7jow: Difference between revisions

Line 8:

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7jow FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7jow OCA], [https://pdbe.org/7jow PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7jow RCSB], [https://www.ebi.ac.uk/pdbsum/7jow PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7jow ProSAT]</span></td></tr>

</table>

~~== Disease ==~~

[https://www.uniprot.org/uniprot/KLK4_HUMAN KLK4_HUMAN] Defects in KLK4 are the cause of amelogenesis imperfecta hypomaturation type 2A1 (AI2A1) [MIM:[https://omim.org/entry/204700 204700]. AI2A1 is an autosomal recessive defect of enamel formation. The disorder involves both primary and secondary dentitions. The teeth have a shiny agar jelly appearance and the enamel is softer than normal. Brown pigment is present in middle layers of enamel.<ref>PMID:15235027</ref>

== Function ==

[https://www.uniprot.org/uniprot/~~KLK4_HUMAN KLK4_HUMAN~~] ~~Involved in enamel formation.<ref>PMID:15235027</ref>~~

[https://www.uniprot.org/uniprot/BBKI_BAUBA BBKI_BAUBA]

==See Also==

*[[Kallikrein 3D structures|Kallikrein 3D structures]]

~~== References ==~~

~~<references/>~~

__TOC__

</StructureSection>

Navigation menu

Page actions

Page actions

Personal tools

Navigation

Search

Tools

@@ Line 8: / Line 8: @@
 <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7jow FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7jow OCA], [https://pdbe.org/7jow PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7jow RCSB], [https://www.ebi.ac.uk/pdbsum/7jow PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7jow ProSAT]</span></td></tr>
 </table>
-== Disease ==
-[https://www.uniprot.org/uniprot/KLK4_HUMAN KLK4_HUMAN] Defects in KLK4 are the cause of amelogenesis imperfecta hypomaturation type 2A1 (AI2A1) [MIM:[https://omim.org/entry/204700 204700]. AI2A1 is an autosomal recessive defect of enamel formation. The disorder involves both primary and secondary dentitions. The teeth have a shiny agar jelly appearance and the enamel is softer than normal. Brown pigment is present in middle layers of enamel.<ref>PMID:15235027</ref>
 == Function ==
-[https://www.uniprot.org/uniprot/KLK4_HUMAN KLK4_HUMAN] Involved in enamel formation.<ref>PMID:15235027</ref>
+[https://www.uniprot.org/uniprot/BBKI_BAUBA BBKI_BAUBA]
 ==See Also==
 *[[Kallikrein 3D structures|Kallikrein 3D structures]]
-== References ==
-<references/>
 __TOC__
 </StructureSection>