S100 Family: 3.40.1190.20.13.1.1.1

Representative domain: 2yxtA00

Classification Lineage (3.40.1190.20.13.1.1.1)

CATH Code	Level Description	Links
3	Alpha Beta
3.40	3-Layer(aba) Sandwich
3.40.1190	UDP-N-acetylmuramoyl-L-alanine:D-glutamate ligase
3.40.1190.20		Gene3D
3.40.1190.20.13
3.40.1190.20.13.1
3.40.1190.20.13.1.1
3.40.1190.20.13.1.1.1

Summary of Non-Redundant Representatives


-	-	-	-	-	-	-	-	8

Non-Redundant Representatives (8)
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 3.40.1190.20.13.1.1.1 (8)

CATH code	Domain ID	Keywords
3.40.1190.20.13.1.1.1.1	2yxtA00	Homo sapiens, sodium ion binding, lithium ion binding, Metabolic pathways, magnesium ion binding, protein homodimerization activity, Pyridoxal kinase, pyridoxal phosphate biosynthetic process, pyridoxal phosphate binding, cytosol, pyridoxal kinase activity, ATP binding, Pyridoxal kinase., cell proliferation, zinc ion binding, pyridoxine kinase [EC:2.7.1.35], potassium ion binding, Vitamin B6 metabolism
3.40.1190.20.13.1.1.1.2	2yxtB00	cytosol, pyridoxal phosphate binding, pyridoxal kinase activity, ATP binding, Pyridoxal kinase., cell proliferation, zinc ion binding, Vitamin B6 metabolism, pyridoxine kinase [EC:2.7.1.35], potassium ion binding, Homo sapiens, sodium ion binding, lithium ion binding, protein homodimerization activity, Metabolic pathways, magnesium ion binding, Pyridoxal kinase, pyridoxal phosphate biosynthetic process
3.40.1190.20.13.1.1.1.3	3keuA00	Homo sapiens, lithium ion binding, sodium ion binding, protein homodimerization activity, Metabolic pathways, magnesium ion binding, pyridoxal phosphate biosynthetic process, Pyridoxal kinase, pyridoxal kinase activity, ATP binding, cytosol, pyridoxal phosphate binding, Pyridoxal kinase., cell proliferation, Vitamin B6 metabolism, pyridoxine kinase [EC:2.7.1.35], potassium ion binding, zinc ion binding
3.40.1190.20.13.1.1.1.4	3keuB00	Pyridoxal kinase., cell proliferation, pyridoxal kinase activity, ATP binding, cytosol, pyridoxal phosphate binding, Vitamin B6 metabolism, pyridoxine kinase [EC:2.7.1.35], potassium ion binding, zinc ion binding, lithium ion binding, sodium ion binding, Homo sapiens, pyridoxal phosphate biosynthetic process, Pyridoxal kinase, protein homodimerization activity, Metabolic pathways, magnesium ion binding
3.40.1190.20.13.1.1.1.5	2yxuA00	Pyridoxal kinase., cell proliferation, cytosol, pyridoxal phosphate binding, pyridoxal kinase activity, ATP binding, zinc ion binding, Vitamin B6 metabolism, pyridoxine kinase [EC:2.7.1.35], potassium ion binding, sodium ion binding, lithium ion binding, Homo sapiens, Pyridoxal kinase, pyridoxal phosphate biosynthetic process, protein homodimerization activity, Metabolic pathways, magnesium ion binding
3.40.1190.20.13.1.1.1.6	2yxuB00	cell proliferation, Pyridoxal kinase., pyridoxal phosphate binding, cytosol, ATP binding, pyridoxal kinase activity, zinc ion binding, pyridoxine kinase [EC:2.7.1.35], potassium ion binding, Vitamin B6 metabolism, sodium ion binding, lithium ion binding, Homo sapiens, Pyridoxal kinase, pyridoxal phosphate biosynthetic process, Metabolic pathways, magnesium ion binding, protein homodimerization activity
3.40.1190.20.13.1.1.1.7	2f7kA00	cytosol, pyridoxal phosphate binding, ATP binding, pyridoxal kinase activity, cell proliferation, Pyridoxal kinase., zinc ion binding, Vitamin B6 metabolism, pyridoxine kinase [EC:2.7.1.35], potassium ion binding, Homo sapiens, sodium ion binding, lithium ion binding, protein homodimerization activity, Metabolic pathways, magnesium ion binding, Pyridoxal kinase, pyridoxal phosphate biosynthetic process
3.40.1190.20.13.1.1.1.8	2f7kB00	Pyridoxal kinase., cell proliferation, pyridoxal kinase activity, ATP binding, pyridoxal phosphate binding, cytosol, pyridoxine kinase [EC:2.7.1.35], potassium ion binding, Vitamin B6 metabolism, zinc ion binding, lithium ion binding, sodium ion binding, Homo sapiens, pyridoxal phosphate biosynthetic process, Pyridoxal kinase, Metabolic pathways, magnesium ion binding, protein homodimerization activity

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=3.40.1190.20.13.1.1.1

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: 3.40.1190.20.13.1.1.1

Classification Lineage (3.40.1190.20.13.1.1.1)

Summary of Non-Redundant Representatives

What is a Non-Redundant Representative?

S100 Count Entries in S100 Family 3.40.1190.20.13.1.1.1 (8)

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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