P450 Protein:
| P450 Symbol | Cyp24a1 |
| Protein Name | 1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial |
| Uniprot ID | Q09128 |
| EC Number | 1.14.15.16 |
| Gene ID | 25279 |
| Species | Rattus norvegicus (Rat) |
| Txid | 10116 |
| P450 Protein Structure |
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
|
| Subcellular Location | Mitochondrion |
| Protein Sequence | GO |
Reaction Scheme:
| Chemical Conversion | C27H44O4 + Fe2S2 + O2 + H+ → C27H42O4 + Fe2S2 + H2O |
| Reaction Type | Oxidation |
| Chemical Bond | CH-OH |
| RheaID | 24972 |
Cyp24a1
Substrate Information:
| Substrate Name | Calcitetrol |
| Substrate Chemical Formula | C27H44O4 |
| Substrate PubChem CID | 9910685 |
| Substrate Smiles | C[C@H](CCC(C(C)(C)O)O)[C@H]1CC[C@@H]2[C@@]1(CCC/C2=CC=C/3C[C@H](C[C@@H](C3=C)O)O)C |
| Substrate Structure |
| Substrate Name | [2Fe-2S]1+ |
| Substrate Chemical Formula | Fe2S2 |
| Substrate Smiles | S1[Fe]S[Fe+]1 |
| Substrate Structure |
| Substrate Name | O2 |
| Substrate Chemical Formula | O2 |
| Substrate PubChem CID | 977 |
| Substrate CAS Number | 7782-44-7 |
| Substrate Smiles | O=O |
| Substrate Structure |
| Substrate Name | H+ |
| Substrate Chemical Formula | H+ |
| Substrate PubChem CID | 1038 |
| Substrate CAS Number | 12408-02-5 |
| Substrate Smiles | [H+] |
| Substrate Structure |
Product Information:
| Product Name | (1S)-1,25-Dihydroxy-24-Oxocalciol |
| Product Chemical Formula | C27H42O4 |
| Product PubChem CID | 5283703 |
| Product Smiles | C[C@H](CCC(=O)C(C)(C)O)[C@H]1CC[C@@H]2[C@@]1(CCC/C2=CC=C/3C[C@H](C[C@@H](C3=C)O)O)C |
| Product Structure |
| Product Name | [2Fe-2S]2+ |
| Product Chemical Formula | Fe2S2 |
| Product Smiles | S1[Fe+]S[Fe+]1 |
| Product Structure |
| Product Name | H2O |
| Product Chemical Formula | H2O |
| Product PubChem CID | 962 |
| Product CAS Number | 7732-18-5 |
| Product Smiles | O |
| Product Structure |
References:
| Title: | Metabolic studies using recombinant escherichia coli cells producing rat mitochondrial CYP24 CYP24 can convert 1alpha,25-dihydroxyvitamin D3 to calcitroic acid. |
| PMID: | 10231362 |
| Journal: | European journal of biochemistry |
| Year: | 1999/5/1 |
| Title: | Structure-function analysis of vitamin D 24-hydroxylase (CYP24A1) by site-directed mutagenesis: amino acid residues responsible for species-based difference of CYP24A1 between humans and rats. |
| PMID: | 16617161 |
| Journal: | Molecular pharmacology |
| Year: | 2006/7/1 |