1mf7: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
m Protected "1mf7" [edit=sysop:move=sysop]
No edit summary
Line 1: Line 1:
[[Image:1mf7.png|left|200px]]
{{STRUCTURE_1mf7|  PDB=1mf7  |  SCENE=  }}  
{{STRUCTURE_1mf7|  PDB=1mf7  |  SCENE=  }}  
===INTEGRIN ALPHA M I DOMAIN===
{{ABSTRACT_PUBMED_12611591}}


===INTEGRIN ALPHA M I DOMAIN===
==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.


{{ABSTRACT_PUBMED_12611591}}
==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 14: Line 16:


==Reference==
==Reference==
<ref group="xtra">PMID:012611591</ref><references group="xtra"/>
<ref group="xtra">PMID:012611591</ref><references group="xtra"/><references/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Liddington, R C.]]
[[Category: Liddington, R C.]]
[[Category: McCleverty, C J.]]
[[Category: McCleverty, C J.]]
[[Category: Cell adhesion]]
[[Category: Cell adhesion]]

Revision as of 02:58, 25 March 2013

Template:STRUCTURE 1mf7

INTEGRIN ALPHA M I DOMAININTEGRIN ALPHA M I DOMAIN

Template:ABSTRACT PUBMED 12611591

DiseaseDisease

[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.

FunctionFunction

[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 StructureAbout this Structure

1mf7 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See AlsoSee Also

ReferenceReference

[xtra 1]

  1. McCleverty CJ, Liddington RC. Engineered allosteric mutants of the integrin alphaMbeta2 I domain: structural and functional studies. Biochem J. 2003 May 15;372(Pt 1):121-7. PMID:12611591 doi:http://dx.doi.org/10.1042/BJ20021273

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA