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Nuclear protein AMMECR1 (AMMECR1)

Homo sapiens — UniProt Q9Y4X0

Gene: AMMECR1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Nuclear protein AMMECR1 (AMMECR1) is a protein from Homo sapiens identified by UniProt accession Q9Y4X0, 333 residues long. MolForge cross-references it against 0 known binders and 42 disease associations.

  • UniProt accession: Q9Y4X0; gene symbol AMMECR1.
  • Organism: Homo sapiens.
  • Length: 333 amino acids.
  • Top disease associations (Open Targets): Alport syndrome - intellectual disability - midface hypoplasia - elliptocytosis, Short stature and Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameNuclear protein AMMECR1
UniProt accessionQ9Y4X0
GeneAMMECR1
OrganismHomo sapiens
Length333 residues
Molecular weight—
EC numbers—
Target class—
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 (42)

Diseases linked to this target (Open Targets).

  • Alport syndrome - intellectual disability - midface hypoplasia - elliptocytosis · score 0.65
  • Short stature · score 0.45
  • Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome · score 0.42
  • neurodegenerative disease · score 0.19
  • response to statin · score 0.09
  • low density lipoprotein cholesterol measurement · score 0.08
  • Disorder of lipid metabolism · score 0.07
  • familial hypercholesterolemia · score 0.03
  • psoriasis · score 0.02
  • ovarian carcinoma · score 0.01

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9Y4X0-F1alphafoldPREDICTED71.98—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9Y4X0.

Amino-acid sequence (333 residues)

MAAGCCGVKK QKLSSSPPSG SGGGGGASSS SHCSGESQCR AGELGLGGAG TRLNGLGGLT GGGSGSGCTL SPPQGCGGGG GGIALSPPPS CGVGTLLSTP AAATSSSPSS SSAASSSSPG SRKMVVSAEM CCFCFDVLYC HLYGYQQPRT PRFTNEPYPL FVTWKIGRDK RLRGCIGTFS AMNLHSGLRE YTLTSALKDS RFPPMTRDEL PRLFCSVSLL TNFEDVCDYL DWEVGVHGIR IEFINEKGSK RTATYLPEVA KEQGWDHIQT IDSLLRKGGY KAPITNEFRK TIKLTRYRSE KMTLSYAEYL AHRQHHHFQN GIGHPLPPYN HYS

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with AMMECR1?

The strongest Open Targets associations for AMMECR1 are Alport syndrome - intellectual disability - midface hypoplasia - elliptocytosis, Short stature, Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome, neurodegenerative disease and response to statin.

How long is the AMMECR1 protein?

The Homo sapiens AMMECR1 protein (UniProt Q9Y4X0) is 333 amino acids long.

Browse: Targets: A · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ9Y4X0
GeneAMMECR1
OrganismHomo sapiens
Length333
Binders0
Diseases42
View on UniProt