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4hxx

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{{STRUCTURE_4hxx| PDB=4hxx | SCENE= }}
 
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===Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1===
 
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{{ABSTRACT_PUBMED_23507151}}
 
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==Function==
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==Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1==
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[[http://www.uniprot.org/uniprot/AMPM1_HUMAN AMPM1_HUMAN]] Removes the N-terminal methionine from nascent proteins. Required for normal progression through the cell cycle.<ref>PMID:16274222</ref> <ref>PMID:17114291</ref>
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<StructureSection load='4hxx' size='340' side='right'caption='[[4hxx]], [[Resolution|resolution]] 2.09&Aring;' scene=''>
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== Structural highlights ==
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==About this Structure==
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<table><tr><td colspan='2'>[[4hxx]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4HXX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4HXX FirstGlance]. <br>
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[[4hxx]] 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=4HXX OCA].
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.09&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=1AY:(1R)-N~2~-[5-CHLORO-2-(5-CHLOROPYRIDIN-2-YL)-6-METHYLPYRIMIDIN-4-YL]-1-PHENYL-N~1~-(4-PHENYLBUTYL)ETHANE-1,2-DIAMINE'>1AY</scene>, <scene name='pdbligand=CO:COBALT+(II)+ION'>CO</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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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=4hxx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4hxx OCA], [https://pdbe.org/4hxx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4hxx RCSB], [https://www.ebi.ac.uk/pdbsum/4hxx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4hxx ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/MAP11_HUMAN MAP11_HUMAN] Cotranslationally removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Required for normal progression through the cell cycle.[HAMAP-Rule:MF_03174]<ref>PMID:16274222</ref> <ref>PMID:17114291</ref>
==See Also==
==See Also==
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*[[Aminopeptidase|Aminopeptidase]]
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*[[Aminopeptidase 3D structures|Aminopeptidase 3D structures]]
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== References ==
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==Reference==
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<references/>
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<ref group="xtra">PMID:023507151</ref><references group="xtra"/><references/>
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__TOC__
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[[Category: Human]]
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</StructureSection>
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[[Category: Methionyl aminopeptidase]]
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[[Category: Homo sapiens]]
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[[Category: Amzel, L M.]]
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[[Category: Large Structures]]
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[[Category: Gabelli, S B.]]
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[[Category: Amzel LM]]
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[[Category: Liu, J.]]
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[[Category: Gabelli SB]]
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[[Category: Zhang, F.]]
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[[Category: Liu J]]
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[[Category: Aminopeptidase]]
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[[Category: Zhang F]]
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[[Category: Cell cycle]]
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[[Category: Hydrolase-hydrolase inhibitor complex]]
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[[Category: Pyridinylpyrimidine]]
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[[Category: Pyrimidine]]
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[[Category: Pyrimidyl group]]
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Current revision

Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1

PDB ID 4hxx

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