EcoDrugPlus

Protein Arginine Methyltransferase 5

Ensembl ID : ENSUAMG00000008536
Gene Symbol: PRMT5
2 Cross references
198 Possible Orthologues:

Protein Kinase C Alpha

Ensembl ID : ENSUAMG00000008454
Gene Symbol: PRKCA
2 Cross references
271 Possible Orthologues:

Protein Kinase C Beta

Ensembl ID : ENSUAMG00000006518
Gene Symbol: PRKCB
2 Cross references
284 Possible Orthologues:

Protein Kinase C Delta

Ensembl ID : ENSUAMG00000007384
Gene Symbol: PRKCD
2 Cross references
280 Possible Orthologues:

Protein Kinase C Gamma

Ensembl ID : ENSUAMG00000012828
Gene Symbol: PRKCG
2 Cross references
198 Possible Orthologues:

Protein Kinase C Iota

Ensembl ID : ENSUAMG00000012707
Gene Symbol: PRKCI
2 Cross references
195 Possible Orthologues:

Protein Kinase C Theta

Ensembl ID : ENSUAMG00000003888
Gene Symbol: PRKCQ
2 Cross references
202 Possible Orthologues:

Protein Kinase D1

Ensembl ID : ENSUAMG00000008055
Gene Symbol: PRKD1
2 Cross references
204 Possible Orthologues:

Protein Kinase D3

Ensembl ID : ENSUAMG00000014976
Gene Symbol: PRKD3
2 Cross references
270 Possible Orthologues:

Protein Kinase Camp-Activated Catalytic Subunit Beta

Ensembl ID : ENSUAMG00000025378
Gene Symbol: PRKACB
2 Cross references
297 Possible Orthologues:

Protein Kinase, Dna-Activated, Catalytic Subunit

Ensembl ID : ENSUAMG00000008703
Gene Symbol: PRKDC
2 Cross references
184 Possible Orthologues:

Protein Tyrosine Kinase 2

Ensembl ID : ENSUAMG00000022672
Gene Symbol: PTK2
1 Cross references
320 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).