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PDOC51120

LDL-receptor class B (LDLRB) repeat profile

Description:

The low-density lipoprotein receptor (LDLR) regulates cholesterol homeostasis in mammalian cells. LDLR binds cholesterol-carrying LDL, associates with clathrin-coated pits, and is internalized into acidic endosomes where it separates from its ligand. The ligand is degraded in lysosomes, while the receptor returns to the cell surface [1]. The LDLR has several domains. The ligand-binding domain contains seven LDL receptor class A repeats (see <PDOC00929>), each with three disulfide bonds and a coordinated Ca2+ ion. The second conserved region contains two EGF repeats (see <PDOC00913>), followed by six YWTD or LDL receptor class B repeats and another EGF repeat [2]. This conserved region is critical for ligand release and recycling of the receptor [3].

The structure of the six YWTD repeats of LDL receptor have been solved (see <PDB:1IJQ>) [4]. The six YWTD repeats together fold into a six-bladed β-propeller. Each blade of the propeller consists of four antiparallel β-strands; the innermost strand of each blade is labeled 1 and the outermost strand, 4. The sequence repeats are offset with respect to the blades of the propeller, such that any given 40-residue YWTD repeat spans strands 2–4 of one propeller blade and strand 1 of the subsequent blade. This offset ensures circularization of the propeller because the last strand of the final sequence repeat acts as an innermost strand 1 of the blade that harbors strands 2–4 from the first sequence repeat.

Some proteins known to contain LDL receptor class B repeats:

  • Animal low-density lipoprotein receptor.
  • Mammalian pro-epidermal growth factor precursor (EGF).
  • Mammalian nidogen-2 precursor, a cell adhesion glycoprotein which is widely distributed in basement membranes.
  • Vertebrate sortilin-related receptor precursor.
  • Very low-density lipoprotein receptor precursor (VLDLR). It binds VLDL and transports it into cells by endocytosis.
  • Drosophila Yolkless protein. It is involved in uptake of vitellogenin by endocytosis.

The profile we developed covers the whole LDL receptor class B repeat.

Last update:

May 2005 / First entry.

Technical section:

PROSITE method (with tools and information) covered by this documentation:

LDLRB, PS51120LDL-receptor class B (LDLRB) repeat profile  (MATRIX)
Sequences known to belong to this class detected by the profile: ALL
Other sequence(s) detected in Swiss-Prot: NONE
Domain architecture view of Swiss-Prot proteins matching PS51120
PS51120
• Retrieve an alignment of Swiss-Prot true positive hits:
  Clustal format, color, condensed view  / Clustal format, color  / Clustal format, plain text  / Fasta format
Retrieve the sequence logo from the alignment
Taxonomic tree view of all Swiss-Prot/TrEMBL entries matching PS51120
Retrieve a list of all Swiss-Prot/TrEMBL entries matching PS51120
Scan Swiss-Prot/TrEMBL entries against PS51120
view ligand binding statistics
Matching PDB structures: 1IJQ 1LPX 1LRX 1N7D ... [ALL]

References:

1 AuthorsBrown M.S., Goldstein J.L.
TitleA receptor-mediated pathway for cholesterol homeostasis.
SourceScience 232:34-47(1986).
PubMed ID3513311
2 AuthorsSpringer T.A.
TitleAn extracellular beta-propeller module predicted in lipoprotein and scavenger receptors, tyrosine kinases, epidermal growth factor precursor, and extracellular matrix components.
SourceJ. Mol. Biol. 283:837-862(1998).
PubMed ID9790844
3 AuthorsDavis C.G., Goldstein J.L., Sudhof T.C., Anderson R.G., Russell D.W., Brown M.S.
TitleAcid-dependent ligand dissociation and recycling of LDL receptor mediated by growth factor homology region.
SourceNature 326:760-765(1987).
PubMed ID3494949
DOI10.1038/326760a0
4 AuthorsJeon H., Meng W., Takagi J., Eck M.J., Springer T.A., Blacklow S.C.
TitleImplications for familial hypercholesterolemia from the structure of the LDL receptor YWTD-EGF domain pair.
SourceNat. Struct. Biol. 8:499-504(2001).
PubMed ID11373616
DOI10.1038/88556

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