4b5z

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (11:43, 20 December 2023) (edit) (undo)
 
(4 intermediate revisions not shown.)
Line 1: Line 1:
 +
==Structure of the apo-rFnBPA(189-505) from Staphylococcus aureus==
==Structure of the apo-rFnBPA(189-505) from Staphylococcus aureus==
-
<StructureSection load='4b5z' size='340' side='right' caption='[[4b5z]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
+
<StructureSection load='4b5z' size='340' side='right'caption='[[4b5z]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
-
<table><tr><td colspan='2'>[[4b5z]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Staa8 Staa8]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4B5Z OCA]. <br>
+
<table><tr><td colspan='2'>[[4b5z]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Staphylococcus_aureus_subsp._aureus_NCTC_8325 Staphylococcus aureus subsp. aureus NCTC 8325]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4B5Z OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4B5Z FirstGlance]. <br>
-
</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4b60|4b60]]</td></tr>
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.2&#8491;</td></tr>
-
<tr><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </span></td></tr>
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4b5z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4b5z OCA], [https://pdbe.org/4b5z PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4b5z RCSB], [https://www.ebi.ac.uk/pdbsum/4b5z PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4b5z ProSAT]</span></td></tr>
-
<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=4b5z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4b5z OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4b5z RCSB], [http://www.ebi.ac.uk/pdbsum/4b5z PDBsum]</span></td></tr>
+
</table>
-
<table>
+
== Function ==
 +
[https://www.uniprot.org/uniprot/FNBA_STAA8 FNBA_STAA8] Possesses multiple, substituting fibronectin (Fn) binding regions, each capable of conferring adherence to both soluble and immobilized forms of Fn. This confers to S.aureus the ability to invade endothelial cells both in vivo and in vitro, without requiring additional factors, although in a slow and inefficient way through actin rearrangements in host cells. This invasion process is mediated by integrin alpha-5/beta-1. Promotes bacterial attachment to both soluble and immobilized forms of fibrinogen (Fg) by means of a unique binding site localized within the 17 C-terminal residues of the gamma-chain of human Fg. Both plasma proteins (Fn and Fg) function as a bridge between bacterium and host cell. Promotes attachment to immobilized elastin peptides in a dose-dependent and saturable manner. Promotes attachment to both full-length and segments of immobilized human tropoelastin at multiple sites in a dose and pH-dependent manner. Promotes adherence to and aggregation of activated platelets independently of other S.aureus surface molecules. Is a critical mediator implicated in the induction of experimental endocarditis in rats with catheter-induced aortic vegetations, promoting both colonization and persistence of the bacterium into the host.<ref>PMID:2521391</ref> <ref>PMID:10788510</ref> <ref>PMID:11736995</ref> <ref>PMID:11553573</ref> <ref>PMID:15234962</ref> <ref>PMID:15216468</ref> <ref>PMID:15897276</ref> <ref>PMID:17516661</ref>
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
Line 13: Line 15:
Evidence for Steric Regulation of Fibrinogen binding to Staphylococcus aureus fibronectin-binding protein A (FnBPA).,Stemberk V, Jones RP, Moroz O, Atkin KE, Edwards AM, Turkenburg JP, Leech AP, Massey RC, Potts JR J Biol Chem. 2014 Mar 13. PMID:24627488<ref>PMID:24627488</ref>
Evidence for Steric Regulation of Fibrinogen binding to Staphylococcus aureus fibronectin-binding protein A (FnBPA).,Stemberk V, Jones RP, Moroz O, Atkin KE, Edwards AM, Turkenburg JP, Leech AP, Massey RC, Potts JR J Biol Chem. 2014 Mar 13. PMID:24627488<ref>PMID:24627488</ref>
-
From MEDLINE®/PubMed®, 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>
 +
<div class="pdbe-citations 4b5z" style="background-color:#fffaf0;"></div>
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
-
[[Category: Staa8]]
+
[[Category: Large Structures]]
-
[[Category: Atkin, K E.]]
+
[[Category: Staphylococcus aureus subsp. aureus NCTC 8325]]
-
[[Category: Moroz, O.]]
+
[[Category: Atkin KE]]
-
[[Category: Potts, J R.]]
+
[[Category: Moroz O]]
-
[[Category: Stemberk, V.]]
+
[[Category: Potts JR]]
-
[[Category: Turkenburg, J P.]]
+
[[Category: Stemberk V]]
-
[[Category: Cell adhesion]]
+
[[Category: Turkenburg JP]]
-
[[Category: Fibrinogen binding]]
+

Current revision

Structure of the apo-rFnBPA(189-505) from Staphylococcus aureus

PDB ID 4b5z

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools