1jl9

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[1jl9]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JL9 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1JL9 FirstGlance]. <br>
<table><tr><td colspan='2'>[[1jl9]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JL9 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1JL9 FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1jl9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1jl9 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1jl9 RCSB], [http://www.ebi.ac.uk/pdbsum/1jl9 PDBsum]</span></td></tr>
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</td></tr><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=1jl9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1jl9 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1jl9 RCSB], [http://www.ebi.ac.uk/pdbsum/1jl9 PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/EGF_HUMAN EGF_HUMAN]] Defects in EGF are the cause of hypomagnesemia type 4 (HOMG4) [MIM:[http://omim.org/entry/611718 611718]]; also known as renal hypomagnesemia normocalciuric. HOMG4 is a disorder characterized by massive renal hypomagnesemia and normal levels of serum calcium and calcium excretion. Clinical features include seizures, mild-to mederate psychomotor retardation, and brisk tendon reflexes.<ref>PMID:17671655</ref>
[[http://www.uniprot.org/uniprot/EGF_HUMAN EGF_HUMAN]] Defects in EGF are the cause of hypomagnesemia type 4 (HOMG4) [MIM:[http://omim.org/entry/611718 611718]]; also known as renal hypomagnesemia normocalciuric. HOMG4 is a disorder characterized by massive renal hypomagnesemia and normal levels of serum calcium and calcium excretion. Clinical features include seizures, mild-to mederate psychomotor retardation, and brisk tendon reflexes.<ref>PMID:17671655</ref>
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Bi, R C.]]
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[[Category: Bi, R C]]
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[[Category: Chai, J J.]]
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[[Category: Chai, J J]]
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[[Category: He, C H.]]
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[[Category: He, C H]]
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[[Category: Huang, B R.]]
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[[Category: Huang, B R]]
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[[Category: Li, M.]]
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[[Category: Li, M]]
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[[Category: Lu, H S.]]
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[[Category: Lu, H S]]
[[Category: Dimerization]]
[[Category: Dimerization]]
[[Category: Growth factor]]
[[Category: Growth factor]]
[[Category: Signaling protein]]
[[Category: Signaling protein]]

Revision as of 12:17, 2 January 2015

Crystal Structure of Human Epidermal Growth Factor

1jl9, resolution 3.00Å

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