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The effect of ring currents on carbon chemical shifts in cytochromes
Calculations suggest that some carbon chemical shifts in proteins should have large ring current shifts (> 1 ppm). We present 13C, 15N and 1H assignments for cytochrome C2 from Rhodospirillum rubrum, compare these with shifts for other cytochromes c, and show that the calculated ring current shif...
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Published in: | Journal of biomolecular NMR 1997-06, Vol.9 (4), p.389-395 |
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container_title | Journal of biomolecular NMR |
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creator | Blanchard, L Hunter, C N Williamson, M P |
description | Calculations suggest that some carbon chemical shifts in proteins should have large ring current shifts (> 1 ppm). We present 13C, 15N and 1H assignments for cytochrome C2 from Rhodospirillum rubrum, compare these with shifts for other cytochromes c, and show that the calculated ring current shifts are similar to experimentally observed shifts, but that there remain substantial conformation-dependent shifts of side-chain carbons. Ring current shifts as large as 6 ppm are observed. We show that the ring current effects do not seriously affect the Chemical Shift Index method for delineating secondary structure, but may have an impact on more precise methods for generating structural constraints. |
doi_str_mv | 10.1023/A:1018394410613 |
format | article |
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We show that the ring current effects do not seriously affect the Chemical Shift Index method for delineating secondary structure, but may have an impact on more precise methods for generating structural constraints.</description><identifier>ISSN: 0925-2738</identifier><identifier>EISSN: 1573-5001</identifier><identifier>DOI: 10.1023/A:1018394410613</identifier><identifier>PMID: 9255943</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Amino Acid Sequence ; Bacterial Proteins - chemistry ; Carbon Isotopes ; Cytochrome c Group - chemistry ; Cytochromes c2 ; Hydrogen - chemistry ; Magnetic Resonance Spectroscopy - methods ; Molecular Sequence Data ; Nitrogen Isotopes ; NMR ; Nuclear magnetic resonance ; Protein Structure, Secondary ; Rhodospirillum rubrum - chemistry ; Species Specificity</subject><ispartof>Journal of biomolecular NMR, 1997-06, Vol.9 (4), p.389-395</ispartof><rights>Kluwer Academic Publishers 1997</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c279t-5a74320021b8446edeefdb6584810fd4fd2b5092df6debd12246ff4ef25ffc953</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9255943$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blanchard, L</creatorcontrib><creatorcontrib>Hunter, C N</creatorcontrib><creatorcontrib>Williamson, M P</creatorcontrib><title>The effect of ring currents on carbon chemical shifts in cytochromes</title><title>Journal of biomolecular NMR</title><addtitle>J Biomol NMR</addtitle><description>Calculations suggest that some carbon chemical shifts in proteins should have large ring current shifts (> 1 ppm). 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language | eng |
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subjects | Amino Acid Sequence Bacterial Proteins - chemistry Carbon Isotopes Cytochrome c Group - chemistry Cytochromes c2 Hydrogen - chemistry Magnetic Resonance Spectroscopy - methods Molecular Sequence Data Nitrogen Isotopes NMR Nuclear magnetic resonance Protein Structure, Secondary Rhodospirillum rubrum - chemistry Species Specificity |
title | The effect of ring currents on carbon chemical shifts in cytochromes |
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