Summary
LEM/SAP HeH motif
This superfamily includes protein domains with the helix-extended loop-helix (HeH) structure.
This clan contains 14 families and the total number of domains in the clan is 41265. The clan was built by A Bateman.
Literature references
- Okubo S, Hara F, Tsuchida Y, Shimotakahara S, Suzuki S, Hatanaka H, Yokoyama S, Tanaka H, Yasuda H, Shindo H; , J Biol Chem. 2004;279:31455-31461.: NMR structure of the N-terminal domain of SUMO ligase PIAS1 and its interaction with tumor suppressor p53 and A/T-rich DNA oligomers. PUBMED:15133049 EPMC:15133049
Members
This clan contains the following 14 member families:
ARMET_C BTHB Endonuc-dimeris FANC_SAP HeH LEM LETM1_RBD Lsr2 PADR1 PRP4 Rho_N SAP SAP_new25 ThymopoietinExternal database links
SCOP: | 63450 |
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 |
---|---|---|
SAP (PF02037) | 13967 (33.8%) | View |
Rho_N (PF07498) | 8859 (21.5%) | View |
LETM1_RBD (PF07766) | 4417 (10.7%) | View |
PRP4 (PF08799) | 3296 (8.0%) | View |
Lsr2 (PF11774) | 2890 (7.0%) | View |
LEM (PF03020) | 2800 (6.8%) | View |
PADR1 (PF08063) | 1191 (2.9%) | View |
HeH (PF12949) | 865 (2.1%) | View |
Thymopoietin (PF08198) | 794 (1.9%) | View |
ARMET_C (PF10208) | 770 (1.9%) | View |
BTHB (PF18410) | 713 (1.7%) | View |
SAP_new25 (PF18953) | 366 (0.9%) | View |
FANC_SAP (PF18081) | 238 (0.6%) | View |
Endonuc-dimeris (PF09124) | 99 (0.2%) | View |
Total: 14 | Total: 41265 | 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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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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