2lna

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (05:46, 15 May 2024) (edit) (undo)
 
(One intermediate revision not shown.)
Line 1: Line 1:
==Solution NMR Structure of the mitochondrial inner membrane domain (residues 164-251), FtsH_ext, from the paraplegin-like protein AFG3L2 from Homo sapiens, Northeast Structural Genomics Consortium Target HR6741A==
==Solution NMR Structure of the mitochondrial inner membrane domain (residues 164-251), FtsH_ext, from the paraplegin-like protein AFG3L2 from Homo sapiens, Northeast Structural Genomics Consortium Target HR6741A==
-
<StructureSection load='2lna' size='340' side='right'caption='[[2lna]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
+
<StructureSection load='2lna' size='340' side='right'caption='[[2lna]]' scene=''>
== Structural highlights ==
== Structural highlights ==
-
<table><tr><td colspan='2'>[[2lna]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LNA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LNA FirstGlance]. <br>
+
<table><tr><td colspan='2'>[[2lna]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LNA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LNA FirstGlance]. <br>
-
</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">AFG3L2 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2lna FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lna OCA], [https://pdbe.org/2lna PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lna RCSB], [https://www.ebi.ac.uk/pdbsum/2lna PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lna ProSAT]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2lna FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lna OCA], [https://pdbe.org/2lna PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lna RCSB], [https://www.ebi.ac.uk/pdbsum/2lna PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lna ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
== Disease ==
-
[[https://www.uniprot.org/uniprot/AFG32_HUMAN AFG32_HUMAN]] Spinocerebellar ataxia type 28;Early-onset spastic ataxia-neuropathy syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
+
[https://www.uniprot.org/uniprot/AFG32_HUMAN AFG32_HUMAN] Spinocerebellar ataxia type 28;Early-onset spastic ataxia-neuropathy syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
== Function ==
-
[[https://www.uniprot.org/uniprot/AFG32_HUMAN AFG32_HUMAN]] ATP-dependent protease which is essential for axonal development (By similarity).
+
[https://www.uniprot.org/uniprot/AFG32_HUMAN AFG32_HUMAN] ATP-dependent protease which is essential for axonal development (By similarity).
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
Line 24: Line 24:
__TOC__
__TOC__
</StructureSection>
</StructureSection>
-
[[Category: Human]]
+
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
-
[[Category: Acton, T B]]
+
[[Category: Acton TB]]
-
[[Category: Everett, J K]]
+
[[Category: Everett JK]]
-
[[Category: Janua, H]]
+
[[Category: Janua H]]
-
[[Category: Kennedy, M A]]
+
[[Category: Kennedy MA]]
-
[[Category: Kohan, E]]
+
[[Category: Kohan E]]
-
[[Category: Lee, H]]
+
[[Category: Lee H]]
-
[[Category: MPP, Mitochondrial Protein Partnership]]
+
[[Category: Montelione GT]]
-
[[Category: Montelione, G T]]
+
[[Category: Prestegard JH]]
-
[[Category: Structural genomic]]
+
[[Category: Ramelot TA]]
-
[[Category: Prestegard, J H]]
+
[[Category: Shastry R]]
-
[[Category: Ramelot, T A]]
+
[[Category: Xiao R]]
-
[[Category: Shastry, R]]
+
[[Category: Yang Y]]
-
[[Category: Xiao, R]]
+
-
[[Category: Yang, Y]]
+
-
[[Category: Hydrolase]]
+
-
[[Category: Mitochondrial protein partnership]]
+
-
[[Category: Mpp]]
+
-
[[Category: PSI, Protein structure initiative]]
+
-
[[Category: Psi-biology]]
+

Current revision

Solution NMR Structure of the mitochondrial inner membrane domain (residues 164-251), FtsH_ext, from the paraplegin-like protein AFG3L2 from Homo sapiens, Northeast Structural Genomics Consortium Target HR6741A

PDB ID 2lna

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/2lna"
Personal tools