5x5p: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

~~The~~ entry ~~5x5p~~ is ~~ON HOLD~~ ~~until Paper Publication~~

==Human serum transferrin bound to ruthenium NTA==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[5x5p]] is a 1 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=5X5P OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5X5P FirstGlance]. <br>

~~Description~~:

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=FE:FE+(III)+ION'>FE</scene>, <scene name='pdbligand=MLI:MALONATE+ION'>MLI</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NTA:NITRILOTRIACETIC+ACID'>NTA</scene>, <scene name='pdbligand=RU:RUTHENIUM+ION'>RU</scene></td></tr>

[[Category: ~~Unreleased Structures~~]]

<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=5x5p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5x5p OCA], [http://pdbe.org/5x5p PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5x5p RCSB], [http://www.ebi.ac.uk/pdbsum/5x5p PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5x5p ProSAT]</span></td></tr>

</table>

== Disease ==

[[http://www.uniprot.org/uniprot/TRFE_HUMAN TRFE_HUMAN]] Defects in TF are the cause of atransferrinemia (ATRAF) [MIM:[http://omim.org/entry/209300 209300]]. Atransferrinemia is rare autosomal recessive disorder characterized by iron overload and hypochromic anemia.<ref>PMID:11110675</ref> <ref>PMID:15466165</ref>

== Function ==

[[http://www.uniprot.org/uniprot/TRFE_HUMAN TRFE_HUMAN]] Transferrins are iron binding transport proteins which can bind two Fe(3+) ions in association with the binding of an anion, usually bicarbonate. It is responsible for the transport of iron from sites of absorption and heme degradation to those of storage and utilization. Serum transferrin may also have a further role in stimulating cell proliferation.

== References ==

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Sun, H]]

[[Category: Wang, M]]

[[Category: Metal transport]]

[[Category: Nta]]

[[Category: Ruthenium]]

[[Category: Transferrin]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 5x5p is ON HOLD  until Paper Publication
+==Human serum transferrin bound to ruthenium NTA==
+<StructureSection load='5x5p' size='340' side='right' caption='[[5x5p]], [[Resolution|resolution]] 2.70&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[5x5p]] is a 1 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=5X5P OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5X5P FirstGlance]. <br>
-Description:
+</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=FE:FE+(III)+ION'>FE</scene>, <scene name='pdbligand=MLI:MALONATE+ION'>MLI</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NTA:NITRILOTRIACETIC+ACID'>NTA</scene>, <scene name='pdbligand=RU:RUTHENIUM+ION'>RU</scene></td></tr>
-[[Category: Unreleased Structures]]
+<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=5x5p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5x5p OCA], [http://pdbe.org/5x5p PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5x5p RCSB], [http://www.ebi.ac.uk/pdbsum/5x5p PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5x5p ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[[http://www.uniprot.org/uniprot/TRFE_HUMAN TRFE_HUMAN]] Defects in TF are the cause of atransferrinemia (ATRAF) [MIM:[http://omim.org/entry/209300 209300]]. Atransferrinemia is rare autosomal recessive disorder characterized by iron overload and hypochromic anemia.<ref>PMID:11110675</ref> <ref>PMID:15466165</ref>
+== Function ==
+[[http://www.uniprot.org/uniprot/TRFE_HUMAN TRFE_HUMAN]] Transferrins are iron binding transport proteins which can bind two Fe(3+) ions in association with the binding of an anion, usually bicarbonate. It is responsible for the transport of iron from sites of absorption and heme degradation to those of storage and utilization. Serum transferrin may also have a further role in stimulating cell proliferation.
+== References ==
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Sun, H]]
+[[Category: Wang, M]]
+[[Category: Metal transport]]
+[[Category: Nta]]
+[[Category: Ruthenium]]
+[[Category: Transferrin]]