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{{Infobox_gene}}
{{PBB_Controls
'''Platelet glycoprotein Ib alpha chain''' also known as '''glycoprotein Ib (platelet), alpha polypeptide''' or '''CD42b''' ('''C'''luster of '''D'''ifferentiation '''42b'''), is a [[protein]] that in humans is encoded by the ''GP1BA'' [[gene]].
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| update_protein_box = yes
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}}


<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== Function ==
{{GNF_Protein_box
| image = PBB_Protein_GP1BA_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1gwb.
| PDB = {{PDB2|1gwb}}, {{PDB2|1m0z}}, {{PDB2|1m10}}, {{PDB2|1ook}}, {{PDB2|1p8v}}, {{PDB2|1p9a}}, {{PDB2|1qyy}}, {{PDB2|1sq0}}, {{PDB2|1u0n}}
| Name = Glycoprotein Ib (platelet), alpha polypeptide
| HGNCid = 4439
| Symbol = GP1BA
| AltSymbols =; BSS; CD42B; CD42b-alpha; GP1B; MGC34595
| OMIM = 606672
| ECnumber = 
| Homologene = 143
| MGIid = 1333744
| GeneAtlas_image1 = PBB_GE_GP1BA_207389_at_tn.png
| Function = {{GNF_GO|id=GO:0005515 |text = protein binding}} {{GNF_GO|id=GO:0015057 |text = thrombin receptor activity}}
| Component = {{GNF_GO|id=GO:0005624 |text = membrane fraction}} {{GNF_GO|id=GO:0005886 |text = plasma membrane}} {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}}
| Process = {{GNF_GO|id=GO:0000902 |text = cell morphogenesis}} {{GNF_GO|id=GO:0007155 |text = cell adhesion}} {{GNF_GO|id=GO:0007166 |text = cell surface receptor linked signal transduction}} {{GNF_GO|id=GO:0030168 |text = platelet activation}} {{GNF_GO|id=GO:0030193 |text = regulation of blood coagulation}} {{GNF_GO|id=GO:0042730 |text = fibrinolysis}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 2811
    | Hs_Ensembl = ENSG00000185245
    | Hs_RefseqProtein = NP_000164
    | Hs_RefseqmRNA = NM_000173
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 17
    | Hs_GenLoc_start = 4776680
    | Hs_GenLoc_end = 4778599
    | Hs_Uniprot = P07359
    | Mm_EntrezGene = 14723
    | Mm_Ensembl = ENSMUSG00000050675
    | Mm_RefseqmRNA = NM_010326
    | Mm_RefseqProtein = NP_034456
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 11
    | Mm_GenLoc_start = 70455317
    | Mm_GenLoc_end = 70458253
    | Mm_Uniprot = O35930
  }}
}}
'''Glycoprotein Ib (platelet), alpha polypeptide''' ('''GP1BA''') also known as '''CD42b''' ('''C'''luster of '''D'''ifferentiation '''42b'''), is a human [[gene]].


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that are linked by disulfide bonds. The Gp Ib functions as a receptor for [[von Willebrand factor]] (VWF). The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX and platelet glycoprotein V. The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury, and also initiates signaling events within the platelet that lead to enhanced platelet activation, thrombosis, and hemostasis. This gene encodes the alpha subunit. Several polymorphisms and mutations have been described in this gene, some of which are the cause of [[Bernard-Soulier syndrome]]s and platelet-type [[von Willebrand disease]].<ref>{{cite web | title = Entrez Gene: GP1BA glycoprotein Ib (platelet), alpha polypeptide| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2811| accessdate = }}</ref>
{{PBB_Summary
| section_title =
| summary_text = Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that are linked by disulfide bonds. The Gp Ib functions as a receptor for von Willebrand factor (VWF). The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX and platelet glycoprotein V. The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury, and also initiates signaling events within the platelet that lead to enhanced platelet activation, thrombosis, and hemostasis. This gene encodes the alpha subunit. Several polymorphisms and mutations have been described in this gene, some of which are the cause of [[Bernard-Soulier syndrome]]s and platelet-type [[von Willebrand disease]].<ref>{{cite web | title = Entrez Gene: GP1BA glycoprotein Ib (platelet), alpha polypeptide| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2811| accessdate = }}</ref>
}}


==See also==
== Interactions ==
 
GP1BA has been shown to [[Protein-protein interaction|interact]] with [[YWHAZ]]<ref name=pmid9454760>{{cite journal | vauthors = Calverley DC, Kavanagh TJ, Roth GJ | title = Human signaling protein 14-3-3zeta interacts with platelet glycoprotein Ib subunits Ibalpha and Ibbeta | journal = Blood | volume = 91 | issue = 4 | pages = 1295–303  | date = February 1998 | pmid = 9454760 }}</ref><ref name=pmid8631758>{{cite journal | vauthors = Du X, Fox JE, Pei S | title = Identification of a binding sequence for the 14-3-3 protein within the cytoplasmic domain of the adhesion receptor, platelet glycoprotein Ib alpha | journal = J. Biol. Chem. | volume = 271 | issue = 13 | pages = 7362–7  | date = March 1996 | pmid = 8631758 | doi = 10.1074/jbc.271.13.7362 }}</ref><ref name=pmid10627461>{{cite journal | vauthors = Feng S, Christodoulides N, Reséndiz JC, Berndt MC, Kroll MH | title = Cytoplasmic domains of GpIbalpha and GpIbbeta regulate 14-3-3zeta binding to GpIb/IX/V | journal = Blood | volume = 95 | issue = 2 | pages = 551–7  | date = January 2000 | pmid = 10627461 }}</ref> and [[FLNB]].<ref name=pmid9651345>{{cite journal | vauthors = Takafuta T, Wu G, Murphy GF, Shapiro SS | title = Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha | journal = J. Biol. Chem. | volume = 273 | issue = 28 | pages = 17531–8  | date = July 1998 | pmid = 9651345 | doi = 10.1074/jbc.273.28.17531 }}</ref>
 
== See also ==
* [[Cluster of differentiation]]
* [[Cluster of differentiation]]


==References==
== References ==
{{reflist|2}}
{{reflist}}
{{Clear}}


==Further reading==
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Kunishima S, Kamiya T, Saito H | title = Genetic abnormalities of Bernard-Soulier syndrome | journal = Int. J. Hematol. | volume = 76 | issue = 4 | pages = 319–27 | year = 2002 | pmid = 12463594 | doi = 10.1007/BF02982690 }}
| citations =
* {{cite journal | vauthors = Du X | title = Signaling and regulation of the platelet glycoprotein Ib-IX-V complex | journal = Curr. Opin. Hematol. | volume = 14 | issue = 3 | pages = 262–9 | year = 2007 | pmid = 17414217 | doi = 10.1097/MOH.0b013e3280dce51a }}
*{{cite journal | author=Kunishima S, Kamiya T, Saito H |title=Genetic abnormalities of Bernard-Soulier syndrome. |journal=Int. J. Hematol. |volume=76 |issue= 4 |pages= 319-27 |year= 2003 |pmid= 12463594 |doi= }}
* {{cite journal | vauthors = Clemetson KJ | title = A short history of platelet glycoprotein Ib complex | journal = Thromb. Haemost. | volume = 98 | issue = 1 | pages = 63–8 | year = 2007 | pmid = 17597992 | doi = 10.1160/th07-05-0327 }}
*{{cite journal | author=Du X |title=Signaling and regulation of the platelet glycoprotein Ib-IX-V complex. |journal=Curr. Opin. Hematol. |volume=14 |issue= 3 |pages= 262-9 |year= 2007 |pmid= 17414217 |doi= 10.1097/MOH.0b013e3280dce51a }}
* {{cite journal | vauthors = López JA, Ludwig EH, McCarthy BJ | title = Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications | journal = J. Biol. Chem. | volume = 267 | issue = 14 | pages = 10055–61 | year = 1992 | pmid = 1577776 | doi =  }}
*{{cite journal | author=Clemetson KJ |title=A short history of platelet glycoprotein Ib complex. |journal=Thromb. Haemost. |volume=98 |issue= 1 |pages= 63-8 |year= 2007 |pmid= 17597992 |doi= }}
* {{cite journal | vauthors = Murata M, Furihata K, Ishida F, Russell SR, Ware J, Ruggeri ZM | title = Genetic and structural characterization of an amino acid dimorphism in glycoprotein Ib alpha involved in platelet transfusion refractoriness | journal = Blood | volume = 79 | issue = 11 | pages = 3086–90 | year = 1992 | pmid = 1586750 | doi =  }}
*{{cite journal | author=López JA, Ludwig EH, McCarthy BJ |title=Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications. |journal=J. Biol. Chem. |volume=267 |issue= 14 |pages= 10055-61 |year= 1992 |pmid= 1577776 |doi=  }}
* {{cite journal | vauthors = Girma JP, Takahashi Y, Yoshioka A, Diaz J, Meyer D | title = Ristocetin and botrocetin involve two distinct domains of von Willebrand factor for binding to platelet membrane glycoprotein Ib | journal = Thromb. Haemost. | volume = 64 | issue = 2 | pages = 326–32 | year = 1990 | pmid = 1702906 | doi =  }}
*{{cite journal | author=Murata M, Furihata K, Ishida F, ''et al.'' |title=Genetic and structural characterization of an amino acid dimorphism in glycoprotein Ib alpha involved in platelet transfusion refractoriness. |journal=Blood |volume=79 |issue= 11 |pages= 3086-90 |year= 1992 |pmid= 1586750 |doi=  }}
* {{cite journal | vauthors = Miller JL, Lyle VA, Cunningham D | title = Mutation of leucine-57 to phenylalanine in a platelet glycoprotein Ib alpha leucine tandem repeat occurring in patients with an autosomal dominant variant of Bernard-Soulier disease | journal = Blood | volume = 79 | issue = 2 | pages = 439–46 | year = 1992 | pmid = 1730088 | doi =  }}
*{{cite journal | author=Girma JP, Takahashi Y, Yoshioka A, ''et al.'' |title=Ristocetin and botrocetin involve two distinct domains of von Willebrand factor for binding to platelet membrane glycoprotein Ib. |journal=Thromb. Haemost. |volume=64 |issue= 2 |pages= 326-32 |year= 1991 |pmid= 1702906 |doi=  }}
* {{cite journal | vauthors = Modderman PW, Admiraal LG, Sonnenberg A, von dem Borne AE | title = Glycoproteins V and Ib-IX form a noncovalent complex in the platelet membrane | journal = J. Biol. Chem. | volume = 267 | issue = 1 | pages = 364–9 | year = 1992 | pmid = 1730602 | doi =  }}
*{{cite journal | author=Miller JL, Lyle VA, Cunningham D |title=Mutation of leucine-57 to phenylalanine in a platelet glycoprotein Ib alpha leucine tandem repeat occurring in patients with an autosomal dominant variant of Bernard-Soulier disease. |journal=Blood |volume=79 |issue= 2 |pages= 439-46 |year= 1992 |pmid= 1730088 |doi=  }}
* {{cite journal | vauthors = Miller JL, Cunningham D, Lyle VA, Finch CN | title = Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 88 | issue = 11 | pages = 4761–5 | year = 1991 | pmid = 2052556 | pmc = 51746 | doi = 10.1073/pnas.88.11.4761 }}
*{{cite journal | author=Modderman PW, Admiraal LG, Sonnenberg A, von dem Borne AE |title=Glycoproteins V and Ib-IX form a noncovalent complex in the platelet membrane. |journal=J. Biol. Chem. |volume=267 |issue= 1 |pages= 364-9 |year= 1992 |pmid= 1730602 |doi=  }}
* {{cite journal | vauthors = Hess D, Schaller J, Rickli EE, Clemetson KJ | title = Identification of the disulphide bonds in human platelet glycocalicin | journal = Eur. J. Biochem. | volume = 199 | issue = 2 | pages = 389–93 | year = 1991 | pmid = 2070794 | doi = 10.1111/j.1432-1033.1991.tb16135.x }}
*{{cite journal | author=Miller JL, Cunningham D, Lyle VA, Finch CN |title=Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=88 |issue= 11 |pages= 4761-5 |year= 1991 |pmid= 2052556 |doi= }}
* {{cite journal | vauthors = Du X, Beutler L, Ruan C, Castaldi PA, Berndt MC | title = Glycoprotein Ib and glycoprotein IX are fully complexed in the intact platelet membrane | journal = Blood | volume = 69 | issue = 5 | pages = 1524–7 | year = 1987 | pmid = 2436691 | doi =  }}
*{{cite journal | author=Hess D, Schaller J, Rickli EE, Clemetson KJ |title=Identification of the disulphide bonds in human platelet glycocalicin. |journal=Eur. J. Biochem. |volume=199 |issue= 2 |pages= 389-93 |year= 1991 |pmid= 2070794 |doi= }}
* {{cite journal | vauthors = Andrews RK, Booth WJ, Gorman JJ, Castaldi PA, Berndt MC | title = Purification of botrocetin from Bothrops jararaca venom. Analysis of the botrocetin-mediated interaction between von Willebrand factor and the human platelet membrane glycoprotein Ib-IX complex | journal = Biochemistry | volume = 28 | issue = 21 | pages = 8317–26 | year = 1989 | pmid = 2557900 | doi = 10.1021/bi00447a009 }}
*{{cite journal | author=Du X, Beutler L, Ruan C, ''et al.'' |title=Glycoprotein Ib and glycoprotein IX are fully complexed in the intact platelet membrane. |journal=Blood |volume=69 |issue= 5 |pages= 1524-7 |year= 1987 |pmid= 2436691 |doi=  }}
* {{cite journal | vauthors = Wenger RH, Wicki AN, Kieffer N, Adolph S, Hameister H, Clemetson KJ | title = The 5' flanking region and chromosomal localization of the gene encoding human platelet membrane glycoprotein Ib alpha | journal = Gene | volume = 85 | issue = 2 | pages = 517–24 | year = 1989 | pmid = 2628181 | doi = 10.1016/0378-1119(89)90446-0 }}
*{{cite journal | author=Andrews RK, Booth WJ, Gorman JJ, ''et al.'' |title=Purification of botrocetin from Bothrops jararaca venom. Analysis of the botrocetin-mediated interaction between von Willebrand factor and the human platelet membrane glycoprotein Ib-IX complex. |journal=Biochemistry |volume=28 |issue= 21 |pages= 8317-26 |year= 1990 |pmid= 2557900 |doi= }}
* {{cite journal | vauthors = Wenger RH, Kieffer N, Wicki AN, Clemetson KJ | title = Structure of the human blood platelet membrane glycoprotein Ib alpha gene | journal = Biochem. Biophys. Res. Commun. | volume = 156 | issue = 1 | pages = 389–95 | year = 1988 | pmid = 2845978 | doi = 10.1016/S0006-291X(88)80853-2 }}
*{{cite journal | author=Wenger RH, Wicki AN, Kieffer N, ''et al.'' |title=The 5' flanking region and chromosomal localization of the gene encoding human platelet membrane glycoprotein Ib alpha. |journal=Gene |volume=85 |issue= 2 |pages= 517-24 |year= 1990 |pmid= 2628181 |doi= }}
* {{cite journal | vauthors = Wicki AN, Clemetson KJ | title = Structure and function of platelet membrane glycoproteins Ib and V. Effects of leukocyte elastase and other proteases on platelets response to von Willebrand factor and thrombin | journal = Eur. J. Biochem. | volume = 153 | issue = 1 | pages = 1–11 | year = 1985 | pmid = 2933256 | doi = 10.1111/j.1432-1033.1985.tb09259.x }}
*{{cite journal | author=Wenger RH, Kieffer N, Wicki AN, Clemetson KJ |title=Structure of the human blood platelet membrane glycoprotein Ib alpha gene. |journal=Biochem. Biophys. Res. Commun. |volume=156 |issue= 1 |pages= 389-95 |year= 1988 |pmid= 2845978 |doi= }}
* {{cite journal | vauthors = Adelman B, Michelson AD, Greenberg J, Handin RI | title = Proteolysis of platelet glycoprotein Ib by plasmin is facilitated by plasmin lysine-binding regions | journal = Blood | volume = 68 | issue = 6 | pages = 1280–4 | year = 1986 | pmid = 2946332 | doi =  }}
*{{cite journal | author=Wicki AN, Clemetson KJ |title=Structure and function of platelet membrane glycoproteins Ib and V. Effects of leukocyte elastase and other proteases on platelets response to von Willebrand factor and thrombin. |journal=Eur. J. Biochem. |volume=153 |issue= 1 |pages= 1-11 |year= 1985 |pmid= 2933256 |doi= }}
* {{cite journal | vauthors = Lopez JA, Chung DW, Fujikawa K, Hagen FS, Papayannopoulou T, Roth GJ | title = Cloning of the alpha chain of human platelet glycoprotein Ib: a transmembrane protein with homology to leucine-rich alpha 2-glycoprotein | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 84 | issue = 16 | pages = 5615–9 | year = 1987 | pmid = 3303030 | pmc = 298913 | doi = 10.1073/pnas.84.16.5615 }}
*{{cite journal | author=Adelman B, Michelson AD, Greenberg J, Handin RI |title=Proteolysis of platelet glycoprotein Ib by plasmin is facilitated by plasmin lysine-binding regions. |journal=Blood |volume=68 |issue= 6 |pages= 1280-4 |year= 1987 |pmid= 2946332 |doi=  }}
* {{cite journal | vauthors = Lopez JA, Chung DW, Fujikawa K, Hagen FS, Davie EW, Roth GJ | title = The alpha and beta chains of human platelet glycoprotein Ib are both transmembrane proteins containing a leucine-rich amino acid sequence | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 85 | issue = 7 | pages = 2135–9 | year = 1988 | pmid = 3353370 | pmc = 279943 | doi = 10.1073/pnas.85.7.2135 }}
*{{cite journal | author=Lopez JA, Chung DW, Fujikawa K, ''et al.'' |title=Cloning of the alpha chain of human platelet glycoprotein Ib: a transmembrane protein with homology to leucine-rich alpha 2-glycoprotein. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=84 |issue= 16 |pages= 5615-9 |year= 1987 |pmid= 3303030 |doi= }}
* {{cite journal | vauthors = Titani K, Takio K, Handa M, Ruggeri ZM | title = Amino acid sequence of the von Willebrand factor-binding domain of platelet membrane glycoprotein Ib | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 84 | issue = 16 | pages = 5610–4 | year = 1987 | pmid = 3497398 | pmc = 298912 | doi = 10.1073/pnas.84.16.5610 }}
*{{cite journal | author=Lopez JA, Chung DW, Fujikawa K, ''et al.'' |title=The alpha and beta chains of human platelet glycoprotein Ib are both transmembrane proteins containing a leucine-rich amino acid sequence. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=85 |issue= 7 |pages= 2135-9 |year= 1988 |pmid= 3353370 |doi= }}
* {{cite journal | vauthors = Harmon JT, Jamieson GA | title = The glycocalicin portion of platelet glycoprotein Ib expresses both high and moderate affinity receptor sites for thrombin. A soluble radioreceptor assay for the interaction of thrombin with platelets | journal = J. Biol. Chem. | volume = 261 | issue = 28 | pages = 13224–9 | year = 1986 | pmid = 3759960 | doi =  }}
*{{cite journal | author=Titani K, Takio K, Handa M, Ruggeri ZM |title=Amino acid sequence of the von Willebrand factor-binding domain of platelet membrane glycoprotein Ib. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=84 |issue= 16 |pages= 5610-4 |year= 1987 |pmid= 3497398 |doi= }}
*{{cite journal | author=Harmon JT, Jamieson GA |title=The glycocalicin portion of platelet glycoprotein Ib expresses both high and moderate affinity receptor sites for thrombin. A soluble radioreceptor assay for the interaction of thrombin with platelets. |journal=J. Biol. Chem. |volume=261 |issue= 28 |pages= 13224-9 |year= 1986 |pmid= 3759960 |doi=  }}
}}
{{refend}}
{{refend}}


==External links==
== External links ==
* {{MeshName|GP1BA+protein,+human}}
* {{MeshName|GP1BA+protein,+human}}


{{membrane-protein-stub}}
{{PDB Gallery|geneid=2811}}
{{Coagulation}}
{{Clusters of differentiation}}
 
{{NLM content}}
{{NLM content}}
{{Clusters of differentiation}}
 
[[Category:Clusters of differentiation]]
[[Category:Clusters of differentiation]]
{{WikiDoc Sources}}
 
 
{{membrane-protein-stub}}

Latest revision as of 00:41, 27 October 2017

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Identifiers
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External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
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Ensembl

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RefSeq (mRNA)

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RefSeq (protein)

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Platelet glycoprotein Ib alpha chain also known as glycoprotein Ib (platelet), alpha polypeptide or CD42b (Cluster of Differentiation 42b), is a protein that in humans is encoded by the GP1BA gene.

Function

Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that are linked by disulfide bonds. The Gp Ib functions as a receptor for von Willebrand factor (VWF). The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX and platelet glycoprotein V. The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury, and also initiates signaling events within the platelet that lead to enhanced platelet activation, thrombosis, and hemostasis. This gene encodes the alpha subunit. Several polymorphisms and mutations have been described in this gene, some of which are the cause of Bernard-Soulier syndromes and platelet-type von Willebrand disease.[1]

Interactions

GP1BA has been shown to interact with YWHAZ[2][3][4] and FLNB.[5]

See also

References

  1. ↑ "Entrez Gene: GP1BA glycoprotein Ib (platelet), alpha polypeptide".
  2. ↑ Calverley DC, Kavanagh TJ, Roth GJ (February 1998). "Human signaling protein 14-3-3zeta interacts with platelet glycoprotein Ib subunits Ibalpha and Ibbeta". Blood. 91 (4): 1295–303. PMID 9454760.
  3. ↑ Du X, Fox JE, Pei S (March 1996). "Identification of a binding sequence for the 14-3-3 protein within the cytoplasmic domain of the adhesion receptor, platelet glycoprotein Ib alpha". J. Biol. Chem. 271 (13): 7362–7. doi:10.1074/jbc.271.13.7362. PMID 8631758.
  4. ↑ Feng S, Christodoulides N, Reséndiz JC, Berndt MC, Kroll MH (January 2000). "Cytoplasmic domains of GpIbalpha and GpIbbeta regulate 14-3-3zeta binding to GpIb/IX/V". Blood. 95 (2): 551–7. PMID 10627461.
  5. ↑ Takafuta T, Wu G, Murphy GF, Shapiro SS (July 1998). "Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha". J. Biol. Chem. 273 (28): 17531–8. doi:10.1074/jbc.273.28.17531. PMID 9651345.

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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