Entity Details
| Primary name |
PERT_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | P07202 |
| EntryName | PERT_HUMAN |
| FullName | Thyroid peroxidase |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 933 |
| SequenceStatus | complete |
| DateCreated | 1988-04-01 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell surface |
| Membrane |
Domains
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| Domain | Name | Category | Type |
| IPR000152 | EGF-type aspartate/asparagine hydroxylation site | PTM | PTM |
| IPR000436 | Sushi/SCR/CCP domain | Domain | Domain |
| IPR000742 | EGF-like domain | Domain | Domain |
| IPR001881 | EGF-like calcium-binding domain | Domain | Domain |
| IPR010255 | Haem peroxidase superfamily | Family | Homologous superfamily |
| IPR018097 | EGF-like calcium-binding, conserved site | Site | Conserved site |
| IPR019791 | Haem peroxidase, animal-type | Family | Family |
| IPR029589 | Thyroid peroxidase | Family | Family |
| IPR035976 | Sushi/SCR/CCP superfamily | Family | Homologous superfamily |
| IPR037120 | Haem peroxidase domain superfamily, animal type | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 274500 | OMIM | Thyroid dyshormonogenesis 2A (TDH2A) | A disorder due to defective conversion of accumulated iodide to organically bound iodine. The iodide organification defect can be partial or complete. The disease is caused by variants affecting the gene represented in this entry. |
Drugs
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| Drug | Name | Source | Type |
| DB00389 | Carbimazole | Drugbank | small molecule |
| DB00509 | Dextrothyroxine | Drugbank | small molecule |
| DB00550 | Propylthiouracil | Drugbank | small molecule |
| DB00763 | Methimazole | Drugbank | small molecule |
| DB05382 | Iodine | Drugbank | small molecule |
| DB08604 | Triclosan | Drugbank | small molecule |
| DB11085 | Resorcinol | Drugbank | small molecule |
| DB11496 | 2-mercaptobenzothiazole | Drugbank | small molecule |
Interactions
2 interactions