Bleomycin hydrolase

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Bleomycin hydrolase is an enzyme that in humans is encoded by the BLMH gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesBLMH, BH, BMH, bleomycin hydrolase
Quick facts BLMH, Available structures ...
BLMH
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesBLMH, BH, BMH, bleomycin hydrolase
External IDsOMIM: 602403; MGI: 1345186; HomoloGene: 330; GeneCards: BLMH; OMA:BLMH - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000386

NM_178645

RefSeq (protein)

NP_000377

NP_848760

Location (UCSC)Chr 17: 30.25 – 30.29 MbChr 11: 76.82 – 76.88 Mb
PubMed search[3][4]
Wikidata
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Bleomycin hydrolase (BMH) is a cytoplasmic cysteine peptidase that is highly conserved through evolution. Its biological function is hydrolysis of the reactive electrophile homocysteine thiolactone.[8] Another of its activities is metabolic inactivation of the glycopeptide bleomycin (BLM), an essential component of combination chemotherapy regimens for cancer. The protein contains the signature active site residues of the cysteine protease papain superfamily.[7]

Interactions

References

Further reading

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