General Information of Drug Therapeutic Target (DTT) (ID: TTAS2UO)

DTT Name Bacterial Urease (Bact ureC)
Synonyms Urease subunit alpha; Urea amidohydrolase subunit alpha
Gene Name Bact ureC
DTT Type
Successful target
[1]
BioChemical Class
Carbon-nitrogen hydrolase
UniProt ID
URE1_KLEAE
TTD ID
T28869
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Sequence
MSNISRQAYADMFGPTVGDKVRLADTELWIEVEDDLTTYGEEVKFGGGKVIRDGMGQGQM
LAADCVDLVLTNALIVDHWGIVKADIGVKDGRIFAIGKAGNPDIQPNVTIPIGAATEVIA
AEGKIVTAGGIDTHIHWICPQQAEEALVSGVTTMVGGGTGPAAGTHATTCTPGPWYISRM
LQAADSLPVNIGLLGKGNVSQPDALREQVAAGVIGLKIHEDWGATPAAIDCALTVADEMD
IQVALHSDTLNESGFVEDTLAAIGGRTIHTFHTEGAGGGHAPDIITACAHPNILPSSTNP
TLPYTLNTIDEHLDMLMVCHHLDPDIAEDVAFAESRIRRETIAAEDVLHDLGAFSLTSSD
SQAMGRVGEVILRTWQVAHRMKVQRGALAEETGDNDNFRVKRYIAKYTINPALTHGIAHE
VGSIEVGKLADLVVWSPAFFGVKPATVIKGGMIAIAPMGDINASIPTPQPVHYRPMFGAL
GSARHHCRLTFLSQAAAANGVAERLNLRSAIAVVKGCRTVQKADMVHNSLQPNITVDAQT
YEVRVDGELITSEPADVLPMAQRYFLF
Function
Catalyzes the hydrolysis of urea, leading to the production of carbon dioxide and ammonia. Allows many soil bacteria to use urea as a nitrogen source. An important virulence factor that improves survival of pathogenic bacteria under acidic conditions within the host and can also cause direct damage to the host tissue due to ammonia, CO2 or alkali production.

Molecular Interaction Atlas (MIA) of This DTT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DTT
1 Approved Drug(s) Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
Acetohydroxamic Acid DMYX7NI Urinary tract infection GC08 Approved [1]
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5 Investigative Drug(s) Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
1-cyclohexyl-1-isopropyl-3,3-dimethylselenourea DMS10LE Discovery agent N.A. Investigative [2]
3-(4-bromobenzyl)-1,1-dimethylselenourea DMAKMIJ Discovery agent N.A. Investigative [2]
3-(4-bromophenyl)-1,1-dimethylthiourea DMXMZRE Discovery agent N.A. Investigative [2]
3-dodecyl-1,1-dimethylthiourea DMO5EBI Discovery agent N.A. Investigative [2]
N-glycylglycinehydroxamic acid DMPEZHC Discovery agent N.A. Investigative [3]
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References

1 Enzymatic, immunological and phylogenetic characterization of Brucella suis urease. BMC Microbiol. 2008 Jul 19;8:121.
2 Facile one-pot synthesis of thio and selenourea derivatives: a new class of potent urease inhibitors. Bioorg Med Chem Lett. 2007 Nov 15;17(22):6387-91.
3 Design, synthesis, and evaluation of novel organophosphorus inhibitors of bacterial ureases. J Med Chem. 2008 Sep 25;51(18):5736-44.