Sequence of SUMF1_HUMAN

formylglycine-generating enzyme

Q8NBK3

374

40556

1259314

Dierks T.,Schmidt B.,Borissenko L.V.,Peng J.,Preusser A.,Mariappan M.,von Figura K.

Multiple sulfatase deficiency is caused by mutations in the gene encoding the Homo sapiens C-alpha-formyglycine-generating enzyme.

Cell

113

435-444

2003

1259315

Cosma M.P.,Pepe S.,Annunziata I.,Newbold R.F.,Grompe M.,Parenti G.,Ballabio A.

The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases.

Cell

113

445-456

2003

1259316

Oshikawa M.,Usami R.,Kato S.

Characterization of the arylsulfatase I (ARSI) gene preferentially expressed in the human retinal pigment epithelium cell line ARPE-19.

Mol. Vis.

15

482-494

2009

1259317

Clark H.F.,Gurney A.L.,Abaya E.,Baker K.,Baldwin D.T.,Brush J.,Chen J.,Chow B.,Chui C.,Crowley C.,Currell B.,Deuel B.,Dowd P.,Eaton D.,Foster J.S.,Grimaldi C.,Gu Q.,Hass P.E.,Heldens S.,Huang A.,Kim H.S.,Klimowski L.,Jin Y.,Johnson S.,Lee J.,Lewis L.,Liao D.,Mark M.R.,Robbie E.,Sanchez C.,Schoenfeld J.,Seshagiri S.,Simmons L.,Singh J.,Smith V.,Stinson J.,Vagts A.,Vandlen R.L.,Watanabe C.,Wieand D.,Woods K.,Xie M.-H.,Yansura D.G.,Yi S.,Yu G.,Yuan J.,Zhang M.,Zhang Z.,Goddard A.D.,Wood W.I.,Godowski P.J.,Gray A.M.

The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.

Genome Res.

13

2265-2270

2003

1259318

Ota T.,Suzuki Y.,Nishikawa T.,Otsuki T.,Sugiyama T.,Irie R.,Wakamatsu A.,Hayashi K.,Sato H.,Nagai K.,Kimura K.,Makita H.,Sekine M.,Obayashi M.,Nishi T.,Shibahara T.,Tanaka T.,Ishii S.,Yamamoto J.,Saito K.,Kawai Y.,Isono Y.,Nakamura Y.,Nagahari K.,Murakami K.,Yasuda T.,Iwayanagi T.,Wagatsuma M.,Shiratori A.,Sudo H.,Hosoiri T.,Kaku Y.,Kodaira H.,Kondo H.,Sugawara M.,Takahashi M.,Kanda K.,Yokoi T.,Furuya T.,Kikkawa E.,Omura Y.,Abe K.,Kamihara K.,Katsuta N.,Sato K.,Tanikawa M.,Yamazaki M.,Ninomiya K.,Ishibashi T.,Yamashita H.,Murakawa K.,Fujimori K.,Tanai H.,Kimata M.,Watanabe M.,Hiraoka S.,Chiba Y.,Ishida S.,Ono Y.,Takiguchi S.,Watanabe S.,Yosida M.,Hotuta T.,Kusano J.,Kanehori K.,Takahashi-Fujii A.,Hara H.,Tanase T.-O.,Nomura Y.,Togiya S.,Komai F.,Hara R.,Takeuchi K.,Arita M.,Imose N.,Musashino K.,Yuuki H.,Oshima A.,Sasaki N.,Aotsuka S.,Yoshikawa Y.,Matsunawa H.,Ichihara T.,Shiohata N.,Sano S.,Moriya S.,Momiyama H.,Satoh N.,Takami S.,Terashima Y.,Suzuki O.,Nakagawa S.,Senoh A.,Mizoguchi H.,Goto Y.,Shimizu F.,Wakebe H.,Hishigaki H.,Watanabe T.,Sugiyama A.,Takemoto M.,Kawakami B.,Yamazaki M.,Watanabe K.,Kumagai A.,Itakura S.,Fukuzumi Y.,Fujimori Y.,Komiyama M.,Tashiro H.,Tanigami A.,Fujiwara T.,Ono T.,Yamada K.,Fujii Y.,Ozaki K.,Hirao M.,Ohmori Y.,Kawabata A.,Hikiji T.,Kobatake N.,Inagaki H.,Ikema Y.,Okamoto S.,Okitani R.,Kawakami T.,Noguchi S.,Itoh T.,Shigeta K.,Senba T.,Matsumura K.,Nakajima Y.,Mizuno T.,Morinaga M.,Sasaki M.,Togashi T.,Oyama M.,Hata H.,Watanabe M.,Komatsu T.,Mizushima-Sugano J.,Satoh T.,Shirai Y.,Takahashi Y.,Nakagawa K.,Okumura K.,Nagase T.,Nomura N.,Kikuchi H.,Masuho Y.,Yamashita R.,Nakai K.,Yada T.,Nakamura Y.,Ohara O.,Isogai T.,Sugano S.

Complete sequencing and characterization of 21,243 full-length human cDNAs.

Nat. Genet.

36

40-45

2004

1259319

Otsuki T.,Ota T.,Nishikawa T.,Hayashi K.,Suzuki Y.,Yamamoto J.,Wakamatsu A.,Kimura K.,Sakamoto K.,Hatano N.,Kawai Y.,Ishii S.,Saito K.,Kojima S.,Sugiyama T.,Ono T.,Okano K.,Yoshikawa Y.,Aotsuka S.,Sasaki N.,Hattori A.,Okumura K.,Nagai K.,Sugano S.,Isogai T.

Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.

DNA Res.

12

117-126

2005

1259320

Muzny D.M.,Scherer S.E.,Kaul R.,Wang J.,Yu J.,Sudbrak R.,Buhay C.J.,Chen R.,Cree A.,Ding Y.,Dugan-Rocha S.,Gill R.,Gunaratne P.,Harris R.A.,Hawes A.C.,Hernandez J.,Hodgson A.V.,Hume J.,Jackson A.,Khan Z.M.,Kovar-Smith C.,Lewis L.R.,Lozado R.J.,Metzker M.L.,Milosavljevic A.,Miner G.R.,Morgan M.B.,Nazareth L.V.,Scott G.,Sodergren E.,Song X.-Z.,Steffen D.,Wei S.,Wheeler D.A.,Wright M.W.,Worley K.C.,Yuan Y.,Zhang Z.,Adams C.Q.,Ansari-Lari M.A.,Ayele M.,Brown M.J.,Chen G.,Chen Z.,Clendenning J.,Clerc-Blankenburg K.P.,Chen R.,Chen Z.,Davis C.,Delgado O.,Dinh H.H.,Dong W.,Draper H.,Ernst S.,Fu G.,Gonzalez-Garay M.L.,Garcia D.K.,Gillett W.,Gu J.,Hao B.,Haugen E.,Havlak P.,He X.,Hennig S.,Hu S.,Huang W.,Jackson L.R.,Jacob L.S.,Kelly S.H.,Kube M.,Levy R.,Li Z.,Liu B.,Liu J.,Liu W.,Lu J.,Maheshwari M.,Nguyen B.-V.,Okwuonu G.O.,Palmeiri A.,Pasternak S.,Perez L.M.,Phelps K.A.,Plopper F.J.,Qiang B.,Raymond C.,Rodriguez R.,Saenphimmachak C.,Santibanez J.,Shen H.,Shen Y.,Subramanian S.,Tabor P.E.,Verduzco D.,Waldron L.,Wang J.,Wang J.,Wang Q.,Williams G.A.,Wong G.K.-S.,Yao Z.,Zhang J.,Zhang X.,Zhao G.,Zhou J.,Zhou Y.,Nelson D.,Lehrach H.,Reinhardt R.,Naylor S.L.,Yang H.,Olson M.,Weinstock G.,Gibbs R.A.

The DNA sequence, annotation and analysis of human chromosome 3.

Nature

440

1194-1198

2006

1259322

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Genome Res.

14

2121-2127

2004

1259323

Zito E.,Fraldi A.,Pepe S.,Annunziata I.,Kobinger G.,Di Natale P.,Ballabio A.,Cosma M.P.

Sulphatase activities are regulated by the interaction of sulphatase-modifying factor 1 with SUMF2.

EMBO Rep.

6

655-660

2005

1259324

Preusser-Kunze A.,Mariappan M.,Schmidt B.,Gande S.L.,Mutenda K.,Wenzel D.,von Figura K.,Dierks T.

Molecular characterization of the human Calpha-formylglycine-generating enzyme.

J. Biol. Chem.

280

14900-14910

2005

1259325

Dierks T.,Dickmanns A.,Preusser-Kunze A.,Schmidt B.,Mariappan M.,von Figura K.,Ficner R.,Rudolph M.G.

Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme.

Cell

121

541-552

2005

1259326

Gande S.L.,Mariappan M.,Schmidt B.,Pringle T.H.,von Figura K.,Dierks T.

Paralog of the formylglycine-generating enzyme--retention in the endoplasmic reticulum by canonical and noncanonical signals.

FEBS J.

275

1118-1130

2008

1259327

Chen R.,Jiang X.,Sun D.,Han G.,Wang F.,Ye M.,Wang L.,Zou H.

Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.

J. Proteome Res.

8

651-661

2009

1259328

Vaca Jacome A.S.,Rabilloud T.,Schaeffer-Reiss C.,Rompais M.,Ayoub D.,Lane L.,Bairoch A.,Van Dorsselaer A.,Carapito C.

N-terminome analysis of the human mitochondrial proteome.

Proteomics

15

2519-2524

2015

1259329

Holder P.G.,Jones L.C.,Drake P.M.,Barfield R.M.,Banas S.,de Hart G.W.,Baker J.,Rabuka D.

Reconstitution of formylglycine-generating enzyme with copper(II) for aldehyde tag conversion.

J. Biol. Chem.

290

15730-15745

2015

1259330

Roeser D.,Preusser-Kunze A.,Schmidt B.,Gasow K.,Wittmann J.G.,Dierks T.,von Figura K.,Rudolph M.G.

A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme.

Proc. Natl. Acad. Sci. U.S.A.

103

81-86

2006

1259331

Cosma M.P.,Pepe S.,Parenti G.,Settembre C.,Annunziata I.,Wade-Martins R.,Domenico C.D.,Natale P.D.,Mankad A.,Cox B.,Uziel G.,Mancini G.M.,Zammarchi E.,Donati M.A.,Kleijer W.J.,Filocamo M.,Carrozzo R.,Carella M.,Ballabio A.

Molecular and functional analysis of SUMF1 mutations in multiple sulfatase deficiency.

Hum. Mutat.

23

576-581

2004

1259332

Schlotawa L.,Steinfeld R.,von Figura K.,Dierks T.,Gaertner J.

Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency.

Hum. Mutat.

29

205-205

2008

1259333

Schlotawa L.,Ennemann E.C.,Radhakrishnan K.,Schmidt B.,Chakrapani A.,Christen H.J.,Moser H.,Steinmann B.,Dierks T.,Gaertner J.

SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency.

Eur. J. Hum. Genet.

19

253-261

2011