Type |
Details |
Score |
Publication |
First Author: |
Zandl-Lang M |
Year: |
2018 |
Journal: |
Biochim Biophys Acta |
Title: |
Regulatory effects of simvastatin and apoJ on APP processing and amyloid-β clearance in blood-brain barrier endothelial cells. |
Volume: |
1863 |
Issue: |
1 |
Pages: |
40-60 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fears CY |
Year: |
2005 |
Journal: |
Cancer Res |
Title: |
Low-density lipoprotein receptor-related protein contributes to the antiangiogenic activity of thrombospondin-2 in a murine glioma model. |
Volume: |
65 |
Issue: |
20 |
Pages: |
9338-46 |
|
•
•
•
•
•
|
Publication |
First Author: |
Magat J |
Year: |
2022 |
Journal: |
J Biol Chem |
Title: |
Intracerebroventricular dosing of N-sulfoglucosamine sulfohydrolase in mucopolysaccharidosis IIIA mice reduces markers of brain lysosomal dysfunction. |
Volume: |
298 |
Issue: |
12 |
Pages: |
102625 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sui L |
Year: |
2022 |
Journal: |
Nat Commun |
Title: |
PRSS2 remodels the tumor microenvironment via repression of Tsp1 to stimulate tumor growth and progression. |
Volume: |
13 |
Issue: |
1 |
Pages: |
7959 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hernandez-Garzón E |
Year: |
2016 |
Journal: |
Glia |
Title: |
The insulin-like growth factor I receptor regulates glucose transport by astrocytes. |
Volume: |
64 |
Issue: |
11 |
Pages: |
1962-71 |
|
•
•
•
•
•
|
Publication |
First Author: |
Moore KM |
Year: |
2016 |
Journal: |
Neurobiol Dis |
Title: |
A spectrum of exercise training reduces soluble Aβ in a dose-dependent manner in a mouse model of Alzheimer's disease. |
Volume: |
85 |
|
Pages: |
218-224 |
|
•
•
•
•
•
|
Publication |
First Author: |
Shang J |
Year: |
2019 |
Journal: |
Brain Res |
Title: |
Chronic cerebral hypoperfusion alters amyloid-β transport related proteins in the cortical blood vessels of Alzheimer's disease model mouse. |
Volume: |
1723 |
|
Pages: |
146379 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kurokawa S |
Year: |
2012 |
Journal: |
J Biol Chem |
Title: |
Long isoform mouse selenoprotein P (Sepp1) supplies rat myoblast L8 cells with selenium via endocytosis mediated by heparin binding properties and apolipoprotein E receptor-2 (ApoER2). |
Volume: |
287 |
Issue: |
34 |
Pages: |
28717-26 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kapustin A |
Year: |
2012 |
Journal: |
Biochem J |
Title: |
Fibulin-5 binds urokinase-type plasminogen activator and mediates urokinase-stimulated β1-integrin-dependent cell migration. |
Volume: |
443 |
Issue: |
2 |
Pages: |
491-503 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gorski DJ |
Year: |
2015 |
Journal: |
Matrix Biol |
Title: |
Deletion of ADAMTS5 does not affect aggrecan or versican degradation but promotes glucose uptake and proteoglycan synthesis in murine adipose derived stromal cells. |
Volume: |
47 |
|
Pages: |
66-84 |
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•
•
•
•
•
|
Publication |
First Author: |
Fava M |
Year: |
2018 |
Journal: |
Arterioscler Thromb Vasc Biol |
Title: |
Role of ADAMTS-5 in Aortic Dilatation and Extracellular Matrix Remodeling. |
Volume: |
38 |
Issue: |
7 |
Pages: |
1537-1548 |
|
•
•
•
•
•
|
Publication |
First Author: |
Prasad H |
Year: |
2018 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Amyloid clearance defect in ApoE4 astrocytes is reversed by epigenetic correction of endosomal pH. |
Volume: |
115 |
Issue: |
28 |
Pages: |
E6640-E6649 |
|
•
•
•
•
•
|
Publication |
First Author: |
Dumanis SB |
Year: |
2012 |
Journal: |
Mol Neurodegener |
Title: |
FE65 as a link between VLDLR and APP to regulate their trafficking and processing. |
Volume: |
7 |
|
Pages: |
9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Elfakhri KH |
Year: |
2018 |
Journal: |
Neuroscience |
Title: |
Characterization of Hit Compounds Identified from High-throughput Screening for their Effect on Blood-brain Barrier Integrity and Amyloid-β Clearance: In Vitro and In Vivo Studies. |
Volume: |
379 |
|
Pages: |
269-280 |
|
•
•
•
•
•
|
Publication |
First Author: |
Barucker C |
Year: |
2014 |
Journal: |
J Biol Chem |
Title: |
Nuclear translocation uncovers the amyloid peptide Aβ42 as a regulator of gene transcription. |
Volume: |
289 |
Issue: |
29 |
Pages: |
20182-91 |
|
•
•
•
•
•
|
Publication |
First Author: |
Quan W |
Year: |
2021 |
Journal: |
Glia |
Title: |
Haploinsufficiency of microglial MyD88 ameliorates Alzheimer's pathology and vascular disorders in APP/PS1-transgenic mice. |
Volume: |
69 |
Issue: |
8 |
Pages: |
1987-2005 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mills J |
Year: |
2019 |
Journal: |
Biochim Biophys Acta Mol Cell Res |
Title: |
LDL receptor related protein 1 requires the I3 domain of discs-large homolog 1/DLG1 for interaction with the kinesin motor protein KIF13B. |
Volume: |
1866 |
Issue: |
12 |
Pages: |
118552 |
|
•
•
•
•
•
|
Publication |
First Author: |
Schilperoort M |
Year: |
2023 |
Journal: |
Nat Metab |
Title: |
PFKFB2-mediated glycolysis promotes lactate-driven continual efferocytosis by macrophages. |
Volume: |
5 |
Issue: |
3 |
Pages: |
431-444 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rushworth JV |
Year: |
2013 |
Journal: |
J Biol Chem |
Title: |
Prion protein-mediated toxicity of amyloid-β oligomers requires lipid rafts and the transmembrane LRP1. |
Volume: |
288 |
Issue: |
13 |
Pages: |
8935-51 |
|
•
•
•
•
•
|
Publication |
First Author: |
Garg AD |
Year: |
2012 |
Journal: |
EMBO J |
Title: |
A novel pathway combining calreticulin exposure and ATP secretion in immunogenic cancer cell death. |
Volume: |
31 |
Issue: |
5 |
Pages: |
1062-79 |
|
•
•
•
•
•
|
Publication |
First Author: |
Xu J |
Year: |
2021 |
Journal: |
Biomed Pharmacother |
Title: |
Effects of DHA dietary intervention on hepatic lipid metabolism in apolipoprotein E-deficient and C57BL/6J wild-type mice. |
Volume: |
144 |
|
Pages: |
112329 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kegulian NC |
Year: |
2019 |
Journal: |
Arterioscler Thromb Vasc Biol |
Title: |
ApoC-III Glycoforms Are Differentially Cleared by Hepatic TRL (Triglyceride-Rich Lipoprotein) Receptors. |
Volume: |
39 |
Issue: |
10 |
Pages: |
2145-2156 |
|
•
•
•
•
•
|
Publication |
First Author: |
Auderset L |
Year: |
2020 |
Journal: |
Front Cell Dev Biol |
Title: |
Low-Density Lipoprotein Receptor-Related Protein 1 (LRP1) Is a Negative Regulator of Oligodendrocyte Progenitor Cell Differentiation in the Adult Mouse Brain. |
Volume: |
8 |
|
Pages: |
564351 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hu Y |
Year: |
2021 |
Journal: |
Dev Dyn |
Title: |
Single-cell analysis of nonhuman primate preimplantation development in comparison to humans and mice. |
Volume: |
250 |
Issue: |
7 |
Pages: |
974-985 |
|
•
•
•
•
•
|
Publication |
First Author: |
Smith DL |
Year: |
1995 |
Journal: |
Plant Cell |
Title: |
LRP1, a gene expressed in lateral and adventitious root primordia of arabidopsis. |
Volume: |
7 |
Issue: |
6 |
Pages: |
735-45 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
Zinc finger (Znf) domains are relatively small protein motifs which contain multiple finger-like protrusions that make tandem contacts with their target molecule. Some of these domains bind zinc, but many do not; instead binding other metals such as iron, or no metal at all. For example, some family members form salt bridges to stabilise the finger-like folds. They were first identified as a DNA-binding motif in transcription factor TFIIIA from Xenopus laevis (African clawed frog), however they are now recognised to bind DNA, RNA, protein and/or lipid substrates [, , , , ]. Their binding properties depend on the amino acid sequence of the finger domains and of the linker between fingers, as well as on the higher-order structures and the number of fingers. Znf domains are often found in clusters, where fingers can have different binding specificities. There are many superfamilies of Znf motifs, varying in both sequence and structure. They display considerable versatility in binding modes, even between members of the same class (e.g. some bind DNA, others protein), suggesting that Znf motifs are stable scaffolds that have evolved specialised functions. For example, Znf-containing proteins function in gene transcription, translation, mRNA trafficking, cytoskeleton organisation, epithelial development, cell adhesion, protein folding, chromatin remodelling and zinc sensing, to name but a few []. Zinc-binding motifs are stable structures, and they rarely undergo conformational changes upon binding their target. These sequences contain a putative zinc finger domain found predominantly in plants. Arabidopsis thaliana (Mouse-ear cress) has at least 10 distinct members. Proteins containing this domain, including LRP1 (lateral root primordium 1)[], generally share the same size, about 300 amino acids, and architecture. This 43-residue domain, and a more C-terminal companion domain of similar size, appear as tightly conserved islands of sequence similarity. The remainder consists largely of low-complexity sequence. Several animal proteins have regions with matching patterns of Cys, Gly, and His residues. But are excluded from this family because of their low similarity. |
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•
•
•
•
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Publication |
First Author: |
Zhou Y |
Year: |
2019 |
Journal: |
Exp Neurol |
Title: |
A neutral lipid-enriched diet improves myelination and alleviates peripheral nerve pathology in neuropathic mice. |
Volume: |
321 |
|
Pages: |
113031 |
|
•
•
•
•
•
|
Publication |
First Author: |
Eisenbaum M |
Year: |
2024 |
Journal: |
Exp Neurol |
Title: |
Repetitive head trauma and apoE4 induce chronic cerebrovascular alterations that impair tau elimination from the brain. |
Volume: |
374 |
|
Pages: |
114702 |
|
•
•
•
•
•
|
Publication |
First Author: |
Vos DY |
Year: |
2023 |
Journal: |
Arterioscler Thromb Vasc Biol |
Title: |
Cargo-Specific Role for Retriever Subunit VPS26C in Hepatocyte Lipoprotein Receptor Recycling to Control Postprandial Triglyceride-Rich Lipoproteins. |
Volume: |
43 |
Issue: |
1 |
Pages: |
e29-e45 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pan Y |
Year: |
2018 |
Journal: |
Brain Behav Immun |
Title: |
Cognitive benefits of lithium chloride in APP/PS1 mice are associated with enhanced brain clearance of β-amyloid. |
Volume: |
70 |
|
Pages: |
36-47 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tachibana M |
Year: |
2018 |
Journal: |
Exp Neurol |
Title: |
Pericyte implantation in the brain enhances cerebral blood flow and reduces amyloid-β pathology in amyloid model mice. |
Volume: |
300 |
|
Pages: |
13-21 |
|
•
•
•
•
•
|
Publication |
First Author: |
Shiroshima T |
Year: |
2009 |
Journal: |
FEBS Lett |
Title: |
Identification of LRP1B-interacting proteins and inhibition of protein kinase Calpha-phosphorylation of LRP1B by association with PICK1. |
Volume: |
583 |
Issue: |
1 |
Pages: |
43-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Krieger M |
Year: |
1994 |
Journal: |
Annu Rev Biochem |
Title: |
Structures and functions of multiligand lipoprotein receptors: macrophage scavenger receptors and LDL receptor-related protein (LRP). |
Volume: |
63 |
|
Pages: |
601-37 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bieri S |
Year: |
1995 |
Journal: |
Biochemistry |
Title: |
Disulfide bridges of a cysteine-rich repeat of the LDL receptor ligand-binding domain. |
Volume: |
34 |
Issue: |
40 |
Pages: |
13059-65 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mahley RW |
Year: |
1988 |
Journal: |
Science |
Title: |
Apolipoprotein E: cholesterol transport protein with expanding role in cell biology. |
Volume: |
240 |
Issue: |
4852 |
Pages: |
622-30 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Conserved_site |
Description: |
Low-density lipoprotein (LDL) receptors are the major cholesterol-carrying lipoproteins of plasma. Seven successive cysteine-rich repeats of about 40 amino acids are present in the N-terminal of this multidomain membrane protein []. Similar domains have been found (see references in []) in other extracellular and membrane proteins which are listed below: Vertebrate very low density lipoprotein (VLDL) receptor, which binds and transports VLDL. Its extracellular domain is composed of 8 LDLRA domains, 3 EGF-like domains and 6 LDL-receptor class B domains (LDLRB). Vertebrate low-density lipoprotein receptor-related protein 1 (LRP1) (reviewed in []), which may act as a receptor for the endocytosis of extracellular ligands. LRP1 contains 31 LDLRA domains and 22 EGF-like domains. Vertebrate low-density lipoprotein receptor-related protein 2 (LRP2) (also known as gp330 or megalin). LRP2 contains 36 LDLRA domains and 17 EGF-like domains. A LRP-homologue from Caenorhabditis elegans, which contains 35 LDLRA domains and 17 EGF-like domains. Drosophila putative vitellogenin receptor, with 13 copies of LDLRA domains and 17 EGF-like repeats. Complement factor I, which is responsible for cleaving the alpha-chains of C4b and C3b. It consists of a FIMAC domain (Factor I/MAC proteins C6/C7), a scavenger receptor-like domain, 2 copies of LDLRA and a C-terminal serine protease domain. Complement components C6, C7, C8 and C9. They contain each one LDLRA domain. Perlecan, a large multidomain basement membrane heparan sulphate proteoglycan composed of 4 LDLRA domains, 3 LamB domains, 12 laminin EGF- like domains, 14-21 IG-like domains, 3 LamG domains, and 4 EGF-like domains. A similar but shorter proteoglycan (UNC52) is found in Caenorhabditis elegans which has 3 repeats of LDLRA. Invertebrate giant extracellular hemoglobin linker chains, which allow heme-containing chains to construct giant hemoglobin (1 LDLRA domain). G-protein coupled receptor Grl101 of the snail Lymnaea stagnalis, which might directly transduce signals carried by large extracellular proteins. Vertebrate enterokinase (EC 3.4.21.9), a type II membrane protein of the intestinal brush border, which activates trypsinogen. It consists at least of a catalytic light chain and a multidomain heavy chain which has 2 LDLRA, a MAM domain (see ), a SRCR domain (see ) and a CUB domain (see ).Human autosomal dominant polycystic kidney disease protein 1 (PKD1), which is involved in adhesive protein-protein and protein-carbohydrate interactions. The potential calcium-binding site of its single LDLRA domain is missing. Vertebrate integral membrane protein DGCR2/IDD, a potential adhesion receptor with 1 LDLRA domain, a C-type lectin and a VWFC domain (see ).Drosophila serine protease nudel (EC 3.4.21.-), which is involved in the induction of dorsoventral polarity of the embryo. It has 11 LDLRA domains, 3 of which miss the first disulphide bond (C1-C3). Avian subgroup A rous sarcoma virus receptor (1 copy of LDLRA). Bovine Sco-spondin, which is secreted by the subcommissural organ in embryos and is involved in the modulation of neuronal aggregation. It contains at least 2 EGF-like domains and 3 LDLRA domains. The LDL-receptor class A domain contains 6 disulphide-bound cysteines []and a highly conserved cluster of negatively charged amino acids, of which many are clustered on one face of the module []. A schematic representation of this domain is shown here: +---------------------+ +--------------------------------+| | | |-CxxxxxxxxxxxxCxxxxxxxxCxxxxxxxxCxxxxxxxxxxCxxxxxxxxxxxxxxxxxxxxxC-|*******************************************| |+----------------------------+'C': conserved cysteine involved in a disulphide bond.'x': any residue.'*': position of the pattern.In LDL-receptors the class A domains form the binding site for LDL []and calcium. The acidic residues between the fourth and sixth cysteines are important for high-affinity binding of positively charged sequences in LDLR's ligands []. The repeat has been shown []to consist of a β-hairpin structure followed by a series of β-turns. The binding of calcium seems to induce no significant conformational change. |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
260
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
345
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
306
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
249
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
246
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
98
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
102
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
89
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
344
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
260
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
175
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
70
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
345
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
306
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
426
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1228
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
525
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
533
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
713
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
483
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
858
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
584
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1614
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
2123
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
548
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
507
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1613
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
261
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
549
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
478
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
682
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
713
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
285
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
546
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
438
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
466
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
546
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
619
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
781
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
769
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1232
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
580
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
713
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1614
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
324
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1037
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1639
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
584
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1457
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
638
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
770
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
498
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1130
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1613
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
790
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
413
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
548
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
580
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
507
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
518
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
743
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Yamamoto T |
Year: |
1984 |
Journal: |
Cell |
Title: |
The human LDL receptor: a cysteine-rich protein with multiple Alu sequences in its mRNA. |
Volume: |
39 |
Issue: |
1 |
Pages: |
27-38 |
|
•
•
•
•
•
|
Publication |
First Author: |
Daly NL |
Year: |
1995 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Three-dimensional structure of a cysteine-rich repeat from the low-density lipoprotein receptor. |
Volume: |
92 |
Issue: |
14 |
Pages: |
6334-8 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
603
 |
Fragment?: |
false |
|
•
•
•
•
•
|