1h92

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[1h92]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1H92 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1H92 FirstGlance]. <br>
<table><tr><td colspan='2'>[[1h92]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1H92 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1H92 FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1fbz|1fbz]], [[1lcj|1lcj]], [[1lck|1lck]], [[1qpc|1qpc]], [[1qpd|1qpd]], [[1qpe|1qpe]], [[1qpj|1qpj]], [[3lck|3lck]]</td></tr>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1fbz|1fbz]], [[1lcj|1lcj]], [[1lck|1lck]], [[1qpc|1qpc]], [[1qpd|1qpd]], [[1qpe|1qpe]], [[1qpj|1qpj]], [[3lck|3lck]]</td></tr>
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<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=1h92 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1h92 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1h92 RCSB], [http://www.ebi.ac.uk/pdbsum/1h92 PDBsum]</span></td></tr>
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<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=1h92 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1h92 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1h92 RCSB], [http://www.ebi.ac.uk/pdbsum/1h92 PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/LCK_HUMAN LCK_HUMAN]] Severe combined immunodeficiency due to LCK deficiency. Note=A chromosomal aberration involving LCK is found in leukemias. Translocation t(1;7)(p34;q34) with TCRB.
[[http://www.uniprot.org/uniprot/LCK_HUMAN LCK_HUMAN]] Severe combined immunodeficiency due to LCK deficiency. Note=A chromosomal aberration involving LCK is found in leukemias. Translocation t(1;7)(p34;q34) with TCRB.
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Biesinger, B.]]
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[[Category: Biesinger, B]]
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[[Category: Friedrich, U.]]
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[[Category: Friedrich, U]]
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[[Category: Hoffmann, S.]]
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[[Category: Hoffmann, S]]
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[[Category: Roesch, P.]]
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[[Category: Roesch, P]]
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[[Category: Schweimer, K.]]
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[[Category: Schweimer, K]]
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[[Category: Sticht, H.]]
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[[Category: Sticht, H]]
[[Category: Lck]]
[[Category: Lck]]
[[Category: Sh3 domain]]
[[Category: Sh3 domain]]

Revision as of 22:13, 22 December 2014

SH3 DOMAIN OF HUMAN LCK TYROSINE KINASE

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