Summary
Protein kinase C, C1 domain
The members of this clan are all variations of the protein kinase C1 domain that is characterised by a rich cysteine and histidine content. The C1 domain is the N-terminal region of conservation found in protein kinase C domains. This domain is involved in binding many ligands, which include diacylglycerol, phorbol esters and zinc [1].
This clan contains 5 families and the total number of domains in the clan is 10495. The clan was built by RD Finn.
Literature references
- Azzi A, Boscoboinik D, Hensey C; , Eur J Biochem 1992;208:547-557.: The protein kinase C family. PUBMED:1396661 EPMC:1396661
Members
This clan contains the following 5 member families:
C1_1 C1_2 C1_3 C1_4 ZZExternal database links
| CATH: | 3.30.60.20 |
| SCOP: | 57889 |
Domain organisation
Below is a listing of the unique domain organisations or architectures from this clan. More...
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Alignments
The table below shows the number of occurrences of each domain throughout the sequence database. More...
| Pfam family | Num. domains | Alignment |
|---|---|---|
| C1_1 (PF00130) | 6123 (58.3%) | View |
| ZZ (PF00569) | 2746 (26.2%) | View |
| C1_3 (PF07649) | 800 (7.6%) | View |
| C1_2 (PF03107) | 558 (5.3%) | View |
| C1_4 (PF07975) | 268 (2.6%) | View |
| Total: 5 | Total: 10495 | Clan alignment |
Please note: Clan alignments can be very large and can cause problems for some browsers. Read the note above before viewing.
Family relationships
This diagram shows the relationships between members of this clan. More...
Species distribution
Tree controls
HideThis tree shows the occurrence of the domains in this clan across different species. More...
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Interactions
Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the MSD group, to allow us to map Pfam domains onto UniProt three-dimensional structures. The table below shows the mapping between the Pfam families in this clan, the corresponding UniProt entries, and the region of the three-dimensional structures that are available for that sequence.
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