1sd1

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==About this Structure==
==About this Structure==
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1SD1 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=1SD1 OCA].
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1SD1 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=1SD1 OCA].
==Reference==
==Reference==
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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]
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<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]]
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[[Category: Single protein]]
 
[[Category: Cornell, K A.]]
[[Category: Cornell, K A.]]
[[Category: Ealick, S E.]]
[[Category: Ealick, S E.]]
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[[Category: Purine salvage,formycin some]]
[[Category: Purine salvage,formycin some]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 17:26:00 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 12:58:15 2009''

Revision as of 10:58, 17 February 2009

Template:STRUCTURE 1sd1

STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE COMPLEXED WITH FORMYCIN A

Template:ABSTRACT PUBMED 15122881

About this Structure

1SD1 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • 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:http://dx.doi.org/10.1021/bi035492h

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