2cs4
From Proteopedia
(Difference between revisions)
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==Solution structure of N-terminal domain of chromosome 12 open reading frame 2== | ==Solution structure of N-terminal domain of chromosome 12 open reading frame 2== | ||
| - | <StructureSection load='2cs4' size='340' side='right' caption='[[2cs4]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | + | <StructureSection load='2cs4' size='340' side='right'caption='[[2cs4]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2cs4]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[2cs4]] 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=2CS4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2CS4 FirstGlance]. <br> |
| - | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">C12orf2 ([ | + | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">C12orf2 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2cs4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2cs4 OCA], [https://pdbe.org/2cs4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2cs4 RCSB], [https://www.ebi.ac.uk/pdbsum/2cs4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2cs4 ProSAT], [https://www.topsan.org/Proteins/RSGI/2cs4 TOPSAN]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [[ | + | [[https://www.uniprot.org/uniprot/RASF8_HUMAN RASF8_HUMAN]] Note=A chromosomal aberration involving RASSF8 is found in a complex type of synpolydactyly referred to as 3/3-prime/4 synpolydactyly associated with metacarpal and metatarsal synostoses. Reciprocal translocation t(12;22)(p11.2;q13.3) with FBLN1. |
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Human]] | [[Category: Human]] | ||
| + | [[Category: Large Structures]] | ||
[[Category: Hayashi, F]] | [[Category: Hayashi, F]] | ||
[[Category: Nagashima, T]] | [[Category: Nagashima, T]] | ||
Revision as of 11:48, 3 February 2021
Solution structure of N-terminal domain of chromosome 12 open reading frame 2
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