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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, PS51120; LDL-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 |
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| Matching PDB structures:
1IJQ 1LPX 1LRX 1N7D ... [ALL] |
References:
| 1 |
Authors | Brown M.S., Goldstein J.L. |
| Title | A receptor-mediated pathway for cholesterol homeostasis. |
| Source | Science 232:34-47(1986). |
| PubMed ID | 3513311 |
| 2 |
Authors | Springer T.A. |
| Title | An extracellular beta-propeller module predicted in lipoprotein and scavenger receptors, tyrosine kinases, epidermal growth factor precursor, and extracellular matrix components. |
| Source | J. Mol. Biol. 283:837-862(1998). |
| PubMed ID | 9790844 |
| 3 |
Authors | Davis C.G., Goldstein J.L., Sudhof T.C., Anderson R.G., Russell D.W., Brown M.S. |
| Title | Acid-dependent ligand dissociation and recycling of LDL receptor mediated by growth factor homology region. |
| Source | Nature 326:760-765(1987). |
| PubMed ID | 3494949 |
| DOI | 10.1038/326760a0 |
| 4 |
Authors | Jeon H., Meng W., Takagi J., Eck M.J., Springer T.A., Blacklow S.C. |
| Title | Implications for familial hypercholesterolemia from the structure of the LDL receptor YWTD-EGF domain pair. |
| Source | Nat. Struct. Biol. 8:499-504(2001). |
| PubMed ID | 11373616 |
| DOI | 10.1038/88556 |
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