S100 Family: 1.10.268.10.2.1.1.1

Molscript image for 3l4jA05
Representative domain: 3l4jA05
PDB coordinates for domain 3l4jA05

Classification Lineage (1.10.268.10.2.1.1.1)

CATH CodeLevel DescriptionLinks
1 Mainly Alpha
1.10 Orthogonal Bundle
1.10.268 Topoisomerase; domain 3
1.10.268.10 Topoisomerase, domain 3 Gene3D
1.10.268.10.2
1.10.268.10.2.1
1.10.268.10.2.1.1
1.10.268.10.2.1.1.1

Summary of Non-Redundant Representatives

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S100 Count Entries in S100 Family 1.10.268.10.2.1.1.1 (3)

CATH Level CATH code Domain ID Keywords Thumbnail
1.10.268.10.2.1.1.1.1 3l4jA05 chromatin remodeling at centromere, DNA strand elongation involved in DNA replication, reciprocal meiotic recombination, Saccharomyces cerevisiae, DNA topoisomerase (ATP-hydrolyzing)., DNA topoisomerase II [EC:5.99.1.3], protein binding, chromatin assembly or disassembly, regulation of mitotic recombination, synaptonemal complex, DNA topoisomerase (ATP-hydrolyzing) activity, DNA topological change, mitochondrion, DNA topoisomerase 2 Molscript image for 3l4jA05
1.10.268.10.2.1.1.1.2 2rgrA05 mitochondrion, DNA topoisomerase 2, DNA topoisomerase (ATP-hydrolyzing) activity, DNA topological change, regulation of mitotic recombination, synaptonemal complex, chromatin assembly or disassembly, protein binding, Saccharomyces cerevisiae, DNA topoisomerase (ATP-hydrolyzing)., DNA topoisomerase II [EC:5.99.1.3], chromatin remodeling at centromere, DNA strand elongation involved in DNA replication, reciprocal meiotic recombination Molscript image for 2rgrA05
1.10.268.10.2.1.1.1.3 3l4kA05 chromatin assembly or disassembly, protein binding, synaptonemal complex, regulation of mitotic recombination, DNA topological change, DNA topoisomerase (ATP-hydrolyzing) activity, DNA topoisomerase 2, mitochondrion, reciprocal meiotic recombination, chromatin remodeling at centromere, DNA strand elongation involved in DNA replication, DNA topoisomerase II [EC:5.99.1.3], Saccharomyces cerevisiae, DNA topoisomerase (ATP-hydrolyzing). Molscript image for 3l4kA05

The information on Functional Families (FunFams) is currently being updated and will be released by the end of March 2012. The pages will include the following features:
  • Multiple alignments for each functional family
  • Representative structure for each functional with known catalytic and interface residues highlighted, along with conserved residues predicted by scorecons
  • Detailed functional information on diversity and conservation within Functional families
  • Multi-domain architectures
In the meantime, please find a summary of information on the FunFams and protein networks within this superfamily on the Gene3D pages: