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Protein Name: Osteopetrosis-associated transmembrane protein 1

UniprotKB/SwissProt ID: OSTM1_HUMAN (Q86WC4)

Gene Name: OSTM1

Synonyms: GL

Organism: Homo sapiens (Human).

Function: Required for osteoclast and melanocyte maturation and function (By similarity).

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Lysosome membrane; Single-pass type I membrane protein. Note=Requires CLCN7 to travel to lysosomes.

Graphical Visualization of Ubiquitination Sites:
Overview of Protein Ubiquitination Sites with Functional and Structural Information


The ubiquitination sites of OSTM1_HUMAN

No. Position Ubiquitinated Peptide Secondary Structure Solvent Accessibility Substrate Motifs PubMed ID
1321ILPKRL K SSTSFA CCHHHH C CCCCHH 46.52%2190698

The interacting network mediated by proteins: OSTM1_HUMAN


Disease:
Disease database Database Entry Disease information
KEGGH00436 Osteopetrosis, including: Osteopetrosis, severe neonatal or infantile forms; Osteopetrosis, intermed
OMIM259720OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5 ;;OSTEOPETROSIS, INFANTILE MALIGNANT 3
OMIM607649OSTEOPETROSIS-ASSOCIATED TRANSMEMBRANE PROTEIN 1; OSTM1 ;;GREY-LETHAL, MOUSE, HOMOLOG OF; GL
HPRD09628Osteopetrosis, autosomal recessive
Metabolic pathway:
Kegg map ID Pathway
map03008Ribosome biogenesis in eukaryotes