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Article title matches

  1. Category:Finer-Moore, J S (47 bytes)
    1: List of pages with the keyword Finer-Moore, J S
  2. Category:Moore D (38 bytes)
    1: List of pages with the keyword Moore D
  3. Category:Finer-Moore JS (45 bytes)
    1: List of pages with the keyword Finer-Moore JS
  4. Category:Moore MM (39 bytes)
    1: List of pages with the keyword Moore MM
  5. Category:Moore RJ (39 bytes)
    1: List of pages with the keyword Moore RJ
  6. Category:Moore GR (39 bytes)
    1: List of pages with the keyword Moore GR
  7. Category:Moore BA (39 bytes)
    1: List of pages with the keyword Moore BA
  8. Category:Moore GS (39 bytes)
    1: List of pages with the keyword Moore GS
  9. Category:Moore, P B. (47 bytes)
    1: List of structures with the keyword Moore, P B.
  10. Category:Moore, G R. (42 bytes)
    1: List of pages with the keyword Moore, G R.
  11. Category:Moore, P B (41 bytes)
    1: List of pages with the keyword Moore, P B
  12. Category:Moore DT (39 bytes)
    1: List of pages with the keyword Moore DT
  13. Category:Moore M (38 bytes)
    1: List of pages with the keyword Moore M
  14. Category:Moore JM (39 bytes)
    1: List of pages with the keyword Moore JM
  15. Category:Moore JP (39 bytes)
    1: List of pages with the keyword Moore JP
  16. User:Reta Moore Shiver (531 bytes)
    1: * Full Real Name: Reta Moore Shiver
    3: ...nd DNA results that have been given to me which I believe are flawed or incorrect.
    5: * Institution (NO ABBREVIATIONS): None
    10: ... Biology, M.ED. (Social Work Foundations), PhD, Public Adminatration
  17. Category:Moore JD (39 bytes)
    1: List of pages with the keyword Moore JD
  18. Category:Moore JE (39 bytes)
    1: List of pages with the keyword Moore JE
  19. Category:Moore, J G (41 bytes)
    1: List of pages with the keyword Moore, J G
  20. Category:Moore, R S (41 bytes)
    1: List of pages with the keyword Moore, R S

Page text matches

  1. 1jmh (2,602 bytes)
    2: ==CONTRIBUTIONS OF ORIENTATION AND HYDROGEN BONDING TO CATALYSIS IN ASN-229 MUTANTS OF THYMIDYL...
    5: ...oteopedia.org/fgij/fg.htm?mol=1JMH FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...d class="sblockDat" id="ligandDat"><scene name='pdbligand=UMP:2-DEOXYURIDINE+5-MONOPHOSPHATE'>UMP</sc...
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1jmh ProSAT]</span></td></tr>
  2. 1jmf (2,602 bytes)
    2: ==CONTRIBUTIONS OF ORIENTATION AND HYDROGEN BONDING TO CATALYSIS IN ASN-229 MUTANTS OF THYMIDYL...
    5: ...oteopedia.org/fgij/fg.htm?mol=1JMF FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...d class="sblockDat" id="ligandDat"><scene name='pdbligand=UMP:2-DEOXYURIDINE+5-MONOPHOSPHATE'>UMP</sc...
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1jmf ProSAT]</span></td></tr>
  3. 1jmg (2,602 bytes)
    2: ==CONTRIBUTIONS OF ORIENTATION AND HYDROGEN BONDING TO CATALYSIS IN ASN-229 MUTANTS OF THYMIDYL...
    5: ...oteopedia.org/fgij/fg.htm?mol=1JMG FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...d class="sblockDat" id="ligandDat"><scene name='pdbligand=UMP:2-DEOXYURIDINE+5-MONOPHOSPHATE'>UMP</sc...
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1jmg ProSAT]</span></td></tr>
  4. 1jmi (2,602 bytes)
    2: ==CONTRIBUTIONS OF ORIENTATION AND HYDROGEN BONDING TO CATALYSIS IN ASN-229 MUTANTS OF THYMIDYL...
    5: ...oteopedia.org/fgij/fg.htm?mol=1JMI FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...d class="sblockDat" id="ligandDat"><scene name='pdbligand=UMP:2-DEOXYURIDINE+5-MONOPHOSPHATE'>UMP</sc...
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1jmi ProSAT]</span></td></tr>
  5. 1a8e (3,463 bytes)
    2: ...HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE==
    5: ...oteopedia.org/fgij/fg.htm?mol=1A8E FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...nd=CO3:CARBONATE+ION'>CO3</scene>, <scene name='pdbligand=FE:FE+(III)+ION'>FE</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1a8e ProSAT]</span></td></tr>
  6. 1a8f (3,463 bytes)
    2: ...HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE==
    5: ...oteopedia.org/fgij/fg.htm?mol=1A8F FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...nd=CO3:CARBONATE+ION'>CO3</scene>, <scene name='pdbligand=FE:FE+(III)+ION'>FE</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1a8f ProSAT]</span></td></tr>
  7. 2uze (8,262 bytes)
    2: ...of human CDK2 complexed with a thiazolidinone inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2UZE FirstGlance]. <br>
    6: ...4-OXO-1,3-THIAZOLIDIN-5-YLIDENE)METHYL]FURAN-2-YL}BENZOIC+ACID'>C95</scene></td></tr>
    7: ...s:]]</b></td><td class="sblockDat"><scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
    8: ...8|2iw8]], [[2iw9|2iw9]], [[2uue|2uue]], [[2uzb|2uzb]], [[2uzd|2uzd]], [[2uzl|2uzl]], [[2uzn|2uzn]], [...
  8. 2uzb (9,421 bytes)
    2: ...of human CDK2 complexed with a thiazolidinone inhibitor==
    3: ... load='2uzb' size='340' side='right'caption='[[2uzb]], [[Resolution|resolution]] 2.70&Aring;' scene='...
    5: ...oteopedia.org/fgij/fg.htm?mol=2UZB FirstGlance]. <br>
    6: ...,3-THIAZOLIDIN-5-YLIDENE)METHYL]-2-FURYL}-N-METHYLBENZENESULFONAMIDE'>C75</scene></td></tr>
    7: ...s:]]</b></td><td class="sblockDat"><scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
  9. 2uzl (9,479 bytes)
    2: ...of human CDK2 complexed with a thiazolidinone inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2UZL FirstGlance]. <br>
    6: ...N-5-YLIDENE)METHYL]FURAN-2-YL}-2-(TRIFLUOROMETHYL)BENZENESULFONAMIDE'>C94</scene></td></tr>
    7: ...s:]]</b></td><td class="sblockDat"><scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
    8: ...m|2j9m]], [[2jgz|2jgz]], [[2uue|2uue]], [[2uzb|2uzb]], [[2uzd|2uzd]], [[2uze|2uze]], [[2uzn|2uzn]], [...
  10. 2uzo (6,871 bytes)
    2: ...of human CDK2 complexed with a thiazolidinone inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2UZO FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...DIOXO-1,3-THIAZOLIDIN-5-YLIDENE)METHYL]FURAN-2-YL}BENZENESULFONAMIDE'>C62</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2uzo ProSAT]</span></td></tr>
  11. 2uzn (6,875 bytes)
    2: ...of human CDK2 complexed with a thiazolidinone inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2UZN FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...NO-4-OXO-1,3-THIAZOLIDIN-5-YLIDENE)ETHYL]-2-FURYL}BENZENESULFONAMIDE'>C96</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2uzn ProSAT]</span></td></tr>
  12. 2uzd (9,459 bytes)
    2: ...of human CDK2 complexed with a thiazolidinone inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2UZD FirstGlance]. <br>
    6: ...4-OXO-1,3-THIAZOLIDIN-5-YLIDENE)METHYL]FURAN-2-YL}BENZENESULFONAMIDE'>C85</scene></td></tr>
    7: ...s:]]</b></td><td class="sblockDat"><scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
    8: ...9|2iw9]], [[2j9m|2j9m]], [[2jgz|2jgz]], [[2uzb|2uzb]], [[2uue|2uue]], [[2uze|2uze]], [[2uzl|2uzl]], [...
  13. 2c69 (6,514 bytes)
    2: ...an CDK2 complexed with the triazolopyrimidine inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2C69 FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...="ligandDat"><scene name='pdbligand=CT8:(5Z)-5-(3-BROMOCYCLOHEXA-2,5-DIEN-1-YLIDENE)-N-(PYRIDIN-4-YLM...
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c69 ProSAT]</span></td></tr>
  14. 2c6l (6,489 bytes)
    2: ...an CDK2 complexed with the triazolopyrimidine inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2C6L FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...)AMINO][1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-YL}AMINO)BENZENESULFONAMIDE'>DT4</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c6l ProSAT]</span></td></tr>
  15. 2c6m (6,478 bytes)
    2: ...an CDK2 complexed with the triazolopyrimidine inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2C6M FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...XYLOXY)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-YL]AMINO}BENZENESULFONAMIDE'>DT5</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c6m ProSAT]</span></td></tr>
  16. 2c6i (6,482 bytes)
    2: ...an CDK2 complexed with the triazolopyrimidine inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2C6I FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...ETHOXY)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-YL]AMINO}BENZENESULFONAMIDE'>DT1</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c6i ProSAT]</span></td></tr>
  17. 2c6k (6,480 bytes)
    2: ...an CDK2 complexed with the triazolopyrimidine inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2C6K FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...LAMINO)[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-YL]AMINO}BENZENESULFONAMIDE'>DT2</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c6k ProSAT]</span></td></tr>
  18. 2c68 (6,508 bytes)
    2: ...an CDK2 complexed with the triazolopyrimidine inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2C68 FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...="ligandDat"><scene name='pdbligand=CT6:(5Z)-5-(3-BROMOCYCLOHEXA-2,5-DIEN-1-YLIDENE)-N-(PYRIDIN-4-YLM...
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c68 ProSAT]</span></td></tr>
  19. 2c6o (6,447 bytes)
    2: ...an CDK2 complexed with the triazolopyrimidine inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2C6O FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...d class="sblockDat" id="ligandDat"><scene name='pdbligand=4SP:O6-CYCLOHEXYLMETHOXY-2-(4-SULPHAMOYLANI...
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c6o ProSAT]</span></td></tr>
  20. 2c6t (6,584 bytes)
    2: ...an CDK2 complexed with the triazolopyrimidine inhibitor==
    5: ...oteopedia.org/fgij/fg.htm?mol=2C6T FirstGlance]. <br>
    6: ...>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resol...
    7: ...O}BENZENESULFONAMIDE'>DT5</scene>, <scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
    8: ...um], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2c6t ProSAT]</span></td></tr>

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