| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-99 |
Sentence |
denotes |
Cloning and expression of a proteoglycan UDP-galactose:beta-xylose beta1,4-galactosyltransferase I. |
| T2 |
100-170 |
Sentence |
denotes |
A seventh member of the human beta4-galactosyltransferase gene family. |
| T3 |
171-310 |
Sentence |
denotes |
A seventh member of the human beta4-galactosyltransferase family, beta4Gal-T7, was identified by BLAST analysis of expressed sequence tags. |
| T4 |
311-590 |
Sentence |
denotes |
The coding region of beta4Gal-T7 depicts a type II transmembrane protein with sequence similarity to beta4-galactosyltransferases, but the sequence was distinct in known motifs and did not contain the cysteine residues conserved in the other six members of the beta4Gal-T family. |
| T5 |
591-671 |
Sentence |
denotes |
The genomic organization of beta4Gal-T7 was different from previous beta4Gal-Ts. |
| T6 |
672-848 |
Sentence |
denotes |
Expression of beta4Gal-T7 in insect cells showed that the gene product had beta1,4-galactosyltransferase activity with beta-xylosides, and the linkage formed was Galbeta1-4Xyl. |
| T7 |
849-1088 |
Sentence |
denotes |
Thus, beta4Gal-T7 represents galactosyltransferase I enzyme (xylosylprotein beta1, 4-galactosyltransferase; EC 2.4.1.133), which attaches the first galactose in the proteoglycan linkage region GlcAbeta1-3Galbeta1-3Galbeta1-4Xylbeta1-O-Ser. |
| T8 |
1089-1363 |
Sentence |
denotes |
Sequence analysis of beta4Gal-T7 from a fibroblast cell line of a patient with a progeroid syndrome and signs of the Ehlers-Danlos syndrome, previously shown to exhibit reduced galactosyltransferase I activity (Quentin, E., Gladen, A., Rodén, L., and Kresse, H. (1990) Proc. |
| T9 |
1364-1369 |
Sentence |
denotes |
Natl. |
| T10 |
1370-1375 |
Sentence |
denotes |
Acad. |
| T11 |
1376-1380 |
Sentence |
denotes |
Sci. |
| T12 |
1381-1383 |
Sentence |
denotes |
U. |
| T13 |
1384-1386 |
Sentence |
denotes |
S. |
| T14 |
1387-1389 |
Sentence |
denotes |
A. |
| T15 |
1390-1725 |
Sentence |
denotes |
87, 1342-1346), revealed two inherited allelic variants, beta4Gal-T7(186D) and beta4Gal-T7(206P), each with a single missense substitution in the putative catalytic domain of the enzyme. beta4Gal-T7(186D) exhibited a 4-fold elevated K(m) for the donor substrate, whereas essentially no activity was demonstrated with beta4Gal-T7(206P). |
| T16 |
1726-1911 |
Sentence |
denotes |
Molecular cloning of beta4Gal-T7 should facilitate general studies of its pathogenic role in progeroid syndromes and connective tissue disorders with affected proteoglycan biosynthesis. |