Type |
Details |
Score |
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
frog, western clawed |
|
•
•
•
•
•
|
Gene |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chimpanzee |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
macaque, rhesus |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Publication |
First Author: |
Bufe B |
Year: |
2019 |
Journal: |
Nat Commun |
Title: |
Bacterial MgrB peptide activates chemoreceptor Fpr3 in mouse accessory olfactory system and drives avoidance behaviour. |
Volume: |
10 |
Issue: |
1 |
Pages: |
4889 |
|
•
•
•
•
•
|
Publication |
First Author: |
Stempel H |
Year: |
2016 |
Journal: |
J Biol Chem |
Title: |
Strain-specific Loss of Formyl Peptide Receptor 3 in the Murine Vomeronasal and Immune Systems. |
Volume: |
291 |
Issue: |
18 |
Pages: |
9762-75 |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus caroli |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus pahari |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus spretus |
|
•
•
•
•
•
|
Publication |
First Author: |
Gao JL |
Year: |
1998 |
Journal: |
Genomics |
Title: |
Differential expansion of the N-formylpeptide receptor gene cluster in human and mouse. |
Volume: |
51 |
Issue: |
2 |
Pages: |
270-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rivière S |
Year: |
2009 |
Journal: |
Nature |
Title: |
Formyl peptide receptor-like proteins are a novel family of vomeronasal chemosensors. |
Volume: |
459 |
Issue: |
7246 |
Pages: |
574-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Liberles SD |
Year: |
2009 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Formyl peptide receptors are candidate chemosensory receptors in the vomeronasal organ. |
Volume: |
106 |
Issue: |
24 |
Pages: |
9842-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Vaughn MW |
Year: |
2002 |
Journal: |
J Immunol |
Title: |
Identification, cloning, and functional characterization of a murine lipoxin A4 receptor homologue gene. |
Volume: |
169 |
Issue: |
6 |
Pages: |
3363-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kurosaka K |
Year: |
2005 |
Journal: |
J Immunol |
Title: |
Mouse cathelin-related antimicrobial peptide chemoattracts leukocytes using formyl peptide receptor-like 1/mouse formyl peptide receptor-like 2 as the receptor and acts as an immune adjuvant. |
Volume: |
174 |
Issue: |
10 |
Pages: |
6257-65 |
|
•
•
•
•
•
|
Publication |
First Author: |
Takano T |
Year: |
1997 |
Journal: |
J Exp Med |
Title: |
Aspirin-triggered 15-epi-lipoxin A4 (LXA4) and LXA4 stable analogues are potent inhibitors of acute inflammation: evidence for anti-inflammatory receptors. |
Volume: |
185 |
Issue: |
9 |
Pages: |
1693-704 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wang ZG |
Year: |
2002 |
Journal: |
Gene |
Title: |
Characterization of two new members of the formyl peptide receptor gene family from 129S6 mice. |
Volume: |
299 |
Issue: |
1-2 |
Pages: |
57-63 |
|
•
•
•
•
•
|
Publication |
First Author: |
Adams DJ |
Year: |
2024 |
Journal: |
Nature |
Title: |
Genetic determinants of micronucleus formation in vivo. |
Volume: |
627 |
Issue: |
8002 |
Pages: |
130-136 |
|
•
•
•
•
•
|
Publication |
First Author: |
MGD Nomenclature Committee |
Year: |
1995 |
|
Title: |
Nomenclature Committee Use |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Perniss A |
Year: |
2020 |
Journal: |
Immunity |
Title: |
Chemosensory Cell-Derived Acetylcholine Drives Tracheal Mucociliary Clearance in Response to Virulence-Associated Formyl Peptides. |
Volume: |
52 |
Issue: |
4 |
Pages: |
683-699.e11 |
|
•
•
•
•
•
|
Publication |
First Author: |
Birkl D |
Year: |
2019 |
Journal: |
FASEB J |
Title: |
Formyl peptide receptor 2 regulates monocyte recruitment to promote intestinal mucosal wound repair. |
Volume: |
33 |
Issue: |
12 |
Pages: |
13632-13643 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gavins FN |
Year: |
2003 |
Journal: |
Blood |
Title: |
Leukocyte antiadhesive actions of annexin 1: ALXR- and FPR-related anti-inflammatory mechanisms. |
Volume: |
101 |
Issue: |
10 |
Pages: |
4140-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics and the International Mouse Phenotyping Consortium (IMPC) |
Year: |
2014 |
Journal: |
Database Release |
Title: |
Obtaining and Loading Phenotype Annotations from the International Mouse Phenotyping Consortium (IMPC) Database |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
International Mouse Strain Resource |
Year: |
2014 |
Journal: |
Database Download |
Title: |
MGI download of germline transmission data for alleles from IMSR strain data |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Dickinson ME |
Year: |
2016 |
Journal: |
Nature |
Title: |
High-throughput discovery of novel developmental phenotypes. |
Volume: |
537 |
Issue: |
7621 |
Pages: |
508-514 |
|
•
•
•
•
•
|
Publication |
First Author: |
International Knockout Mouse Consortium |
Year: |
2014 |
Journal: |
Database Download |
Title: |
MGI download of modified allele data from IKMC and creation of new knockout alleles |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Helmholtz Zentrum Muenchen GmbH |
Year: |
2010 |
Journal: |
MGI Direct Data Submission |
Title: |
Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu) |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Gobbetti T |
Year: |
2014 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Nonredundant protective properties of FPR2/ALX in polymicrobial murine sepsis. |
Volume: |
111 |
Issue: |
52 |
Pages: |
18685-90 |
|
•
•
•
•
•
|
Publication |
First Author: |
Brancaleone V |
Year: |
2013 |
Journal: |
Blood |
Title: |
A vasculo-protective circuit centered on lipoxin A4 and aspirin-triggered 15-epi-lipoxin A4 operative in murine microcirculation. |
Volume: |
122 |
Issue: |
4 |
Pages: |
608-17 |
|
•
•
•
•
•
|
Publication |
First Author: |
The Gene Ontology Consortium |
Year: |
2010 |
|
Title: |
Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
The Gene Ontology Consortium |
Year: |
2014 |
|
Title: |
Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Lavigne MC |
Year: |
2002 |
Journal: |
Cell Immunol |
Title: |
The N-formylpeptide receptor (FPR) and a second G(i)-coupled receptor mediate fMet-Leu-Phe-stimulated activation of NADPH oxidase in murine neutrophils. |
Volume: |
218 |
Issue: |
1-2 |
Pages: |
7-12 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bufe B |
Year: |
2012 |
Journal: |
J Biol Chem |
Title: |
Formyl peptide receptors from immune and vomeronasal system exhibit distinct agonist properties. |
Volume: |
287 |
Issue: |
40 |
Pages: |
33644-55 |
|
•
•
•
•
•
|
Publication |
First Author: |
UniProt-GOA |
Year: |
2012 |
|
Title: |
Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
UniProt-GOA |
Year: |
2012 |
|
Title: |
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas |
Year: |
2010 |
|
Title: |
Annotation inferences using phylogenetic trees |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Levy BD |
Year: |
2002 |
Journal: |
Nat Med |
Title: |
Multi-pronged inhibition of airway hyper-responsiveness and inflammation by lipoxin A(4). |
Volume: |
8 |
Issue: |
9 |
Pages: |
1018-23 |
|
•
•
•
•
•
|
Publication |
First Author: |
Coffelt SB |
Year: |
2009 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
The pro-inflammatory peptide LL-37 promotes ovarian tumor progression through recruitment of multipotent mesenchymal stromal cells. |
Volume: |
106 |
Issue: |
10 |
Pages: |
3806-11 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wu J |
Year: |
2011 |
Journal: |
Biochem Biophys Res Commun |
Title: |
Lipoxin A4 inhibits the production of proinflammatory cytokines induced by β-amyloid in vitro and in vivo. |
Volume: |
408 |
Issue: |
3 |
Pages: |
382-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Elias I |
Year: |
2016 |
Journal: |
Diabetes |
Title: |
ALOX5AP Overexpression in Adipose Tissue Leads to LXA4 Production and Protection Against Diet-Induced Obesity and Insulin Resistance. |
Volume: |
65 |
Issue: |
8 |
Pages: |
2139-50 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kang JW |
Year: |
2016 |
Journal: |
Biochim Biophys Acta |
Title: |
Resolvin D1 protects the liver from ischemia/reperfusion injury by enhancing M2 macrophage polarization and efferocytosis. |
Volume: |
1861 |
Issue: |
9 Pt A |
Pages: |
1025-1035 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Database and National Center for Biotechnology Information |
Year: |
2000 |
Journal: |
Database Release |
Title: |
Entrez Gene Load |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Allen Institute for Brain Science |
Year: |
2004 |
Journal: |
Allen Institute |
Title: |
Allen Brain Atlas: mouse riboprobes |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2009 |
Journal: |
Database Download |
Title: |
Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI) |
Year: |
2010 |
Journal: |
Database Download |
Title: |
Consensus CDS project |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Bairoch A |
Year: |
1999 |
Journal: |
Database Release |
Title: |
SWISS-PROT Annotated protein sequence database |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2005 |
|
Title: |
Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2010 |
Journal: |
Database Download |
Title: |
Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome U74 Array Platform (A, B, C v2). |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2005 |
|
Title: |
Obtaining and loading genome assembly coordinates from NCBI annotations |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2009 |
Journal: |
Database Download |
Title: |
Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2003 |
|
Title: |
MGI Sequence Curation Reference |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Mouse Genome Informatics Scientific Curators |
Year: |
2002 |
|
Title: |
Chromosome assignment of mouse genes using the Mouse Genome Sequencing Consortium (MGSC) assembly and the ENSEMBL Database |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Park SK |
Year: |
2014 |
Journal: |
Mol Genet Genomics |
Title: |
Nuclear FKBPs, Fpr3 and Fpr4 affect genome-wide genes transcription. |
Volume: |
289 |
Issue: |
2 |
Pages: |
125-36 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wilson LK |
Year: |
1995 |
Journal: |
J Biol Chem |
Title: |
The yeast immunophilin Fpr3 is a physiological substrate of the tyrosine-specific phosphoprotein phosphatase Ptp1. |
Volume: |
270 |
Issue: |
42 |
Pages: |
25185-93 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
351
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Yang D |
Year: |
2002 |
Journal: |
J Leukoc Biol |
Title: |
Human dendritic cells express functional formyl peptide receptor-like-2 (FPRL2) throughout maturation. |
Volume: |
72 |
Issue: |
3 |
Pages: |
598-607 |
|
•
•
•
•
•
|
Publication |
First Author: |
Migeotte I |
Year: |
2005 |
Journal: |
J Exp Med |
Title: |
Identification and characterization of an endogenous chemotactic ligand specific for FPRL2. |
Volume: |
201 |
Issue: |
1 |
Pages: |
83-93 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Formyl peptide receptors (FPR) are members of the rhodopsin-like G-protein coupled receptor family and are involved in chemotaxis [, ]. They were originally identified by their ability to bind N-formyl peptides (typified by fMet-Leu-Phe (fMLP)), produced by the degradation of either bacterial or host cells [, ]but subsequent ligands have been discovered, containing many microbial agonists derived from both bacteria and viruses [, ].FPRs were initially found on leukocytes, but they are expressed in other cells, for example, immature dendritic cells, platelets, microglial cells, astrocytes, fibroblasts and platelets [, ]. FPRs are expressed at high levels on polymorphonuclear and mononuclear phagocytes. Formyl peptide receptors are not only involved in mediating immune cell response to infection, but also act to suppress the immune system under certain conditions []. The main responses elicited upon ligation of formylated peptides, are those of morphological polarization, locomotion, production of reactive-oxygen species and release of proteolytic enzymes []. There are three formyl peptide receptor subtypes, FPR1, FPR2 and FPR3 [, ]. The sequence similarity between FPR1 and FPR2 is high (69%), and although there is a large sequence similarity also between FPR2 and FPR3 (83%), FPR3 can not bind formylated peptides [, ]. Formyl peptide receptor 3 (FPR3) is primarily a receptor of monocytes, macrophages and dendritic cells. It is also expressed on mouse, but not human, neutrophils [, , ]. Although FPR3 is found in human monocytes, studies have shown that approximately one third of individuals lack cell surface expression of this receptor [, ]. The functions of FPR3, other than directing cell migration, remain to be characterised [, ]. |
|
•
•
•
•
•
|
Publication |
First Author: |
Gantz I |
Year: |
1996 |
Journal: |
Cytogenet Cell Genet |
Title: |
Molecular cloning of a novel receptor (CMKLR1) with homology to the chemotactic factor receptors. |
Volume: |
74 |
Issue: |
4 |
Pages: |
286-90 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Formyl peptide receptors (FPR) are members of the rhodopsin-like G-protein coupled receptor family and are involved in chemotaxis [, ]. They were originally identified by their ability to bind N-formyl peptides (typified by fMet-Leu-Phe (fMLP)), produced by the degradation of either bacterial or host cells [, ]but subsequent ligands have been discovered, containing many microbial agonists derived from both bacteria and viruses [, ].FPRs were initially found on leukocytes, but they are expressed in other cells, for example, immature dendritic cells, platelets, microglial cells, astrocytes, fibroblasts and platelets [, ]. FPRs are expressed at high levels on polymorphonuclear and mononuclear phagocytes. Formyl peptide receptors are not only involved in mediating immune cell response to infection, but also act to suppress the immune system under certain conditions []. The main responses elicited upon ligation of formylated peptides, are those of morphological polarization, locomotion, production of reactive-oxygen species and release of proteolytic enzymes []. There are three formyl peptide receptor subtypes, FPR1, FPR2 and FPR3 [, ]. The sequence similarity between FPR1 and FPR2 is high (69%), and although there is a large sequence similarity also between FPR2 and FPR3 (83%), FPR3 can not bind formylated peptides [, ]. This entry includes the formyl peptide receptors and other related receptors such as C3a and C5a anaphylatoxin chemotactic receptors []and G-protein-coupled receptor CMKlR1 []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Migeotte I |
Year: |
2006 |
Journal: |
Cytokine Growth Factor Rev |
Title: |
Formyl peptide receptors: a promiscuous subfamily of G protein-coupled receptors controlling immune responses. |
Volume: |
17 |
Issue: |
6 |
Pages: |
501-19 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ye RD |
Year: |
2009 |
Journal: |
Pharmacol Rev |
Title: |
International Union of Basic and Clinical Pharmacology. LXXIII. Nomenclature for the formyl peptide receptor (FPR) family. |
Volume: |
61 |
Issue: |
2 |
Pages: |
119-61 |
|
•
•
•
•
•
|
Publication |
First Author: |
Le Y |
Year: |
2002 |
Journal: |
Trends Immunol |
Title: |
Formyl-peptide receptors revisited. |
Volume: |
23 |
Issue: |
11 |
Pages: |
541-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Panaro MA |
Year: |
2006 |
Journal: |
Immunopharmacol Immunotoxicol |
Title: |
Biological role of the N-formyl peptide receptors. |
Volume: |
28 |
Issue: |
1 |
Pages: |
103-27 |
|
•
•
•
•
•
|
Publication |
First Author: |
Braun MC |
Year: |
2001 |
Journal: |
Blood |
Title: |
Activation of the formyl peptide receptor by the HIV-derived peptide T-20 suppresses interleukin-12 p70 production by human monocytes. |
Volume: |
97 |
Issue: |
11 |
Pages: |
3531-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
He HQ |
Year: |
2013 |
Journal: |
Mol Pharmacol |
Title: |
Functional characterization of three mouse formyl peptide receptors. |
Volume: |
83 |
Issue: |
2 |
Pages: |
389-98 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fu H |
Year: |
2006 |
Journal: |
J Leukoc Biol |
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Ligand recognition and activation of formyl peptide receptors in neutrophils. |
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79 |
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Year: |
2015 |
Journal: |
FASEB J |
Title: |
Targeting the annexin 1-formyl peptide receptor 2/ALX pathway affords protection against bacterial LPS-induced pathologic changes in the murine adrenal cortex. |
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7 |
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2016 |
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PLoS One |
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11 |
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e0156092 |
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First Author: |
Cooray SN |
Year: |
2013 |
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Proc Natl Acad Sci U S A |
Title: |
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Front Biosci |
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Year: |
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Nat Struct Mol Biol |
Title: |
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Volume: |
11 |
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3 |
Pages: |
275-83 |
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Protein Domain |
Type: |
Family |
Description: |
FK506-binding proteins (FKBPs) are a particular class of peptidyl-prolyl cis-trans isomerases (PPIases) () []. This entry represents a group of nuclear FK506-binding proteins that act as histone chaperones. They each containing an extended acidic domain in addition to the conserved FK506-binding/peptidylprolyl isomerase (PPIase) domain. The PPIase domain has been shown to regulate histone H3 methylation, while the acidic domain has been shown to facilitate histone deposition and may regulate rDNA silencing [, ]. This entry includes Fpr3 and its paralogue, Fpr4, from budding yeasts. They have been shown to affect genome-wide genes transcription [].This entry also includes AtFKBP53 from Arabidopsis and SpFkbp39p from Schizosaccharomyces pombe. AtFKBP53 possesses histone chaperone activity and is required for repressing ribosomal gene expression in Arabidopsis []. SpFkbp39p is a histone chaperone regulating rDNA silencing []. |
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Title: |
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448-52 |
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