Renin receptor (ATP6AP2)

Homo sapiens — UniProt O75787

Gene: ATP6AP2Homo sapiensSwissProt reviewed

About Renin receptor

Renin receptor (ATP6AP2) is a protein from Homo sapiens identified by UniProt accession O75787, 350 residues long. MolForge cross-references it against 0 known binders and 243 disease associations.

Target properties

Protein nameRenin receptor
UniProt accessionO75787
GeneATP6AP2
OrganismHomo sapiens
Length350 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (243)

Diseases linked to this target (Open Targets).

  • syndromic X-linked intellectual disability Hedera type · score 0.67
  • neurodegenerative disease · score 0.54
  • congenital disorder of glycosylation type II · score 0.53
  • X-linked parkinsonism-spasticity syndrome · score 0.51
  • X-linked intellectual disability, Hedera type · score 0.50
  • ATP6AP2-related disorder · score 0.41
  • X-linked intellectual disability - epilepsy · score 0.37
  • endometrial cancer · score 0.18
  • genetic disorder · score 0.18
  • cutaneous melanoma · score 0.13

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-O75787-F1alphafoldPREDICTED79.16—

Amino-acid sequence (350 residues)

MAVFVVLLAL VAGVLGNEFS ILKSPGSVVF RNGNWPIPGE RIPDVAALSM GFSVKEDLSW PGLAVGNLFH RPRATVMVMV KGVNKLALPP GSVISYPLEN AVPFSLDSVA NSIHSLFSEE TPVVLQLAPS EERVYMVGKA NSVFEDLSVT LRQLRNRLFQ ENSVLSSLPL NSLSRNNEVD LLFLSELQVL HDISSLLSRH KHLAKDHSPD LYSLELAGLD EIGKRYGEDS EQFRDASKIL VDALQKFADD MYSLYGGNAV VELVTVKSFD TSLIRKTRTI LEAKQAKNPA SPYNLAYKYN FEYSVVFNMV LWIMIALALA VIITSYNIWN MDPGYDSIIY RMTNQKIRMD

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Quick facts

UniProtO75787
GeneATP6AP2
OrganismHomo sapiens
Length350
Binders0
Diseases243
View on UniProt