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Reviewed, UniProtKB/Swiss-Prot Q86V21 (AACS_HUMAN)

Last modified July 22, 2008. Version 46. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Acetoacetyl-CoA synthetase
    EC=6.2.1.16
Alternative name(s):
    Acyl-CoA synthetase family member 1
    Protein sur-5 homolog
Gene names
Name: AACS
Synonyms: ACSF1
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length672 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

General annotation (Comments)

Function

Activates acetoacetate to acetoacetyl-CoA. May be involved in utilizing ketone body for the fatty acid-synthesis during adipose tissue development By similarity.

Catalytic activity

ATP + acetoacetate + CoA = AMP + diphosphate + acetoacetyl-CoA.

Subcellular location

CytoplasmcytosolBy similarity.

Tissue specificity

Highly expressed in kidney, heart and brain, but low in liver.

Sequence similarities

Belongs to the ATP-dependent AMP-binding enzyme family.

Sequence caution

The sequence AAH41000.1 differs from that shown. Reason: Frameshift at position 201.

The sequence BAB14793.1 differs from that shown. Reason: Frameshift at position 519.

Ontologies

Keywords

   Biological processFatty acid metabolism
Lipid metabolism
   Cellular componentCytoplasm
   Coding sequence diversityAlternative splicing
Polymorphism
   Molecular functionLigase
   PTMPhosphoprotein

Gene Ontology (GO)

None. [Check GOA]

Alternative products

This entry describes 3 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q86V21-1)

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
Isoform 2 (identifier: Q86V21-2)

The sequence of this isoform differs from the canonical sequence as follows:
     561-672: ESFEEVEDSL...YRDIPELQGF → YAQRQESGSC...RDPGSVPGHP
Notes: No experimental confirmation available.
Isoform 3 (identifier: Q86V21-3)

The sequence of this isoform differs from the canonical sequence as follows:
     1-402: Missing.
Notes: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical view

Molecule processing

Chain1 – 672672Acetoacetyl-CoA synthetase

Amino acid modifications

Modified residue5241Phosphotyrosine By similarity

Natural variations

Alternative sequence1 – 402402Missing in isoform 3.
Alternative sequence561 – 672112ESFEE…ELQGF → YAQRQESGSCRQTDHRWKSR GARRCFLEPRDPGSVPGHP in isoform 2.
Natural variant1181I → V: dbSNP rs12831803.

Experimental info

Sequence conflict701G → E in BAB14793. Ref.2
Sequence conflict1191A → V in BAB14040. Ref.2
Sequence conflict1281K → E in BAB14793. Ref.2
Sequence conflict1371E → G in BAB14040. Ref.2
Sequence conflict1501V → A in BAB14040. Ref.2
Sequence conflict3911K → E in AAH41000. Ref.4

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified June 1, 2003. Version 1.
Checksum: 36006739EE4857D9

FASTA67275,144
        10         20         30         40         50         60 
MSKEERPGRE EILECQVMWE PDSKKNTQMD RFRAAVGAAC GLALESYDDL YHWSVESYSD 

        70         80         90        100        110        120 
FWAEFWKFSG IVFSRVYDEV VDTSKGIADV PEWFKGSRLN YAENLLRHKE NDRVALYIAR 

       130        140        150        160        170        180 
EGKEEIVKVT FEELRQEVAL FAAAMRKMGV KKGDRVVGYL PNSEHAVEAM LAAASIGAIW 

       190        200        210        220        230        240 
SSTSPDFGVN GVLDRFSQIQ PKLIFSVEAV VYNGKEHNHM EKLQQVVKGL PDLKKVVVIP 

       250        260        270        280        290        300 
YVSSRENIDL SKIPNSVFLD DFLATGTSEQ APQLEFEQLP FSHPLFIMFS SGTTGAPKCM 

       310        320        330        340        350        360 
VHSAGGTLIQ HLKEHLLHGN MTSSDILLCY TTVGWMMWNW MVSLLATGAA MVLYDGSPLV 

       370        380        390        400        410        420 
PTPNVLWDLV DRIGITVLVT GAKWLSVLEE KAMKPVETHS LQMLHTILST GSPLKAQSYE 

       430        440        450        460        470        480 
YVYRCIKSSI LLGSISGGTD IISCFMGHNF SLPVYKGEIQ ARNLGMAVEA WNEEGKAVWG 

       490        500        510        520        530        540 
ESGELVCTKP IPCQPTHFWN DENGNKYRKA YFSKFPGIWA HGDYCRINPK TGGIVMLGRS 

       550        560        570        580        590        600 
DGTLNPNGVR FGSSEIYNIV ESFEEVEDSL CVPQYNKYRE ERVILFLKMA SGHAFQPDLV 

       610        620        630        640        650        660 
KRIRDAIRMG LSARHVPSLI LETKGIPYTL NGKKVEVAVK QIIAGKAVEQ GGAFSNPETL 

       670 
DLYRDIPELQ GF 

« Hide

Isoform 2 [UniParc].

Checksum: 1C454CA0635CB5C5
Show »

59967,035
Isoform 3 [UniParc].

Checksum: 930E1C6E82B5061D
Show »

27030,061

References

« Hide 'large scale' references
[1]"Expression of acetoacetyl-CoA synthetase, a novel cytosolic ketone body-utilizing enzyme, in human brain."
Ohgami M., Takahashi N., Yamasaki M., Fukui T.
Biochem. Pharmacol. 65:989-994(2003) [PubMed: 12623130] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), TISSUE SPECIFICITY.
[2]"Complete sequencing and characterization of 21,243 full-length human cDNAs."
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. expand/collapse author list , 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.
Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
Tissue: Mammary gland and Retinoblastoma.
[3]Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. expand/collapse author list , Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W., Venter J.C.
Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[4]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1; 2 AND 3), VARIANT VAL-118.
Tissue: Brain, Kidney and Testis.
[5]"Caenorhabditis elegans SUR-5, a novel but conserved protein, negatively regulates LET-60 Ras activity during vulval induction."
Gu T., Orita S., Han M.
Mol. Cell. Biol. 18:4556-4564(1998) [PubMed: 9671465] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 12-672 (ISOFORM 1).
[6]The German cDNA consortium
Submitted (SEP-2004) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 48-672 (ISOFORM 1).
Tissue: Stomach.
[7]"Evidence for 26 distinct acyl-coenzyme A synthetase genes in the human genome."
Watkins P.A., Maiguel D., Jia Z., Pevsner J.
J. Lipid Res. 48:2736-2750(2007) [PubMed: 17762044] [Abstract]
Cited for: IDENTIFICATION.

Cross-references

Sequence databases

AB054121 mRNA. Translation: BAD22560.1.
AK022451 mRNA. Translation: BAB14040.1.
AK024036 mRNA. Translation: BAB14793.1. Frameshift.
CH471054 Genomic DNA. Translation: EAW98474.1.
BC004997 mRNA. Translation: AAH04997.1.
BC040490 mRNA. Translation: AAH40490.2.
BC040574 mRNA. Translation: AAH40574.1.
BC041000 mRNA. Translation: AAH41000.1. Frameshift.
BC051862 mRNA. Translation: AAH51862.1.
AY091468 mRNA. Translation: AAM44124.1.
AL833047 mRNA. Translation: CAH56309.1.
RefSeqNP_076417.2.
UniGeneHs.656073

3D structure databases

ModBaseSearch...

PTM databases

PhosphoSiteQ86V21.

Genome annotation databases

EnsemblENSG00000081760. Homo sapiens. [Contig view]
GeneID65985.
KEGGhsa:65985.
NMPDRfig|9606.3.peg.8499.

Organism-specific databases

HGNCHGNC:21298. AACS.
PharmGKBPA134940696.
GenAtlasSearch...
GeneCardsSearch...

Phylogenomic databases

HOVERGENQ86V21.

Gene expression databases

ArrayExpressQ86V21.
CleanExHS_AACS.

Family and domain databases

InterProIPR005914. Acac_CoA_synth.
IPR000873. AMP-dep_Synth/Lig.
[Graphical view]
PfamPF00501. AMP-binding. 1 hit.
[Graphical view]
PRINTSPR00154. AMPBINDING.
TIGRFAMsTIGR01217. ac_ac_CoA_syn. 1 hit.
PROSITEPS00455. AMP_BINDING. 1 hit.
[Graphical view]
ProDomQ86V21.
[Graphical view] [Entries sharing at least one domain]
BLOCKSSearch...

Other Resources

ProtoNetSearch...

Entry information

Entry nameAACS_HUMAN
AccessionPrimary (citable) accession number: Q86V21
Secondary accession number(s): Q49AB9 expand/collapse secondary AC list , Q49AC3, Q658Q8, Q8IWD2, Q8NEW5, Q9BSJ9, Q9H829, Q9HA19
Entry history
Integrated into UniProtKB/Swiss-Prot: January 15, 2008
Last sequence update: June 1, 2003
Last modified: July 22, 2008
This is version 46 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)

Relevant documents

Human chromosome 12

Human chromosome 12: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

UniProtKB secondary accession numbers

Index of UniProtKB secondary accession numbers

SIMILARITY comments

Index of protein domains and families

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents