EcoDrugPlus

Protein Kinase C Delta

Ensembl ID : ENSMPUG00000016815
Gene Symbol: PRKCD
3 Cross references
280 Possible Orthologues:

Protein Kinase C Epsilon

Ensembl ID : ENSMPUG00000012014
Gene Symbol: PRKCE
4 Cross references
316 Possible Orthologues:

Protein Kinase C Eta

Ensembl ID : ENSMPUG00000006500
Gene Symbol: PRKCH
1 Cross references
237 Possible Orthologues:

Protein Kinase C Gamma

Ensembl ID : ENSMPUG00000010153
Gene Symbol: PRKCG
2 Cross references
198 Possible Orthologues:

Protein Kinase C Iota

Ensembl ID : ENSMPUG00000017108
Gene Symbol: PRKCI
2 Cross references
195 Possible Orthologues:

Protein Kinase C Theta

Ensembl ID : ENSMPUG00000016362
Gene Symbol: PRKCQ
2 Cross references
203 Possible Orthologues:

Protein Kinase C Zeta

Ensembl ID : ENSMPUG00000007773
Gene Symbol: PRKCZ
2 Cross references
198 Possible Orthologues:

Protein Kinase D1

Ensembl ID : ENSMPUG00000005409
Gene Symbol: PRKD1
2 Cross references
204 Possible Orthologues:

Protein Kinase D3

Ensembl ID : ENSMPUG00000010243
Gene Symbol: PRKD3
2 Cross references
270 Possible Orthologues:

Protein Kinase Camp-Activated Catalytic Subunit Alpha

Ensembl ID : ENSMPUG00000003076
Gene Symbol: PRKACA
2 Cross references
283 Possible Orthologues:

Protein Kinase Camp-Activated Catalytic Subunit Beta

Ensembl ID : ENSMPUG00000005765
Gene Symbol: PRKACB
4 Cross references
297 Possible Orthologues:

Protein Kinase, Dna-Activated, Catalytic Subunit

Ensembl ID : ENSMPUG00000001020
Gene Symbol: PRKDC
2 Cross references
184 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 from 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 from 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).