| ACP5 |
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| Available structures |
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| PDB | Ortholog search: PDBe RCSB |
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| Identifiers |
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| Aliases | ACP5, HPAP, SPENCDI, TRAP, TRACP5a, TRACP5b, TrATPase, acid phosphatase 5, tartrate resistant, TRAcP |
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| External IDs | OMIM: 171640; MGI: 87883; HomoloGene: 115578; GeneCards: ACP5; OMA:ACP5 - orthologs |
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| Gene location (Human) |
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| | Chr. | Chromosome 19 (human) |
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| | Band | 19p13.2 | Start | 11,574,653 bp |
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| End | 11,579,993 bp |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 9 (mouse) |
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| | Band | 9 A3|9 8.38 cM | Start | 22,038,023 bp |
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| End | 22,047,007 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - periodontal fiber
- upper lobe of left lung
- right lung
- lower lobe of lung
- tibia
- granulocyte
- lymph node
- spleen
- rectum
- appendix
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| | Top expressed in | - body of femur
- tibiofemoral joint
- white adipose tissue
- subcutaneous adipose tissue
- fetal liver hematopoietic progenitor cell
- brown adipose tissue
- spleen
- intercostal muscle
- tunica adventitia of aorta
- large intestine
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| | More reference expression data |
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| BioGPS | |
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| Gene ontology |
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| Molecular function | | | Cellular component | | | Biological process | | | Sources:Amigo / QuickGO |
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| Wikidata |
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Tartrate-resistant acid phosphatase (TRAP or TRAPase), also called acid phosphatase 5, tartrate resistant (ACP5) or TRAP5b, is a glycosylated monomeric metalloprotein enzyme expressed in mammals. It has a molecular weight of approximately 35kDa, a basic isoelectric point (7.6–9.5), and optimal activity in acidic conditions. TRAP is synthesized as latent proenzyme and activated by proteolytic cleavage and reduction. It is differentiated from other mammalian acid phosphatases by its resistance to inhibition by tartrate and by its molecular weight.
The mechanism of phosphate ester hydrolysis by TRAP is through a nucleophilic attack mechanism, whereby, catalysis occurs with the binding of a phosphate-substrate to the Fe2+ in the active site of TRAP. This is then followed by a nucleophilic attack by a hydroxide ligand on the bound phosphorus atom, resulting in cleavage of the phosphate ester bond and production of an alcohol. The exact identity and mechanism of the hydroxide ligand is unclear, but it is thought to be either a hydroxide that bridges the metal ions within the active site or a terminal hydroxide bound to Fe3+, with conflicting reports for both mechanisms.