Id |
Subject |
Object |
Predicate |
Lexical cue |
T1 |
0-62 |
Sentence |
denotes |
Nitric oxide-stimulated guanine nucleotide exchange on p21ras. |
T1 |
0-62 |
Sentence |
denotes |
Nitric oxide-stimulated guanine nucleotide exchange on p21ras. |
T2 |
63-222 |
Sentence |
denotes |
The protooncogene p21ras, a monomeric G protein family member, plays a critical role in converting extracellular signals into intracellular biochemical events. |
T2 |
63-222 |
Sentence |
denotes |
The protooncogene p21ras, a monomeric G protein family member, plays a critical role in converting extracellular signals into intracellular biochemical events. |
T3 |
223-344 |
Sentence |
denotes |
Here, we report that nitric oxide (NO) activates p21ras in human T cells as evidenced by an increase in GTP-bound p21ras. |
T3 |
223-344 |
Sentence |
denotes |
Here, we report that nitric oxide (NO) activates p21ras in human T cells as evidenced by an increase in GTP-bound p21ras. |
T4 |
345-449 |
Sentence |
denotes |
In vitro studies using pure recombinant p21ras demonstrate that the activation is direct and reversible. |
T4 |
345-449 |
Sentence |
denotes |
In vitro studies using pure recombinant p21ras demonstrate that the activation is direct and reversible. |
T5 |
450-582 |
Sentence |
denotes |
Circular dichroism analysis reveals that NO induces a profound conformational change in p21ras in association with GDP/GTP exchange. |
T5 |
450-582 |
Sentence |
denotes |
Circular dichroism analysis reveals that NO induces a profound conformational change in p21ras in association with GDP/GTP exchange. |
T6 |
583-713 |
Sentence |
denotes |
The mechanism of activation is due to S-nitrosylation of a critical cysteine residue which stimulates guanine nucleotide exchange. |
T6 |
583-713 |
Sentence |
denotes |
The mechanism of activation is due to S-nitrosylation of a critical cysteine residue which stimulates guanine nucleotide exchange. |
T7 |
714-895 |
Sentence |
denotes |
Furthermore, we demonstrate that p21ras is essential for NO-induced downstream signaling, such as NF-kappa B activation, and that endogenous NO can activate p21ras in the same cell. |
T7 |
714-895 |
Sentence |
denotes |
Furthermore, we demonstrate that p21ras is essential for NO-induced downstream signaling, such as NF-kappa B activation, and that endogenous NO can activate p21ras in the same cell. |
T8 |
896-955 |
Sentence |
denotes |
These studies identify p21ras as a target of the same cell. |
T8 |
896-955 |
Sentence |
denotes |
These studies identify p21ras as a target of the same cell. |
T9 |
956-1122 |
Sentence |
denotes |
These studies identify p21ras as a target of NO in T cells and suggest that NO activates p21ras by an action which mimics that of guanine nucleotide exchange factors. |
T9 |
956-1122 |
Sentence |
denotes |
These studies identify p21ras as a target of NO in T cells and suggest that NO activates p21ras by an action which mimics that of guanine nucleotide exchange factors. |