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Article title matches
- Category:Turk B (37 bytes)
1: List of pages with the keyword Turk B - Category:Turk, D (38 bytes)
1: List of pages with the keyword Turk, D - Category:Turk, S (38 bytes)
1: List of pages with the keyword Turk, S - Category:Turk, V (38 bytes)
1: List of pages with the keyword Turk, V - Category:Turk, B (38 bytes)
1: List of pages with the keyword Turk, B - Category:Turk, D A (40 bytes)
1: List of pages with the keyword Turk, D A - Category:Turk, M (38 bytes)
1: List of pages with the keyword Turk, M - Category:Turk V (37 bytes)
1: List of pages with the keyword Turk V - Category:Turk S (37 bytes)
1: List of pages with the keyword Turk S - Category:Turk, L S (40 bytes)
1: List of pages with the keyword Turk, L S - Category:Turk M (37 bytes)
1: List of pages with the keyword Turk M - Category:Turk D (37 bytes)
1: List of pages with the keyword Turk D - Category:Turk DA (38 bytes)
1: List of pages with the keyword Turk DA - Category:Turk BE (38 bytes)
1: List of pages with the keyword Turk BE - Category:Turk LS (38 bytes)
1: List of pages with the keyword Turk LS
Page text matches
- 8pch (4,913 bytes)
2: ...AL CARBOXYL GROUP DEFINES CATHEPSIN H AMINOPEPTIDASE FUNCTION==
3: ...'[[8pch]], [[Resolution|resolution]] 2.10Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=8PCH FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1Å</td></tr> - 2j90 (7,182 bytes)
2: ==Crystal structure of human ZIP kinase in complex with a tetracyclic pyridone inhibitor...
3: ...'[[2j90]], [[Resolution|resolution]] 2.00Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=2J90 FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2Å</td></tr> - 1ai8 (8,605 bytes)
2: ...LEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG==
3: ...'[[1ai8]], [[Resolution|resolution]] 1.85Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1AI8 FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.85Å</td></tr> - 2j51 (4,662 bytes)
2: ...an STE20-like kinase bound to 5-Amino-3-((4-(aminosulfonyl)phenyl)amino) -N-(2,6-difluorophenyl)-1H-1...
3: ...'[[2j51]], [[Resolution|resolution]] 2.10Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=2J51 FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1Å</td></tr> - 2jfl (4,823 bytes)
2: ...HOSPHORYLATED FORM) BOUND TO 5- AMINO-3-((4-(AMINOSULFONYL)PHENYL)AMINO)-N-(2,6- DIFLUOROPHENYL)-1H-1...
3: ...'[[2jfl]], [[Resolution|resolution]] 2.20Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=2JFL FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.2Å</td></tr> - 2jfm (4,276 bytes)
2: ==CRYSTAL STRUCTURE OF HUMAN STE20-LIKE KINASE (UNLIGANDED FORM)==
3: ...'[[2jfm]], [[Resolution|resolution]] 2.85Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=2JFM FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.85Å</td></tr> - 1qj7 (6,939 bytes)
2: ==Novel Covalent Active Site Thrombin Inhibitors==
3: ...'[[1qj7]], [[Resolution|resolution]] 2.20Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1QJ7 FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.2Å</td></tr> - 4iyb (1,781 bytes)
2: ... ricin B-like lectin (MPL) in complex with galactose==
3: ...'[[4iyb]], [[Resolution|resolution]] 1.59Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=4IYB FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.59Å</td></tr> - 2uv2 (4,935 bytes)
2: ==Crystal Structure Of Human Ste20-Like Kinase Bound To 4-(4-(5- Cyclopropyl-1H-pyrazol-3-ylami...
3: ...'[[2uv2]], [[Resolution|resolution]] 2.30Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=2UV2 FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.3Å</td></tr> - 2j7t (5,481 bytes)
2: ...ture of human serine threonine kinase-10 bound to SU11274==
3: ...'[[2j7t]], [[Resolution|resolution]] 2.00Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=2J7T FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2Å</td></tr> - 1a3b (8,275 bytes)
3: ...'[[1a3b]], [[Resolution|resolution]] 1.80Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1A3B FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8Å</td></tr>
7: ...29:TRI166+(BIFUNCTIONAL+BORONATE+INHIBITOR)'>T29</scene></td></tr> - 1a3e (6,024 bytes)
3: ...'[[1a3e]], [[Resolution|resolution]] 1.85Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1A3E FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.85Å</td></tr>
7: ...andDat"><scene name='pdbligand=T16:BOROLOG2'>T16</scene></td></tr> - 1aix (8,626 bytes)
2: ...COMPLEX WITH EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROVAL==
3: ...'[[1aix]], [[Resolution|resolution]] 2.10Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1AIX FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1Å</td></tr> - 1bbr (5,004 bytes)
2: ...NOGEN BOUND TO BOVINE THROMBIN AT 2.3 ANGSTROMS RESOLUTION==
3: ...'[[1bbr]], [[Resolution|resolution]] 2.30Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1BBR FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.3Å</td></tr> - 1buv (5,163 bytes)
2: ==CRYSTAL STRUCTURE OF THE MT1-MMP-TIMP-2 COMPLEX==
3: ...'[[1buv]], [[Resolution|resolution]] 2.75Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1BUV FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.75Å</td></tr> - 1csb (4,293 bytes)
2: ...for the design of specific epoxysuccinyl inhibitors==
3: ...'[[1csb]], [[Resolution|resolution]] 2.00Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1CSB FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2Å</td></tr> - 1dvc (5,094 bytes)
2: ...EFIN A AT PH 5.5 AND 308K, NMR, MINIMIZED AVERAGE STRUCTURE==
3: ...='1dvc' size='340' side='right'caption='[[1dvc]]' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1DVC FirstGlance]. <br>
6: ...d:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> - 1dvd (5,080 bytes)
2: ...MAN STEFIN A AT PH 5.5 AND 308K, NMR, 17 STRUCTURES==
3: ...='1dvd' size='340' side='right'caption='[[1dvd]]' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1DVD FirstGlance]. <br>
6: ...d:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> - 1ef7 (4,435 bytes)
2: ==CRYSTAL STRUCTURE OF HUMAN CATHEPSIN X==
3: ...'[[1ef7]], [[Resolution|resolution]] 2.67Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1EF7 FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.67Å</td></tr> - 1huc (5,042 bytes)
2: ...N LIVER CATHEPSIN B: THE STRUCTURAL BASIS FOR ITS SPECIFICITY==
3: ...'[[1huc]], [[Resolution|resolution]] 2.10Å' scene=''>
4: == Structural highlights ==
5: ... [https://proteopedia.org/fgij/fg.htm?mol=1HUC FirstGlance]. <br>
6: ... id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1Å</td></tr>
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