1sd2: Difference between revisions

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==About this Structure==
==About this Structure==
1SD2 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=1SD2 OCA].  
1SD2 is a 1 chain 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=1SD2 OCA].  


==Reference==
==Reference==
Structural comparison of MTA phosphorylase and MTA/AdoHcy nucleosidase explains substrate preferences and identifies regions exploitable for inhibitor design., Lee JE, Settembre EC, Cornell KA, Riscoe MK, Sufrin JR, Ealick SE, Howell PL, Biochemistry. 2004 May 11;43(18):5159-69. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15122881 15122881]
<ref group="xtra">PMID:15122881</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: S-methyl-5-thioadenosine phosphorylase]]
[[Category: S-methyl-5-thioadenosine phosphorylase]]
[[Category: Single protein]]
[[Category: Cornell, K A.]]
[[Category: Cornell, K A.]]
[[Category: Ealick, S E.]]
[[Category: Ealick, S E.]]
Line 40: Line 39:
[[Category: Sulfate]]
[[Category: Sulfate]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 11:56:41 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 08:31:03 2009''

Revision as of 06:31, 17 February 2009

File:1sd2.png

Template:STRUCTURE 1sd2

STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE COMPLEXED WITH 5'-METHYLTHIOTUBERCIDIN

Template:ABSTRACT PUBMED 15122881

About this Structure

1SD2 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  1. Lee JE, Settembre EC, Cornell KA, Riscoe MK, Sufrin JR, Ealick SE, Howell PL. Structural comparison of MTA phosphorylase and MTA/AdoHcy nucleosidase explains substrate preferences and identifies regions exploitable for inhibitor design. Biochemistry. 2004 May 11;43(18):5159-69. PMID:15122881 doi:https://dx.doi.org/10.1021/bi035492h

Page seeded by OCA on Tue Feb 17 08:31:03 2009

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