BAT5

Protein BAT5 is a protein that in humans is encoded by the BAT5 gene.[5][6][7]

ABHD16A
Identifiers
AliasesABHD16A, BAT5, D6S82E, NG26, PP199, abhydrolase domain containing 16A, hBAT5, abhydrolase domain containing 16A, phospholipase, SPG86
External IDsOMIM: 142620 MGI: 99476 HomoloGene: 10904 GeneCards: ABHD16A
Orthologs
SpeciesHumanMouse
Entrez

7920

193742

Ensembl

ENSMUSG00000007036

UniProt

O95870

Q9Z1Q2

RefSeq (mRNA)

NM_001177515
NM_021160

NM_178592

RefSeq (protein)

NP_001170986
NP_066983

NP_848707

Location (UCSC)Chr 6: 31.69 – 31.7 MbChr 17: 35.31 – 35.32 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity.[7]

Bat5 structure

Amino Acid Sequence

Cross examination of BAT5 Amino Acid sequence in humans and mice

BAT5 (also known as ABHD16A) has been found to be 558 amino acid residues. It was fist identified in 1992 in the gene domain of TNF alpha and TNF beta. BAT5 (ABHD 16A) in different species has been found to be different lengths of amino acid sequence.

Structural prediction of human BAT5 (ABHD 16A) protein

BAT5 has been determined to be highly conserved when compared to human, mice and other mammalian ontologies.[8] It is found to be expressed in multiple different tissue cells. According to molecular evolutionary genetic analysis, in comparison of 13 mammalian species, the noticeable differences in amino acid sequence length is due to splicing in post transcriptional processing of mRNA.[9]

Human chromosome 6 and Mouse chromosome 17 BAT5 location

BAT5 gene location

Human Bat5 (ABHD16A) is located on chromosome 6. Mice Bat5 (ABHD 16A) is located between TNF and Heat shock protein near the Ck2b protein kinase gene.[9]

BAT5 molecular weight

BAT5 molecular weight comparison of Humans (H) and Mice (m)

BAT5 in humans and mice has been found to be around 63kDA.

Bat5 implications in recent studies

BAT5 has been linked to neurological, immune regulation, Kawasaki's disease and coronary artery disease.[9]

References

  1. ENSG00000231488, ENSG00000204427, ENSG00000235676, ENSG00000230475, ENSG00000206403, ENSG00000224552 GRCh38: Ensembl release 89: ENSG00000236063, ENSG00000231488, ENSG00000204427, ENSG00000235676, ENSG00000230475, ENSG00000206403, ENSG00000224552 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000007036 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Spies T, Blanck G, Bresnahan M, Sands J, Strominger JL (Feb 1989). "A new cluster of genes within the human major histocompatibility complex". Science. 243 (4888): 214–7. Bibcode:1989Sci...243..214S. doi:10.1126/science.2911734. PMID 2911734.
  6. Spies T, Bresnahan M, Strominger JL (Dec 1989). "Human major histocompatibility complex contains a minimum of 19 genes between the complement cluster and HLA-B". Proc Natl Acad Sci U S A. 86 (22): 8955–8. Bibcode:1989PNAS...86.8955S. doi:10.1073/pnas.86.22.8955. PMC 298409. PMID 2813433.
  7. "Entrez Gene: BAT5 HLA-B associated transcript 5".
  8. Savinainen, Juha R.; Patel, Jayendra Z.; Parkkari, Teija; Navia-Paldanius, Dina; Marjamaa, Joona J. T.; Laitinen, Tuomo; Nevalainen, Tapio; Laitinen, Jarmo T. (2014-10-07). "Biochemical and Pharmacological Characterization of the Human Lymphocyte Antigen B-Associated Transcript 5 (BAT5/ABHD16A)". PLOS ONE. 9 (10): e109869. doi:10.1371/journal.pone.0109869. ISSN 1932-6203.
  9. Xu, Jun; Gu, Weizhen; Ji, Kai; Xu, Zhao; Zhu, Haihua; Zheng, Wenming. "Sequence analysis and structure prediction of ABHD16A and the roles of the ABHD family members in human disease". Open Biology. 8 (5): 180017. doi:10.1098/rsob.180017. PMC 5990648. PMID 29794032.

Further reading


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