7jow
From Proteopedia
(Difference between revisions)
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<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> | <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> | </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 == | == Function == | ||
| - | [https://www.uniprot.org/uniprot/ | + | [https://www.uniprot.org/uniprot/BBKI_BAUBA BBKI_BAUBA] |
==See Also== | ==See Also== | ||
*[[Kallikrein 3D structures|Kallikrein 3D structures]] | *[[Kallikrein 3D structures|Kallikrein 3D structures]] | ||
| - | == References == | ||
| - | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
Current revision
Crystal structure of BbKI complexed with Human Kallikrein 4
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