EcoDrugPlus

Protein Arginine Methyltransferase 5

Ensembl ID : ENSUPAG00010011261
Gene Symbol: PRMT5
3 Cross references
198 Possible Orthologues:

Protein Kinase C Alpha

Ensembl ID : ENSUPAG00010001212
Gene Symbol: PRKCA
1 Cross references
289 Possible Orthologues:

Protein Kinase C Beta

Ensembl ID : ENSUPAG00010011021
Gene Symbol: PRKCB
1 Cross references
284 Possible Orthologues:

Protein Kinase C Delta

Ensembl ID : ENSUPAG00010012847
Gene Symbol: PRKCD
3 Cross references
280 Possible Orthologues:

Protein Kinase C Epsilon

Ensembl ID : ENSUPAG00010020686
Gene Symbol: PRKCE
1 Cross references
315 Possible Orthologues:

Protein Kinase C Eta

Ensembl ID : ENSUPAG00010009074
Gene Symbol: PRKCH
1 Cross references
237 Possible Orthologues:

Protein Kinase C Gamma

Ensembl ID : ENSUPAG00010001264
Gene Symbol: PRKCG
3 Cross references
198 Possible Orthologues:

Protein Kinase C Iota

Ensembl ID : ENSUPAG00010020789
Gene Symbol: PRKCI
3 Cross references
150 Possible Orthologues:

Protein Kinase C Theta

Ensembl ID : ENSUPAG00010001641
Gene Symbol: PRKCQ
1 Cross references
203 Possible Orthologues:

Protein Kinase C Zeta

Ensembl ID : ENSUPAG00010004383
Gene Symbol: PRKCZ
1 Cross references
201 Possible Orthologues:

Protein Kinase D1

Ensembl ID : ENSUPAG00010012522
Gene Symbol: PRKD1
3 Cross references
204 Possible Orthologues:

Protein Kinase D3

Ensembl ID : ENSUPAG00010004617
Gene Symbol: PRKD3
1 Cross references
270 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).