Summary
ATP synthase F0 subunit
This clan contains subunits of the F0 complex of ATP-synthase. The F0 complex is the non-catalytic unit of ATPase and is involved in proton translocation across membranes.
This clan contains 13 families and the total number of domains in the clan is 35379. The clan was built by J Mistry.
Literature references
- Cross RL, Muller V; , FEBS Lett. 2004;576:1-4.: The evolution of A-, F-, and V-type ATP synthases and ATPases: reversals in function and changes in the H+/ATP coupling ratio. PUBMED:15473999 EPMC:15473999
- Rappas M, Niwa H, Zhang X; , Curr Protein Pept Sci. 2004;5:89-105.: Mechanisms of ATPases--a multi-disciplinary approach. PUBMED:15078220 EPMC:15078220
Members
This clan contains the following 13 member families:
ATP-synt_8 ATP-synt_B FliH Fun_ATP-synt_8 HrpE Mt_ATP-synt_B OSCP T3SS_SCTL V-ATPase_G V-ATPase_G_2 vATP-synt_E Yae1_N YMF19Domain 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 |
---|---|---|
ATP-synt_B (PF00430) | 10521 (29.7%) | View |
OSCP (PF00213) | 10264 (29.0%) | View |
vATP-synt_E (PF01991) | 3593 (10.2%) | View |
FliH (PF02108) | 3488 (9.9%) | View |
Yae1_N (PF09811) | 2674 (7.6%) | View |
V-ATPase_G (PF03179) | 2434 (6.9%) | View |
Mt_ATP-synt_B (PF05405) | 1694 (4.8%) | View |
YMF19 (PF02326) | 168 (0.5%) | View |
Fun_ATP-synt_8 (PF05933) | 143 (0.4%) | View |
ATP-synt_8 (PF00895) | 124 (0.4%) | View |
V-ATPase_G_2 (PF16999) | 100 (0.3%) | View |
HrpE (PF06188) | 97 (0.3%) | View |
T3SS_SCTL (PF06635) | 79 (0.2%) | View |
Total: 13 | Total: 35379 | 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
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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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