| Interacting proteins: Q9NV31 and Q96G21 |
Pubmed |
SVM Score :0.0 |
| NA |
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| Interacting proteins: Q9NV31 and Q96G21 |
Pubmed |
SVM Score :0.0 |
| Similarly , other 90 S particle components such as Imp 3 and Imp 4 do not associate with the pre rRNA precursor in the absence of Pwp 2 . ^^^ |
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| Interacting proteins: Q9NV31 and Q96G21 |
Pubmed |
SVM Score :0.0 |
| Two of the strains ( imp 3 and imp 4 ) carry leaky mutations that affect cell fusion ; neither mutation is found by tetrad analysis to be linked to mt or to the other . ^^^ |
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| Interacting proteins: Q9NV31 and Q96G21 |
Pubmed |
SVM Score :0.0 |
| IMP 5 beta lactamase showed a greater homology with IMP 1 , IMP 3 and IMP 4 ( identified in Southeast Asia ) , than with IMP 2 , found in Italy ( 93 % , 92 % , 91 % and 87 % of amino acid identity , respectively ) . bla ( IMP 5 ) was the only gene cassette inserted into a class 1 integron , named In 76 . ^^^ |
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| Interacting proteins: Q9NV31 and Q96G21 |
Pubmed |
SVM Score :0.0 |
| The human Imp 3 and Imp 4 proteins form a ternary complex with hMpp 10 , which only interacts with the U 3 snoRNA in 60 80S ribonucleoprotein complexes . ^^^ We have cloned cDNAs encoding the human and mouse homologs of the yeast U 3 snoRNP associated proteins Imp 3 and Imp 4 . ^^^ The results of complementation experiments show that , in contrast to mouse Imp 4 , mouse Imp 3 can partially alleviate the growth defect of the corresponding yeast null strain , indicating that the role of Imp 3 in pre rRNA processing is evolutionarily conserved . ^^^ The results of density gradient centrifugation experiments show that , in contrast to hU 3 55K , the human Imp 3 and Imp 4 proteins predominantly interact with the U 3 snoRNA in 60 80S ribonucleoprotein complexes . ^^^ |
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