2v3q: Difference between revisions

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[[Image:2v3q.png|left|200px]]


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==Serendipitous discovery and X-ray structure of a human phosphate binding apolipoprotein==
The line below this paragraph, containing "STRUCTURE_2v3q", creates the "Structure Box" on the page.
<StructureSection load='2v3q' size='340' side='right'caption='[[2v3q]], [[Resolution|resolution]] 1.89&Aring;' scene=''>
You may change the PDB parameter (which sets the PDB file loaded into the applet)
== Structural highlights ==
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
<table><tr><td colspan='2'>[[2v3q]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=2cap 2cap]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2V3Q OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2V3Q FirstGlance]. <br>
or leave the SCENE parameter empty for the default display.
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</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=2v3q FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2v3q OCA], [https://pdbe.org/2v3q PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2v3q RCSB], [https://www.ebi.ac.uk/pdbsum/2v3q PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2v3q ProSAT]</span></td></tr>
{{STRUCTURE_2v3q|  PDB=2v3q  |  SCENE=  }}
</table>
== Disease ==
[[https://www.uniprot.org/uniprot/PHBP_UNKP PHBP_UNKP]] May be involved in atherosclerosis.
== Function ==
[[https://www.uniprot.org/uniprot/PHBP_UNKP PHBP_UNKP]] Phosphate-binding protein.<ref>PMID:18076037</ref> 
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/v3/2v3q_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=2v3q ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The Human Phosphate Binding Protein (HPBP) is a serendipitously discovered apolipoprotein from human plasma that binds phosphate. Amino acid sequence relates HPBP to an intriguing protein family that seems ubiquitous in eukaryotes. These proteins, named DING according to the sequence of their four conserved N-terminal residues, are systematically absent from eukaryotic genome databases. As a consequence, HPBP amino acids sequence had to be first assigned from the electronic density map. Then, an original approach combining X-ray crystallography and mass spectrometry provides the complete and a priori exact sequence of the 38-kDa HPBP. This first complete sequence of a eukaryotic DING protein will be helpful to study HPBP and the entire DING protein family.


===SERENDIPITOUS DISCOVERY AND X-RAY STRUCTURE OF A HUMAN PHOSPHATE BINDING APOLIPOPROTEIN===
Tandem use of X-ray crystallography and mass spectrometry to obtain ab initio the complete and exact amino acids sequence of HPBP, a human 38-kDa apolipoprotein.,Diemer H, Elias M, Renault F, Rochu D, Contreras-Martel C, Schaeffer C, Van Dorsselaer A, Chabriere E Proteins. 2008 Jun;71(4):1708-20. PMID:18076037<ref>PMID:18076037</ref>


From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 2v3q" style="background-color:#fffaf0;"></div>


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==See Also==
The line below this paragraph, {{ABSTRACT_PUBMED_16531243}}, adds the Publication Abstract to the page
*[[Phosphate-binding protein|Phosphate-binding protein]]
(as it appears on PubMed at http://www.pubmed.gov), where 16531243 is the PubMed ID number.
== References ==
-->
<references/>
{{ABSTRACT_PUBMED_16531243}}
__TOC__
 
</StructureSection>
==About this Structure==
[[2v3q]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=2cap 2cap]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2V3Q OCA].
 
==Reference==
<ref group="xtra">PMID:16531243</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Berna, A.]]
[[Category: Large Structures]]
[[Category: Bernier, F.]]
[[Category: Berna, A]]
[[Category: Carpentier, P.]]
[[Category: Bernier, F]]
[[Category: Chabriere, E.]]
[[Category: Carpentier, P]]
[[Category: Chesne-Seck, M L.]]
[[Category: Chabriere, E]]
[[Category: Contreras-Martel, C.]]
[[Category: Chesne-Seck, M L]]
[[Category: Diemer, H.]]
[[Category: Contreras-Martel, C]]
[[Category: Dorsselaer, A Van.]]
[[Category: Diemer, H]]
[[Category: Dupuy, J.]]
[[Category: Dorsselaer, A Van]]
[[Category: Elias, M.]]
[[Category: Dupuy, J]]
[[Category: Fontecilla, J C.]]
[[Category: Elias, M]]
[[Category: Masson, P.]]
[[Category: Fontecilla, J C]]
[[Category: Morales, R.]]
[[Category: Masson, P]]
[[Category: Nicodeme, M.]]
[[Category: Morales, R]]
[[Category: Renault, F.]]
[[Category: Nicodeme, M]]
[[Category: Rochu, D.]]
[[Category: Renault, F]]
[[Category: Schaeffer, C.]]
[[Category: Rochu, D]]
[[Category: Schaeffer, C]]
[[Category: Atherosclerosis]]
[[Category: Atherosclerosis]]
[[Category: Hdl]]
[[Category: Hdl]]

Latest revision as of 15:37, 23 March 2022

Serendipitous discovery and X-ray structure of a human phosphate binding apolipoproteinSerendipitous discovery and X-ray structure of a human phosphate binding apolipoprotein

Structural highlights

2v3q is a 1 chain structure with sequence from Homo sapiens. This structure supersedes the now removed PDB entry 2cap. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Ligands:, ,
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Disease

[PHBP_UNKP] May be involved in atherosclerosis.

Function

[PHBP_UNKP] Phosphate-binding protein.[1]

Evolutionary Conservation

Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf.

Publication Abstract from PubMed

The Human Phosphate Binding Protein (HPBP) is a serendipitously discovered apolipoprotein from human plasma that binds phosphate. Amino acid sequence relates HPBP to an intriguing protein family that seems ubiquitous in eukaryotes. These proteins, named DING according to the sequence of their four conserved N-terminal residues, are systematically absent from eukaryotic genome databases. As a consequence, HPBP amino acids sequence had to be first assigned from the electronic density map. Then, an original approach combining X-ray crystallography and mass spectrometry provides the complete and a priori exact sequence of the 38-kDa HPBP. This first complete sequence of a eukaryotic DING protein will be helpful to study HPBP and the entire DING protein family.

Tandem use of X-ray crystallography and mass spectrometry to obtain ab initio the complete and exact amino acids sequence of HPBP, a human 38-kDa apolipoprotein.,Diemer H, Elias M, Renault F, Rochu D, Contreras-Martel C, Schaeffer C, Van Dorsselaer A, Chabriere E Proteins. 2008 Jun;71(4):1708-20. PMID:18076037[2]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

See Also

References

  1. Diemer H, Elias M, Renault F, Rochu D, Contreras-Martel C, Schaeffer C, Van Dorsselaer A, Chabriere E. Tandem use of X-ray crystallography and mass spectrometry to obtain ab initio the complete and exact amino acids sequence of HPBP, a human 38-kDa apolipoprotein. Proteins. 2008 Jun;71(4):1708-20. PMID:18076037 doi:10.1002/prot.21866
  2. Diemer H, Elias M, Renault F, Rochu D, Contreras-Martel C, Schaeffer C, Van Dorsselaer A, Chabriere E. Tandem use of X-ray crystallography and mass spectrometry to obtain ab initio the complete and exact amino acids sequence of HPBP, a human 38-kDa apolipoprotein. Proteins. 2008 Jun;71(4):1708-20. PMID:18076037 doi:10.1002/prot.21866

2v3q, resolution 1.89Å

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