2q9f

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(New page: '''Unreleased structure''' The entry 2q9f is ON HOLD until Jun 12 2009 Authors: White, M.A., Mast, N.V., Johnson, E.F., Stout, C.D., Pikuleva, I.A. Description: Crystal structure of hu...)
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'''Unreleased structure'''
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[[Image:2q9f.jpg|left|200px]]
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The entry 2q9f is ON HOLD until Jun 12 2009
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{{STRUCTURE_2q9f| PDB=2q9f | SCENE= }}
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Authors: White, M.A., Mast, N.V., Johnson, E.F., Stout, C.D., Pikuleva, I.A.
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'''Crystal structure of human cytochrome P450 46A1 in complex with cholesterol-3-sulphate'''
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Description: Crystal structure of human cytochrome P450 46A1 in complex with cholestrol-3-sulphate
 
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==Overview==
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Human cytochrome P450 46A1 (CYP46A1) is one of the key enzymes in cholesterol homeostasis in the brain. The crystallization and heavy-atom structure solution of an active truncated CYP46A1 in complex with the high-affinity substrate analogue cholesterol-3-sulfate (CH-3S) is reported. The 2.6 angstroms structure of CYP46A1-CH-3S was solved using both anion and cation heavy-atom salts. In addition to the native anomalous signal from the haem iron, an NaI anion halide salt derivative and a complementary CsCl alkali-metal cation salt derivative were used. The general implications of the use of halide and alkali-metal quick soaks are discussed. The importance of using isoionic strength buffers, the titration of heavy-atom salts into different ionic species and the role of concentration are considered. It was observed that cation/anion-binding sites will occasionally overlap, which could negatively impact upon mixed RbBr soaks used for multiple anomalous scatterer MAD (MMAD). The use of complementary cation and anion heavy-atom salt derivatives is a convenient and powerful tool for MIR(AS) structure solution.
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 11 08:37:10 2008''
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==About this Structure==
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2Q9F is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Q9F OCA].
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==Reference==
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Use of complementary cation and anion heavy-atom salt derivatives to solve the structure of cytochrome P450 46A1., White MA, Mast N, Bjorkhem I, Johnson EF, Stout CD, Pikuleva IA, Acta Crystallogr D Biol Crystallogr. 2008 May;64(Pt 5):487-95. Epub 2008, Apr 19. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18453684 18453684]
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[[Category: Cholesterol 24-hydroxylase]]
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[[Category: Homo sapiens]]
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[[Category: Single protein]]
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[[Category: Johnson, E F.]]
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[[Category: Mast, N V.]]
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[[Category: Pikuleva, I A.]]
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[[Category: Stout, C D.]]
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[[Category: White, M A.]]
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[[Category: Cholesterol metabolic enzyme]]
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[[Category: Cholesterol-3-sulphate]]
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[[Category: Cyp46a1]]
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[[Category: Heme]]
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[[Category: Monooxygenase]]
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[[Category: Oxidoreductase]]
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[[Category: P450]]
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[[Category: P450 46a1]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 18 12:03:06 2008''

Revision as of 09:03, 18 June 2008

Template:STRUCTURE 2q9f

Crystal structure of human cytochrome P450 46A1 in complex with cholesterol-3-sulphate


Overview

Human cytochrome P450 46A1 (CYP46A1) is one of the key enzymes in cholesterol homeostasis in the brain. The crystallization and heavy-atom structure solution of an active truncated CYP46A1 in complex with the high-affinity substrate analogue cholesterol-3-sulfate (CH-3S) is reported. The 2.6 angstroms structure of CYP46A1-CH-3S was solved using both anion and cation heavy-atom salts. In addition to the native anomalous signal from the haem iron, an NaI anion halide salt derivative and a complementary CsCl alkali-metal cation salt derivative were used. The general implications of the use of halide and alkali-metal quick soaks are discussed. The importance of using isoionic strength buffers, the titration of heavy-atom salts into different ionic species and the role of concentration are considered. It was observed that cation/anion-binding sites will occasionally overlap, which could negatively impact upon mixed RbBr soaks used for multiple anomalous scatterer MAD (MMAD). The use of complementary cation and anion heavy-atom salt derivatives is a convenient and powerful tool for MIR(AS) structure solution.

About this Structure

2Q9F is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Use of complementary cation and anion heavy-atom salt derivatives to solve the structure of cytochrome P450 46A1., White MA, Mast N, Bjorkhem I, Johnson EF, Stout CD, Pikuleva IA, Acta Crystallogr D Biol Crystallogr. 2008 May;64(Pt 5):487-95. Epub 2008, Apr 19. PMID:18453684 Page seeded by OCA on Wed Jun 18 12:03:06 2008

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