S100 Family: 2.60.40.10.16.1.1.1

Representative domain: 1my7A00

Classification Lineage (2.60.40.10.16.1.1.1)

CATH Code	Level Description	Links
2	Mainly Beta
2.60	Sandwich
2.60.40	Immunoglobulin-like
2.60.40.10	Immunoglobulins	Gene3D
2.60.40.10.16
2.60.40.10.16.1
2.60.40.10.16.1.1
2.60.40.10.16.1.1.1

Summary of Non-Redundant Representatives


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Non-Redundant Representatives (2)
Functional Families
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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 2.60.40.10.16.1.1.1 (2)

CATH Level	CATH code	Domain ID	Keywords	Thumbnail
	2.60.40.10.16.1.1.1.1	1my7A00	Adipocytokine signaling pathway, sequence-specific enhancer binding RNA polymerase II transcription factor activity, RIG-I-like receptor signaling pathway, Apoptosis, Toll-like receptor signaling pathway, liver development, Chronic myeloid leukemia, Leishmaniasis, NOD-like receptor signaling pathway, positive regulation of interleukin-12 biosynthetic process, Transcription factor p65, hair follicle development, B cell receptor signaling pathway, Chagas disease, response to muramyl dipeptide, Neurotrophin signaling pathway, Mus musculus, transcription factor p65, transcription activator activity, Pancreatic cancer, Chemokine signaling pathway, Cytosolic DNA-sensing pathway, T cell receptor signaling pathway, Pathways in cancer, organ morphogenesis, Acute myeloid leukemia, Prostate cancer, Small cell lung cancer, MAPK signaling pathway, negative regulation of protein catabolic process
	2.60.40.10.16.1.1.1.2	1my7B00	negative regulation of protein catabolic process, MAPK signaling pathway, Small cell lung cancer, Prostate cancer, Acute myeloid leukemia, organ morphogenesis, Pathways in cancer, T cell receptor signaling pathway, Cytosolic DNA-sensing pathway, Chemokine signaling pathway, Pancreatic cancer, transcription activator activity, transcription factor p65, Mus musculus, Neurotrophin signaling pathway, B cell receptor signaling pathway, Chagas disease, response to muramyl dipeptide, hair follicle development, Transcription factor p65, positive regulation of interleukin-12 biosynthetic process, NOD-like receptor signaling pathway, Leishmaniasis, Chronic myeloid leukemia, liver development, Apoptosis, Toll-like receptor signaling pathway, RIG-I-like receptor signaling pathway, sequence-specific enhancer binding RNA polymerase II transcription factor activity, Adipocytokine signaling pathway

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=2.60.40.10.16.1.1.1

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: 2.60.40.10.16.1.1.1

Classification Lineage (2.60.40.10.16.1.1.1)

Summary of Non-Redundant Representatives

What is a Non-Redundant Representative?

S100 Count Entries in S100 Family 2.60.40.10.16.1.1.1 (2)

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?

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