EcoDrugPlus

Proteasome 26s Subunit, Non-Atpase 3

Ensembl ID : ENSOPRG00000007186
Gene Symbol: PSMD3
3 Cross references
212 Possible Orthologues:

Proteasome 26s Subunit, Non-Atpase 6

Ensembl ID : ENSOPRG00000016439
Gene Symbol: PSMD6
1 Cross references
213 Possible Orthologues:

Proteasome 26s Subunit, Non-Atpase 8

Ensembl ID : ENSOPRG00000009910
Gene Symbol: PSMD8
1 Cross references
202 Possible Orthologues:

Protein Arginine Methyltransferase 5

Ensembl ID : ENSOPRG00000001113
Gene Symbol: PRMT5
3 Cross references
198 Possible Orthologues:

Protein Kinase C Alpha

Ensembl ID : ENSOPRG00000015694
Gene Symbol: PRKCA
1 Cross references
289 Possible Orthologues:

Protein Kinase C Beta

Ensembl ID : ENSOPRG00000002672
Gene Symbol: PRKCB
1 Cross references
284 Possible Orthologues:

Protein Kinase C Delta

Ensembl ID : ENSOPRG00000011041
Gene Symbol: PRKCD
3 Cross references
280 Possible Orthologues:

Protein Kinase C Epsilon

Ensembl ID : ENSOPRG00000010173
Gene Symbol: PRKCE
1 Cross references
315 Possible Orthologues:

Protein Kinase C Eta

Ensembl ID : ENSOPRG00000007737
Gene Symbol: PRKCH
1 Cross references
237 Possible Orthologues:

Protein Kinase C Gamma

Ensembl ID : ENSOPRG00000013209
Gene Symbol: PRKCG
1 Cross references
199 Possible Orthologues:

Protein Kinase C Iota

Ensembl ID : ENSOPRG00000015588
Gene Symbol: PRKCI
1 Cross references
193 Possible Orthologues:

Protein Kinase C Theta

Ensembl ID : ENSOPRG00000003065
Gene Symbol: PRKCQ
1 Cross references
203 Possible Orthologues:

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PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).