EcoDrugPlus

Proteasome Subunit Beta Type-9

Ensembl ID : ENSXMAG00000014611
Gene Symbol: LOC102218720
3 Cross references
201 Possible Orthologues:

Protein Arginine Methyltransferase 5

Ensembl ID : ENSXMAG00000000469
Gene Symbol: PRMT5
3 Cross references
198 Possible Orthologues:

Protein Farnesyltransferase Subunit Beta-Like

Ensembl ID : ENSXMAG00000007833
Gene Symbol: LOC102235994
3 Cross references
209 Possible Orthologues:

Protein Kinase C Alpha

Ensembl ID : ENSXMAG00000006578
Gene Symbol: PRKCA
3 Cross references
213 Possible Orthologues:

Protein Kinase C Beta

Ensembl ID : ENSXMAG00000000201
Gene Symbol: PRKCB
4 Cross references
207 Possible Orthologues:

Protein Kinase C Beta Type-Like

Ensembl ID : ENSXMAG00000005339
Gene Symbol: LOC102228928
3 Cross references
223 Possible Orthologues:

Protein Kinase C Delta

Ensembl ID : ENSXMAG00000001861
Gene Symbol: PRKCD
3 Cross references
204 Possible Orthologues:

Protein Kinase C Delta

Ensembl ID : ENSXMAG00000010429
Gene Symbol: PRKCD
3 Cross references
203 Possible Orthologues:

Protein Kinase C Epsilon

Ensembl ID : ENSXMAG00000001760
Gene Symbol: PRKCE
3 Cross references
246 Possible Orthologues:

Protein Kinase C Epsilon

Ensembl ID : ENSXMAG00000015967
Gene Symbol: PRKCE
2 Cross references
249 Possible Orthologues:

Protein Kinase C Eta

Ensembl ID : ENSXMAG00000025270
Gene Symbol: PRKCH
3 Cross references
224 Possible Orthologues:

Protein Kinase C Iota

Ensembl ID : ENSXMAG00000000481
Gene Symbol: PRKCI
3 Cross references
87 Possible Orthologues:


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).