1frq

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{{STRUCTURE_1frq| PDB=1frq | SCENE= }}
{{STRUCTURE_1frq| PDB=1frq | SCENE= }}
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'''FERREDOXIN:NADP+ OXIDOREDUCTASE (FERREDOXIN REDUCTASE) MUTANT E312A'''
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===FERREDOXIN:NADP+ OXIDOREDUCTASE (FERREDOXIN REDUCTASE) MUTANT E312A===
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==Overview==
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Ferredoxin-NADP+ reductase, the prototype of a large family of structurally related flavoenzymes, pairs single electrons carried by ferredoxin I and transfers them as a hydride to NADP+. Four mutants of the enzyme, in which Glu-312 was replaced with Asp, Gln, Leu, and Ala to probe the role of the residue charge, size, and polarity in the enzyme activity, have been heterologously expressed, purified, and characterized through steady-state, rapid kinetic studies, ligand-binding experiments, and three-dimensional structure determination by x-ray crystallography. The E312L mutant was the only one that was almost inactive (approximately 1%), whereas unexpectedly the E312A reductase was 10-100% active with the various acceptors tested. Rapid kinetic absorption spectroscopy studies demonstrated that flavin reduction by NADPH was impaired in the mutants. Furthermore, NADP(H) binding was partially perturbed. These functional and structural studies lead us to conclude that Glu-312 does not fulfil the role of proton donor during catalysis, but it is required for proper binding of the nicotinamide ring of NADP(H). In addition, its charge modulates the two one-electron redox potentials of the flavin to stabilize the semiquinone form.
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(as it appears on PubMed at http://www.pubmed.gov), where 9852055 is the PubMed ID number.
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{{ABSTRACT_PUBMED_9852055}}
==About this Structure==
==About this Structure==
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[[Category: Zanetti, G.]]
[[Category: Zanetti, G.]]
[[Category: Flavoprotein]]
[[Category: Flavoprotein]]
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Revision as of 00:50, 1 July 2008

Template:STRUCTURE 1frq

FERREDOXIN:NADP+ OXIDOREDUCTASE (FERREDOXIN REDUCTASE) MUTANT E312A

Template:ABSTRACT PUBMED 9852055

About this Structure

1FRQ is a Single protein structure of sequence from Spinacia oleracea. Full crystallographic information is available from OCA.

Reference

Probing the function of the invariant glutamyl residue 312 in spinach ferredoxin-NADP+ reductase., Aliverti A, Deng Z, Ravasi D, Piubelli L, Karplus PA, Zanetti G, J Biol Chem. 1998 Dec 18;273(51):34008-15. PMID:9852055

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