Prestin (SLC26A5)

Homo sapiens — UniProt P58743

Gene: SLC26A5Homo sapiensSwissProt reviewed

About Prestin

Prestin (SLC26A5) is a protein from Homo sapiens identified by UniProt accession P58743, 744 residues long. MolForge cross-references it against 0 known binders and 108 disease associations.

Target properties

Protein namePrestin
UniProt accessionP58743
GeneSLC26A5
OrganismHomo sapiens
Length744 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 (108)

Diseases linked to this target (Open Targets).

  • deafness · score 0.60
  • hearing loss, autosomal recessive · score 0.59
  • hearing loss · score 0.50
  • hearing measurement · score 0.43
  • chronotype measurement · score 0.31
  • genetic disorder · score 0.19
  • blood protein measurement · score 0.17
  • Hearing impairment · score 0.12
  • diet measurement · score 0.09
  • intraocular pressure measurement · score 0.09

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P58743-F1alphafoldPREDICTED83.70—

Amino-acid sequence (744 residues)

MDHAEENEIL AATQRYYVER PIFSHPVLQE RLHTKDKVPD SIADKLKQAF TCTPKKIRNI IYMFLPITKW LPAYKFKEYV LGDLVSGIST GVLQLPQGLA FAMLAAVPPI FGLYSSFYPV IMYCFLGTSR HISIGPFAVI SLMIGGVAVR LVPDDIVIPG GVNATNGTEA RDALRVKVAM SVTLLSGIIQ FCLGVCRFGF VAIYLTEPLV RGFTTAAAVH VFTSMLKYLF GVKTKRYSGI FSVVYSTVAV LQNVKNLNVC SLGVGLMVFG LLLGGKEFNE RFKEKLPAPI PLEFFAVVMG TGISAGFNLK ESYNVDVVGT LPLGLLPPAN PDTSLFHLVY VDAIAIAIVG FSVTISMAKT LANKHGYQVD GNQELIALGL CNSIGSLFQT FSISCSLSRS LVQEGTGGKT QLAGCLASLM ILLVILATGF LFESLPQAVL SAIVIVNLKG MFMQFSDLPF FWRTSKIELT IWLTTFVSSL FLGLDYGLIT AVIIALLTVI YRTQSPSYKV LGKLPETDVY IDIDAYEEVK EIPGIKIFQI NAPIYYANSD LYSNALKRKT GVNPAVIMGA RRKAMRKYAK EVGNANMANA TVVKADAEVD GEDATKPEEE DGEVKYPPIV IKSTFPEEMQ RFMPPGDNVH TVILDFTQVN FIDSVGVKTL AGIVKEYGDV GIYVYLAGCS AQVVNDLTRN RFFENPALWE LLFHSIHDAV LGSQLREALA EQEASAPPSQ EDLEPNATPA TPEA

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Quick facts

UniProtP58743
GeneSLC26A5
OrganismHomo sapiens
Length744
Binders0
Diseases108
View on UniProt