MATCH (Memetic Algorithm and Combinatorial Optimization Heuristics) is a new memetic algorithm for automated sequence-specific polypeptide backbone NMR assignment of proteins. MATCH employs local optimization for tracing partial sequence-specific assignments within a global, population-based search environment, where the simultaneous application of local and global optimization heuristics guarantees high efficiency and robustness. MATCH thus makes combined use of the two predominant concepts in use for automated NMR assignment of proteins. Dynamic transition and inherent mutation are new techniques that enable automatic adaptation to variable quality of the experimental input data. The concept of dynamic transition is incorporated in all ma...
Protein NMR peak assignment refers to the process of assigning a group of “spin systems” obtained ex...
Protein NMR peak assignment refers to the process of assigning a group of “spin systems” obtained ex...
Over the past decade, a number of methods have been developed to determine the approximate structure...
<div><p>ADAPT-NMR (Assignment-directed Data collection Algorithm utilizing a Probabilistic Toolkit i...
NMR spectroscopy is one of the two methods for determining the structures of proteins. The producti...
NMR spectroscopy is one of the two methods for determining the structures of proteins. The producti...
We present a new program, PASA (Program for Automated Sequential Assignment), for assigning protein ...
The sequential assignment of backbone resonances is the first step in the structure determination of...
A novel automated approach for the sequence specific NMR assignments of 1HN, 13Cα, 13Cβ, 1...
Despite significant advances in automated nuclear magnetic resonance-based protein structure determi...
Nuclear magnetic resonance spectroscopy of proteins (protein NMR) is a powerful analytical technique...
Nuclear magnetic resonance spectroscopy of proteins (protein NMR) is a powerful analytical technique...
The necessity to acquire large multidimensional datasets, a basis for assignment of NMR resonances, ...
Nuclear magnetic resonance spectroscopy of proteins (protein NMR) is a powerful analytical technique...
High-throughput NMR structural biology can play an important role in structural genomics. We report ...
Protein NMR peak assignment refers to the process of assigning a group of “spin systems” obtained ex...
Protein NMR peak assignment refers to the process of assigning a group of “spin systems” obtained ex...
Over the past decade, a number of methods have been developed to determine the approximate structure...
<div><p>ADAPT-NMR (Assignment-directed Data collection Algorithm utilizing a Probabilistic Toolkit i...
NMR spectroscopy is one of the two methods for determining the structures of proteins. The producti...
NMR spectroscopy is one of the two methods for determining the structures of proteins. The producti...
We present a new program, PASA (Program for Automated Sequential Assignment), for assigning protein ...
The sequential assignment of backbone resonances is the first step in the structure determination of...
A novel automated approach for the sequence specific NMR assignments of 1HN, 13Cα, 13Cβ, 1...
Despite significant advances in automated nuclear magnetic resonance-based protein structure determi...
Nuclear magnetic resonance spectroscopy of proteins (protein NMR) is a powerful analytical technique...
Nuclear magnetic resonance spectroscopy of proteins (protein NMR) is a powerful analytical technique...
The necessity to acquire large multidimensional datasets, a basis for assignment of NMR resonances, ...
Nuclear magnetic resonance spectroscopy of proteins (protein NMR) is a powerful analytical technique...
High-throughput NMR structural biology can play an important role in structural genomics. We report ...
Protein NMR peak assignment refers to the process of assigning a group of “spin systems” obtained ex...
Protein NMR peak assignment refers to the process of assigning a group of “spin systems” obtained ex...
Over the past decade, a number of methods have been developed to determine the approximate structure...