4an3

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[4an3]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4AN3 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4AN3 FirstGlance]. <br>
<table><tr><td colspan='2'>[[4an3]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4AN3 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4AN3 FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5Y0:N-[(2S)-2,3-BIS(OXIDANYL)PROPOXY]-3,4-BIS(FLUORANYL)-2-[(2-FLUORANYL-4-IODANYL-PHENYL)AMINO]BENZAMIDE'>5Y0</scene>, <scene name='pdbligand=ATP:ADENOSINE-5-TRIPHOSPHATE'>ATP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene><br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=5Y0:N-[(2S)-2,3-BIS(OXIDANYL)PROPOXY]-3,4-BIS(FLUORANYL)-2-[(2-FLUORANYL-4-IODANYL-PHENYL)AMINO]BENZAMIDE'>5Y0</scene>, <scene name='pdbligand=ATP:ADENOSINE-5-TRIPHOSPHATE'>ATP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
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<tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1s9j|1s9j]], [[4an2|4an2]], [[4an9|4an9]], [[4anb|4anb]]</td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1s9j|1s9j]], [[4an2|4an2]], [[4an9|4an9]], [[4anb|4anb]]</td></tr>
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<tr><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Mitogen-activated_protein_kinase_kinase Mitogen-activated protein kinase kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.12.2 2.7.12.2] </span></td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Mitogen-activated_protein_kinase_kinase Mitogen-activated protein kinase kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.12.2 2.7.12.2] </span></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=4an3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4an3 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4an3 RCSB], [http://www.ebi.ac.uk/pdbsum/4an3 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=4an3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4an3 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4an3 RCSB], [http://www.ebi.ac.uk/pdbsum/4an3 PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/MP2K1_HUMAN MP2K1_HUMAN]] Defects in MAP2K1 are a cause of cardiofaciocutaneous syndrome (CFC syndrome) [MIM:[http://omim.org/entry/115150 115150]]; also known as cardio-facio-cutaneous syndrome. CFC syndrome is characterized by a distinctive facial appearance, heart defects and mental retardation. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. The inheritance of CFC syndrome is autosomal dominant.
[[http://www.uniprot.org/uniprot/MP2K1_HUMAN MP2K1_HUMAN]] Defects in MAP2K1 are a cause of cardiofaciocutaneous syndrome (CFC syndrome) [MIM:[http://omim.org/entry/115150 115150]]; also known as cardio-facio-cutaneous syndrome. CFC syndrome is characterized by a distinctive facial appearance, heart defects and mental retardation. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. The inheritance of CFC syndrome is autosomal dominant.
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
</div>
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==See Also==
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*[[Mitogen-activated protein kinase kinase|Mitogen-activated protein kinase kinase]]
== References ==
== References ==
<references/>
<references/>
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[[Category: Human]]
[[Category: Human]]
[[Category: Mitogen-activated protein kinase kinase]]
[[Category: Mitogen-activated protein kinase kinase]]
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[[Category: Aay, N.]]
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[[Category: Aay, N]]
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[[Category: Anand, N K.]]
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[[Category: Anand, N K]]
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[[Category: Blazey, C M.]]
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[[Category: Blazey, C M]]
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[[Category: Bowles, O J.]]
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[[Category: Bowles, O J]]
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[[Category: Bussenius, J.]]
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[[Category: Bussenius, J]]
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[[Category: Costanzo, S.]]
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[[Category: Costanzo, S]]
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[[Category: Curtis, J K.]]
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[[Category: Curtis, J K]]
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[[Category: Defina, S C.]]
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[[Category: Defina, S C]]
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[[Category: Dubenko, L.]]
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[[Category: Dubenko, L]]
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[[Category: Engst, S.]]
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[[Category: Engst, S]]
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[[Category: Johnston, S.]]
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[[Category: Johnston, S]]
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[[Category: Joshi, A A.]]
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[[Category: Joshi, A A]]
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[[Category: Kennedy, A R.]]
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[[Category: Kennedy, A R]]
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[[Category: Kim, A I.]]
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[[Category: Kim, A I]]
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[[Category: Koltun, E S.]]
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[[Category: Koltun, E S]]
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[[Category: Lougheed, J C.]]
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[[Category: Lougheed, J C]]
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[[Category: Manalo, J C.L.]]
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[[Category: Manalo, J C.L]]
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[[Category: Martini, J F.]]
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[[Category: Martini, J F]]
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[[Category: Nuss, J M.]]
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[[Category: Nuss, J M]]
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[[Category: Peto, C J.]]
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[[Category: Peto, C J]]
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[[Category: Rice, K D.]]
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[[Category: Rice, K D]]
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[[Category: Tsang, T H.]]
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[[Category: Tsang, T H]]
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[[Category: Yu, P.]]
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[[Category: Yu, P]]
[[Category: Allosteric inhibition]]
[[Category: Allosteric inhibition]]
[[Category: Atp-binding]]
[[Category: Atp-binding]]
[[Category: Map2k1]]
[[Category: Map2k1]]
[[Category: Transferase]]
[[Category: Transferase]]

Revision as of 14:00, 4 January 2015

Crystal structures of human MEK1 with carboxamide-based allosteric inhibitor XL518 (GDC-0973), or related analogs.

4an3, resolution 2.10Å

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