1nl9: Difference between revisions
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[[Image:1nl9.png|left|200px]] | [[Image:1nl9.png|left|200px]] | ||
{{STRUCTURE_1nl9| PDB=1nl9 | SCENE= }} | {{STRUCTURE_1nl9| PDB=1nl9 | SCENE= }} | ||
===Potent, Selective Protein Tyrosine Phosphatase 1B Inhibitor Compound 12 Using a Linked-Fragment Strategy=== | ===Potent, Selective Protein Tyrosine Phosphatase 1B Inhibitor Compound 12 Using a Linked-Fragment Strategy=== | ||
{{ABSTRACT_PUBMED_12670229}} | {{ABSTRACT_PUBMED_12670229}} | ||
==About this Structure== | ==About this Structure== | ||
[[1nl9]] is a 1 chain structure of [[Proten tyrosine phosphatase]] and [[Tyrosine phosphatase]] with 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=1NL9 OCA]. | |||
==See Also== | |||
*[[Proten tyrosine phosphatase|Proten tyrosine phosphatase]] | |||
*[[Tyrosine phosphatase|Tyrosine phosphatase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:012670229</ref><ref group="xtra">PMID:015258570</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Protein-tyrosine-phosphatase]] | [[Category: Protein-tyrosine-phosphatase]] | ||
| Line 42: | Line 34: | ||
[[Category: Xin, Z.]] | [[Category: Xin, Z.]] | ||
[[Category: Dual-site oxamic acid inhibitor bound to p-loop]] | [[Category: Dual-site oxamic acid inhibitor bound to p-loop]] | ||
[[Category: Hydrolase]] | |||
[[Category: Protein tyrosine phosphatase fold]] | [[Category: Protein tyrosine phosphatase fold]] | ||
Revision as of 14:57, 25 July 2012
Potent, Selective Protein Tyrosine Phosphatase 1B Inhibitor Compound 12 Using a Linked-Fragment StrategyPotent, Selective Protein Tyrosine Phosphatase 1B Inhibitor Compound 12 Using a Linked-Fragment Strategy
Template:ABSTRACT PUBMED 12670229
About this StructureAbout this Structure
1nl9 is a 1 chain structure of Proten tyrosine phosphatase and Tyrosine phosphatase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See AlsoSee Also
ReferenceReference
- ↑ Szczepankiewicz BG, Liu G, Hajduk PJ, Abad-Zapatero C, Pei Z, Xin Z, Lubben TH, Trevillyan JM, Stashko MA, Ballaron SJ, Liang H, Huang F, Hutchins CW, Fesik SW, Jirousek MR. Discovery of a potent, selective protein tyrosine phosphatase 1B inhibitor using a linked-fragment strategy. J Am Chem Soc. 2003 Apr 9;125(14):4087-96. PMID:12670229 doi:10.1021/ja0296733
- ↑ Wiesmann C, Barr KJ, Kung J, Zhu J, Erlanson DA, Shen W, Fahr BJ, Zhong M, Taylor L, Randal M, McDowell RS, Hansen SK. Allosteric inhibition of protein tyrosine phosphatase 1B. Nat Struct Mol Biol. 2004 Aug;11(8):730-7. Epub 2004 Jul 18. PMID:15258570 doi:10.1038/nsmb803
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- Homo sapiens
- Protein-tyrosine-phosphatase
- Abad-Zapatero, C.
- Ballaron, S J.
- Fesik, S W.
- Hajduk, P J.
- Huang, F.
- Hutchins, C W.
- Jirousek, M R.
- Liang, H.
- Liu, G.
- Lubben, T.
- Pei, Z.
- Stashko, M A.
- Szczepankiewicz, B G.
- Trevillyan, J M.
- Xin, Z.
- Dual-site oxamic acid inhibitor bound to p-loop
- Hydrolase
- Protein tyrosine phosphatase fold