Search Results - "Hartog, A.F"

Modification of membrane-bound F1 by p-fluorosulfonylbenzoyl-5′-adenosine: sites of binding and effect on activity by van der Zwet-de Graaff, I, Hartog, A.F, Berden, J.A

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Hydrolysis of ATP by F1 can be described only on the basis of a dual-site mechanism by Berden, J A, Hartog, A F, Edel, C M

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Antimicrobial activity of vanadium chloroperoxidase on planktonic Streptococcus mutans cells and Streptococcus mutans biofilms by Hoogenkamp, M A, Crielaard, W, ten Cate, J M, Wever, R, Hartog, A F, Renirie, R

“…The aim of this study was to investigate the antimicrobial activity of vanadium chloroperoxidase (VCPO) reaction products on planktonic and biofilm cells of…”
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A new crosslinker for mass spectrometric analysis of the quaternary structure of protein complexes by Back, J.W, Hartog, A.F, Dekker, H.L, Muijsers, Anton O, de Koning, L.J, de Jong, Luitzen

“…Mass spectrometric structural analysis of crosslinked peptides is a powerful method to elucidate the spatial arrangement of polypeptides in protein complexes…”
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One of the non-exchangeable nucleotides of the mitochondrial F1-ATPase is bound at a β-subunit: evidence for a non-rotatory two-site catalytic mechanism by Hartog, A.F., Berden, J.A.

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One of the non-exchangeable nucleotides of the mitochondrial F 1-ATPase is bound at a β-subunit: evidence for a non-rotatory two-site catalytic mechanism by Hartog, A.F., Berden, J.A.

“…In active MF 1, one of the two non-exchangeable tightly bound adenine nucleotides is an ATP, while the other is an ADP. The respective sites are called the…”
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Analysis of the nucleotide binding sites of mitochondrial ATP synthase provides evidence for a two-site catalytic mechanism by Berden, J.A, Hartog, A.F

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Characterization of the respiratory chain from cultured Crithidia fasciculata by Speijer, Dave, Breek, Cornelis K.D., Muijsers, Anton O., Hartog, Aloysius F., Berden, Jan A., Albracht, Simon P.J., Samyn, Bart, Van Beeumen, Jozef, Benne, Rob

“…Mitochondrial mRNAs encoding subunits of respiratory-chain complexes in kinetoplstids are post-transcriptionally edited by uridine insertion and deletion. In…”
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Synthesis of 8-N 3-[2'- 32P]NADP(H), a new photoaffinity label for NADP(H)-specific enzymes by Hartog, A.F., Berden, J.A.

“…The synthesis of the photoaffinity label 8-N 3-[2'- 32P]NADP + is described. The synthesis consists of the following steps: first 8-N 3-AMP is synthesized from…”
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FSBA modifies both α- and β-subunits of F 1 specifically and can be bound together with AXP at the same α-subunit by Hartog, A.F, Edel, C.M, Braham, J, Muijsers, A.O, Berden, J.A

“…Binding of 1 mole 5′-fluorosulfonylbenzoyladenosine (FSBA) per mol F 1 induces about 50% inhibition of ATPase activity and 80% inhibition of ITPase activity…”
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Analysis of the inhibitory non-catalytic ADP binding site on mitochondrial F1, using NAP3-2N3ADP as probe. Effects of the modification on ATPase and ITPase activity by Edel, C.M., Hartog, A.F., Berden, J.A.

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FSBA modifies both α- and β-subunits of F1 specifically and can be bound together with AXP at the same α-subunit by Hartog, A.F, Edel, C.M, Braham, J, Muijsers, A.O, Berden, J.A

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Modification of membrane-bound F 1 by p-fluorosulfonylbenzoyl-5′-adenosine: sites of binding and effect on activity by van der Zwet-de Graaff, I, Hartog, A.F, Berden, J.A

“…Bovine heart submitochondrial particles (smp) were incubated with p-fluorosulfonylbenzoyl-5′-adenosine (FSBA) in order to study the binding of this ligand and…”
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Synthesis of 8‐N3‐[2'‐32P]NADP(H), a new photoaffinity label for NADP(H)‐specific enzymes by Hartog, A.F., Berden, J.A.

“…The synthesis of the photoaffinity label 8‐N3‐[2'‐32P]NADP+ is described. The synthesis consists of the following steps: first 8‐N3‐AMP is synthesized from AMP…”
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Energy-linked transhydrogenase. Characterization of a nucleotide-binding sequence in nicotinamide nucleotide transhydrogenase from beef heart by Hu, P S, Persson, B, Höög, J O, Jörnvall, H, Hartog, A F, Berden, J A, Holmberg, E, Rydström, J

“…Purified nicotinamide nucleotide transhydrogenase from beef heart was investigated with respect to labeling and subsequent sequence analysis of a nicotinamide…”
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