scholarly article | Q13442814 |
P819 | ADS bibcode | 2012PNAS..10917772G |
P356 | DOI | 10.1073/PNAS.1201794109 |
P932 | PMC publication ID | 3497760 |
P698 | PubMed publication ID | 22652570 |
P5875 | ResearchGate publication ID | 225085918 |
P50 | author | Angela Morrone | Q114448145 |
Carlo Travaglini Allocatelli | Q33273334 | ||
Maurizio Brunori | Q33274063 | ||
Rajanish Giri | Q37367373 | ||
Stefano Gianni | Q42424774 | ||
P2093 | author name string | Per Jemth | |
P2860 | cites work | The design and characterization of two proteins with 88% sequence identity but different structure and function | Q24680766 |
NMR structures of two designed proteins with high sequence identity but different fold and function | Q27652181 | ||
A minimal sequence code for switching protein structure and function | Q27658235 | ||
The folding of an enzyme. I. Theory of protein engineering analysis of stability and pathway of protein folding | Q28306201 | ||
Lever-arm mechanics of processive myosins | Q28743071 | ||
Unfolding free energy changes determined by the linear extrapolation method. 1. Unfolding of phenylmethanesulfonyl alpha-chymotrypsin using different denaturants | Q29617228 | ||
Funnels, pathways, and the energy landscape of protein folding: a synthesis | Q29617521 | ||
Experiment and theory highlight role of native state topology in SH3 folding | Q30175284 | ||
The folding transition state between SH3 domains is conformationally restricted and evolutionarily conserved. | Q30175285 | ||
Changes of protein folding pathways by circular permutation. Overlapping nuclei promote global cooperativity | Q81475972 | ||
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Comparison of successive transition states for folding reveals alternative early folding pathways of two homologous proteins | Q30485355 | ||
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A conserved folding mechanism for PDZ domains | Q33275051 | ||
Optimization of rates of protein folding: the nucleation-condensation mechanism and its implications | Q33739669 | ||
Phi-value analysis and the nature of protein-folding transition states | Q34330816 | ||
The denatured state dictates the topology of two proteins with almost identical sequence but different native structure and function | Q34537052 | ||
GB1 is not a two-state folder: identification and characterization of an on-pathway intermediate | Q35342463 | ||
The family feud: do proteins with similar structures fold via the same pathway? | Q36046430 | ||
Transient aggregates in protein folding are easily mistaken for folding intermediates | Q36178839 | ||
Malleability of protein folding pathways: a simple reason for complex behaviour | Q36717597 | ||
Folding dynamics and mechanism of beta-hairpin formation | Q36890665 | ||
From the first protein structures to our current knowledge of protein folding: delights and scepticisms | Q37199653 | ||
Folding and stability of globular proteins and implications for function | Q37373854 | ||
Characterisation of transition state structures for protein folding using 'high', 'medium' and 'low' {Phi}-values | Q38632179 | ||
Exploring the cytochrome c folding mechanism: cytochrome c552 from thermus thermophilus folds through an on-pathway intermediate | Q42169209 | ||
Structural analysis of the rate-limiting transition states in the folding of Im7 and Im9: similarities and differences in the folding of homologous proteins | Q44290691 | ||
A common folding mechanism in the cytochrome c family | Q45079922 | ||
Engineering subtilisin into a fluoride-triggered processing protease useful for one-step protein purification. | Q51581149 | ||
Development of the multiple sequence approximation within the AGADIR model of alpha-helix formation: comparison with Zimm-Bragg and Lifson-Roig formalisms. | Q52267131 | ||
An integrated kinetic analysis of intermediates and transition states in protein folding reactions. | Q52323750 | ||
Specific nucleus as the transition state for protein folding: evidence from the lattice model. | Q52372545 | ||
The Structure of the Transition State for Folding of Chymotrypsin Inhibitor 2 Analysed by Protein Engineering Methods: Evidence for a Nucleation-condensation Mechanism for Protein Folding | Q57823358 | ||
Structural characterization of a misfolded intermediate populated during the folding process of a PDZ domain | Q58069943 | ||
Engineered Symmetric Connectivity of Secondary Structure Elements Highlights Malleability of Protein Folding Pathways | Q58069954 | ||
Folding studies of immunoglobulin-like β-sandwich proteins suggest that they share a common folding pathway | Q60162505 | ||
Three-state model for lysozyme folding: triangular folding mechanism with an energetically trapped intermediate | Q73542293 | ||
P433 | issue | 44 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | protein structure | Q735188 |
protein folding | Q847556 | ||
P1104 | number of pages | 5 | |
P304 | page(s) | 17772-17776 | |
P577 | publication date | 2012-05-31 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Folding pathways of proteins with increasing degree of sequence identities but different structure and function | |
P478 | volume | 109 |
Q42161709 | Better theoretical models and protein design experiments can help to understand protein folding |
Q85319860 | Chemical physics of protein folding |
Q89727245 | Effects of Topology and Sequence in Protein Folding Linked via Conformational Fluctuations |
Q51654036 | Examination of the quality of various force fields and solvation models for the equilibrium simulations of GA88 and GB88. |
Q38927110 | How cooperative are protein folding and unfolding transitions? |
Q61813463 | Investigating the Molecular Basis of the Aggregation Propensity of the Pathological D76N Mutant of Beta-2 Microglobulin: Role of the Denatured State |
Q41149978 | Kinetic and thermodynamic studies reveal chemokine homologues CC11 and CC24 with an almost identical tertiary structure have different folding pathways |
Q51601311 | Molecular dynamics simulations on the conformational transitions from the GA 98 (GA 88) to GB 98 (GB 88) proteins. |
Q35875154 | Protein folding of the SAP domain, a naturally occurring two-helix bundle |
Q41702344 | Protein folding, misfolding and aggregation: The importance of two-electron stabilizing interactions. |
Q34319454 | Take home lessons from studies of related proteins |
Q30388845 | Theoretical Insights into the Biophysics of Protein Bi-stability and Evolutionary Switches |
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