EcoDrugPlus

Proteasome Subunit Beta Type-7

Ensembl ID : ENSELUG00000028849
Gene Symbol: PSB7
2 Cross references
172 Possible Orthologues:

Proteasome Subunit Beta Type-9

Ensembl ID : ENSELUG00000019630
Gene Symbol: LOC105009101
3 Cross references
211 Possible Orthologues:

Protein Arginine Methyltransferase 5

Ensembl ID : ENSELUG00000004788
Gene Symbol: PRMT5
3 Cross references
199 Possible Orthologues:

Protein Farnesyltransferase Subunit Beta

Ensembl ID : ENSELUG00000019978
Gene Symbol: LOC105024336
3 Cross references
204 Possible Orthologues:

Protein Kinase C Beta

Ensembl ID : ENSELUG00000018024
Gene Symbol: PRKCB
1 Cross references
205 Possible Orthologues:

Protein Kinase C Beta

Ensembl ID : ENSELUG00000013970
Gene Symbol: PRKCB
3 Cross references
203 Possible Orthologues:

Protein Kinase C Delta

Ensembl ID : ENSELUG00000016499
Gene Symbol: PRKCD
1 Cross references
204 Possible Orthologues:

Protein Kinase C Epsilon

Ensembl ID : ENSELUG00000012528
Gene Symbol: PRKCE
3 Cross references
265 Possible Orthologues:

Protein Kinase C Epsilon Type

Ensembl ID : ENSELUG00000002584
Gene Symbol: LOC105006029
2 Cross references
251 Possible Orthologues:

Protein Kinase C Eta

Ensembl ID : ENSELUG00000011477
Gene Symbol: PRKCH
3 Cross references
224 Possible Orthologues:

Protein Kinase C Iota

Ensembl ID : ENSELUG00000013218
Gene Symbol: PRKCI
3 Cross references
270 Possible Orthologues:

Protein Kinase C Zeta

Ensembl ID : ENSELUG00000013042
Gene Symbol: PRKCZ
3 Cross references
205 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).