EcoDrugPlus

Proteasome 26s Subunit, Non-Atpase 7

Ensembl ID : ENSUMAG00000018624
Gene Symbol: PSMD7
4 Cross references
243 Possible Orthologues:

Proteasome 26s Subunit, Non-Atpase 8

Ensembl ID : ENSUMAG00000018535
Gene Symbol: PSMD8
4 Cross references
202 Possible Orthologues:

Protein Arginine Methyltransferase 5

Ensembl ID : ENSUMAG00000014079
Gene Symbol: PRMT5
4 Cross references
198 Possible Orthologues:

Protein Kinase C Alpha

Ensembl ID : ENSUMAG00000019423
Gene Symbol: PRKCA
4 Cross references
289 Possible Orthologues:

Protein Kinase C Beta

Ensembl ID : ENSUMAG00000008721
Gene Symbol: PRKCB
4 Cross references
284 Possible Orthologues:

Protein Kinase C Delta

Ensembl ID : ENSUMAG00000020236
Gene Symbol: PRKCD
4 Cross references
280 Possible Orthologues:

Protein Kinase C Eta

Ensembl ID : ENSUMAG00000013719
Gene Symbol: PRKCH
4 Cross references
237 Possible Orthologues:

Protein Kinase C Gamma

Ensembl ID : ENSUMAG00000011272
Gene Symbol: PRKCG
4 Cross references
198 Possible Orthologues:

Protein Kinase C Iota

Ensembl ID : ENSUMAG00000010638
Gene Symbol: PRKCI
4 Cross references
195 Possible Orthologues:

Protein Kinase C Theta

Ensembl ID : ENSUMAG00000012477
Gene Symbol: PRKCQ
4 Cross references
203 Possible Orthologues:

Protein Kinase C Zeta

Ensembl ID : ENSUMAG00000010365
Gene Symbol: PRKCZ
4 Cross references
198 Possible Orthologues:

Protein Kinase D1

Ensembl ID : ENSUMAG00000005703
Gene Symbol: PRKD1
4 Cross references
204 Possible Orthologues:

Select Keywords:


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).