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1.
J Bacteriol ; 195(16): 3714-23, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23772067

RESUMO

NodD1, a member of the NodD family of LysR-type transcriptional regulators (LTTRs), mediates nodulation (nod) gene expression in the soil bacterium Sinorhizobium meliloti in response to the plant-secreted flavonoid luteolin. We used genetic screens and targeted approaches to identify NodD1 residues that show altered responses to luteolin during the activation of nod gene transcription. Here we report four types of NodD1 mutants. Type I (NodD1 L69F, S104L, D134N, and M193I mutants) displays reduced or no activation of nod gene expression. Type II (NodD1 K205N) is constitutively active but repressed by luteolin. Type III (NodD1 L280F) demonstrates enhanced activity with luteolin compared to that of wild-type NodD1. Type IV (NodD1 D284N) shows moderate constitutive activity yet can still be induced by luteolin. In the absence of luteolin, many mutants display a low binding affinity for nod gene promoter DNA in vitro. Several mutants also show, as does wild-type NodD1, increased affinity for nod gene promoters with added luteolin. All of the NodD1 mutant proteins can homodimerize and heterodimerize with wild-type NodD1. Based on these data and the crystal structures of several LTTRs, we present a structural model of wild-type NodD1, identifying residues important for inducer binding, protein multimerization, and interaction with RNA polymerase at nod gene promoters.


Assuntos
Regulação Bacteriana da Expressão Gênica/efeitos dos fármacos , Luteolina/farmacologia , Sinorhizobium meliloti/metabolismo , Fatores de Transcrição/metabolismo , Alelos , Proteínas de Bactérias , DNA Bacteriano/metabolismo , Modelos Moleculares , Mutação , Ligação Proteica , Conformação Proteica , Sinorhizobium meliloti/genética , Fatores de Transcrição/genética
2.
J Comput Biol ; 18(1): 17-26, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21210729

RESUMO

Most current template-based structure prediction methods concentrate on finding the correct backbone conformation and then packing sidechains within that backbone. Our packing-based method derives distance constraints from conserved relative packing groups (RPGs). In our refinement approach, the RPGs provide a level of resolution that restrains global topology while allowing conformational sampling. In this study, we test our template-based structure prediction method using 51 prediction units from CASP7 experiments. RPG-based constraints are able to substantially improve approximately two-thirds of starting templates. Upon deeper investigation, we find that true positive spatial constraints, especially those non-local in sequence, derived from the RPGs were important to building nearer native models. Surprisingly, the fraction of incorrect or false positive constraints does not strongly influence the quality of the final candidate. This result indicates that our RPG-based true positive constraints sample the self-consistent, cooperative interactions of the native structure. The lack of such reinforcing cooperativity explains the weaker effect of false positive constraints. Generally, these findings are encouraging indications that RPGs will improve template-based structure prediction.


Assuntos
Caspase 7/química , Modelos Moleculares , Homologia Estrutural de Proteína , Algoritmos , Simulação por Computador , Humanos , Conformação Proteica
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