Latexin (LXN)

Homo sapiens — UniProt Q9BS40

Gene: LXNHomo sapiensSwissProt reviewed

About Latexin

Latexin (LXN) is a protein from Homo sapiens identified by UniProt accession Q9BS40, 222 residues long. MolForge cross-references it against 0 known binders and 92 disease associations.

Target properties

Protein nameLatexin
UniProt accessionQ9BS40
GeneLXN
OrganismHomo sapiens
Length222 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 (92)

Diseases linked to this target (Open Targets).

  • hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 · score 0.57
  • Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 · score 0.57
  • combined oxidative phosphorylation deficiency · score 0.34
  • diastolic blood pressure · score 0.29
  • systolic blood pressure · score 0.20
  • genetic disorder · score 0.19
  • PR interval · score 0.13
  • Developmental regression · score 0.12
  • Relative macrocephaly · score 0.12
  • Severe muscular hypotonia · score 0.12

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9BS40-F1alphafoldPREDICTED95.96—

Amino-acid sequence (222 residues)

MEIPPTNYPA SRAALVAQNY INYQQGTPHR VFEVQKVKQA SMEDIPGRGH KYHLKFAVEE IIQKQVKVNC TAEVLYPSTG QETAPEVNFT FEGETGKNPD EEDNTFYQRL KSMKEPLEAQ NIPDNFGNVS PEMTLVLHLA WVACGYIIWQ NSTEDTWYKM VKIQTVKQVQ RNDDFIELDY TILLHNIASQ EIIPWQMQVL WHPQYGTKVK HNSRLPKEVQ LE

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Quick facts

UniProtQ9BS40
GeneLXN
OrganismHomo sapiens
Length222
Binders0
Diseases92
View on UniProt