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What is MEROPS ?. Database of Peptidases and their Inhibitors More Specific than Pfam, containing in depth, expert details about each entry Hierarchical classification Accessed at http://merops.sanger.ac.uk/. “SLEDGEHAMMER” PEPTIDASES.
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What is MEROPS ? • Database of Peptidases and their Inhibitors • More Specific than Pfam, containing in depth, expert details about each entry • Hierarchical classification • Accessed at http://merops.sanger.ac.uk/
“SLEDGEHAMMER” PEPTIDASES Peptidases that cleave many bonds in a protein, reducing it to peptides • Physiological food digestion (pepsin) intracellular protein turnover (proteasome, cathepsin D) tissue remodelling (collagenase 1, gelatinases A and B) • Pathological parasite invasion (cruzipain) arthritis, emphysema, tumour invasion • Biotechnological cheese making (chymosin) biological washing powders (subtilisin) meat tenderizer (papain) protein sequencing (trypsin, chymotrypsin, pepsin)
“CHISEL” PEPTIDASES Peptidases that cleave just one or two bonds in a protein • Physiological protein biosynthesis (methionyl aminopeptidase, signal peptidase) apoptosis (caspases, granzyme B) blood coagulation (factor Xa) complement assembly (C1r, C1s) activation of bioactive peptides and hormones (furin, kexin, renin) destruction of bioactive peptides (neprilysin) • Pathological RNA viral polyprotein processing (retropepsin) DNA virus protein processing (adenain, assemblin) bacterial lethal factors (tetanus, anthrax) Alzheimer’s disease • Biotechnological Purification of expressed proteins (enteropeptidase, TEV proteinase)
CD Family C11 C13 C14 C25 C50 Peptidase Species C14.001 human (MER00850) mouse (MER00851) rat (MER00852) pig (MER12113) horse (MER06237) gerbil (MER20111) The MEROPS hierarchy 37 Clan 180 1942 24896
Calpain I C H Calpain 7 C H Calpain 10 C H SOL C H THE PEPTIDASE UNIT I II III IV Peptidase unit (domain II) zinc finger domain III PBH domain calcium-binding (domain IV) MIT domain
caspase 1 (rat) TYPE PEPTIDASES DIRECT E < 0.001 caspase 1 (human) caspase 2 (human) caspase 9 (human) caspase 3 (dog) E > 0.001 TRANSITIVE E < 0.001 DIRECT caspase 3 (human)
DATA SOURCES • FastA searches of UniProt • FastA searches of proteomes from completely sequenced genomes • TBlastN searches of EMBL • FastPan searches of human and mouse ESTs • Sequences in papers
CD Family C11 C13 C14 C25 C50 Peptidase Species C14.001 human (MER00850) mouse (MER00851) rat (MER00852) pig (MER12113) horse (MER06237) gerbil (MER20111) The MEROPS hierarchy 37 Clan 180 1942 24896
ADDING FAMILIES TO CLANS • Every clan has a type peptidase • A peptidase family is added to a clan if • a peptidase has a similar tertiary structure to the clan type example, as defined by • the crystallographers • DALI (z score > 5.99) • SCOP • the active site residues are in the same order in the sequence as that of the clan type example
CD Family C11 C13 C14 C25 C50 Peptidase Species C14.001 human (MER00850) mouse (MER00851) rat (MER00852) pig (MER12113) horse (MER06237) gerbil (MER20111) The MEROPS hierarchy 37 Clan 180 1942 24896
WHAT IS A PEPTIDASE? • Similar substrate specificity (known or predicted) • Sequence homology from amino to carboxy terminus • Derived from the same node on a cladogram
Inhibitors • MEROPS also contains information about peptidase inhibitors • There is a hierarchical classification of inhibitors. • The design and look of the inhibitor pages is very similar to the peptidase.
SUMMARY • Peptidases are enzymes that are difficult to classify by substrate specificity. The MEROPS database provides an alternative, hierarchical classification by domain structure (CLAN), sequence (FAMILY) and specificity (PEPTIDASE). • There are no families of hypothetical proteins in MEROPS. • A family contains peptidases of only one catalytic type. • A clan, however, can consist of families of peptidases of different catalytic types. • Homologues can be predicted to be peptidases
Further Reading Rawlings ND, Tolle DP, Barrett AJ. MEROPS: the peptidase database. Nucleic Acids Res. 2004 Jan 1;32 Database issue:D160-4. PMID: 14681384 Rawlings ND, Tolle DP, Barrett AJ. Evolutionary families of peptidase inhibitors. Biochem J. 2004 Mar 15; (Pt 3):705-16. Review. PMID: 14705960 Handbook of Proteolyic Enzymes. Neil D. Rawlings et al. Academic Press Or mail: merops@sanger.ac.uk
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