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CCR4-NOT transcription complex subunit 2 (CNOT2)

Homo sapiens — UniProt Q9NZN8

Gene: CNOT2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

CCR4-NOT transcription complex subunit 2 (CNOT2) is a protein from Homo sapiens identified by UniProt accession Q9NZN8, 540 residues long. MolForge cross-references it against 0 known binders and 57 disease associations.

  • UniProt accession: Q9NZN8; gene symbol CNOT2.
  • Organism: Homo sapiens.
  • Length: 540 amino acids.
  • Top disease associations (Open Targets): intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies, genetic disorder and neurodegenerative disease.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameCCR4-NOT transcription complex subunit 2
UniProt accessionQ9NZN8
GeneCNOT2
OrganismHomo sapiens
Length540 residues
Molecular weight—
EC numbers—
Target class—
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 (57)

Diseases linked to this target (Open Targets).

  • intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies · score 0.51
  • genetic disorder · score 0.41
  • neurodegenerative disease · score 0.40
  • Neurodevelopmental disorder · score 0.27
  • glioblastoma multiforme · score 0.25
  • breast adenocarcinoma · score 0.25
  • gastric adenocarcinoma · score 0.23
  • lung adenocarcinoma · score 0.23
  • squamous cell lung carcinoma · score 0.23
  • urinary bladder cancer · score 0.23

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NZN8-F1alphafoldPREDICTED59.07—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9NZN8.

Amino-acid sequence (540 residues)

MVRTDGHTLS EKRNYQVTNS MFGASRKKFV EGVDSDYHDE NMYYSQSSMF PHRSEKDMLA SPSTSGQLSQ FGASLYGQQS ALGLPMRGMS NNTPQLNRSL SQGTQLPSHV TPTTGVPTMS LHTPPSPSRG ILPMNPRNMM NHSQVGQGIG IPSRTNSMSS SGLGSPNRSS PSIICMPKQQ PSRQPFTVNS MSGFGMNRNQ AFGMNNSLSS NIFNGTDGSE NVTGLDLSDF PALADRNRRE GSGNPTPLIN PLAGRAPYVG MVTKPANEQS QDFSIHNEDF PALPGSSYKD PTSSNDDSKS NLNTSGKTTS STDGPKFPGD KSSTTQNNNQ QKKGIQVLPD GRVTNIPQGM VTDQFGMIGL LTFIRAAETD PGMVHLALGS DLTTLGLNLN SPENLYPKFA SPWASSPCRP QDIDFHVPSE YLTNIHIRDK LAAIKLGRYG EDLLFYLYYM NGGDVLQLLA AVELFNRDWR YHKEERVWIT RAPGMEPTMK TNTYERGTYY FFDCLNWRKV AKEFHLEYDK LEERPHLPST FNYNPAQQAF

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with CNOT2?

The strongest Open Targets associations for CNOT2 are intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies, genetic disorder, neurodegenerative disease, Neurodevelopmental disorder and glioblastoma multiforme.

How long is the CNOT2 protein?

The Homo sapiens CNOT2 protein (UniProt Q9NZN8) is 540 amino acids long.

Browse: Targets: C · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ9NZN8
GeneCNOT2
OrganismHomo sapiens
Length540
Binders0
Diseases57
View on UniProt