Nucleotide sequence encoding a slow allele of Adh1 in pearl millet

1990 ◽  
Vol 14 (3) ◽  
pp. 453-455 ◽  
Author(s):  
Duc Bui Dang Ha ◽  
Dominique Buffard ◽  
Fr�d�rik Berger ◽  
Colette Br�da ◽  
Robert Esnault
Keyword(s):  
Nucleotide Sequence ◽  
Pearl Millet ◽  
Sequence Encoding ◽  
Slow Allele

The nucleotide sequence encoding bovine opsin

1984 ◽  
Vol 24 (11) ◽  
pp. 1695 ◽  
Author(s):  
W. Baehr ◽  
M.L. Applebury
Keyword(s):  
Nucleotide Sequence ◽  
Sequence Encoding

Nucleotide sequence encoding human pancreatic ribonuclease

1994 ◽  
Vol 1218 (3) ◽  
pp. 466-468 ◽  
Author(s):  
Masaharu Seno ◽  
Jun-ichiro Futami ◽  
Megumi Kosaka ◽  
Satimaru Seno ◽  
Hidenori Yamada
Keyword(s):  
Nucleotide Sequence ◽  
Pancreatic Ribonuclease ◽  
Sequence Encoding ◽  
Human Pancreatic Ribonuclease

Cloning and molecular analysis of the human citrate synthase gene

Genome ◽  
1998 ◽  
Vol 41 (5) ◽  
pp. 733-738 ◽  
Author(s):  
Michael J Goldenthal ◽  
Jose Marin-Garcia ◽  
Radha Ananthakrishnan
Keyword(s):  
Amino Acids ◽  
Nucleotide Sequence ◽  
Human Heart ◽  
Citrate Synthase ◽  
Krebs Cycle ◽  
Chromosome 12 ◽  
Primary Sequence ◽  
Key Words Human ◽  
Human Genomic ◽  
Sequence Encoding

The nucleotide sequence encoding the citrate synthase (CS) gene was determined from the sequencing of the CS cDNA isolated from a human heart cDNA library. The primary sequence of CS deduced from its nucleotide sequence reveals a highly conserved, albeit slightly larger, protein of 466 amino acids, with 95% homology to its pig homologue. The data also indicate that the human genomic CS gene contains no introns, and confirms the location of the human CS gene on chromosome 12.Key words: human, citrate synthase, Krebs' cycle.

Structure and expression of a tandem gene pair in Leishmania donovani that encodes a protein structurally homologous to eucaryotic cation-transporting ATPases

1987 ◽  
Vol 7 (11) ◽  
pp. 3937-3946
Author(s):  
J C Meade ◽  
J Shaw ◽  
S Lemaster ◽  
G Gallagher ◽  
J R Stringer
Keyword(s):  
Amino Acids ◽  
Nucleotide Sequence ◽  
Tandem Repeat ◽  
Base Pair ◽  
Leishmania Donovani ◽  
Oligonucleotide Probe ◽  
Open Reading Frame ◽  
Reading Frame ◽  
Atpase Gene ◽  
Sequence Encoding

An oligonucleotide probe was used to clone a cation-transporting ATPase gene from the genome of Leishmania donovani. The nucleotide sequence of the gene contained a 2,922-base-pair open reading frame that was predicted to encode a 107,406-dalton protein composed of 974 amino acids. The predicted L. donovani protein contained all the structural and functional domains expected to be present in a cation-transporting ATPase of the aspartyl phosphate class. The nucleotide sequence encoding the ATPase gene was duplicated in tandem in the parasite genome. Partial sequenation of the second member of the tandem repeat, which lay 2 kilobase pairs downstream of the ATPase gene, indicated that it was either identical to the first gene or very closely related to it. RNA homologous to either the ATPase gene or its adjacent relative was 5 kilobases in size and was approximately equally abundant in both promastigote and amastigote forms of the organism.

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