Homo sapiens Protein: HP
Summary
InnateDB Protein IDBP-233821.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HP
Protein Name haptoglobin
Synonyms BP; HP2ALPHA2; HPA1S;
Species Homo sapiens
Ensembl Protein ENSP00000381199
InnateDB Gene IDBG-547150 (HP)
Protein Structure
UniProt Annotation
Function As a result of hemolysis, hemoglobin is found to accumulate in the kidney and is secreted in the urine. Haptoglobin captures, and combines with free plasma hemoglobin to allow hepatic recycling of heme iron and to prevent kidney damage. Haptoglobin also acts as an Antimicrobial; Antioxidant, has antibacterial activity and plays a role in modulating many aspects of the acute phase response. Hemoglobin/haptoglobin complexes are rapidely cleared by the macrophage CD163 scavenger receptor expressed on the surface of liver Kupfer cells through an endocytic lysosomal degradation pathway. {ECO:0000269PubMed:21248165}.Uncleaved haptoglogin, also known as zonulin, plays a role in intestinal permeability, allowing intercellular tight junction disassembly, and controlling the equilibrium between tolerance and immunity to non-self antigens. {ECO:0000269PubMed:21248165}.
Subcellular Localization Secreted.
Disease Associations Anhaptoglobinemia (AHP) [MIM:614081]: A condition characterized by the absence of the serum glycoprotein haptoglobin. Serum levels of haptoglobin vary among normal persons: levels are low in the neonatal period and in the elderly, differ by population, and can be influenced by environmental factors, such as infection. Secondary hypohaptoglobinemia can occur as a consequence of hemolysis, during which haptoglobin binds to free hemoglobin. Congenital haptoglobin deficiency is a risk factor for anaphylactic non-hemolytic transfusion reactions. {ECO:0000269PubMed:14999562}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed by the liver and secreted in plasma.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 21 experimentally validated interaction(s) in this database.
Experimentally validated
Total 21 [view]
Protein-Protein 20 [view]
Protein-DNA 0
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004252 serine-type endopeptidase activity
GO:0005515 protein binding
GO:0016209 antioxidant activity
GO:0030492 hemoglobin binding
Biological Process
GO:0002376 immune system process
GO:0006508 proteolysis
GO:0006952 defense response
GO:0006953 acute-phase response
GO:0008152 metabolic process
GO:0010942 positive regulation of cell death
GO:0042542 response to hydrogen peroxide
GO:0042742 defense response to bacterium
GO:0051354 negative regulation of oxidoreductase activity
GO:2000296 negative regulation of hydrogen peroxide catabolic process
Cellular Component
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0031838 haptoglobin-hemoglobin complex
GO:0070062 extracellular vesicular exosome
GO:0071682 endocytic vesicle lumen
GO:0072562 blood microparticle
Protein Structure and Domains
PDB ID
InterPro IPR000436 Sushi/SCR/CCP
IPR001254 Peptidase S1
IPR001314 Peptidase S1A, chymotrypsin-type
IPR008292 Haptoglobin
IPR009003 Trypsin-like cysteine/serine peptidase domain
PFAM PF00084
PF00089
PRINTS PR00722
PIRSF PIRSF001137
SMART SM00032
SM00020
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P00738
PhosphoSite PhosphoSite-P00738
TrEMBL Q6PEJ8
UniProt Splice Variant
Entrez Gene 3250
UniGene Hs.513711
RefSeq NP_001119574
HUGO HGNC:5141
OMIM 140210
CCDS CCDS45525
HPRD 00772
IMGT
EMBL AC004682 AC009087 AK314700 BC017862 BC058031 BC107587 BC121124 BC121125 DQ314870 K00422 K01763 L29394 M10935 M13192 M69197 X00606 X00637 X01786 X01789 X01791 X01793 X02206
GenPept AAA52684 AAA52685 AAA52687 AAA88078 AAA88080 AAC27432 AAH17862 AAH58031 AAI07588 AAI21125 AAI21126 ABC40729 BAF98793 CAA25248 CAA25267 CAA25926