Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
A new phenomenon has been detected in the time-resolved electron-nuclear double resonance (ENDOR) spectra of the spin-correlated radical pairs in photosynthetic reaction center proteins. The observed effects result from both increased resolution and orientational selectivity provided by high magnetic field EPR and are manifest as specific, derivative-type lines in the ENDOR spectrum. Importantly, the positions and amplitudes of these lines contain information on the interaction of a particular nucleus with both correlated electron spins. Thus, spin density delocalization in the protein environment between the donor and acceptor in the SCRP can be revealed via SCRP ENDOR, providing a unique opportunity to probe the electron-transfer pathways in natural and artificial photosynthetic assemblies.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/ja039309j | DOI Listing |
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