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4 leucine --> valine distal pocket mutants of nitrophorin 2 (NP2) and their NO complexes have been inv
5 ter in the NO-storage and -transport protein Nitrophorin 2 (NP2) from the salivary glands of the bloo
7 substituents of the low-spin Fe(III) form of nitrophorin 2, as its complexes with N-methylimidazole (
10 have refined atomic resolution structures of nitrophorin 4 (NP4) from Rhodnius prolixus complexed wit
14 porphine-halides (Fe(P)(X), X = Cl, Br) and nitrophorin 4 (NP4) using femtosecond coherence spectros
17 etermined the crystal structures of Rhodnius nitrophorin 4 to ultrahigh resolution in four functional
18 blood-sucking insect Rhodnius prolixus uses nitrophorin 4, a heme protein, to deliver nitric oxide (
21 serving to stabilize the ferric state of the nitrophorins, a requirement for their physiological func
26 structure are completely unlike those of the nitrophorins from Rhodnius prolixus, where NO protection
28 o acid alignments, it is most similar to the nitrophorin group of lipocalins found in the same insect
30 urprisingly, NO binds not only to the ferric nitrophorin heme, but it can also be stored as an S-nitr
33 nding and absorption spectra for recombinant nitrophorin I were indistinguishable from those of the i
36 sults suggest that tighter NO binding in the nitrophorins is due to the trapping of the molecule in a
37 blood-sucking insect that uses a mixture of nitrophorin (NP) proteins to deliver nitric oxide (NO) f
39 ared 13 site-directed mutants of three major nitrophorins, NP2, NP1, and NP4, to investigate the stab
45 ea, expressly discussed for the heme protein nitrophorin, that porphyrin core distortions could lead
46 structure of the Cimex lectularius (bedbug) nitrophorin, the protein responsible for NO storage and
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