Sequence of AT1A1_HUMAN

Na+/K+-exchanging ATPase

P05023

1023

112896

7603

Kawakami K.,Ohta T.,Nojima H.,Nagano K.

Primary structure of the alpha-subunit of human Na,K-ATPase deduced from cDNA sequence.

J. Biochem.

100

389-397

1986

7604

Ruiz A.,Bhat S.P.,Bok D.

Characterization and quantification of full-length and truncated Na,K-ATPase alpha 1 and beta 1 RNA transcripts expressed in human retinal pigment epithelium.

Gene

155

179-184

1995

7605

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

7606

Gregory S.G.,Barlow K.F.,McLay K.E.,Kaul R.,Swarbreck D.,Dunham A.,Scott C.E.,Howe K.L.,Woodfine K.,Spencer C.C.A.,Jones M.C.,Gillson C.,Searle S.,Zhou Y.,Kokocinski F.,McDonald L.,Evans R.,Phillips K.,Atkinson A.,Cooper R.,Jones C.,Hall R.E.,Andrews T.D.,Lloyd C.,Ainscough R.,Almeida J.P.,Ambrose K.D.,Anderson F.,Andrew R.W.,Ashwell R.I.S.,Aubin K.,Babbage A.K.,Bagguley C.L.,Bailey J.,Beasley H.,Bethel G.,Bird C.P.,Bray-Allen S.,Brown J.Y.,Brown A.J.,Buckley D.,Burton J.,Bye J.,Carder C.,Chapman J.C.,Clark S.Y.,Clarke G.,Clee C.,Cobley V.,Collier R.E.,Corby N.,Coville G.J.,Davies J.,Deadman R.,Dunn M.,Earthrowl M.,Ellington A.G.,Errington H.,Frankish A.,Frankland J.,French L.,Garner P.,Garnett J.,Gay L.,Ghori M.R.J.,Gibson R.,Gilby L.M.,Gillett W.,Glithero R.J.,Grafham D.V.,Griffiths C.,Griffiths-Jones S.,Grocock R.,Hammond S.,Harrison E.S.I.,Hart E.,Haugen E.,Heath P.D.,Holmes S.,Holt K.,Howden P.J.,Hunt A.R.,Hunt S.E.,Hunter G.,Isherwood J.,James R.,Johnson C.,Johnson D.,Joy A.,Kay M.,Kershaw J.K.,Kibukawa M.,Kimberley A.M.,King A.,Knights A.J.,Lad H.,Laird G.,Lawlor S.,Leongamornlert D.A.,Lloyd D.M.,Loveland J.,Lovell J.,Lush M.J.,Lyne R.,Martin S.,Mashreghi-Mohammadi M.,Matthews L.,Matthews N.S.W.,McLaren S.,Milne S.,Mistry S.,Moore M.J.F.,Nickerson T.,O'Dell C.N.,Oliver K.,Palmeiri A.,Palmer S.A.,Parker A.,Patel D.,Pearce A.V.,Peck A.I.,Pelan S.,Phelps K.,Phillimore B.J.,Plumb R.,Rajan J.,Raymond C.,Rouse G.,Saenphimmachak C.,Sehra H.K.,Sheridan E.,Shownkeen R.,Sims S.,Skuce C.D.,Smith M.,Steward C.,Subramanian S.,Sycamore N.,Tracey A.,Tromans A.,Van Helmond Z.,Wall M.,Wallis J.M.,White S.,Whitehead S.L.,Wilkinson J.E.,Willey D.L.,Williams H.,Wilming L.,Wray P.W.,Wu Z.,Coulson A.,Vaudin M.,Sulston J.E.,Durbin R.M.,Hubbard T.,Wooster R.,Dunham I.,Carter N.P.,McVean G.,Ross M.T.,Harrow J.,Olson M.V.,Beck S.,Rogers J.,Bentley D.R.

The DNA sequence and biological annotation of human chromosome 1.

Nature

441

315-321

2006

7608

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

Genome Res.

14

2121-2127

2004

7609

Shull M.M.,Pugh D.G.,Lingrel J.B.

The human Na, K-ATPase alpha 1 gene: characterization of the 5'-flanking region and identification of a restriction fragment length polymorphism.

Genomics

6

451-460

1990

7611

Shull M.M.,Lingrel J.B.

Multiple genes encode the human Na+,K+-ATPase catalytic subunit.

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

84

4039-4043

1987

7612

Chehab F.F.,Kan Y.W.,Law M.L.,Hartz J.,Kao F.T.,Blostein R.

Human placental Na+,K+-ATPase alpha subunit: cDNA cloning, tissue expression, DNA polymorphism, and chromosomal localization.

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

84

7901-7905

1987

7613

Chicz R.M.,Urban R.G.,Lane W.S.,Gorga J.C.,Stern L.J.,Vignali D.A.A.,Strominger J.L.

Predominant naturally processed peptides bound to HLA-DR1 are derived from MHC-related molecules and are heterogeneous in size.

Nature

358

764-768

1992

7614

Sverdlov E.D.,Monastyrskaya G.S.,Broude N.E.,Ushkaryov Y.A.,Allikmets R.L.,Melkov A.M.,Smirnov Y.V.,Malyshev I.V.,Dulubova I.E.,Petrukhin K.E.,Gryshin A.V.,Kiyatkin N.I.,Kostina M.B.,Sverdlov V.E.,Modyanov N.N.,Ovchinnikov Y.A.

The family of human Na+,K+-ATPase genes. No less than five genes and/or pseudogenes related to the alpha-subunit.

FEBS Lett.

217

275-278

1987

7616

Hundal H.S.,Maxwell D.L.,Ahmed A.,Darakhshan F.,Mitsumoto Y.,Klip A.

Subcellular distribution and immunocytochemical localization of Na,K-ATPase subunit isoforms in human skeletal muscle.

Mol. Membr. Biol.

11

255-262

1994

7617

Hillman R.T.,Green R.E.,Brenner S.E.

An unappreciated role for RNA surveillance.

Genome Biol.

5

0-0

2004

7618

Chi A.,Valencia J.C.,Hu Z.-Z.,Watabe H.,Yamaguchi H.,Mangini N.J.,Huang H.,Canfield V.A.,Cheng K.C.,Yang F.,Abe R.,Yamagishi S.,Shabanowitz J.,Hearing V.J.,Wu C.,Appella E.,Hunt D.F.

Proteomic and bioinformatic characterization of the biogenesis and function of melanosomes.

J. Proteome Res.

5

3135-3144

2006

7619

Uusi-Rauva K.,Luiro K.,Tanhuanpaeae K.,Kopra O.,Martin-Vasallo P.,Kyttaelae A.,Jalanko A.

Novel interactions of CLN3 protein link Batten disease to dysregulation of fodrin-Na+, K+ ATPase complex.

Exp. Cell Res.

314

2895-2905

2008

7620

Gauci S.,Helbig A.O.,Slijper M.,Krijgsveld J.,Heck A.J.,Mohammed S.

Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.

Anal. Chem.

81

4493-4501

2009

7621

Mayya V.,Lundgren D.H.,Hwang S.-I.,Rezaul K.,Wu L.,Eng J.K.,Rodionov V.,Han D.K.

Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.

Sci. Signal.

2

0-0

2009

7622

Burkard T.R.,Planyavsky M.,Kaupe I.,Breitwieser F.P.,Buerckstuemmer T.,Bennett K.L.,Superti-Furga G.,Colinge J.

Initial characterization of the human central proteome.

BMC Syst. Biol.

5

17-17

2011

7623

Bibert S.,Liu C.C.,Figtree G.A.,Garcia A.,Hamilton E.J.,Marassi F.M.,Sweadner K.J.,Cornelius F.,Geering K.,Rasmussen H.H.

FXYD proteins reverse inhibition of the Na+-K+ pump mediated by glutathionylation of its beta1 subunit.

J. Biol. Chem.

286

18562-18572

2011

7624

Krapivinsky G.,Krapivinsky L.,Stotz S.C.,Manasian Y.,Clapham D.E.

POST, partner of stromal interaction molecule 1 (STIM1), targets STIM1 to multiple transporters.

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

108

19234-19239

2011

7625

Zhou H.,Di Palma S.,Preisinger C.,Peng M.,Polat A.N.,Heck A.J.,Mohammed S.

Toward a comprehensive characterization of a human cancer cell phosphoproteome.

J. Proteome Res.

12

260-271

2013

7626

Bian Y.,Song C.,Cheng K.,Dong M.,Wang F.,Huang J.,Sun D.,Wang L.,Ye M.,Zou H.

An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

J. Proteomics

96

253-262

2014

7627

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

7628

Lassuthova P.,Rebelo A.P.,Ravenscroft G.,Lamont P.J.,Davis M.R.,Manganelli F.,Feely S.M.,Bacon C.,Brozkova D.S.,Haberlova J.,Mazanec R.,Tao F.,Saghira C.,Abreu L.,Courel S.,Powell E.,Buglo E.,Bis D.M.,Baxter M.F.,Ong R.W.,Marns L.,Lee Y.C.,Bai Y.,Isom D.G.,Barro-Soria R.,Chung K.W.,Scherer S.S.,Larsson H.P.,Laing N.G.,Choi B.O.,Seeman P.,Shy M.E.,Santoro L.,Zuchner S.

Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2.

Am. J. Hum. Genet.

102

505-514

2018

7629

Schlingmann K.P.,Bandulik S.,Mammen C.,Tarailo-Graovac M.,Holm R.,Baumann M.,Koenig J.,Lee J.J.Y.,Droegemoeller B.,Imminger K.,Beck B.B.,Altmueller J.,Thiele H.,Waldegger S.,Van't Hoff W.,Kleta R.,Warth R.,van Karnebeek C.D.M.,Vilsen B.,Bockenhauer D.,Konrad M.

Germline de novo mutations in ATP1A1 cause renal hypomagnesemia, refractory seizures, and intellectual disability.

Am. J. Hum. Genet.

103

808-816

2018