Human Gene LPA (ENST00000447678.2) Description and Page Index
  Description: Apo(a) is the main constituent of lipoprotein(a) (Lp(a)). It has serine proteinase activity and is able of autoproteolysis. Inhibits tissue-type plasminogen activator 1. Lp(a) may be a ligand for megalin/Gp 330. (from UniProt P08519)
Gencode Transcript: ENST00000447678.2
Gencode Gene: ENSG00000198670.12
Transcript (Including UTRs)
   Position: hg38 chr6:160,586,480-160,613,115 Size: 26,636 Total Exon Count: 11 Strand: -
Coding Region
   Position: hg38 chr6:160,586,480-160,613,115 Size: 26,636 Coding Exon Count: 11 

Page IndexSequence and LinksUniProtKB CommentsProtein StructureOther NamesMethods
Data last updated at UCSC: 2021-06-20 19:51:40

+  Sequence and Links to Tools and Databases
  Press "+" in the title bar above to open this section.

-  Comments and Description Text from UniProtKB
  ID: APOA_HUMAN
DESCRIPTION: RecName: Full=Apolipoprotein(a); Short=Apo(a); Short=Lp(a); EC=3.4.21.-; Flags: Precursor;
FUNCTION: Apo(a) is the main constituent of lipoprotein(a) (Lp(a)). It has serine proteinase activity and is able of autoproteolysis. Inhibits tissue-type plasminogen activator 1. Lp(a) may be a ligand for megalin/Gp 330.
SUBUNIT: Disulfide-linked to apo-B100. Binds to fibronectin and decorin.
PTM: N- and O-glycosylated. The N-glycans are complex biantennary structures present in either a mono- or disialylated state. The O- glycans are mostly (80%) represented by the monosialylated core type I structure, NeuNAcalpha2-3Galbeta1-3GalNAc, with smaller amounts of disialylated and non-sialylated O-glycans also detected.
POLYMORPHISM: The reference genome sequence encodes a variant that contains 16 Kringle domains and that lack residues 533 to 3040. Depending on the individual, the encoded protein contains 2-43 copies of kringle-type domains. The allele represented here contains 38 copies of the kringle-type repeats.
MISCELLANEOUS: Apo(a) is known to be proteolytically cleaved, leading to the formation of the so-called mini-Lp(a). Apo(a) fragments accumulate in atherosclerotic lesions, where they may promote thrombogenesis. O-glycosylation may limit the extent of proteolytic fragmentation. Homology with plasminogen kringles IV and V is thought to underlie the atherogenicity of the protein, because the fragments are competing with plasminogen for fibrin(ogen) binding.
SIMILARITY: Belongs to the peptidase S1 family. Plasminogen subfamily.
SIMILARITY: Contains 38 kringle domains.
SIMILARITY: Contains 1 peptidase S1 domain.
WEB RESOURCE: Name=SHMPD; Note=The Singapore human mutation and polymorphism database; URL="http://shmpd.bii.a-star.edu.sg/gene.php?genestart=A&genename=APOA";

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR000001 - Kringle
IPR013806 - Kringle-like
IPR018056 - Kringle_CS
IPR009003 - Pept_cys/ser_Trypsin-like
IPR018114 - Peptidase_S1/S6_AS
IPR001254 - Peptidase_S1_S6
IPR001314 - Peptidase_S1A

Pfam Domains:
PF00051 - Kringle domain
PF00089 - Trypsin

Protein Data Bank (PDB) 3-D Structure
MuPIT help

1I71
- X-ray

1JFN
- NMR

1KIV
- X-ray
To conserve bandwidth, only the images from the first 3 structures are shown.
2FEB - NMR 3KIV - X-ray 4KIV - X-ray


ModBase Predicted Comparative 3D Structure on P08519
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

+  Other Names for This Gene
  Press "+" in the title bar above to open this section.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.