Reviewed, UniProtKB/Swiss-Prot P22557 (HEM0_HUMAN)

Names and origin

Protein names

Recommended name:
    5-aminolevulinate synthase, erythroid-specific, mitochondrial
    EC=2.3.1.37
Alternative name(s):
    5-aminolevulinic acid synthase
    Delta-aminolevulinate synthase
    Delta-ALA synthetase
      Short name=ALAS-E

Gene names

Name:	ALAS2
Synonyms:	ALASE, ASB

Organism

Homo sapiens (Human)

Taxonomic identifier

9606 [NCBI]

Taxonomic lineage

Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo

Protein attributes

Sequence length	587 AA.
Sequence status	Complete.
Sequence processing	The displayed sequence is further processed into a mature form.
Protein existence	Evidence at protein level.

General annotation (Comments)

Catalytic activity	Succinyl-CoA + glycine = 5-aminolevulinate + CoA + CO(2).
Cofactor	Pyridoxal phosphate.
Pathway	Porphyrin metabolism; protoporphyrin-IX biosynthesis; 5-aminolevulinate from glycine: step 1/1.
Subunit structure	Homodimer.
Subcellular location	Mitochondrion matrix.
Tissue specificity	Erythroid specific.
Involvement in disease	Defects in ALAS2 are a cause of X-linked sideroblastic anemia (XLSA) [MIM:301300]. Sideroblastic anemia is characterized by anemia of varying severity, hypochromic peripheral erythrocytes, progressive accumulation of iron, and the presence of ringed sideroblasts in the bone marrow.
Miscellaneous	There are two delta-ALA synthetase in vertebrates: an erythroid- specific form and one (housekeeping) which is expressed in all tissues.
Sequence similarities	Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family.

Ontologies

Keywords
Biological process	Heme biosynthesis
Cellular component	Mitochondrion
Disease	Disease mutation
Domain	Transit peptide
Ligand	Pyridoxal phosphate
Molecular function	Acyltransferase Transferase
Gene Ontology (GO)
Biological process	erythrocyte differentiation Ref.2 Non-traceable author statement. Source: UniProtKB heme biosynthetic process Non-traceable author statement. Source: UniProtKB hemoglobin biosynthetic process Inferred from sequence or structural similarity. Source: UniProtKB oxygen homeostasis Non-traceable author statement. Source: UniProtKB response to hypoxia Inferred from direct assay. Source: UniProtKB
Cellular component	mitochondrial inner membrane Inferred from direct assay. Source: UniProtKB
Molecular function	5-aminolevulinate synthase activity Inferred from direct assay. Source: UniProtKB protein binding Inferred from physical interaction. Source: UniProtKB
Complete GO annotation...

Sequence annotation (Features)

	Feature key	Position(s)	Length	Description	Graphical view
Molecule processing
	Transit peptide	1 – ?49	49	Mitochondrion
	Chain	?50 – 587	538	5-aminolevulinate synthase, erythroid-specific, mitochondrial
Sites
	Binding site	391	1	Pyridoxal phosphate (covalent) Probable
Natural variations
	Natural variant	159	1	D → Y in XLSA.
	Natural variant	199	1	Y → H in XLSA.
	Natural variant	204	1	R → Q in XLSA; 15% to 35% activity of wild-type.
	Natural variant	388	1	T → S in XLSA.
	Natural variant	411	1	R → C in XLSA; 12% to 25% activity of wild-type.
	Natural variant	448	1	R → Q in XLSA.
	Natural variant	452	1	R → C in XLSA.
	Natural variant	476	1	I → N in XLSA.
	Natural variant	560	1	R → H in XLSA.
Experimental info
	Sequence conflict	182	1	S → F in CAA39795. Ref.1

Sequences

	Sequence		Length	Mass (Da)
	P22557-1 [UniParc]. Last modified January 23, 2002. Version 2. Checksum: FD821BE245C440B5	FASTA	587	64,633
	10 20 30 40 50 60 MVTAAMLLQC CPVLARGPTS LLGKVVKTHQ FLFGIGRCPI LATQGPNCSQ IHLKATKAGG 70 80 90 100 110 120 DSPSWAKGHC PFMLSELQDG KSKIVQKAAP EVQEDVKAFK TDLPSSLVSV SLRKPFSGPQ 130 140 150 160 170 180 EQEQISGKVT HLIQNNMPGN YVFSYDQFFR DKIMEKKQDH TYRVFKTVNR WADAYPFAQH 190 200 210 220 230 240 FSEASVASKD VSVWCSNDYL GMSRHPQVLQ ATQETLQRHG AGAGGTRNIS GTSKFHVELE 250 260 270 280 290 300 QELAELHQKD SALLFSSCFV ANDSTLFTLA KILPGCEIYS DAGNHASMIQ GIRNSGAAKF 310 320 330 340 350 360 VFRHNDPDHL KKLLEKSNPK IPKIVAFETV HSMDGAICPL EELCDVSHQY GALTFVDEVH 370 380 390 400 410 420 AVGLYGSRGA GIGERDGIMH KIDIISGTLG KAFGCVGGYI ASTRDLVDMV RSYAAGFIFT 430 440 450 460 470 480 TSLPPMVLSG ALESVRLLKG EEGQALRRAH QRNVKHMRQL LMDRGLPVIP CPSHIIPIRV 490 500 510 520 530 540 GNAALNSKLC DLLLSKHGIY VQAINYPTVP RGEELLRLAP SPHHSPQMME DFVEKLLLAW 550 560 570 580 TAVGLPLQDV SVAACNFCRR PVHFELMSEW ERSYFGNMGP QYVTTYA

References

	« Hide 'large scale' referencesShow 'large scale' references »
[1]	"Two different genes encode delta-aminolevulinate synthase in humans: nucleotide sequences of cDNAs for the housekeeping and erythroid genes." Bishop D.F. Nucleic Acids Res. 18:7187-7188(1990) [PubMed: 2263504] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Liver.
[2]	"Human erythroid 5-aminolevulinate synthase: promoter analysis and identification of an iron-responsive element in the mRNA." Cox T.C., Bawden M.J., Martin A., May B.K. EMBO J. 10:1891-1902(1991) [PubMed: 2050125] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Liver.
[3]	"Identification and characterization of a conserved erythroid-specific enhancer located in intron 8 of the human 5-aminolevulinate synthase 2 gene." Surinya K.H., Cox T.C., May B.K. J. Biol. Chem. 273:16798-16809(1998) [PubMed: 9642238] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
[4]	"The DNA sequence of the human X chromosome." Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P., Frankish A., Lovell F.L., Howe K.L., Ashurst J.L., Fulton R.S., Sudbrak R., Wen G., Jones M.C. , Hurles M.E., Andrews T.D., Scott C.E., Searle S., Ramser J., Whittaker A., Deadman R., Carter N.P., Hunt S.E., Chen R., Cree A., Gunaratne P., Havlak P., Hodgson A., Metzker M.L., Richards S., Scott G., Steffen D., Sodergren E., Wheeler D.A., Worley K.C., Ainscough R., Ambrose K.D., Ansari-Lari M.A., Aradhya S., Ashwell R.I., Babbage A.K., Bagguley C.L., Ballabio A., Banerjee R., Barker G.E., Barlow K.F., Barrett I.P., Bates K.N., Beare D.M., Beasley H., Beasley O., Beck A., Bethel G., Blechschmidt K., Brady N., Bray-Allen S., Bridgeman A.M., Brown A.J., Brown M.J., Bonnin D., Bruford E.A., Buhay C., Burch P., Burford D., Burgess J., Burrill W., Burton J., Bye J.M., Carder C., Carrel L., Chako J., Chapman J.C., Chavez D., Chen E., Chen G., Chen Y., Chen Z., Chinault C., Ciccodicola A., Clark S.Y., Clarke G., Clee C.M., Clegg S., Clerc-Blankenburg K., Clifford K., Cobley V., Cole C.G., Conquer J.S., Corby N., Connor R.E., David R., Davies J., Davis C., Davis J., Delgado O., Deshazo D., Dhami P., Ding Y., Dinh H., Dodsworth S., Draper H., Dugan-Rocha S., Dunham A., Dunn M., Durbin K.J., Dutta I., Eades T., Ellwood M., Emery-Cohen A., Errington H., Evans K.L., Faulkner L., Francis F., Frankland J., Fraser A.E., Galgoczy P., Gilbert J., Gill R., Gloeckner G., Gregory S.G., Gribble S., Griffiths C., Grocock R., Gu Y., Gwilliam R., Hamilton C., Hart E.A., Hawes A., Heath P.D., Heitmann K., Hennig S., Hernandez J., Hinzmann B., Ho S., Hoffs M., Howden P.J., Huckle E.J., Hume J., Hunt P.J., Hunt A.R., Isherwood J., Jacob L., Johnson D., Jones S., de Jong P.J., Joseph S.S., Keenan S., Kelly S., Kershaw J.K., Khan Z., Kioschis P., Klages S., Knights A.J., Kosiura A., Kovar-Smith C., Laird G.K., Langford C., Lawlor S., Leversha M., Lewis L., Liu W., Lloyd C., Lloyd D.M., Loulseged H., Loveland J.E., Lovell J.D., Lozado R., Lu J., Lyne R., Ma J., Maheshwari M., Matthews L.H., McDowall J., McLaren S., McMurray A., Meidl P., Meitinger T., Milne S., Miner G., Mistry S.L., Morgan M., Morris S., Mueller I., Mullikin J.C., Nguyen N., Nordsiek G., Nyakatura G., O'dell C.N., Okwuonu G., Palmer S., Pandian R., Parker D., Parrish J., Pasternak S., Patel D., Pearce A.V., Pearson D.M., Pelan S.E., Perez L., Porter K.M., Ramsey Y., Reichwald K., Rhodes S., Ridler K.A., Schlessinger D., Schueler M.G., Sehra H.K., Shaw-Smith C., Shen H., Sheridan E.M., Shownkeen R., Skuce C.D., Smith M.L., Sotheran E.C., Steingruber H.E., Steward C.A., Storey R., Swann R.M., Swarbreck D., Tabor P.E., Taudien S., Taylor T., Teague B., Thomas K., Thorpe A., Timms K., Tracey A., Trevanion S., Tromans A.C., d'Urso M., Verduzco D., Villasana D., Waldron L., Wall M., Wang Q., Warren J., Warry G.L., Wei X., West A., Whitehead S.L., Whiteley M.N., Wilkinson J.E., Willey D.L., Williams G., Williams L., Williamson A., Williamson H., Wilming L., Woodmansey R.L., Wray P.W., Yen J., Zhang J., Zhou J., Zoghbi H., Zorilla S., Buck D., Reinhardt R., Poustka A., Rosenthal A., Lehrach H., Meindl A., Minx P.J., Hillier L.W., Willard H.F., Wilson R.K., Waterston R.H., Rice C.M., Vaudin M., Coulson A., Nelson D.L., Weinstock G., Sulston J.E., Durbin R.M., Hubbard T., Gibbs R.A., Beck S., Rogers J., Bentley D.R. Nature 434:325-337(2005) [PubMed: 15772651] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[5]	"X-linked pyridoxine-responsive sideroblastic anemia due to a Thr388-to-Ser substitution in erythroid 5-aminolevulinate synthase." Cox T.C., Bottomley S.S., Wiley J.S., Bawden M.J., Matthews C.S., May B.K. N. Engl. J. Med. 330:675-679(1994) [PubMed: 8107717] [Abstract] Cited for: VARIANT XLSA SER-388.
[6]	"Enzymatic defect in 'X-linked' sideroblastic anemia: molecular evidence for erythroid delta-aminolevulinate synthase deficiency." Cotter P.D., Baumann M., Bishop D.F. Proc. Natl. Acad. Sci. U.S.A. 89:4028-4032(1992) [PubMed: 1570328] [Abstract] Cited for: VARIANT XLSA ASN-476.
[7]	"R411C mutation of the ALAS2 gene encodes a pyridoxine-responsive enzyme with low activity." Furuyama K., Uno R., Urabe A., Hayashi N., Fujita H., Kondo M., Sassa S., Yamamoto M. Br. J. Haematol. 103:839-841(1998) [PubMed: 9858242] [Abstract] Cited for: VARIANT XLSA CYS-411.
[8]	"A novel mutation of the erythroid-specific gamma-aminolevulinate synthase gene in a patient with non-inherited pyridoxine-responsive sideroblastic anemia." Harigae H., Furuyama K., Kudo K., Hayashi N., Yamamoto M., Sassa S., Sasaki T. Am. J. Hematol. 62:112-114(1999) [PubMed: 10577279] [Abstract] Cited for: VARIANT XLSA GLN-204.
[9]	"Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis." Cotter P.D., May A., Li L., Al-Sabah A.I., Fitzsimons E.J., Cazzola M., Bishop D.F. Blood 93:1757-1769(1999) [PubMed: 10029606] [Abstract] Cited for: VARIANTS XLSA HIS-199; CYS-411; GLN-448 AND CYS-452.
[10]	"Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation." Cazzola M., May A., Bergamaschi G., Cerani P., Ferrillo S., Bishop D.F. Blood 100:4236-4238(2002) [PubMed: 12393718] [Abstract] Cited for: VARIANT XLSA HIS-560.
[11]	"A novel mutation in exon 5 of the ALAS2 gene results in X-linked sideroblastic anemia." Hurford M.T., Marshall-Taylor C., Vicki S.L., Zhou J.Z., Silverman L.M., Rezuke W.N., Altman A., Tsongalis G.J. Clin. Chim. Acta 321:49-53(2002) [PubMed: 12031592] [Abstract] Cited for: VARIANT XLSA TYR-159.
+	Additional computationally mapped references.

Web resources

GeneReviews

Cross-references

Sequence databases
EMBLGenBankDDBJ	X56352 mRNA. Translation: CAA39795.1. Different initiation. X60364 mRNA. Translation: CAA42916.1. AF068624 Genomic DNA. Translation: AAC39838.1. Z83821 Genomic DNA. No translation available. AL020991 Genomic DNA. Translation: CAA15886.1.
PIR	SYHUAE. S16347.
RefSeq	NP_000023.2.
UniGene	Hs.522666
3D structure databases
HSSP	HSSP built from PDB template 1H7D based on UniProtKB P08680.
SMR	P22557. Positions 1-49.
ModBase	Search...
Genome annotation databases
Ensembl	ENSG00000158578. Homo sapiens. [Contig view]
GeneID	212.
KEGG	hsa:212.
Organism-specific databases
HGNC	HGNC:397. ALAS2.
HPA	HPA001638.
MIM	301300. gene+phenotype.
Orphanet	1047. Sideroblastic anaemia. 75563. Sideroblastic anaemia, X-linked.
PharmGKB	PA24689.
GenAtlas	Search...
GeneCards	Search...
Phylogenomic databases
HOGENOM	P22557.
HOVERGEN	P22557.
Enzyme and pathway databases
Reactome	REACT_9431. Porphyrin metabolism.
Gene expression databases
ArrayExpress	P22557.
CleanEx	HS_ALAS2.
GermOnline	ENSG00000158578. Homo sapiens.
Family and domain databases
InterPro	IPR010961. 4pyrrol_synth_NH2levulA_synth. IPR015118. 5aminolev_synth_preseq. IPR004839. Aminotrans_I/II. IPR001917. Aminotrans_II_pyridoxalP_BS. IPR015421. PyrdxlP-dep_Trfase_major_sub1. [Graphical view]
Gene3D	G3DSA:3.40.640.10. PyrdxlP-dep_Trfase_major_sub1. 1 hit.
Pfam	PF00155. Aminotran_1_2. 1 hit. PF09029. Preseq_ALAS. 1 hit. [Graphical view]
TIGRFAMs	TIGR01821. 5aminolev_synth. 1 hit.
PROSITE	PS00599. AA_TRANSFER_CLASS_2. 1 hit. [Graphical view]
ProDom	P22557. [Graphical view] [Entries sharing at least one domain]
BLOCKS	Search...
Other Resources
DrugBank	DB00145. Glycine.
SOURCE	Search...
ProtoNet	Search...

Entry information

Entry name

HEM0_HUMAN

Accession

Primary (citable) accession number: P22557
Secondary accession number(s): Q13735

Entry history

Integrated into UniProtKB/Swiss-Prot:	August 1, 1991
Last sequence update:	January 23, 2002
Last modified:	September 2, 2008
This is version 96 of the entry and version 2 of the sequence. [Complete history]

Entry status

Reviewed (UniProtKB/Swiss-Prot)

Annotation project

HPI (Human Proteome Initiative)