2cl6
From Proteopedia
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| - | [[Image:2cl6.gif|left|200px]]<br /> | + | [[Image:2cl6.gif|left|200px]]<br /><applet load="2cl6" size="450" color="white" frame="true" align="right" spinBox="true" |
| - | <applet load="2cl6" size="450" color="white" frame="true" align="right" spinBox="true" | + | |
caption="2cl6, resolution 1.24Å" /> | caption="2cl6, resolution 1.24Å" /> | ||
'''CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH S-CAGED GTP'''<br /> | '''CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH S-CAGED GTP'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
| - | 2CL6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with MG, CAG and XY2 as [http://en.wikipedia.org/wiki/ligands ligands]. | + | 2CL6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with MG, CAG and XY2 as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=AC1:Xy2 Binding Site For Chain X'>AC1</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2CL6 OCA]. |
==Reference== | ==Reference== | ||
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[[Category: proto-oncogene]] | [[Category: proto-oncogene]] | ||
| - | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 19:26:47 2007'' |
Revision as of 17:17, 18 December 2007
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CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH S-CAGED GTP
Contents |
Overview
We present a new design for a fluorescence microspectrophotometer for use, in kinetic crystallography in combination with x-ray diffraction, experiments. The FLUMIX device (Fluorescence spectroscopy to monitor, intermediates in x-ray crystallography) is built for 0 degrees, fluorescence detection, which has several advantages in comparison to a, conventional fluorometer with 90 degrees design. Due to the reduced, spatial requirements and the need for only one objective, the system is, highly versatile, easy to handle, and can be used for many different, applications. In combination with a conventional stereomicroscope, fluorescence measurements or reaction initiation can be performed directly, in a hanging drop crystallization setup. The FLUMIX device can be combined, with most x-ray sources, normally without the need of a specialized, mechanical support. As a biological model system, we have used H-Ras p21, with an artificially introduced photo-labile GTP precursor (caged GTP) and, a covalently attached fluorophore (IANBD amide). Using the FLUMIX system, detailed information about the state of photolyzed crystals of the, modified H-Ras p21 (p21(mod)) could be obtained. Measurements in, combination with a synchrotron beamline showed significant fluorescence, changes in p21(mod) crystals even within a few seconds of x-ray exposure, at 100 K.
Disease
Known diseases associated with this structure: Bladder cancer, somatic OMIM:[190020], Costello syndrome OMIM:[190020], Thyroid carcinoma, follicular, somatic OMIM:[190020]
About this Structure
2CL6 is a Single protein structure of sequence from Homo sapiens with MG, CAG and XY2 as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.
Reference
A newly designed microspectrofluorometer for kinetic studies on protein crystals in combination with x-ray diffraction., Klink BU, Goody RS, Scheidig AJ, Biophys J. 2006 Aug 1;91(3):981-92. Epub 2006 May 12. PMID:16698776
Page seeded by OCA on Tue Dec 18 19:26:47 2007
Categories: Homo sapiens | Single protein | Goody, R.S. | Klink, B.U. | Scheidig, A.J. | CAG | MG | XY2 | Disease mutation | Fluorescence | Golgi apparatus | Gppnhp | Gtp-binding | Guanine nucleotide binding protein | Lipoprotein | Membrane | Methylation | Nucleotide-binding | Palmitate | Prenylation | Proto-oncogene
