Details of Protein
General Information of Protein (ID: PRT00658) | |||||
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Name | FMLP-related receptor I (FPR2) | ||||
Synonyms |
Click to Show/Hide Synonyms of This Protein
FMLP-related receptor I; FMLP-R-I; Formyl peptide receptor-like 1; HM63; Lipoxin A4 receptor; LXA4 receptor; RFP; FPR2; FPRH1; FPRL1; LXA4R
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Gene Name | FPR2 | Gene ID | |||
UniProt ID | |||||
Family | GPCR rhodopsin (GPCR-1) | ||||
Click to Show/Hide the Molecular/Functional Data (Sequence/Structure/Function) of This Protein | |||||
Sequence |
METNFSTPLNEYEEVSYESAGYTVLRILPLVVLGVTFVLGVLGNGLVIWVAGFRMTRTVT
TICYLNLALADFSFTATLPFLIVSMAMGEKWPFGWFLCKLIHIVVDINLFGSVFLIGFIA LDRCICVLHPVWAQNHRTVSLAMKVIVGPWILALVLTLPVFLFLTTVTIPNGDTYCTFNF ASWGGTPEERLKVAITMLTARGIIRFVIGFSLPMSIVAICYGLIAAKIHKKGMIKSSRPL RVLTAVVASFFICWFPFQLVALLGTVWLKEMLFYGKYKIIDILVNPTSSLAFFNSCLNPM LYVFVGQDFRERLIHSLPTSLERALSEDSAPTNDTAANSASPPAETELQAM |
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Structure | |||||
Function | Low affinity receptor for N-formyl-methionyl peptides, which are powerful neutrophil chemotactic factors. Binding of FMLP to the receptor causes activation of neutrophils. This response is mediated via a G-protein that activates a phosphatidylinositol-calcium second messenger system. The activation of LXA4R could result in an anti-inflammatory outcome counteracting the actions of proinflammatory signals such as LTB4 (leukotriene B4). Receptor for the chemokine-like protein FAM19A5, mediating FAM19A5-stimulated macrophage chemotaxis and the inhibitory effect on TNFSF11/RANKL-induced osteoclast differentiation. | ||||
Regulatory Network | |||||
Full List of Metabolite(s) Regulating This Protein | ||||||
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Lipids and lipid-like molecules | ||||||
AT-Resolvin D1 | Click to Show/Hide the Full List of Regulating Pair(s): 1 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair |
Experim Info
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[1] | ||||
Introduced Variation | AT-Resolvin D1 addition (1 hours) | |||||
Induced Change | FPR2 protein activity levels: increase | |||||
Summary | Introduced Variation
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Disease Status | Peritonitis [ICD-11: DC50] | |||||
Details | It is reported that AT-resolvin D1 addition causes the increase of FPR2 protein activity compared with control group. | |||||
Lipoxin A4 | Click to Show/Hide the Full List of Regulating Pair(s): 1 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair |
Experim Info
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[2] | ||||
Introduced Variation | Lipoxin A4 addition (1 hours) | |||||
Induced Change | FPR2 protein affinity activity levels: increase | |||||
Summary | Introduced Variation
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Disease Status | Peritonitis [ICD-11: DC50] | |||||
Details | It is reported that lipoxin A4 addition causes the increase of FPR2 protein affinity activity compared with control group. | |||||
Resolvin D1 | Click to Show/Hide the Full List of Regulating Pair(s): 2 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair (1) |
Experim Info
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[1] | ||||
Introduced Variation | Resolvin D1 addition (1 hours) | |||||
Induced Change | FPR2 protein activity levels: increase | |||||
Summary | Introduced Variation
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Disease Status | Peritonitis [ICD-11: DC50] | |||||
Details | It is reported that resolvin D1 addition causes the increase of FPR2 protein activity compared with control group. | |||||
Regulating Pair (2) |
Experim Info
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[2] | ||||
Introduced Variation | Resolvin D1 addition (1 hours) | |||||
Induced Change | FPR2 protein affinity activity levels: increase | |||||
Summary | Introduced Variation
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Disease Status | Peritonitis [ICD-11: DC50] | |||||
Details | It is reported that resolvin D1 addition causes the increase of FPR2 protein affinity activity compared with control group. | |||||
RvD1-ME | Click to Show/Hide the Full List of Regulating Pair(s): 1 Pair(s) | |||||
Detailed Information |
Metabo Info
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Regulating Pair |
Experim Info
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[1] | ||||
Introduced Variation | RvD1-ME addition (1 hours) | |||||
Induced Change | FPR2 protein activity levels: increase | |||||
Summary | Introduced Variation
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Disease Status | Peritonitis [ICD-11: DC50] | |||||
Details | It is reported that RvD1-ME addition causes the increase of FPR2 protein activity compared with control group. | |||||
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