TCDB is operated by the Saier Lab Bioinformatics Group
Transporter Information:
Name: ATP synthase, H+ transporting, mitochondrial F0 complex, subunit s (factor B)
Symbol: ATP5S
Locations: 14q21.3
Aliases: HSU79253, ATPW
MGI: MGI:1915305
GenBank: U79253
Swiss-Prot: Q99766
Accession Number: NM_015684
PubMed (11744738): Belogrudov GI, Hatefi Y. Factor B and the mitochondrial ATP synthase complex.J Biol Chem. 2002 Feb 22;277(8):6097-103. Epub 2001 Dec 14. PMID: 11744738 [PubMed - indexed for MEDLINE]

Factor B is a subunit of the mammalian ATP synthase complex, whose existence has been controversial. This paper describes the molecular and functional properties of a recombinant human factor B, which when added to bovine submitochondrial particles depleted of their factor B restores the energy coupling activity of the ATP synthase complexes. The mature human factor B has 175 amino acids and a molecular mass of 20,341 Da. The preparation is water-soluble, monomeric, and is inactivated by monothiol- and especially dithiol-modifying reagents, probably reacting at its cysteine residues Cys-92 and Cys-94. A likely factor B gene composed of 5 exons has been identified on chromosome 14q21.3, and the functional role of factor B in the mammalian ATP synthase complex has been discussed.

PubMed (8619474):

The efficiency of shotgun DNA sequencing depends to a great extent on the quality of the random-subclone libraries used. We here describe a novel "double adaptor" strategy for efficient construction of high-quality shotgun libraries. In this method, randomly sheared and end-repaired fragments are ligated to oligonucleotide adaptors creating 12-base overhangs. Nonphosphorylated oligonucleotides are used, which prevents formation of adaptor dimers and ensures efficient ligation of insert to adaptor. The vector is prepared from a modified M13 vector, by KpnI/PstI digestion followed by ligation to oligonucleotides with ends complementary to the overhangs created in the digest. These adaptors create 5'-overhangs complementary to those on the inserts. Following annealing of insert to vector, the DNA is directly used for transformation without a ligation step. This protocol is robust and shows three- to fivefold higher yield of clones compared to previous protocols. No chimeric clones can be detected and the background of clones without an insert is <1%. The procedure is rapid and shows potential for automation.