|
|
|
|
| LEADER |
01000naa a22002652 4500 |
| 001 |
NLM334981433 |
| 003 |
DE-627 |
| 005 |
20231225224840.0 |
| 007 |
cr uuu---uuuuu |
| 008 |
231225s2022 xx |||||o 00| ||eng c |
| 024 |
7 |
|
|a 10.1002/jcc.26799
|2 doi
|
| 028 |
5 |
2 |
|a pubmed24n1116.xml
|
| 035 |
|
|
|a (DE-627)NLM334981433
|
| 035 |
|
|
|a (NLM)34962296
|
| 040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
| 041 |
|
|
|a eng
|
| 100 |
1 |
|
|a Barletta, German P
|e verfasserin
|4 aut
|
| 245 |
1 |
0 |
|a Analysis of changes of cavity volumes in predefined directions of protein motions and cavity flexibility
|
| 264 |
|
1 |
|c 2022
|
| 336 |
|
|
|a Text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
| 338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
| 500 |
|
|
|a Date Completed 07.03.2022
|
| 500 |
|
|
|a Date Revised 07.03.2022
|
| 500 |
|
|
|a published: Print-Electronic
|
| 500 |
|
|
|a Citation Status MEDLINE
|
| 520 |
|
|
|a © 2021 Wiley Periodicals LLC.
|
| 520 |
|
|
|a Dynamics of protein cavities associated with protein fluctuations and conformational plasticity is essential for their biological function. NMR ensembles, molecular dynamics (MD) simulations, and normal mode analysis (NMA) provide appropriate frameworks to explore functionally relevant protein dynamics and cavity changes relationships. Within this context, we have recently developed analysis of null areas (ANA), an efficient method to calculate cavity volumes. ANA is based on a combination of algorithms that guarantees its robustness against numerical differentiations. This is a unique feature with respect to other methods. Herein, we present an updated and improved version that expands it use to quantify changes in cavity features, like volume and flexibility, due to protein structural distortions performed on predefined biologically relevant directions, for example, directions of largest contribution to protein fluctuations (principal component analysis [PCA modes]) obtained by MD simulations or ensembles of NMR structures, collective NMA modes or any other direction of motion associated with specific conformational changes. A web page has been developed where its facilities are explained in detail. First, we show that ANA can be useful to explore gradual changes of cavity volume and flexibility associated with protein ligand binding. Secondly, we perform a comparison study of the extent of variability between protein backbone structural distortions, and changes in cavity volumes and flexibilities evaluated for an ensemble of NMR active and inactive conformers of the epidermal growth factor receptor structures. Finally, we compare changes in size and flexibility between sets of NMR structures for different homologous chains of dynein
|
| 650 |
|
4 |
|a Journal Article
|
| 650 |
|
4 |
|a Research Support, Non-U.S. Gov't
|
| 650 |
|
4 |
|a NMA
|
| 650 |
|
4 |
|a Normal Mode Analysis
|
| 650 |
|
4 |
|a PCA
|
| 650 |
|
4 |
|a Principal Component Analysis
|
| 650 |
|
4 |
|a cavities
|
| 650 |
|
4 |
|a flexibility
|
| 650 |
|
4 |
|a protein cavity
|
| 650 |
|
7 |
|a ErbB Receptors
|2 NLM
|
| 650 |
|
7 |
|a EC 2.7.10.1
|2 NLM
|
| 700 |
1 |
|
|a Barletta, Matias
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Saldaño, Tadeo E
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Fernandez-Alberti, Sebastian
|e verfasserin
|4 aut
|
| 773 |
0 |
8 |
|i Enthalten in
|t Journal of computational chemistry
|d 1984
|g 43(2022), 6 vom: 05. März, Seite 391-401
|w (DE-627)NLM098138448
|x 1096-987X
|7 nnns
|
| 773 |
1 |
8 |
|g volume:43
|g year:2022
|g number:6
|g day:05
|g month:03
|g pages:391-401
|
| 856 |
4 |
0 |
|u http://dx.doi.org/10.1002/jcc.26799
|3 Volltext
|
| 912 |
|
|
|a GBV_USEFLAG_A
|
| 912 |
|
|
|a SYSFLAG_A
|
| 912 |
|
|
|a GBV_NLM
|
| 912 |
|
|
|a GBV_ILN_350
|
| 951 |
|
|
|a AR
|
| 952 |
|
|
|d 43
|j 2022
|e 6
|b 05
|c 03
|h 391-401
|