Cytochrome b · SINGLE PROTEIN · Plasmodium falciparum
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Structured disease, protein, and project context should read before the lower-level identity rail.
As of 2026-09-14Cytochrome b shows approved-linked disease relevance led by amebiasis. 5 more disease programs remain visible in the same review block. 1 linked drug keeps the current disease frame grounded. Protein identity stays anchored to UniProt Q02768. Start with amebiasis, then reuse UniProt Q02768 as the stable protein anchor across project notes and exports.
Start with amebiasis, then reuse UniProt Q02768 as the stable protein anchor across project notes and exports.
Cytochrome b shows approved-linked disease relevance led by amebiasis. 5 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.
Start review with amebiasis because it currently carries approved-linked support. Linked drugs include ATOVAQUONE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
Disease source · ChEMBL drug mechanism + indication proxyCytochrome b
Review this target as Cytochrome b, mapped to UniProt Q02768. Sequence length is 376 aa.
Protein source · UniProt accession via ChEMBL component mappingKeep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Cytochrome b as ChEMBL target CHEMBL1777, mapped to UniProt Q02768. Disease framing currently uses the Open Targets-ready proxy contract.
Reuse the same identifiers in notes, watch rules, exports, and review packs so provenance stays stable across surfaces.
Choose the first block or source based on the question you are trying to answer.
Start here when your first question is whether Cytochrome b is the right protein anchor across sources, using UniProt Q02768 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why amebiasis is currently framed as approved-linked support. It currently carries 1 linked drug in the same disease frame.
Jump to Disease ContextOpen the one-page evidence card when you want the rationale, activity base, and attribution together.
Open Review-ready CardVerify identity, organism, and the fastest next research jumps from the same page.
| Preferred Name | Cytochrome b |
| Target Type | SINGLE PROTEIN |
| Organism | Plasmodium falciparum |
| UniProt | Q02768 |
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | Cytochrome b |
| UniProt Accession | Q02768 |
| Component Type | Protein |
| Sequence Length | 376 aa |
Cytochrome b
Review this target as Cytochrome b, mapped to UniProt Q02768. Sequence length is 376 aa.
Open Targets-ready disease context using the current target-indication evidence contract.
Cytochrome b shows approved-linked disease relevance led by amebiasis. 5 more disease programs remain visible in the same review block.
Start review with amebiasis because it currently carries approved-linked support. Linked drugs include ATOVAQUONE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.