Peroxisomal multifunctional enzyme type 2 (HSD17B4)

Homo sapiens — UniProt P51659

Gene: HSD17B4Homo sapiensSwissProt reviewed

About Peroxisomal multifunctional enzyme type 2

Peroxisomal multifunctional enzyme type 2 (HSD17B4) is a protein from Homo sapiens identified by UniProt accession P51659, 736 residues long. MolForge cross-references it against 0 known binders and 165 disease associations.

Target properties

Protein namePeroxisomal multifunctional enzyme type 2
UniProt accessionP51659
GeneHSD17B4
OrganismHomo sapiens
Length736 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 (165)

Diseases linked to this target (Open Targets).

  • d-bifunctional protein deficiency · score 0.84
  • Perrault syndrome 1 · score 0.75
  • Perrault syndrome · score 0.72
  • genetic disorder · score 0.49
  • Perrault syndrome 2 · score 0.37
  • hearing loss · score 0.37
  • neurofibrillary tangles measurement · score 0.30
  • neurodegenerative disease · score 0.29
  • Abnormality of the nervous system · score 0.27
  • Rare genetic deafness · score 0.27

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P51659-F1alphafoldPREDICTED88.99—

Amino-acid sequence (736 residues)

MGSPLRFDGR VVLVTGAGAG LGRAYALAFA ERGALVVVND LGGDFKGVGK GSLAADKVVE EIRRRGGKAV ANYDSVEEGE KVVKTALDAF GRIDVVVNNA GILRDRSFAR ISDEDWDIIH RVHLRGSFQV TRAAWEHMKK QKYGRIIMTS SASGIYGNFG QANYSAAKLG LLGLANSLAI EGRKSNIHCN TIAPNAGSRM TQTVMPEDLV EALKPEYVAP LVLWLCHESC EENGGLFEVG AGWIGKLRWE RTLGAIVRQK NHPMTPEAVK ANWKKICDFE NASKPQSIQE STGSIIEVLS KIDSEGGVSA NHTSRATSTA TSGFAGAIGQ KLPPFSYAYT ELEAIMYALG VGASIKDPKD LKFIYEGSSD FSCLPTFGVI IGQKSMMGGG LAEIPGLSIN FAKVLHGEQY LELYKPLPRA GKLKCEAVVA DVLDKGSGVV IIMDVYSYSE KELICHNQFS LFLVGSGGFG GKRTSDKVKV AVAIPNRPPD AVLTDTTSLN QAALYRLSGD WNPLHIDPNF ASLAGFDKPI LHGLCTFGFS ARRVLQQFAD NDVSRFKAIK ARFAKPVYPG QTLQTEMWKE GNRIHFQTKV QETGDIVISN AYVDLAPTSG TSAKTPSEGG KLQSTFVFEE IGRRLKDIGP EVVKKVNAVF EWHITKGGNI GAKWTIDLKS GSGKVYQGPA KGAADTTIIL SDEDFMEVVL GKLDPQKAFF SGRLKARGNI MLSQKLQMIL KDYAKL

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Quick facts

UniProtP51659
GeneHSD17B4
OrganismHomo sapiens
Length736
Binders0
Diseases165
View on UniProt