About Tudor domain-containing protein 15
Tudor domain-containing protein 15 (TDRD15) is a protein
from Homo sapiens identified by UniProt accession
B5MCY1, 1934 residues long.
MolForge cross-references it against 0 known binders and
46 disease associations.
Target properties
| Protein name | Tudor domain-containing protein 15 |
| UniProt accession | B5MCY1 |
| Gene | TDRD15 |
| Organism | Homo sapiens |
| Length | 1934 residues |
| Molecular weight | — |
| EC numbers | — |
| Target class | UNCLASSIFIED |
| Subcellular location | — |
| Keywords | — |
Druggability
Target tractability assessment (Open Targets + pocket analysis). No approved drug
| Druggability tier | MEDIUM |
| Druggability score | — |
| Pocket score | — |
| Max clinical phase | — |
Disease associations (46)
Diseases linked to this target (Open Targets).
- low density lipoprotein cholesterol measurement · score 0.51
- total cholesterol measurement · score 0.45
- alcohol drinking · score 0.38
- hematocrit · score 0.37
- free cholesterol measurement · score 0.35
- coronary artery disease · score 0.35
- alcohol consumption measurement · score 0.34
- vitamin D measurement · score 0.34
- self reported educational attainment · score 0.33
- triglyceride measurement · score 0.32
3D Structure (1)
Experimental (PDB) and predicted (AlphaFold) structures for this protein.
| Structure | Source | Method | Mean pLDDT | Resolution (Å) |
| AF-B5MCY1-F1 | alphafold | PREDICTED | 71.66 | — |
Amino-acid sequence (1934 residues)
MDSTSFLPTF LDVDLTISHI KCLPKDILVK FQGIKSNECE FDYHVLQREI QHTPKVKNNV EIDEFCLVEE RVSGEWQRGR VMEKKNELYT VLLIDRGEEL RVAGPQIASA CGNLFELPPR VVFGIFANIL PVGEKWSPKA LNYFKSLVGI QVKGYVQAIL PLQMFLFEVP KIISQALELQ LGRLVDGDSF RLIVEMLEEF PQQMPDLLQH KRPELSLGNK DTSLDIQHVL DKLQPSLSVG STESVKVSSA LSPSKFYCQL IKWTPELENL TAHMTLHYDT VCQETSPTCD NFGLLCVARR RNGQWHRGIL QQLLPPNQVK IWFMDYGSSE AIPSIYVKKL KQDFILVPLF SFPCSLTCLH SPDRDARIFQ LSIFKQALLG QVVYAHIDWF NKDECLYYVT LQTQESTVNS KCLLKTVGTQ VLCPMSDSKI SNILSETSVS DVNSFAVESF MGNIEWSIDS LNKKGILKVG FPIKTVQMEI EAAYIAFIAY VLNPSNFWVR TNDHRNEFQE IMKNINKFYD LCENDEMILR KPEPGLFCCA RYSKDRRFYR AVITEINGYK INVYFLDYGN TDSIPFFDVK ILLPEFCELP ALAMCCSLAH IFPVEDLWTK AAIDYFKKLV LNKAILLQVI AKKDDKYTVN IQSVEASENI DVISLMLQAG YAEYFQVELE YFPKSVSEYS MLNSESKNKV NIKKVISALL EGPKSKKYHS NNLVENNLSL PKSLAVNISE FKNPFTLSVG PESSWPYKEY IFRPGTVLEV KCSCYYGPGD FSCQLQCKSE DLKLLMEQIQ NYYSIHSDPY EIGQTACVAK YSGKWCRAAV LTQVSKEVDI VFVDYGYQKR VLIEDLCAIN PRFLLLESQA FRCCLNHFIE PVSCKLFSWT RKAFRDLWNF ISSSRGLLTC IIYALVIIHP NHLYNLVDLQ SSFTSAKEFL MNRGSAQYIT LSETFPSLFS LYSYCYSSFN IQIGSEEEVY ISHIYSPQKF YCQLGRNNKD LEMIETKITE SVNLQNFPKY DSNKMRVCIS KYVEDGLSYR ALAIPTDSSS EFQVYFVDFG NKQLVGENML RAISAQFPEL LFTPMQAIKC FLSDLRDVDI PAEISSWFKD NFLGRSLKAI ILSQESDGQL GIELYDGSQY INEKIKVLLH AYGKRHCDQA CCMEKSNKIN ENKRFTTSLK GKTGNNYRHN VINKPSPVTY SERKIDQLMH PKNIHARFLK PSVCYKMEPV SKNKMKTSLN DGLKGIKIVP GAAHILENRR VGQKSVKVVS QSFIRALNQT TSQNPYDLIR PQIKDLPQPQ IYLNAKVKGY VSNISNPANF HIQLAENESV IIRLADALNA TARRLRERKS VKPLVGDLVV AEYSGDNAIY RAVIKKILPG NSFEVEFIDY GNSAIVNTSK IYELQREFLT VPQLGIHAFL SGVKWNEPDE IWDDKTVDYF TSKVHNKTVY CEFLKKHDQK WEVNMICDEK CVINELLKWK ACSKLQKSAL QMPQVLSQKV RPGDNEMKKG KSNESEGSMN SNQQLFKIPL EEFKLGQLEK AEMLNVSKSG RFYVKLSKNK KILSDLIVLI TKEEKKSPFL SMESIEKGLE CLAKSKNTLK WHRSKVEEKY VDDKVLVFLV DCGIYEIVPV CNTKLLSNEI RNIPRQAVPC KWIWFENSKN ISFECLFADL EINILFLKYL DAVWEVEILV DDLLLLEYLN LNTVPVEENK LRLAEIVYNI ESKTPVSSCT IKSFTWVQFQ NDRQYSGIAT AVSDPSDFSI QLEDFFDIMK YLFMLLSDLP ETLQTLPQEF IIPGSSCLFK YKSEDQWNRV EISEVSPQSL CLVLVDYGFS FYIRYSEIIN LKVVPEELLN LPRLSYPCIL YGILPAKGKH WSEEAKIFFR DFLSKPDLVF QFREYHSETK LKVDVIHEKN NLADILVASG LATYSKDSPH LDAITATESA KNPI
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