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Low-density lipoprotein receptor class A domain-containing protein 2 (LDLRAD2)

Homo sapiens — UniProt Q5SZI1

Gene: LDLRAD2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Low-density lipoprotein receptor class A domain-containing protein 2 (LDLRAD2) is a protein from Homo sapiens identified by UniProt accession Q5SZI1, 272 residues long. MolForge cross-references it against 0 known binders and 14 disease associations.

  • UniProt accession: Q5SZI1; gene symbol LDLRAD2.
  • Organism: Homo sapiens.
  • Length: 272 amino acids.
  • Top disease associations (Open Targets): Schwartz-Jampel syndrome, Dyssegmental dysplasia, Silverman-Handmaker type and alkaline phosphatase measurement.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameLow-density lipoprotein receptor class A domain-containing protein 2
UniProt accessionQ5SZI1
GeneLDLRAD2
OrganismHomo sapiens
Length272 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 (14)

Diseases linked to this target (Open Targets).

  • Schwartz-Jampel syndrome · score 0.46
  • Dyssegmental dysplasia, Silverman-Handmaker type · score 0.41
  • alkaline phosphatase measurement · score 0.26
  • genetic disorder · score 0.19
  • connective tissue disease · score 0.15
  • Microcephaly · score 0.11
  • von Willebrand factor measurement · score 0.08
  • Immature Reticulocyte Fraction Measurement · score 0.08
  • gonorrhea · score 0.07
  • gastric carcinoma · score 0.02

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q5SZI1-F1alphafoldPREDICTED78.73—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q5SZI1.

Amino-acid sequence (272 residues)

MEACCLLQLP QRLLLLGAAA LTATALETAD LAELCGQTWQ GDGLLLRSHA ASRRFYFVAP DTDCGLWVQA AAPGDRIRFQ FRFFLVYSLT PAPPALNTSS PAPADPCAPG SYLQFYEGPP GAPRPLGSPL CGLNIPVPVA SSGPFLGLRL VTRGRQPRVD FVGEVTSFRL GPCGAYFRCQ NGRCIPSSLV CDPWGMDNCG DGSDQGSWSP ADCRGPSPVP SQTGSTDAHT SRSLTPSPAL GSAGSLWIAA ERSSPAGRDP TRQDAALEGS TE

Frequently asked questions

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

Which diseases are associated with LDLRAD2?

The strongest Open Targets associations for LDLRAD2 are Schwartz-Jampel syndrome, Dyssegmental dysplasia, Silverman-Handmaker type, alkaline phosphatase measurement, genetic disorder and connective tissue disease.

How long is the LDLRAD2 protein?

The Homo sapiens LDLRAD2 protein (UniProt Q5SZI1) is 272 amino acids long.

Browse: Targets: L · 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

UniProtQ5SZI1
GeneLDLRAD2
OrganismHomo sapiens
Length272
Binders0
Diseases14
View on UniProt