1n94: Difference between revisions

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|PDB= 1n94 |SIZE=350|CAPTION= <scene name='initialview01'>1n94</scene>, resolution 3.50&Aring;
|PDB= 1n94 |SIZE=350|CAPTION= <scene name='initialview01'>1n94</scene>, resolution 3.50&Aring;
|SITE=  
|SITE=  
|LIGAND= <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>, <scene name='pdbligand=HFP:ALPHA-HYDROXYFARNESYLPHOSPHONIC+ACID'>HFP</scene> and <scene name='pdbligand=TIN:2-{(5-{[BUTYL-(2-CYCLOHEXYL-ETHYL)-AMINO]-METHYL}-2&#39;-METHYL-BIPHENYL-2-CARBONYL)-AMINO]-4-METHYLSULFANYL-BUTYRIC ACID'>TIN</scene>
|LIGAND= <scene name='pdbligand=HFP:ALPHA-HYDROXYFARNESYLPHOSPHONIC+ACID'>HFP</scene>, <scene name='pdbligand=TIN:2-{(5-{[BUTYL-(2-CYCLOHEXYL-ETHYL)-AMINO]-METHYL}-2&#39;-METHYL-BIPHENYL-2-CARBONYL)-AMINO]-4-METHYLSULFANYL-BUTYRIC+ACID'>TIN</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
|ACTIVITY=  
|ACTIVITY=  
|GENE=  
|GENE=  
|DOMAIN=
|RELATEDENTRY=[[1n95|1N95]], [[1n9a|1N9A]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1n94 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1n94 OCA], [http://www.ebi.ac.uk/pdbsum/1n94 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1n94 RCSB]</span>
}}
}}


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[[Category: Sullivan, G M.]]
[[Category: Sullivan, G M.]]
[[Category: Wang, W.]]
[[Category: Wang, W.]]
[[Category: HFP]]
[[Category: TIN]]
[[Category: ZN]]
[[Category: farnesyltransferase]]
[[Category: farnesyltransferase]]
[[Category: prenyltransferase]]
[[Category: prenyltransferase]]


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Revision as of 22:27, 30 March 2008

File:1n94.gif


PDB ID 1n94

Drag the structure with the mouse to rotate
, resolution 3.50Å
Ligands: , ,
Related: 1N95, 1N9A


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Aryl Tetrahydropyridine Inhbitors of Farnesyltransferase: Glycine, Phenylalanine and Histidine Derivates


OverviewOverview

Inhibitors of farnesyltransferase are effective against a variety of tumors in mouse models of cancer. Clinical trials to evaluate these agents in humans are ongoing. In our effort to develop new farnesyltransferase inhibitors, we have discovered a series of aryl tetrahydropyridines that incorporate substituted glycine, phenylalanine and histidine residues. The design, synthesis, SAR and biological properties of these compounds will be discussed.

About this StructureAbout this Structure

1N94 is a Protein complex structure of sequences from Rattus norvegicus. Full crystallographic information is available from OCA.

ReferenceReference

Aryl tetrahydropyridine inhibitors of farnesyltransferase: glycine, phenylalanine and histidine derivatives., Gwaltney SL 2nd, O'Connor SJ, Nelson LT, Sullivan GM, Imade H, Wang W, Hasvold L, Li Q, Cohen J, Gu WZ, Tahir SK, Bauch J, Marsh K, Ng SC, Frost DJ, Zhang H, Muchmore S, Jakob CG, Stoll V, Hutchins C, Rosenberg SH, Sham HL, Bioorg Med Chem Lett. 2003 Apr 7;13(7):1359-62. PMID:12657282

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