Identification and structure-function analysis of protein-protein interactions in the plant pathogen Xanthomonas axonopodis pv citri (2003)
- Autor:
- Autor USP: FARAH, SHAKER CHUCK - IQ
- Unidade: IQ
- Subjects: BIOQUÍMICA; XANTHOMONAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Programa e Resumos
- Conference titles: Reunião Anual da Sociedade Brasileira de Bioquímica e Biologia Molecular
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ABNT
FARAH, Chuck Shaker. Identification and structure-function analysis of protein-protein interactions in the plant pathogen Xanthomonas axonopodis pv citri. 2003, Anais.. São Paulo: SBBq, 2003. . Acesso em: 11 out. 2024. -
APA
Farah, C. S. (2003). Identification and structure-function analysis of protein-protein interactions in the plant pathogen Xanthomonas axonopodis pv citri. In Programa e Resumos. São Paulo: SBBq. -
NLM
Farah CS. Identification and structure-function analysis of protein-protein interactions in the plant pathogen Xanthomonas axonopodis pv citri. Programa e Resumos. 2003 ;[citado 2024 out. 11 ] -
Vancouver
Farah CS. Identification and structure-function analysis of protein-protein interactions in the plant pathogen Xanthomonas axonopodis pv citri. Programa e Resumos. 2003 ;[citado 2024 out. 11 ] - Stability of troponin I and T investigated by a hydrophobic fluorescent probe
- A tropomyosin mutant containing a intrinsic fluorescent probe may be used to study head-to-tail interaction thermodynamics
- Structural genomics of the phytopathogen Xanthomonas axonopodis pv citri
- Ca2+-induced rolling of tropomyosin in muscle thin filaments - The alpha- and beta-band hypothesis revisited
- A specific C-terminal deletion in tropomyosin results in a stronger head-to-tail interaction and increased polymerization
- New protein fold from Xanthomonas axonopodis pv citri YaeQ
- Calcium binding to Leptospira outer membrane antigen LipL32 is not necessary for its interaction with plasma fibronectin, collagen type IV, and plasminogen
- High-throughput screening of Xanthomonas axonopodis pv citri targets for structural proteomics using NMR
- Strategy for determining the binding site of tropomyosin on actin
- Deciphering the head-to-tail complex of 'alpha'-tropomyosin using double mutant cycles and molecular docking
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