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.


1s3a

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 18: Line 18:
-->
-->
{{ABSTRACT_PUBMED_15341729}}
{{ABSTRACT_PUBMED_15341729}}
 +
 +
==Disease==
 +
Known disease associated with this structure: Leigh syndrome due to mitochondrial complex I deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602137 602137]]
==About this Structure==
==About this Structure==
-
1S3A is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1S3A OCA].
+
1S3A is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1S3A OCA].
==Reference==
==Reference==
-
The oxidized subunit B8 from human complex I adopts a thioredoxin fold., Brockmann C, Diehl A, Rehbein K, Strauss H, Schmieder P, Korn B, Kuhne R, Oschkinat H, Structure. 2004 Sep;12(9):1645-54. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15341729 15341729]
+
<ref group="xtra">PMID:15341729</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
-
[[Category: Single protein]]
 
[[Category: Brockmann, C.]]
[[Category: Brockmann, C.]]
[[Category: Diehl, A.]]
[[Category: Diehl, A.]]
Line 36: Line 38:
[[Category: Nmr]]
[[Category: Nmr]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 15:15:31 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 12:56:57 2009''

Revision as of 10:56, 16 February 2009

Template:STRUCTURE 1s3a

Contents

NMR Solution Structure of Subunit B8 from Human NADH-Ubiquinone Oxidoreductase Complex I (CI-B8)

Template:ABSTRACT PUBMED 15341729

Disease

Known disease associated with this structure: Leigh syndrome due to mitochondrial complex I deficiency OMIM:[602137]

About this Structure

1S3A is a 1 chain structure of sequence from Homo sapiens. Full experimental information is available from OCA.

Reference

  • Brockmann C, Diehl A, Rehbein K, Strauss H, Schmieder P, Korn B, Kuhne R, Oschkinat H. The oxidized subunit B8 from human complex I adopts a thioredoxin fold. Structure. 2004 Sep;12(9):1645-54. PMID:15341729 doi:http://dx.doi.org/10.1016/j.str.2004.06.021

Page seeded by OCA on Mon Feb 16 12:56:57 2009

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools