Potassium-transporting ATPase
Cross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Potassium-transporting ATPase as ChEMBL target CHEMBL2095173, mapped to UniProt P20648. 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.
Why Potassium-transporting ATPase matters
Potassium-transporting ATPase is reviewed as Potassium-transporting ATPase alpha chain 1 (UniProt P20648); Potassium-transporting ATPase shows approved-linked disease relevance led by gastroesophageal reflux disease. 5 more disease programs remain visible in the same review block.; 13 linked drugs keep this evidence frame grounded.; the current evidence base includes 5 approved drugs, 336 compounds, and 17 assays, with lead potency reaching pChEMBL 7.7.
Potassium-transporting ATPase alpha chain 1 Sequence length is 1035 aa.
Review this target as Potassium-transporting ATPase, mapped to UniProt P20648. ChEMBL maps the protein component as Potassium-transporting ATPase alpha chain 1. Sequence length is 1035 aa.
Protein source · UniProt accession via ChEMBL component mappingPotassium-transporting ATPase shows approved-linked disease relevance led by gastroesophageal reflux disease. 5 more disease programs remain visible in the same review block. 13 linked drugs keep the rationale reviewable. 5 additional disease programs remain visible in the same card. Linked drugs include ABEPRAZAN, DEXLANSOPRAZOLE, ESOMEPRAZOLE MAGNESIUM.
Start review with gastroesophageal reflux disease because it currently carries approved-linked support. Linked drugs include ABEPRAZAN, DEXLANSOPRAZOLE, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE SODIUM. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
ChEMBL target recordChEMBL currently tracks 5 approved drugs, 336 compounds, and 17 assays for this target. The dominant activity type is IC50. CHEMBL1202672 is the current potency anchor at pChEMBL 7.7.
Use CHEMBL1202672 as the tractability anchor when discussing potency (pChEMBL 7.7).
Activity source · ChEMBL 36 via Core EngineStart with the right source
Pick the first block or linked source that matches the review question in front of you.
Start with the review rationale when you need to explain why Potassium-transporting ATPase matters before drilling into raw source blocks.
Jump to Review RationaleGo back to the target snapshot when you need the naming and mapping contract behind UniProt P20648, not just the summarized rationale.
Open Protein ContextUse the target snapshot disease block when you need to see why gastroesophageal reflux disease is currently treated as approved-linked support.
Open Disease ContextSnapshot State
No project snapshot selected. Export uses the live evidence card state.
pChEMBL Activity Distribution
Top 5 Inhibitors (by pChEMBL)
| Structure | Compound | pChEMBL | Type | Phase |
|---|---|---|---|---|
|
|
No preferred name
CHEMBL1202672
|
7.7 | IC50 | — |
|
|
No preferred name
CHEMBL1202661
|
7.5 | IC50 | — |
|
|
No preferred name
CHEMBL1790041
|
7.4 | IC50 | Approved |
|
|
No preferred name
CHEMBL1202621
|
7.3 | IC50 | — |
|
|
No preferred name
CHEMBL1202647
|
7.3 | IC50 | — |
Approved Drugs
| Structure | Compound | First Approval |
|---|---|---|
|
|
PANTOPRAZOLE
CHEMBL1502
|
2000 |
|
|
LANSOPRAZOLE
CHEMBL480
|
1995 |
|
|
OMEPRAZOLE
CHEMBL1503
|
1989 |
|
|
RANITIDINE
CHEMBL1790041
|
1983 |
|
|
CIMETIDINE
CHEMBL30
|
1977 |