ALB

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Generation and annotation of the DNA sequences of human chromosomes 2 and 4

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Genome Res. 13:2265-2270(2003)

The human albumin gene. Characterization of the 5' and 3' flanking regions and the polymorphic gene transcripts

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Complete amino acid sequence of human serum albumin

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FEBS Lett. 58:134-137(1975)

The human myocardial two-dimensional gel protein database: update 1994

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Electrophoresis 15:1459-1465(1994)

Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides

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Structure of a biologically active neurotensin-related peptide obtained from pepsin-treated albumin(s)

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J. Biol. Chem. 262:5968-5973(1987)

Lysine residue 199 of human serum albumin is modified by acetylsalicylic acid

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FEBS Lett. 66:173-175(1976)

Enzymatic digestion and mass spectrometry in the study of advanced glycation end products/peptides

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Lysine residue 240 of human serum albumin is involved in high-affinity binding of bilirubin

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The principal site of nonenzymatic glycosylation of human serum albumin in vivo

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Effect of serum albumin on siderophore-mediated utilization of transferrin iron

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

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Immunoaffinity enrichment and mass spectrometry analysis of protein methylation

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A single kinase generates the majority of the secreted phosphoproteome

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N-terminome analysis of the human mitochondrial proteome

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Hepatic FcRn regulates albumin homeostasis and susceptibility to liver injury

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Three-dimensional structure of human serum albumin

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Science 244:1195-1198(1989)

Structure of human serum albumin

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The sequence of human serum albumin cDNA and its expression in E. coli

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Nucleic Acids Res. 9:6103-6114(1981)

Nucleotide sequence and the encoded amino acids of human serum albumin mRNA

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Genome Res. 11:1392-1403(2001)

A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges

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Eur. J. Biochem. 268:344-352(2001)

Atomic structure and chemistry of human serum albumin

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Crystal structure of human serum albumin complexed with fatty acid reveals an asymmetric distribution of binding sites

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Nat. Struct. Biol. 5:827-835(1998)

Crystal structure of human serum albumin at 2.5-A resolution

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Protein Eng. 12:439-446(1999)

Binding of the general anesthetics propofol and halothane to human serum albumin. High resolution crystal structures

Bhattacharya A.A., Curry S., Franks N.P.,

J. Biol. Chem. 275:38731-38738(2000)

Crystal structures of human serum albumin complexed with monounsaturated and polyunsaturated fatty acids

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J. Mol. Biol. 314:955-960(2001)

Circulatory zinc transport is controlled by distinct interdomain sites on mammalian albumins

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Chem. Sci. 7:6635-6648(2016)

Albumin Canterbury (313 Lys-->Asn). A point mutation in the second domain of serum albumin

Brennan S.O., Herbert P.,

Biochim. Biophys. Acta 912:191-197(1987)

Amino acid substitutions in genetic variants of human serum albumin and in sequences inferred from molecular cloning

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Proc. Natl. Acad. Sci. U.S.A. 84:4413-4417(1987)

Amino acid substitutions in inherited albumin variants from Amerindian and Japanese populations

Takshashi N., Takahashi Y., Isobe T., Putnam F.W., Fujita M., Satoh C., Neel J.V.,

Proc. Natl. Acad. Sci. U.S.A. 84:8001-8005(1987)

Identical structural changes in inherited albumin variants from different populations

Arai K., Ishioka N., Huss K., Madison J., Putnam F.W.,

Proc. Natl. Acad. Sci. U.S.A. 86:434-438(1989)

Point substitutions in Japanese alloalbumins

Arai K., Madison J., Huss K., Ishioka N., Satoh C., Fujita M., Neel J.V., Sakurabayashi I., Putnam F.W.,

Proc. Natl. Acad. Sci. U.S.A. 86:6092-6096(1989)

Point substitutions in albumin genetic variants from Asia

Arai K., Madison J., Shimuzu A., Putnam F.W.,

Proc. Natl. Acad. Sci. U.S.A. 87:497-501(1990)

Albumin Redhill (-1 Arg, 320 Ala-->Thr): a glycoprotein variant of human serum albumin whose precursor has an aberrant signal peptidase cleavage site

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Proc. Natl. Acad. Sci. U.S.A. 87:26-30(1990)

Mutations in genetic variants of human serum albumin found in Italy

Galliano M., Minchiotti L., Porta F., Rossi A., Ferri G., Madison J., Watkins S., Putnam F.W.,

Proc. Natl. Acad. Sci. U.S.A. 87:8721-8725(1990)

Albumin Hawkes Bay; a low level variant caused by loss of a sulphydryl group at position 177

Brennan S.O., Fellowes A.P.,

Biochim. Biophys. Acta 1182:46-50(1993)

Protein and DNA sequence analysis of a 'private' genetic variant: albumin Ortonovo (Glu-505-->Lys)

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Biochim. Biophys. Acta 1225:27-32(1993)

Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant

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Proc. Natl. Acad. Sci. U.S.A. 91:6476-6480(1994)

An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families

Sunthornthepvarakul T., Angkeow P., Weiss R.E., Hayashi Y., Retetoff S.,

Biochem. Biophys. Res. Commun. 202:781-787(1994)

Identification of a human serum albumin species associated with familial dysalbuminemic hyperthyroxinemia

Rushbrook J.I., Becker E., Schussler G.C., Divino C.M.,

J. Clin. Endocrinol. Metab. 80:461-467(1995)

A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred

Wada N., Chiba H., Shimizu C., Kijima H., Kubo M., Koike T.,

J. Clin. Endocrinol. Metab. 82:3246-3250(1997)

Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect

Sunthornthepvarakul T., Likitmaskul S., Ngowngarmratana S., Angsusingha K., Kitvitayasak S., Scherberg N.H., Refetoff S.,

J. Clin. Endocrinol. Metab. 83:1448-1454(1998)

Towards defining the urinary proteome using liquid chromatography-tandem mass spectrometry I. Profiling an unfractionated tryptic digest

Spahr C.S., Davis M.T., McGinley M.D., Robinson J.H., Bures E.J., Beierle J., Mort J., Courchesne P.L., Chen K., Wahl R.C., Yu W., Luethy R., Patterson S.D.,

Proteomics 1:93-107(2001)

Synonyms

Description

KO Status

Drug Information

Human Albumin (SK Plasma)

Human albumin (Guizhou Taibang Biological Products)

Human albumin(Tonrol Bio-Pharmaceutical)

Human Albumin(Guangdong Danxia)

Human Serum Albumin (Green Cross)

Albumin Human(Sanquin Plasma Products)

Human Albumin(Anhui Da'An)

Human Albumin(Hangzhou Tigermed)

Human albumin (Hebei Da'an Pharmaceutical)

Human Albumin(Huhan Nanyue)

Albumin Human(Cis Bio International)

Human albumin (Hualan Biological Engineering)

20% Human albumin (Hemarus Therapeutics)

Albumin Human (Biotest Pharma GmbH)

Vialebex (LFB SA/Swedish Orphan Biovitrum AB)

ND-021

Human Serum Albumin (Baxter)

89 Zirconium labeled GSK-3128349

References

Nonenzymatic glycosylation of human serum albumin alters its conformation and function

Nonenzymatic glycosylation of albumin in vivo. Identification of multiple glycosylated sites

A nucleotide insertion and frameshift cause analbuminemia in an Italian family

Albumin as a zinc carrier: properties of its high-affinity zinc-binding site

Large-scale phosphoproteome analysis of human liver tissue by enrichment and fractionation of phosphopeptides with strong anion exchange chromatography

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

Initial characterization of the human central proteome

The full-ORF clone resource of the German cDNA consortium