2c97: Difference between revisions
No edit summary |
No edit summary |
||
Line 1: | Line 1: | ||
[[Image:2c97.jpg|left|200px]]<br /><applet load="2c97" size=" | [[Image:2c97.jpg|left|200px]]<br /><applet load="2c97" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="2c97, resolution 2.00Å" /> | caption="2c97, resolution 2.00Å" /> | ||
'''LUMAZINE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS BOUND TO 4-(6-CHLORO-2,4-DIOXO-1,2,3,4-TETRAHYDROPYRIMIDIN-5-YL) BUTYL PHOSPHATE'''<br /> | '''LUMAZINE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS BOUND TO 4-(6-CHLORO-2,4-DIOXO-1,2,3,4-TETRAHYDROPYRIMIDIN-5-YL) BUTYL PHOSPHATE'''<br /> | ||
Line 7: | Line 7: | ||
==About this Structure== | ==About this Structure== | ||
2C97 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis] with K, ACT, JCL, DTD and MPD as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Riboflavin_synthase Riboflavin synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.9 2.5.1.9] Known structural/functional Site: <scene name='pdbsite=AC1:Mpd Binding Site For Chain A'>AC1</scene>. Full crystallographic information is available from [http:// | 2C97 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis] with <scene name='pdbligand=K:'>K</scene>, <scene name='pdbligand=ACT:'>ACT</scene>, <scene name='pdbligand=JCL:'>JCL</scene>, <scene name='pdbligand=DTD:'>DTD</scene> and <scene name='pdbligand=MPD:'>MPD</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Riboflavin_synthase Riboflavin synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.9 2.5.1.9] Known structural/functional Site: <scene name='pdbsite=AC1:Mpd+Binding+Site+For+Chain+A'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2C97 OCA]. | ||
==Reference== | ==Reference== | ||
Line 33: | Line 33: | ||
[[Category: transferase]] | [[Category: transferase]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:33:00 2008'' |
Revision as of 11:33, 3 February 2008
|
LUMAZINE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS BOUND TO 4-(6-CHLORO-2,4-DIOXO-1,2,3,4-TETRAHYDROPYRIMIDIN-5-YL) BUTYL PHOSPHATE
OverviewOverview
Recently published genomic investigations of the human pathogen, Mycobacterium tuberculosis have revealed that genes coding the proteins, involved in riboflavin biosynthesis are essential for the growth of the, organism. Because the enzymes involved in cofactor biosynthesis pathways, are not present in humans, they appear to be promising candidates for the, development of therapeutic drugs. The substituted purinetrione compounds, have demonstrated high affinity and specificity to lumazine synthase, which catalyzes the penultimate step of riboflavin biosynthesis in, bacteria and plants. The structure of M. tuberculosis lumazine synthase in, complex with five different inhibitor compounds is presented, together, with studies of the binding reactions by isothermal titration calorimetry., The inhibitors showed the association constants in the micromolar range., The analysis of the structures demonstrated the specific features of the, binding of different inhibitors. The comparison of the structures and, binding modes of five different inhibitors allows us to propose the, ribitylpurinetrione compounds with C4-C5 alkylphosphate chains as most, promising leads for further development of therapeutic drugs against M., tuberculosis.
About this StructureAbout this Structure
2C97 is a Single protein structure of sequence from Mycobacterium tuberculosis with , , , and as ligands. Active as Riboflavin synthase, with EC number 2.5.1.9 Known structural/functional Site: . Full crystallographic information is available from OCA.
ReferenceReference
Structural and thermodynamic insights into the binding mode of five novel inhibitors of lumazine synthase from Mycobacterium tuberculosis., Morgunova E, Illarionov B, Sambaiah T, Haase I, Bacher A, Cushman M, Fischer M, Ladenstein R, FEBS J. 2006 Oct;273(20):4790-804. Epub 2006 Sep 19. PMID:16984393
Page seeded by OCA on Sun Feb 3 10:33:00 2008