Family

Haptoglobin (IPR008292)

Short name: Haptoglobin

Family relationships

Description

Haptoglobin is a plasma protein that binds haemoglobin. The resulting complex is too large to be excreted by the kidney, thereby preventing loss of iron and damage to the kidney. The haptoglobin-haemoglobin complex is degraded in the liver, which is also the site of haptoglobin synthesis. The mature haptoglobin molecule is a tetramer, consisting of two alpha and two beta chains. Alpha and beta chains arise from proteolytic processing of the same precursor. Each beta chain can bind an alpha-beta heterodimer of haemoglobin so that each haptoglobin tetramer binds one haemoglobin tetramer. In Pan troglodytes (Chimpanzee), haptoglobin genes form a small multigene family of three genes: HP, HPR (haptoglobin-related protein, which may be non-functional), and HPP (haptoglobin-primate) [PMID: 3170608]. In contrast, most humans have a two-gene cluster due to an unequal homologous crossover event between HPR and HPP in the human lineage [PMID: 2987228]. Such events may be common among these closely related genes as Macaca mulatta (Rhesus macaque) was found to have haplotypes of one- or two-gene clusters that appear to have formed from unequal crossover among an ancestral three-gene cluster [PMID: 8001969]. The haptoglobin precursor contains a signal sequence, a sushi domain (in mature alpha chain), and a trypsin domain (in mature beta chain) which belongs to the MEROPS peptidase family S1 (clan PA(S)). Haptoglobins have no enzymatic activity as the active site residues typical of trypsin-related proteases are not conserved, they are therefore classed as non-peptidase homologues. A common allelic variant in humans contains two sushi domains.

GO terms

Biological Process

No terms assigned in this category.

Molecular Function

GO:0030492 hemoglobin binding

Cellular Component

GO:0005576 extracellular region

Contributing signatures

Signatures from InterPro member databases are used to construct an entry.
PIRSF
PANTHER