3v8x: Difference between revisions

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~~[[Image:3v8x.png|left|200px]]~~

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~~You may change the PDB parameter (which sets the PDB file loaded into the applet)~~

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===The crystal structure of transferrin binding protein A (TbpA) from Neisserial meningitidis serogroup B in complex with full length human transferrin===

==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>

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==Function==

~~The line below this paragraph, {{ABSTRACT_PUBMED_22327295}}, adds the Publication Abstract to the page~~

[[http://www.uniprot.org/uniprot/TBP1_NEIMB TBP1_NEIMB]] Acts as a transferrin receptor and is required for transferrin utilization (By similarity). [[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.

(~~as it appears on PubMed at~~ http://www.~~pubmed~~.~~gov~~), ~~where 22327295~~ is the ~~PubMed ID number~~.

~~-->~~

~~{{ABSTRACT_PUBMED_22327295}}~~

==About this Structure==

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==Reference==

[[Category: Homo sapiens]]

[[Category: Neisseria meningitidis serogroup b]]

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@@ Line 1: / Line 1: @@
-[[Image:3v8x.png|left|200px]]
-<!--
-The line below this paragraph, containing "STRUCTURE_3v8x", creates the "Structure Box" on the page.
-You may change the PDB parameter (which sets the PDB file loaded into the applet)
-or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
-or leave the SCENE parameter empty for the default display.
--->
 {{STRUCTURE_3v8x|  PDB=3v8x  |  SCENE=  }}
 ===The crystal structure of transferrin binding protein A (TbpA) from Neisserial meningitidis serogroup B in complex with full length human transferrin===
+{{ABSTRACT_PUBMED_22327295}}
+==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==
-The line below this paragraph, {{ABSTRACT_PUBMED_22327295}}, adds the Publication Abstract to the page
+[[http://www.uniprot.org/uniprot/TBP1_NEIMB TBP1_NEIMB]] Acts as a transferrin receptor and is required for transferrin utilization (By similarity). [[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.
-(as it appears on PubMed at http://www.pubmed.gov), where 22327295 is the PubMed ID number.
--->
-{{ABSTRACT_PUBMED_22327295}}
 ==About this Structure==
@@ Line 22: / Line 13: @@
 ==Reference==
-<ref group="xtra">PMID:022327295</ref><references group="xtra"/>
+<ref group="xtra">PMID:022327295</ref><references group="xtra"/><references/>
 [[Category: Homo sapiens]]
 [[Category: Neisseria meningitidis serogroup b]]