| 000 | 03385nam a22004575i 4500 | ||
|---|---|---|---|
| 999 |
_c88221 _d88221 _x1 |
||
| 001 | 88221 | ||
| 003 | ES-MaUEC | ||
| 005 | 20230207040628.0 | ||
| 006 | a||||fo|||| 00| 0 | ||
| 007 | cr nn 008mamaa | ||
| 008 | 170124s2016 gw | s |||| 0|eng d | ||
| 020 | _a9783319473888 | ||
| 024 | 7 |
_a10.1007/978-3-319-47388-8 _2doi |
|
| 040 |
_aES-MaUEC _bspa _cES-MaUEC _dES-MaUEC |
||
| 050 | 4 |
_aQH324.2 _b2016 EB |
|
| 100 | 1 |
_aKoča, Jaroslav _9101774 _0Local |
|
| 245 | 1 | 0 |
_aStructural Bioinformatics Tools for Drug Design : _bExtraction of Biologically Relevant Information from Structural Databases _cby Jaroslav Koca, Radka Svobodová Vareková, Luká Pravda, Karel Berka, Stanislav Geidl, David Sehnal, Michal Otyepka |
| 264 | 1 |
_aCham _bSpringer International Publishing _c2016 |
|
| 300 |
_a1 recurso en línea (XIII, 144 páginas) _b62 ilustraciones |
||
| 336 |
_aTexto (visual) _btxt _2rdacontent |
||
| 337 |
_aelectrónico _bc _2rdamedia |
||
| 338 |
_arecurso electrónico _bcr _2rdacarrier |
||
| 490 | 1 |
_aSpringerBriefs in Biochemistry and Molecular Biology _x2211-9353 |
|
| 505 | 0 | _a1. Introduction -- 2. Biomacromolecular fragments -- 3. Databases -- 4. Detection & Extraction -- a. Biomacromolecular fragments and structural patterns -- b. channels and pores -- 5. Validation -- 6. Characterization -- a. Partial atomic charges -- b. Channel characteristics -- 7. Selected Examples. | |
| 520 | _aA large amount of structural data on biomacromolecules is available and the number of resolved structures is growing rapidly. This implies that we have an increasing opportunity to perform so far unprecedented analyses to obtain crucial biological insight. Biomacromolecular structural fragments such as binding sites or active sites, ligands, channels, pores, secondary structure motifs, etc., become very promising objects for these analyses because such fragments often serve as drug targets or drug templates, or substrate-specific pathways. However, such analyses are very challenging due to their complexity and, consequently, also because they require application of a combination of different software tools. In this book, we describe individual steps necessary for analysis of biomacromolecular fragments and provide a lsit of software tools required to perform such steps. For each step, we also show corresponding web-based tools in detail and provide a few practical examples of their usage. | ||
| 988 | _aEBOOK, EBSPRINGER | ||
| 650 | 7 |
_aBioinformática _2embne _9160489 |
|
| 650 | 7 |
_aDrogas de diseño _2embne _9157991 |
|
| 700 | 1 |
_aSvobodová Vareková, Radka. _9101775 _0Local |
|
| 700 |
_aPravda, Luká _9101776 _0Local |
||
| 700 | 1 |
_aBerka, Karel _0Local _9101777 |
|
| 700 | 1 |
_aGeidl, Stanislav _0Local _9101778 |
|
| 700 | 1 |
_aSehnal, David. _9101779 _0Local |
|
| 700 | 1 |
_aOtyepka, Michal. _9101780 _0Local |
|
| 830 | 0 |
_aSpringerBriefs in Biochemistry and Molecular Biology _x2211-9353 _0http://id.loc.gov/authorities/names/no2012070367 _9133204 |
|
| 856 | 4 | 0 | _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-3-319-47388-8zAcceso a este recurso digital (usuarios Universidad Europea de Madrid) |
| 907 |
_a.b12982258 _b10-10-17 _c08-03-17 |
||
| 942 |
_2lcc _cLE |
||
| 945 |
_g1 _ieBOOK _j0 _lmae _o- _pEUR0.00 _q- _r- _sb _t15 _u0 _v0 _w0 _x0 _y.i11604098 _z06-04-17 |
||
| 998 |
_b06/2020 _dz _eu _feng _ggw _h0 |
||