| Type |
Details |
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Farrell SO |
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J Biol Chem |
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Properties of purified carnitine acyltransferases of mouse liver peroxisomes. |
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Mellon SH |
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Brain Res |
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Neurosteroid biosynthesis: genes for adrenal steroidogenic enzymes are expressed in the brain. |
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Machová E |
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J Neurochem |
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Detection of choline transporter-like 1 protein CTL1 in neuroblastoma x glioma cells and in the CNS, and its role in choline uptake. |
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Biochem Biophys Res Commun |
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Vesicular nucleotide transporter is involved in ATP storage of secretory lysosomes in astrocytes. |
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Stafford CA |
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2022 |
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Nature |
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Phosphorylation of muramyl peptides by NAGK is required for NOD2 activation. |
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Tanaka M |
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2000 |
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Brain Res Mol Brain Res |
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Promoter analysis and characteristics of the 5'-untranslated region of the mouse glial cell line-derived neurotrophic factor gene. |
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Hur J |
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2001 |
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FEBS Lett |
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Induction of caspase-11 by inflammatory stimuli in rat astrocytes: lipopolysaccharide induction through p38 mitogen-activated protein kinase pathway. |
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Satoh K |
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2002 |
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Biochem Biophys Res Commun |
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A novel member of the leucine-rich repeat superfamily induced in rat astrocytes by beta-amyloid. |
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| First Author: |
Faraonio R |
| Year: |
2000 |
| Journal: |
Eur J Biochem |
| Title: |
Characterization of cis-acting elements in the promoter of the mouse metallothionein-3 gene. Activation of gene expression during neuronal differentiation of P19 embryonal carcinoma cells. |
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Clubb BH |
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2000 |
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Biochem Biophys Res Commun |
| Title: |
The 300-kDa intermediate filament-associated protein (IFAP300) is a hamster plectin ortholog. |
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273 |
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| First Author: |
Yu JX |
| Year: |
2000 |
| Journal: |
Immunogenetics |
| Title: |
Molecular cloning of the C6A form cDNA of the mouse sixth complement component: functional integrity despite the absence of factor I modules. |
| Volume: |
51 |
| Issue: |
10 |
| Pages: |
779-87 |
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| First Author: |
Itoh H |
| Year: |
1986 |
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Proc Natl Acad Sci U S A |
| Title: |
Molecular cloning and sequence determination of cDNAs for alpha subunits of the guanine nucleotide-binding proteins Gs, Gi, and Go from rat brain. |
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83 |
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11 |
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3776-80 |
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Ding D |
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1993 |
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Brain Res Mol Brain Res |
| Title: |
Glial cell-specific expression of the serotonin 2 receptor gene: selective reactivation of a repressed promoter. |
| Volume: |
20 |
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3 |
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181-91 |
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| First Author: |
Korkalainen MK |
| Year: |
1995 |
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Chem Biol Interact |
| Title: |
Comparison of expression of aldehyde dehydrogenase 3 and CYP1A1 in dominant and recessive aryl hydrocarbon hydroxylase-deficient mutant mouse hepatoma cells. |
| Volume: |
94 |
| Issue: |
2 |
| Pages: |
121-34 |
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| First Author: |
Qian Y |
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1997 |
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Brain Res Mol Brain Res |
| Title: |
A Menkes P-type ATPase involved in copper homeostasis in the central nervous system of the rat. |
| Volume: |
48 |
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1 |
| Pages: |
60-6 |
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•
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| First Author: |
Luegmayr E |
| Year: |
1998 |
| Journal: |
J Histochem Cytochem |
| Title: |
1,25-Dihydroxy vitamin D3 and tri-iodothyronine stimulate the expression of a protein immunologically related to osteocalcin. |
| Volume: |
46 |
| Issue: |
4 |
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477-86 |
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| First Author: |
Qian Y |
| Year: |
1998 |
| Journal: |
J Nutr |
| Title: |
Copper efflux from murine microvascular cells requires expression of the menkes disease Cu-ATPase. |
| Volume: |
128 |
| Issue: |
8 |
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1276-82 |
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| First Author: |
Stout CE |
| Year: |
2002 |
| Journal: |
J Biol Chem |
| Title: |
Intercellular calcium signaling in astrocytes via ATP release through connexin hemichannels. |
| Volume: |
277 |
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12 |
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10482-8 |
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| First Author: |
Woo HJ |
| Year: |
2002 |
| Journal: |
FEBS Lett |
| Title: |
Escherichia coli 6-pyruvoyltetrahydropterin synthase ortholog encoded by ygcM has a new catalytic activity for conversion of sepiapterin to 7,8-dihydropterin. |
| Volume: |
523 |
| Issue: |
1-3 |
| Pages: |
234-8 |
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| First Author: |
Hammer F |
| Year: |
2004 |
| Journal: |
Endocrinology |
| Title: |
Transcriptional regulation of P450scc gene expression in the embryonic rodent nervous system. |
| Volume: |
145 |
| Issue: |
2 |
| Pages: |
901-12 |
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| First Author: |
Wang Y |
| Year: |
2006 |
| Journal: |
Biochem Pharmacol |
| Title: |
Modulation of mitochondrial metabolic function by phorbol 12-myristate 13-acetate through increased mitochondrial translocation of protein kinase Calpha in C2C12 myocytes. |
| Volume: |
72 |
| Issue: |
7 |
| Pages: |
881-92 |
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| First Author: |
Alam J |
| Year: |
1992 |
| Journal: |
J Biol Chem |
| Title: |
Distal AP-1 binding sites mediate basal level enhancement and TPA induction of the mouse heme oxygenase-1 gene. |
| Volume: |
267 |
| Issue: |
30 |
| Pages: |
21894-900 |
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| First Author: |
Takarada T |
| Year: |
2009 |
| Journal: |
Neurosci Lett |
| Title: |
Transactivation by Runt related factor-2 of matrix metalloproteinase-13 in astrocytes. |
| Volume: |
451 |
| Issue: |
2 |
| Pages: |
99-104 |
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| First Author: |
Furmanski AL |
| Year: |
2010 |
| Journal: |
J Immunol |
| Title: |
Peptide-specific, TCR-alpha-driven, coreceptor-independent negative selection in TCR alpha-chain transgenic mice. |
| Volume: |
184 |
| Issue: |
2 |
| Pages: |
650-7 |
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| First Author: |
Prudencio M |
| Year: |
2012 |
| Journal: |
J Neurochem |
| Title: |
A novel variant of human superoxide dismutase 1 harboring amyotrophic lateral sclerosis-associated and experimental mutations in metal-binding residues and free cysteines lacks toxicity in vivo. |
| Volume: |
121 |
| Issue: |
3 |
| Pages: |
475-85 |
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| First Author: |
Lee CM |
| Year: |
2012 |
| Journal: |
Int J Cancer |
| Title: |
Optical imaging of MMP expression and cancer progression in an inflammation-induced colon cancer model. |
| Volume: |
131 |
| Issue: |
8 |
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1846-53 |
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| First Author: |
Sassa T |
| Year: |
2012 |
| Journal: |
Biochim Biophys Acta |
| Title: |
A shift in sphingolipid composition from C24 to C16 increases susceptibility to apoptosis in HeLa cells. |
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1821 |
| Issue: |
7 |
| Pages: |
1031-7 |
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•
•
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| First Author: |
Voulalas PJ |
| Year: |
2017 |
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Neuroscience |
| Title: |
Loss of dopamine D1 receptors and diminished D1/5 receptor-mediated ERK phosphorylation in the periaqueductal gray after spinal cord lesion. |
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343 |
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94-105 |
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| First Author: |
Huang J |
| Year: |
2011 |
| Journal: |
J Biol Chem |
| Title: |
Type II arginine methyltransferase PRMT5 regulates gene expression of inhibitors of differentiation/DNA binding Id2 and Id4 during glial cell differentiation. |
| Volume: |
286 |
| Issue: |
52 |
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44424-32 |
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| First Author: |
Faouzi A |
| Year: |
2023 |
| Journal: |
Nature |
| Title: |
Structure-based design of bitopic ligands for the µ-opioid receptor. |
| Volume: |
613 |
| Issue: |
7945 |
| Pages: |
767-774 |
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| First Author: |
Suraweera N |
| Year: |
2006 |
| Journal: |
Hum Mol Genet |
| Title: |
Genetic determinants modulate susceptibility to pregnancy-associated tumourigenesis in a recombinant line of Min mice. |
| Volume: |
15 |
| Issue: |
23 |
| Pages: |
3429-35 |
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•
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| First Author: |
Ribes V |
| Year: |
2009 |
| Journal: |
Development |
| Title: |
Early mouse caudal development relies on crosstalk between retinoic acid, Shh and Fgf signalling pathways. |
| Volume: |
136 |
| Issue: |
4 |
| Pages: |
665-76 |
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•
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•
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| First Author: |
Hill TP |
| Year: |
2006 |
| Journal: |
Development |
| Title: |
Multiple roles of mesenchymal beta-catenin during murine limb patterning. |
| Volume: |
133 |
| Issue: |
7 |
| Pages: |
1219-29 |
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| First Author: |
Catela C |
| Year: |
2016 |
| Journal: |
Cell Rep |
| Title: |
Hox Proteins Coordinate Motor Neuron Differentiation and Connectivity Programs through Ret/Gfrα Genes. |
| Volume: |
14 |
| Issue: |
8 |
| Pages: |
1901-15 |
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| First Author: |
Inagawa M |
| Year: |
2013 |
| Journal: |
Mech Dev |
| Title: |
Histone H3 lysine 9 methyltransferases, G9a and GLP are essential for cardiac morphogenesis. |
| Volume: |
130 |
| Issue: |
11-12 |
| Pages: |
519-31 |
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•
•
•
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| First Author: |
Edmond M |
| Year: |
2017 |
| Journal: |
eNeuro |
| Title: |
Topoisomerase IIβ Selectively Regulates Motor Neuron Identity and Peripheral Connectivity through Hox/Pbx-Dependent Transcriptional Programs. |
| Volume: |
4 |
| Issue: |
6 |
|
|
•
•
•
•
•
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| Publication |
| First Author: |
Nowotschin S |
| Year: |
2019 |
| Journal: |
Nature |
| Title: |
The emergent landscape of the mouse gut endoderm at single-cell resolution. |
| Volume: |
569 |
| Issue: |
7756 |
| Pages: |
361-367 |
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•
•
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| First Author: |
Naruse C |
| Year: |
2017 |
| Journal: |
FASEB J |
| Title: |
New insights into the role of Jmjd3 and Utx in axial skeletal formation in mice. |
| Volume: |
31 |
| Issue: |
6 |
| Pages: |
2252-2266 |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
406
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
308
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
404
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
346
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
773
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
350
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
354
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
406
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
584
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
350
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
439
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
157
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
444
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
236
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
202
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
41
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
692
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
267
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
300
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
527
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
188
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
313
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
280
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
605
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
64
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
258
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
150
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
584
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
361
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
303
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
1263
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
167
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
553
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
204
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
350
 |
| Fragment?: |
false |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
77
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
418
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
141
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein |
| Organism: |
Mus musculus/domesticus |
| Length: |
95
 |
| Fragment?: |
true |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Conserved_site |
| Description: |
The membrane attack complex/perforin (MACPF) domain is conserved in bacteria, fungi, mammals and plants. It was originally identified and named as being common to five complement components (C6, C7, C8-alpha, C8-beta, and C9) and perforin. These molecules perform critical functions in innate and adaptive immunity. The MAC family proteins and perforin are known to participate in lytic pore formation. In response to pathogen infection, a sequential and highly specific interaction between the constituent elements occurs to form transmembrane channels which are known as the membrane-attack complex (MAC).Only a few other MACPF proteins have been characterised and several are thought to form pores for invasion or protection [, , ]. Examples are proteins from malarial parasites [], the cytolytic toxins from sea anemones [], and proteins that provide plant immunity [, ]. Functionally uncharacterised MACPF proteins are also evident in pathogenic bacteria such as Chlamydia spp []and Photorhabdus luminescens (Xenorhabdus luminescens) [].The MACPF domain is commonly found to be associated with other N- and C-terminal domains, such as TSP1 (see ), LDLRA (see ), EGF-like (see ),Sushi/CCP/SCR (see ), FIMAC or C2 (see ). They probably control or target MACPF function [, ]. The MACPF domain oligomerizes, undergoes conformational change, and is required for lytic activity.The MACPF domain consists of a central kinked four-stranded antiparallel beta sheet surrounded by alpha helices and beta strands, forming two structural segments. Overall, the MACPF domain hasa thin L-shaped appearance. MACPF domains exhibit limited sequence similarity but contain a signature [YW]-G-[TS]-H-[FY]-x(6)-G-G motif [, , ].Some proteins known to contain a MACPF domain are listed below:Vertebrate complement proteins C6 to C9. Complement factors C6 to C9 assemble to form a scaffold, the membrane attack complex (MAC), that permits C9 polymerisation into pores that lyse Gram-negative pathogens [, ].Vertebrate perforin. It is delivered by natural killer cells and cytotoxic T lymphocytes and forms oligomeric pores (12 to 18 monomers) in the plasma membrane of either virus-infected or transformed cells.Arabidopsis thaliana (Mouse-ear cress) constitutively activated cell death 1 (CAD1) protein. It is likely to act as a mediator that recognises plant signals for pathogen infection [].Arabidopsis thaliana (Mouse-ear cress) necrotic spotted lesions 1 (NSL1) protein [].Venomous sea anemone Phyllodiscus semoni (Night anemone) toxins PsTX-60A and PsTX-60B [].Venomous sea anemone Actineria villosa (Okinawan sea anemone) toxin AvTX-60A [].Plasmodium sporozoite microneme protein essential for cell traversal 2 (SPECT2). It is essential for the membrane-wounding activity of the sporozoite and is involved in its traversal of the sinusoidal cell layer prior to hepatocyte-infection [].P. luminescens Plu-MACPF. Although nonlytic, it was shown to bind to cell membranes [].Chlamydial putative uncharacterised protein CT153 []. |
|
•
•
•
•
•
|
| Protein Domain |
| Type: |
Domain |
| Description: |
The membrane attack complex/perforin (MACPF) domain is conserved in bacteria, fungi, mammals and plants. It was originally identified and named as being common to five complement components (C6, C7, C8-alpha, C8-beta, and C9) and perforin. These molecules perform critical functions in innate and adaptive immunity. The MAC family proteins and perforin are known to participate in lytic pore formation. In response to pathogen infection, a sequential and highly specific interaction between the constituent elements occurs to form transmembrane channels which are known as the membrane-attack complex (MAC).Only a few other MACPF proteins have been characterised and several are thought to form pores for invasion or protection [, , ]. Examples are proteins from malarial parasites [], the cytolytic toxins from sea anemones [], and proteins that provide plant immunity [, ]. Functionally uncharacterised MACPF proteins are also evident in pathogenic bacteria such as Chlamydia spp []and Photorhabdus luminescens (Xenorhabdus luminescens) [].The MACPF domain is commonly found to be associated with other N- and C-terminal domains, such as TSP1 (see ), LDLRA (see ), EGF-like (see ),Sushi/CCP/SCR (see ), FIMAC or C2 (see ). They probably control or target MACPF function [, ]. The MACPF domain oligomerizes, undergoes conformational change, and is required for lytic activity.The MACPF domain consists of a central kinked four-stranded antiparallel beta sheet surrounded by alpha helices and beta strands, forming two structural segments. Overall, the MACPF domain has a thin L-shaped appearance. MACPF domainsexhibit limited sequence similarity but contain a signature [YW]-G-[TS]-H-[FY]-x(6)-G-G motif [, , ].Some proteins known to contain a MACPF domain are listed below:Vertebrate complement proteins C6 to C9. Complement factors C6 to C9 assemble to form a scaffold, the membrane attack complex (MAC), that permits C9 polymerisation into pores that lyse Gram-negative pathogens [, ].Vertebrate perforin. It is delivered by natural killer cells and cytotoxic T lymphocytes and forms oligomeric pores (12 to 18 monomers) in the plasma membrane of either virus-infected or transformed cells.Arabidopsis thaliana (Mouse-ear cress) constitutively activated cell death 1 (CAD1) protein. It is likely to act as a mediator that recognises plant signals for pathogen infection [].Arabidopsis thaliana (Mouse-ear cress) necrotic spotted lesions 1 (NSL1) protein [].Venomous sea anemone Phyllodiscus semoni (Night anemone) toxins PsTX-60A and PsTX-60B [].Venomous sea anemone Actineria villosa (Okinawan sea anemone) toxin AvTX-60A [].Plasmodium sporozoite microneme protein essential for cell traversal 2 (SPECT2). It is essential for the membrane-wounding activity of the sporozoite and is involved in its traversal of the sinusoidal cell layer prior to hepatocyte-infection [].P. luminescens Plu-MACPF. Although nonlytic, it was shown to bind to cell membranes [].Chlamydial putative uncharacterised protein CT153 []. |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
Mus caroli |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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•
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
mouse, laboratory |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
Mus pahari |
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| Protein Coding Gene |
| Type: |
protein_coding_gene |
| Organism: |
Mus spretus |
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| Publication |
| First Author: |
Krumlauf R |
| Year: |
1987 |
| Journal: |
Development |
| Title: |
Developmental and spatial patterns of expression of the mouse homeobox gene, Hox 2.1. |
| Volume: |
99 |
| Issue: |
4 |
| Pages: |
603-17 |
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