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By V.M. Rosenoer

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E. at the end of "loop 1C". Andersson et al. (33) have characterized a peptide from BSA specifically labeled with fluorescein isothiocyanate and from their sequence we can identify the reactive group as Lys-220. This is at the end of loop 2A at the mouth of the binding hole of domain two. This same group is probably the active site residue toward a Meisenheimer complex described by Taylor <47·48-49> and may also be the site of reaction of pyridoxal phosphate (PLP) with BSA. We have found that trinitrobenzene sulfonic acid (TNBS) labels Lys-412 in BSA.

E. at the entrance or mouth of the binding hole. Gambhir et al. e. at the end of "loop 1C". Andersson et al. (33) have characterized a peptide from BSA specifically labeled with fluorescein isothiocyanate and from their sequence we can identify the reactive group as Lys-220. This is at the end of loop 2A at the mouth of the binding hole of domain two. This same group is probably the active site residue toward a Meisenheimer complex described by Taylor <47·48-49> and may also be the site of reaction of pyridoxal phosphate (PLP) with BSA.

2, 705,230. 146. , H. Lefevre, H. Fiedler and L. J. McCarty (1975) An alternative method of large scale plasma fractionation for the isolation of serum albumin. Blut. 30, 121-134. 147. Schultze, H. E. and J. F. Heremans (1966) Molecular Biology of Human Proteins with Special Reference to Plasma Proteins, Vol. 1, pp. 261-270. Elsevier, New York. 148. McMenamy, R. , H. M. Dintzis and F. Watson (1971) Cyanogen bromide fragments of human serum albumin. / . Biol. Chem. 246, 4744-4750. 149. McMenamy, R.

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