Zinc finger protein 729 (ZNF729)

Homo sapiens — UniProt A6NN14

Gene: ZNF729Homo sapiensSwissProt reviewed

About Zinc finger protein 729

Zinc finger protein 729 (ZNF729) is a protein from Homo sapiens identified by UniProt accession A6NN14, 1252 residues long. MolForge cross-references it against 0 known binders and 54 disease associations.

Target properties

Protein nameZinc finger protein 729
UniProt accessionA6NN14
GeneZNF729
OrganismHomo sapiens
Length1252 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 (54)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.37
  • age at menopause · score 0.21
  • smoking status measurement · score 0.21
  • triglyceride measurement · score 0.21
  • sitting height measurement · score 0.09
  • age-related macular degeneration · score 0.07
  • X-linked retinal dysplasia · score 0.06
  • Familial exudative vitreoretinopathy · score 0.06
  • retinitis pigmentosa · score 0.06
  • hereditary persistence of fetal hemoglobin-sickle cell disease syndrome · score 0.06

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-A6NN14-F1alphafoldPREDICTED69.48—

Amino-acid sequence (1252 residues)

MPGAPGSLEM GPLTFRDVTI EFSLEEWQCL DTVQQNLYRD VMLENYRNLV FLGMAVFKPD LITCLKQGKE PWNMKRHEMV TKPPVMRSHF TQDLWPDQST KDSFQEVILR TYARCGHKNL RLRKDCKSAN EGKMHKEGYN KLNQCRTATQ RKIFQCNKHM KVFHKYSNRN KVRHTKKKTF KCIKCSKSFF MLSCLIRHKR IHIRQNIYKC EERGKAFKSF STLTKHKIIH TEDKPYKYKK CGNAFKFSST FTKHKRIHTG ETPFRCEECG KAFNQSSNLT DHKRIHTGEK TYKCEECGKA FKGSSNFNAH KVIHTAEKPY KCEDCGKTFN HFSALRKHKI IHTGKKPYKR EECGKAFSQS STLRKHEIIH TGEKPYKCEE CGKAFKWSSK LTVHKVVHTG EKPYKCEECG KAFSQFSTLK KHKIIHTGKK PYKCEECGKA FNSSSTLMKH KIIHTGEKPY KCEECGKAFR QSSHLTRHKA IHTGEKPYKC EECGKAFNHF SDLRRHKIIH TGKKPYKCEE CGKAFSQSST LRNHQIIHTG EKPYKCEECG KAFKWSSKLT VHKVIHTGEK PCKCEECGKA FKHFSALRKH KVIHTREKLY KCEECGKAFN NSSILAKHKI IHTGKKPYKC EECGKAFRQS SHLTRHKAIH TGEKPYKCEE CGKAFSHFSA LRRHKIIHTG KKPYKCEECG KAFSHFSALR RHKIIHTGEK PYKCEECGKA FKWSSKLTVH KVIHTAEKPC KCEECGKSFK HFSALRKHKV IHTREKLYKC EECVKAFNSF SALMKHKVIH TGEKPYKCEE CGKAFKWSSK LTVHKVIHTG EKPCKCEECG KAFKHFSALR KHKVIHTGKK PYKCEECGKA FSQSSSLRKH EIIHSGEKPY KCEECGKAFK WLSKLTVHKV IHTAEKPCKC EECGKAFKHF SALRKHKIIH TGKKPYKCEE CGKAFNDSST LMKHKIIHTG KKPYKCAECG KAFKQSSHLT RHKAIHTGEK PYKCEECGKD FNNSSTLKKH KLIHTREKLY KCEECVKAFN NFSALMKHKI IHTGEKPYKC EECGKAFKWS SKLTEHKVIH TGEKPCKCEE CDKAFKHFSA LRKHKVIHTG KKPYQCDECG KAFNNSSTLT KHKIIHTGEK PYKCEECGKA FSQSSILTKH KIIHSVEKPY KCEECGKAFN QSSHLTRHKT IHTGEKPYKC EECGKAFIQC SYLIRHKTIH TREKPTNVKK VPKLLSNPHT LLDKTIHTGE KPYKCEECAK AF

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Quick facts

UniProtA6NN14
GeneZNF729
OrganismHomo sapiens
Length1252
Binders0
Diseases54
View on UniProt