+ |
SEMA3A | down-regulates
binding
|
NRP1 |
0.911 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-66661 |
|
|
Homo sapiens |
|
pmid |
sentence |
10196546 |
Semaphorins a and e act as antagonists of neuropilin-1 and agonists of neuropilin-2 receptors. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DLL4 | down-regulates quantity by repression
transcriptional regulation
|
NRP1 |
0.37 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-178029 |
|
|
Homo sapiens |
|
pmid |
sentence |
18339870 |
Dll4 down-regulates vascular endothelial growth factor (vegf)_ receptor_ 2 and nrp1 expression and inhibits vegf function |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SEMA3A | up-regulates activity
binding
|
NRP1 |
0.911 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261815 |
|
|
Homo sapiens |
|
pmid |
sentence |
25335892 |
Further examination of the composition of the functional Sema3B receptor revealed that, unlike Sema3A, which signals exclusively using the NP1 receptor, Sema3B utilizes both NP1 and NP2 for signal transduction. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NRP1 | up-regulates quantity by expression
transcriptional regulation
|
PHACTR1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260061 |
|
|
Homo sapiens |
|
pmid |
sentence |
21939755 |
Recently, we identified a new Vascular Endothelial Growth Factor (VEGF)-A(165)-induced gene Phactr-1, (Phosphatase Actin Regulator-1). We found that neuropilin-1 (NRP-1) and VEGF-R1 depletion inhibited Phactr-1 mRNA expression while NRP-2 and VEGF-R2 depletion had no effect. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
NRP1 | form complex
binding
|
CoV2 spike protein-NRP1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261672 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
other |
Neuropilin-1 facilitates SARS-CoV-2 cell entry and provides a possible pathway into the central nervous system To determine whether SARS-CoV-2 uses NRP1 for virus entry, we generated replication deficient lentiviruses pseudotyped with SARS-CoV-2 spike protein (S) that drive expression of green fluorescent protein (GFP) upon infection. When expressed alone, ACE2 rendered cells susceptible to infection (Fig. 1a). NRP1 alone allowed lower, yet detectable levels of infection, both in HEK-293T and in Caco2 cells (Fig. 1a,b), while cells transfected with plasmids encoding only TMPRSS2 were not infected (Fig. 1a). The co-expression of TMPRSS2 with either ACE2 or NRP1 potentiated the infection, with ACE2 together with TMPRSS2 being twice as efficient as NRP1 with TMPRSS2 (Fig. 1c) |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | SARS-CoV ATTACHMENT AND ENTRY |
+ |
EMX1 | up-regulates quantity by expression
transcriptional regulation
|
NRP1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261593 |
|
|
in vitro |
|
pmid |
sentence |
26534986 |
EMX1 activates the transcription of Nrp1 in vitro. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
SEMA3B | up-regulates activity
binding
|
NRP1 |
0.748 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261814 |
|
|
Homo sapiens |
|
pmid |
sentence |
25335892 |
Further examination of the composition of the functional Sema3B receptor revealed that, unlike Sema3A, which signals exclusively using the NP1 receptor, Sema3B utilizes both NP1 and NP2 for signal transduction. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |