6aax: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 1: | Line 1: | ||
==Crystal structure of TFB1M and h45 with SAM in homo sapiens== | |||
<StructureSection load='6aax' size='340' side='right'caption='[[6aax]], [[Resolution|resolution]] 2.99Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[6aax]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/ ] and [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6AAX OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6AAX FirstGlance]. <br> | |||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene>, <scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene></td></tr> | |||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6aax FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6aax OCA], [http://pdbe.org/6aax PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6aax RCSB], [http://www.ebi.ac.uk/pdbsum/6aax PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6aax ProSAT]</span></td></tr> | ||
[[Category: | </table> | ||
[[Category: | == Disease == | ||
[[http://www.uniprot.org/uniprot/TFB1M_HUMAN TFB1M_HUMAN]] Mitochondrial non-syndromic sensorineural deafness. Variations in TFB1M may influence the clinical expression of aminoglycoside-induced deafness caused by the A1555G mutation in the mitochondrial 12S rRNA. | |||
== Function == | |||
[[http://www.uniprot.org/uniprot/TFB1M_HUMAN TFB1M_HUMAN]] S-adenosyl-L-methionine-dependent methyltransferase which specifically dimethylates mitochondrial 12S rRNA at the conserved stem loop. Also required for basal transcription of mitochondrial DNA, probably via its interaction with POLRMT and TFAM. Stimulates transcription independently of the methyltransferase activity.<ref>PMID:11809803</ref> <ref>PMID:12068295</ref> <ref>PMID:12897151</ref> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Gong, Q]] | |||
[[Category: Li, F]] | |||
[[Category: Liu, X]] | [[Category: Liu, X]] | ||
[[Category: Shen, S]] | [[Category: Shen, S]] | ||
[[Category: Shi, Y]] | [[Category: Shi, Y]] | ||
[[Category: Wu, J]] | |||
[[Category: Wu, P]] | |||
[[Category: Zhang, H]] | |||
[[Category: H45]] | |||
[[Category: Tfb1m]] | |||
[[Category: Transferase-rna complex]] |
Revision as of 01:41, 6 June 2019
Crystal structure of TFB1M and h45 with SAM in homo sapiensCrystal structure of TFB1M and h45 with SAM in homo sapiens
Structural highlights
Disease[TFB1M_HUMAN] Mitochondrial non-syndromic sensorineural deafness. Variations in TFB1M may influence the clinical expression of aminoglycoside-induced deafness caused by the A1555G mutation in the mitochondrial 12S rRNA. Function[TFB1M_HUMAN] S-adenosyl-L-methionine-dependent methyltransferase which specifically dimethylates mitochondrial 12S rRNA at the conserved stem loop. Also required for basal transcription of mitochondrial DNA, probably via its interaction with POLRMT and TFAM. Stimulates transcription independently of the methyltransferase activity.[1] [2] [3] References
|
|