S100 Family: 1.10.10.10.10.1.1.1

Representative domain: 2vooB01

Classification Lineage (1.10.10.10.10.1.1.1)

CATH Code	Level Description	Links
1	Mainly Alpha
1.10	Orthogonal Bundle
1.10.10	Arc Repressor Mutant, subunit A
1.10.10.10	"winged helix" repressor DNA binding domain	Gene3D
1.10.10.10.10
1.10.10.10.10.1
1.10.10.10.10.1.1
1.10.10.10.10.1.1.1

Summary of Non-Redundant Representatives


-	-	-	-	-	-	-	-	7

Non-Redundant Representatives (7)
Functional Families
Help

What is a Non-Redundant Representative?

CATH is a tree-like organisation of nodes that begins with the class node (i.e. the first branch-point of the tree) and ends with the domain nodes (i.e. the leaves of the tree). Each node below the class have a parent that they belong to, e.g. the parent of the H level (Homologous superfamily) is the T (Topology). Additionally, each node above the domains have child nodes that belong to them, e.g. the child nodes of a given H (Homologous superfamily) level are the S35 families (domains clustered at > 35% sequence identity).

S100 Count Entries in S100 Family 1.10.10.10.10.1.1.1 (7)

CATH code	Domain ID	Keywords
1.10.10.10.10.1.1.1.1	2vooB01	Homo sapiens, Systemic lupus erythematosus, lupus La protein, nucleolus, ribonucleoprotein complex, histone mRNA metabolic process, protein binding, tRNA binding, tRNA modification, Lupus La protein, cytoplasm, mRNA binding
1.10.10.10.10.1.1.1.2	2vooA01	nucleolus, lupus La protein, Systemic lupus erythematosus, Homo sapiens, protein binding, histone mRNA metabolic process, ribonucleoprotein complex, Lupus La protein, tRNA modification, tRNA binding, mRNA binding, cytoplasm
1.10.10.10.10.1.1.1.3	2vonB01	mRNA binding, cytoplasm, tRNA modification, Lupus La protein, tRNA binding, protein binding, ribonucleoprotein complex, histone mRNA metabolic process, lupus La protein, nucleolus, Homo sapiens, Systemic lupus erythematosus
1.10.10.10.10.1.1.1.4	2vodA01	Lupus La protein, tRNA modification, tRNA binding, mRNA binding, cytoplasm, nucleolus, lupus La protein, Systemic lupus erythematosus, Homo sapiens, protein binding, histone mRNA metabolic process, ribonucleoprotein complex
1.10.10.10.10.1.1.1.5	2vonA01	mRNA binding, cytoplasm, Lupus La protein, tRNA modification, tRNA binding, protein binding, histone mRNA metabolic process, ribonucleoprotein complex, lupus La protein, nucleolus, Systemic lupus erythematosus, Homo sapiens
1.10.10.10.10.1.1.1.6	2vodB01	cytoplasm, mRNA binding, tRNA binding, tRNA modification, Lupus La protein, ribonucleoprotein complex, histone mRNA metabolic process, protein binding, Homo sapiens, Systemic lupus erythematosus, nucleolus, lupus La protein
1.10.10.10.10.1.1.1.7	2vopA01	cytoplasm, mRNA binding, tRNA binding, tRNA modification, Lupus La protein, ribonucleoprotein complex, histone mRNA metabolic process, protein binding, Homo sapiens, Systemic lupus erythematosus, nucleolus, lupus La protein

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:

http://gene3d.biochem.ucl.ac.uk/superfamily/?accession=1.10.10.10.10.1.1.1

What is a Non-Redundant Representative?

Why can't I have a multiple structural alignment of the whole superfamily?

The simple answer is that some of the larger superfamilies in CATH comprise relatives which are very structurally diverse, having different secondary structure embellishments. Attempting to provide a global alignment of all domains in the superfamily would result in poor quality alignments. As a result, structural alignments in CATH are generated by first clustering together the structures that have at least some recognisable structural similarity using a normalised RMSD score (SIMAX = RMSDxNumber of residues in the largest domain/number of aligned residues) less than a given cutoff.

What is an Close Structural Cluster?

A Close Structural Cluster describes a cluster of two or more CATH domains that have been grouped together due to their close structural similarity (SIMAX score < 5Å where SIMAX = RMSD x Number of residues in the larger domain/number of aligned residues).

What is a Distant Structural Cluster?

A Distant Structural Cluster describes a cluster of two or CATH domains that have been grouped together with a more relaxed structural similarity threshold to investigate more distant evolutionary similarities (SIMAX score < 5Å where SIMAX = RMSD x Number of residues in the larger domain/number of aligned residues).

What is a Structural Neighbour?

The term "structural neighbour" is used here to describe two CATH domains that share a degree of structural similarity. The SSAP algorithm is used to calculate this similarity and works by generating a structure-based pairwise alignment of the two domains then scoring this alignment using a RMSD score which has been normalised by the length of the larger domain divided by the number of aligned residues (SIMAX).

S100 Family: 1.10.10.10.10.1.1.1

Classification Lineage (1.10.10.10.10.1.1.1)

Summary of Non-Redundant Representatives

What is a Non-Redundant Representative?

S100 Count Entries in S100 Family 1.10.10.10.10.1.1.1 (7)

What is a Non-Redundant Representative?

Why can't I have a multiple structural alignment of the whole superfamily?

What is an Close Structural Cluster?

What is a Distant Structural Cluster?

What is a Structural Neighbour?

CATH Shortcuts