Ak2 | ENSMUSG00000028792 | NCBI 11637

Details for: Ak2

Gene ID: 11637

Symbol: Ak2

Ensembl ID: ENSMUSG00000028792

Description: adenylate kinase 2

Associated with

Interconversion of nucleotide di- and triphosphates
(R-MMU-499943)
Metabolism
(R-MMU-1430728)
Metabolism of nucleotides
(R-MMU-15869)
Adenylate kinase activity
(GO:0004017)
Adp biosynthetic process
(GO:0006172)
Amp metabolic process
(GO:0046033)
Atp binding
(GO:0005524)
Cytoplasm
(GO:0005737)
Datp metabolic process
(GO:0046060)
Kinase activity
(GO:0016301)
Mitochondrial inner membrane
(GO:0005743)
Mitochondrion
(GO:0005739)
Nucleobase-containing compound kinase activity
(GO:0019205)
Nucleobase-containing compound metabolic process
(GO:0006139)
Nucleotide binding
(GO:0000166)
Phosphorylation
(GO:0016310)
Phosphotransferase activity, phosphate group as acceptor
(GO:0016776)
Sperm flagellum
(GO:0036126)
Sperm mitochondrial sheath
(GO:0097226)
Transferase activity
(GO:0016740)

Other Information

Proteins

KAD2_MOUSE

Genular Protein ID: 2215343405

Symbol: KAD2_MOUSE

Name: N/A

UniProtKB Accession Codes:

Q9WTP6 A2A820 Q3THT3 Q3TI11 Q3TKI6 Q8C7I9 Q9CY37

Database IDs:

Citations:

PubMed ID: 16141072

Title: The transcriptional landscape of the mammalian genome.

PubMed ID: 16141072

DOI: 10.1126/science.1112014

PubMed ID: 19468303

Title: Lineage-specific biology revealed by a finished genome assembly of the mouse.

PubMed ID: 19468303

DOI: 10.1371/journal.pbio.1000112

PubMed ID: 15489334

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

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 19043416

Title: Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.

PubMed ID: 19043416

DOI: 10.1038/ng.278

PubMed ID: 21183079

Title: A tissue-specific atlas of mouse protein phosphorylation and expression.

PubMed ID: 21183079

DOI: 10.1016/j.cell.2010.12.001

PubMed ID: 23806337

Title: SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways.

PubMed ID: 23806337

DOI: 10.1016/j.molcel.2013.06.001

PubMed ID: 23576753

Title: Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathways.

PubMed ID: 23576753

DOI: 10.1073/pnas.1302961110

Sequence Information:

Length: 239
Mass: 26469
Checksum: CAFF06F053CECE36
Sequence:

MAPNVLASEP EIPKGIRAVL LGPPGAGKGT QAPKLAENFC VCHLATGDML RAMVASGSEL 
GKKLKATMDA GKLVSDEMVV ELIEKNLETP SCKNGFLLDG FPRTVRQAEM LDDLMEKRKE 
KLDSVIEFSI QDSLLIRRIT GRLIHPKSGR SYHEEFNPPK EPMKDDITGE PLIRRSDDNE 
KALKTRLEAY HTQTTPLVEY YRKRGIHCAI DASQTPDIVF ASILAAFSKA TCKDLVMFI

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: Ak2

Associated with

Other Information

The transcriptional landscape of the mammalian genome. PubMed ID: 16141072

Lineage-specific biology revealed by a finished genome assembly of the mouse. PubMed ID: 19468303

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness. PubMed ID: 19043416

A tissue-specific atlas of mouse protein phosphorylation and expression. PubMed ID: 21183079

SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways. PubMed ID: 23806337

Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathways. PubMed ID: 23576753