2lkj
From Proteopedia
Line 1: | Line 1: | ||
- | [[Image:2lkj.png|left|200px]] | ||
- | |||
- | <!-- | ||
- | The line below this paragraph, containing "STRUCTURE_2lkj", 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_2lkj| PDB=2lkj | SCENE= }} | {{STRUCTURE_2lkj| PDB=2lkj | SCENE= }} | ||
- | |||
===Structures and Interaction Analyses of the Integrin Alpha-M Beta-2 Cytoplasmic Tails=== | ===Structures and Interaction Analyses of the Integrin Alpha-M Beta-2 Cytoplasmic Tails=== | ||
+ | {{ABSTRACT_PUBMED_22052909}} | ||
+ | ==Disease== | ||
+ | [[http://www.uniprot.org/uniprot/ITAM_HUMAN ITAM_HUMAN]] Genetic variations in ITGAM has been associated with susceptibility to systemic lupus erythematosus type 6 (SLEB6) [MIM:[http://omim.org/entry/609939 609939]]. Systemic lupus erythematosus (SLE) is a chronic, inflammatory and often febrile multisystemic disorder of connective tissue. It affects principally the skin, joints, kidneys and serosal membranes. It is thought to represent a failure of the regulatory mechanisms of the autoimmune system. | ||
- | + | ==Function== | |
- | + | [[http://www.uniprot.org/uniprot/ITAM_HUMAN ITAM_HUMAN]] Integrin alpha-M/beta-2 is implicated in various adhesive interactions of monocytes, macrophages and granulocytes as well as in mediating the uptake of complement-coated particles. It is identical with CR-3, the receptor for the iC3b fragment of the third complement component. It probably recognizes the R-G-D peptide in C3b. Integrin alpha-M/beta-2 is also a receptor for fibrinogen, factor X and ICAM1. It recognizes P1 and P2 peptides of fibrinogen gamma chain. | |
- | + | ||
- | -- | + | |
- | + | ||
==About this Structure== | ==About this Structure== | ||
Line 22: | Line 13: | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID:022052909</ref><references group="xtra"/> | + | <ref group="xtra">PMID:022052909</ref><references group="xtra"/><references/> |
[[Category: Amalraj, M.]] | [[Category: Amalraj, M.]] | ||
[[Category: Bhattacharjya, S.]] | [[Category: Bhattacharjya, S.]] |
Revision as of 23:35, 24 March 2013
Contents |
Structures and Interaction Analyses of the Integrin Alpha-M Beta-2 Cytoplasmic Tails
Template:ABSTRACT PUBMED 22052909
Disease
[ITAM_HUMAN] Genetic variations in ITGAM has been associated with susceptibility to systemic lupus erythematosus type 6 (SLEB6) [MIM:609939]. Systemic lupus erythematosus (SLE) is a chronic, inflammatory and often febrile multisystemic disorder of connective tissue. It affects principally the skin, joints, kidneys and serosal membranes. It is thought to represent a failure of the regulatory mechanisms of the autoimmune system.
Function
[ITAM_HUMAN] Integrin alpha-M/beta-2 is implicated in various adhesive interactions of monocytes, macrophages and granulocytes as well as in mediating the uptake of complement-coated particles. It is identical with CR-3, the receptor for the iC3b fragment of the third complement component. It probably recognizes the R-G-D peptide in C3b. Integrin alpha-M/beta-2 is also a receptor for fibrinogen, factor X and ICAM1. It recognizes P1 and P2 peptides of fibrinogen gamma chain.
About this Structure
2lkj is a 1 chain structure. Full experimental information is available from OCA.
Reference
- Chua GL, Tang XY, Amalraj M, Tan SM, Bhattacharjya S. Structures and interaction analyses of the integrin alphaMbeta2 cytoplasmic tails. J Biol Chem. 2011 Nov 3. PMID:22052909 doi:10.1074/jbc.M111.280164