
Deacetoxycephalosporin C synthase is an iron(II) 2-oxoglutaratedependent oxygenase that catalyzes the oxidative ring-expansion of penicillin N to deacetoxycephalosporin C. The wild-type enzyme is only able to efficiently utilize 2-oxoglutarate and 2-oxoadipate as a 2-oxoacid co-substrate. Mutation of arginine 258, the side chain of which forms an electrostatic interaction with the 5-carboxylate of the 2-oxoglutarate co-substrate, to a glutamine residue reduced activity to about 5% of the wild-type enzyme with 2-oxoglutarate. However, other aliphatic 2-oxoacids, which were not co-substrates for the wild-type enzyme, were utilized by the R258Q mutant. These 2-oxoacids "rescued" catalytic activity to the level observed for the wild-type enzyme as judged by penicillin N and G conversion. These co-substrates underwent oxidative decarboxylation as observed for 2-oxoglutarate in the normal reaction with the wild-type enzyme. Crystal structures of the iron(II)- 2-oxo-3-methylbutanoate (1.5 A), and iron(II)-2-oxo-4-methylpentanoate (1.6 A) enzyme complexes were obtained, which reveal the molecular basis for this "chemical co-substrate rescue" and help to rationalize the co-substrate selectivity of 2-oxoglutaratedependent oxygenases.
==About this Structure==
==About this Structure==
Line 13: Line 13:
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Streptomyces clavuligerus]]
[[Category: Streptomyces clavuligerus]]
-
[[Category: Baldwin, J.E.]]
+
[[Category: Baldwin, J E.]]
-
[[Category: Clifton, I.J.]]
+
[[Category: Clifton, I J.]]
[[Category: Dubus, A.]]
[[Category: Dubus, A.]]
-
[[Category: Frere, J.M.]]
+
[[Category: Frere, J M.]]
[[Category: Harlos, K.]]
[[Category: Harlos, K.]]
-
[[Category: Lee, H.J.]]
+
[[Category: Lee, H J.]]
-
[[Category: Lloyd, M.D.]]
+
[[Category: Lloyd, M D.]]
-
[[Category: Schofield, C.J.]]
+
[[Category: Schofield, C J.]]
[[Category: COI]]
[[Category: COI]]
[[Category: FE2]]
[[Category: FE2]]
Line 29: Line 29:
[[Category: co-substrate selectivity]]
[[Category: co-substrate selectivity]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 09:49:33 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:01:55 2008''

Revision as of 11:01, 21 February 2008


1hjf, resolution 1.60Å

Drag the structure with the mouse to rotate

ALTERATION OF THE CO-SUBSTRATE SELECTIVITY OF DEACETOXYCEPHALOSPORIN C SYNTHASE: THE ROLE OF ARGININE-258

Overview

Deacetoxycephalosporin C synthase is an iron(II) 2-oxoglutaratedependent oxygenase that catalyzes the oxidative ring-expansion of penicillin N to deacetoxycephalosporin C. The wild-type enzyme is only able to efficiently utilize 2-oxoglutarate and 2-oxoadipate as a 2-oxoacid co-substrate. Mutation of arginine 258, the side chain of which forms an electrostatic interaction with the 5-carboxylate of the 2-oxoglutarate co-substrate, to a glutamine residue reduced activity to about 5% of the wild-type enzyme with 2-oxoglutarate. However, other aliphatic 2-oxoacids, which were not co-substrates for the wild-type enzyme, were utilized by the R258Q mutant. These 2-oxoacids "rescued" catalytic activity to the level observed for the wild-type enzyme as judged by penicillin N and G conversion. These co-substrates underwent oxidative decarboxylation as observed for 2-oxoglutarate in the normal reaction with the wild-type enzyme. Crystal structures of the iron(II)- 2-oxo-3-methylbutanoate (1.5 A), and iron(II)-2-oxo-4-methylpentanoate (1.6 A) enzyme complexes were obtained, which reveal the molecular basis for this "chemical co-substrate rescue" and help to rationalize the co-substrate selectivity of 2-oxoglutaratedependent oxygenases.

About this Structure

1HJF is a Single protein structure of sequence from Streptomyces clavuligerus with and as ligands. Known structural/functional Sites: and . Full crystallographic information is available from OCA.

Reference

Alteration of the co-substrate selectivity of deacetoxycephalosporin C synthase. The role of arginine 258., Lee HJ, Lloyd MD, Clifton IJ, Harlos K, Dubus A, Baldwin JE, Frere JM, Schofield CJ, J Biol Chem. 2001 May 25;276(21):18290-5. Epub 2001 Feb 21. PMID:11279000

Page seeded by OCA on Thu Feb 21 13:01:55 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools