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Article title matches
- Category:Vigers, G P.A (44 bytes)
1: List of pages with the keyword Vigers, G P.A - Category:Vigers GPA (41 bytes)
1: List of pages with the keyword Vigers GPA - Category:Vigers G (39 bytes)
1: List of pages with the keyword Vigers G - Category:Vigers, G (40 bytes)
1: List of pages with the keyword Vigers, G - Category:Vigers, G P (42 bytes)
1: List of pages with the keyword Vigers, G P - Category:Vigers, G.P (42 bytes)
1: List of pages with the keyword Vigers, G.P - Category:Vigers GP (40 bytes)
1: List of pages with the keyword Vigers GP - Category:Vigers, G.P.A (44 bytes)
1: List of pages with the keyword Vigers, G.P.A - Category:Vigers, M (40 bytes)
1: List of pages with the keyword Vigers, M
Page text matches
- 1g0y (2,928 bytes)
2: ...RECEPTOR TYPE 1 COMPLEXED WITH ANTAGONIST PEPTIDE AF10847==
3: ...caption='[[1g0y]], [[Resolution|resolution]] 3.00Å' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=1G0Y FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3&#8491;</td></tr... - 1ilt (3,971 bytes)
2: ...CTURE OF INTERLEUKIN-1 RECEPTOR ANTAGONIST AT 2.0 ANGSTROMS RESOLUTION==
3: ...caption='[[1ilt]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=1ILT FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2&#8491;</td></tr... - 1itb (2,807 bytes)
2: ...LEUKIN-1 RECEPTOR COMPLEXED WITH INTERLEUKIN-1 BETA==
3: ...caption='[[1itb]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=1ITB FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.5&#8491;</td></... - 3omv (8,175 bytes)
2: ==Crystal structure of c-raf (raf-1)==
3: ...caption='[[3omv]], [[Resolution|resolution]] 4.00&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3OMV FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 4&#8491;</td></tr... - 3d4q (5,855 bytes)
2: ==Pyrazole-based inhibitors of B-Raf kinase==
3: ...caption='[[3d4q]], [[Resolution|resolution]] 2.80&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3D4Q FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.8&#8491;</td></... - Category:Vigers, G P.A (44 bytes)
1: List of pages with the keyword Vigers, G P.A - 3o96 (11,113 bytes)
2: ==Crystal Structure of Human AKT1 with an Allosteric Inhibitor==
3: ...caption='[[3o96]], [[Resolution|resolution]] 2.70&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3O96 FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.7&#8491;</td></... - 3ocb (10,811 bytes)
2: ==Akt1 kinase domain with pyrrolopyrimidine inhibitor==
3: ...caption='[[3ocb]], [[Resolution|resolution]] 2.70&Aring;' scene=''>
4: == Structural highlights ==
5: ...izmann.ac.il/oca-docs/fgij/fg.htm?mol=3OCB FirstGlance]. <br>
6: ...ROLO[2,3-D]PYRIMIDIN-4-YL)PIPERAZIN-1-YL]PROPAN-1-AMINE'>XM1</scene></td></tr> - 3ow3 (5,606 bytes)
2: ...othieno- and dihydrofuropyrimidines as potent pan Akt inhibitors==
3: ...caption='[[3ow3]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3OW3 FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9&#8491;</td></... - 3ow4 (9,186 bytes)
2: ...othieno- and dihydrofuropyrimidines as potent pan Akt inhibitors==
3: ...caption='[[3ow4]], [[Resolution|resolution]] 2.60&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3OW4 FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.6&#8491;</td></... - 3ppj (5,147 bytes)
2: ==Human B-Raf Kinase in Complex with a Furopyridine Inhibitor==
3: ...caption='[[3ppj]], [[Resolution|resolution]] 3.70&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3PPJ FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.7&#8491;</td></... - 3ppk (5,156 bytes)
2: ...uman B-Raf Kinase in Complex with a Non-Oxime Furopyridine Inhibitor==
3: ...caption='[[3ppk]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3PPK FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3&#8491;</td></tr... - 3prf (5,166 bytes)
2: ...Raf Kinase Domain in Complex with a Non-Oxime Furopyridine Inhibitor==
3: ...caption='[[3prf]], [[Resolution|resolution]] 2.90&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3PRF FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.9&#8491;</td></... - 3pri (5,175 bytes)
2: ...uman B-Raf Kinase in Complex with a Non-Oxime Furopyridine Inhibitor==
3: ...caption='[[3pri]], [[Resolution|resolution]] 3.50&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3PRI FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.5&#8491;</td></... - 3psb (6,023 bytes)
2: ...-based Indanone Oximes as Potent and Selective B-Raf Inhibitors==
3: ...caption='[[3psb]], [[Resolution|resolution]] 3.40&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3PSB FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.4&#8491;</td></... - 3psd (5,963 bytes)
2: ==Non-oxime pyrazole based inhibitors of B-Raf kinase==
3: ...caption='[[3psd]], [[Resolution|resolution]] 3.60&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3PSD FirstGlance]. <br>
6: ...d><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.6&#8491;</td></... - 3qkk (11,177 bytes)
2: ==Spirochromane Akt Inhibitors==
3: ...caption='[[3qkk]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3QKK FirstGlance]. <br>
6: ...-PIPERIDIN]-1-YL]PROPYL}-2,6-DIMETHYLBENZENESULFONAMIDE'>SMH</scene></td></tr> - 3qkl (11,177 bytes)
2: ==Spirochromane Akt Inhibitors==
3: ...caption='[[3qkl]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3QKL FirstGlance]. <br>
6: ...ROPYL}-N-(2-ETHOXYETHYL)-2,6-DIMETHYLBENZENESULFONAMIDE'>SMR</scene></td></tr> - 3qkm (11,199 bytes)
2: ==Spirocyclic sulfonamides as AKT inhibitors==
3: ...caption='[[3qkm]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=3QKM FirstGlance]. <br>
6: ...IRO[4.5]DEC-7-YL]PROPYL}-2,6-DIMETHYLBENZENESULFONAMIDE'>SM9</scene></td></tr> - 4ekk (10,609 bytes)
2: ==Akt1 with AMP-PNP==
3: ...caption='[[4ekk]], [[Resolution|resolution]] 2.80&Aring;' scene=''>
4: == Structural highlights ==
5: ...tps://proteopedia.org/fgij/fg.htm?mol=4EKK FirstGlance]. <br>
6: ...e>, <scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
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