Corrigendum to: Sulphatase activities are regulated by the interaction of sulphatase-modifying factor 1 with SUMF2 (EMBO reports, (2005), 6, 7, (655-660), 10.1038/sj.embor.7400454);Sulphatase activities are regulated by the interaction of sulphatase-modifying factor 1 with SUMF2

EMBO Reports

Volumn 6, Issue 7, 2005, Pages 655-660

  Zito, Ester ^a   Fraldi, Alessandro ^a   Pepe, Stefano ^a   Annunziata, Ida ^a   Kobinger, Gary ^b   Di Natale, Paola ^c   Ballabio, Andrea ^a,d   Cosma, Maria Pia ^a  

^a TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^d UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

Enzymatic activity; Inborn errors of metabolism; Protein protein interactions

Indexed keywords

CELL PROTEIN; COMPLEMENTARY DNA; CYSTEINE; GLYCINE; SULFATASE; SULFATASE MODIFYING FACTOR 1; SULFATASE MODIFYING FACTOR 2; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CATALYSIS; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; ENZYME ACTIVITY; ENZYME DEFICIENCY; GENE MUTATION; GENE OVEREXPRESSION; GENE SEQUENCE; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; NONHUMAN; PARALOGY; PRIORITY JOURNAL; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN PROCESSING; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM; SEQUENCE HOMOLOGY;

EID: 23744477714     PISSN: 1469221X     EISSN: 14693178     Source Type: Journal    
DOI: 10.15252/embr.201570010     Document Type: Erratum

References (10)

1. Ballabio A, Shapiro LJ (2001) Steroid sulfatase deficiency and X-linked ichthyosis. In The Metabolic and Molecular Basis of Inherited Disease, Scriver CR, Beaudet AL, Sly WS, Valle D (eds) pp 4241-4262. New York, USA: McGraw-Hill
2. Cosma MP, Pepe S, Annunziata I, Newbold RF, Grompe M, Parenti G, Ballabio A (2003) The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases. Cell 113: 445-456
3. Cosma MP et al (2004) Molecular and functional analysis of SUMF1 mutations in multiple sulfatase deficiency. Hum Mutat 23: 576-581
4. Dierks T, Schmidt B, Borissenko LV, Peng J, Preusser A, Mariappan M, von Figura K (2003) Multiple sulfatase deficiency is caused by mutations in the gene encoding the human c(α)-formylglycine generating enzyme. Cell 113: 435-444
5. Franco B et al (1995) A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy. Cell 81: 15-25
6. Hopwood JJ, Ballabio A (2001) Multiple sulfatase deficiency and the nature of the sulfatase family. In The Metabolic and Molecular Basis of Inherited Disease, Scriver CR, Beaudet AL, Valle D, Sly WS (eds) Vol 3, pp 3725-3732. New York, USA: McGraw-Hill
7. Neufeld EF, Muenzer J (2001) The mucopolysaccharidoses. In The Metabolic and Molecular Basis of Inherited Disease, Scriver CR, Beaudet AL, Sly WS, Valle D (eds) pp 3421-3452. New York, USA: McGraw-Hill
8. Schirmer A, Kolter R (1998) Computational analysis of bacterial sulfatases and their modifying enzymes. Chem Biol 5: R181-R186
9. Schmidt B, Selmer T, Ingendoh A, von Figura K (1995) A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency. Cell 82: 271-278
10. Von Figura K, Gieselmann V, Jaeken J (2001) Metachromatic leukodystrophy. In The Metabolic and Molecular Basis of Inherited Disease, Scriver CR, Beaudet AL, Sly WS, Valle D (eds) pp 3695-3724. New York, USA: McGraw-Hill