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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: ...been given to me which I believe are flawed or incorrect.
    5: * Institution (NO ABBREVIATIONS): None
    7: ...untry: Rocky Point, North Carolina, United States of America
    9: * Field of Expertise or Study:
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: ... HYDROGEN BONDING TO CATALYSIS IN ASN-229 MUTANTS OF THYMIDYLATE SYNTHASE==
   3: ...de='right'caption='[[1jmh]], [[Resolution|resolution]] 2.50Å' scene=''>
   5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=1JMH FirstGlance]. <br>
   6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.5&#8491;</td></tr>
   7: ...<scene name='pdbligand=UMP:2-DEOXYURIDINE+5-MONOPHOSPHATE'>UMP</scene></td></tr>
2. 1jmf (2,602 bytes)
   2: ... HYDROGEN BONDING TO CATALYSIS IN ASN-229 MUTANTS OF THYMIDYLATE SYNTHASE==
   3: ...de='right'caption='[[1jmf]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
   5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=1JMF FirstGlance]. <br>
   6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.5&#8491;</td></tr>
   7: ...<scene name='pdbligand=UMP:2-DEOXYURIDINE+5-MONOPHOSPHATE'>UMP</scene></td></tr>
3. 1jmg (2,602 bytes)
   2: ... HYDROGEN BONDING TO CATALYSIS IN ASN-229 MUTANTS OF THYMIDYLATE SYNTHASE==
   3: ...de='right'caption='[[1jmg]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
   5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=1JMG FirstGlance]. <br>
   6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.2&#8491;</td></tr>
   7: ...<scene name='pdbligand=UMP:2-DEOXYURIDINE+5-MONOPHOSPHATE'>UMP</scene></td></tr>
4. 1jmi (2,602 bytes)
   2: ... HYDROGEN BONDING TO CATALYSIS IN ASN-229 MUTANTS OF THYMIDYLATE SYNTHASE==
   3: ...de='right'caption='[[1jmi]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
   5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=1JMI FirstGlance]. <br>
   6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.5&#8491;</td></tr>
   7: ...<scene name='pdbligand=UMP:2-DEOXYURIDINE+5-MONOPHOSPHATE'>UMP</scene></td></tr>
5. 1a8e (5,775 bytes)
   2: ...=HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE==
   3: ...de='right'caption='[[1a8e]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
   5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=1A8E FirstGlance]. <br>
   6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 1.6&#8491;</td></tr>
   7: ...>CO3</scene>, <scene name='pdbligand=FE:FE+(III)+ION'>FE</scene></td></tr>
6. 1a8f (5,775 bytes)
   2: ...=HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE==
   3: ...de='right'caption='[[1a8f]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
   5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=1A8F FirstGlance]. <br>
   6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
   7: ...>CO3</scene>, <scene name='pdbligand=FE:FE+(III)+ION'>FE</scene></td></tr>
7. 2uze (6,927 bytes)
   2: ...human CDK2 complexed with a thiazolidinone inhibitor==
   3: ...de='right'caption='[[2uze]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
   5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2UZE FirstGlance]. <br>
   6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.4&#8491;</td></tr>
   7: ...>, <scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
8. 2uzb (9,421 bytes)
   2: ...human CDK2 complexed with a thiazolidinone inhibitor==
   3: ...de='right'caption='[[2uzb]], [[Resolution|resolution]] 2.70&Aring;' scene=''>
   5: ...ents</b> use [http://proteopedia.org/fgij/fg.htm?mol=2UZB FirstGlance]. <br>
   6: ...DIN-5-YLIDENE)METHYL]-2-FURYL}-N-METHYLBENZENESULFONAMIDE'>C75</scene></td></tr>
   7: ...t&quot;><scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
9. 2uzl (6,953 bytes)
   2: ...human CDK2 complexed with a thiazolidinone inhibitor==
   3: ...de='right'caption='[[2uzl]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
   5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2UZL FirstGlance]. <br>
   6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.4&#8491;</td></tr>
   7: ...>, <scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
10. 2uzo (6,871 bytes)
    2: ...human CDK2 complexed with a thiazolidinone inhibitor==
    3: ...de='right'caption='[[2uzo]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
    5: ...> use [https://proteopedia.org/fgij/fg.htm?mol=2UZO FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.3&#8491;</td></tr>
    7: ...HIAZOLIDIN-5-YLIDENE)METHYL]FURAN-2-YL}BENZENESULFONAMIDE'>C62</scene></td></tr>
11. 2uzn (6,875 bytes)
    2: ...human CDK2 complexed with a thiazolidinone inhibitor==
    3: ...de='right'caption='[[2uzn]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
    5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2UZN FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.3&#8491;</td></tr>
    7: ...3-THIAZOLIDIN-5-YLIDENE)ETHYL]-2-FURYL}BENZENESULFONAMIDE'>C96</scene></td></tr>
12. 2uzd (9,459 bytes)
    2: ...human CDK2 complexed with a thiazolidinone inhibitor==
    3: ...de='right'caption='[[2uzd]], [[Resolution|resolution]] 2.72&Aring;' scene=''>
    5: ...ents</b> use [http://proteopedia.org/fgij/fg.htm?mol=2UZD FirstGlance]. <br>
    6: ...HIAZOLIDIN-5-YLIDENE)METHYL]FURAN-2-YL}BENZENESULFONAMIDE'>C85</scene></td></tr>
    7: ...t&quot;><scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>
13. 2c69 (6,514 bytes)
    2: ...CDK2 complexed with the triazolopyrimidine inhibitor==
    3: ...de='right'caption='[[2c69]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
    5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C69 FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.1&#8491;</td></tr>
    7: ...)-N-(PYRIDIN-4-YLMETHYL)-1,5-DIHYDRO[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-AMINE'>CT8</scene></td></tr>
14. 2c6l (6,489 bytes)
    2: ...CDK2 complexed with the triazolopyrimidine inhibitor==
    3: ...de='right'caption='[[2c6l]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
    5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C6L FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.3&#8491;</td></tr>
    7: ...,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-YL}AMINO)BENZENESULFONAMIDE'>DT4</scene></td></tr>
15. 2c6m (6,478 bytes)
    2: ...CDK2 complexed with the triazolopyrimidine inhibitor==
    3: ...de='right'caption='[[2c6m]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
    5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C6M FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 1.9&#8491;</td></tr>
    7: ...,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-YL]AMINO}BENZENESULFONAMIDE'>DT5</scene></td></tr>
16. 2c6i (6,482 bytes)
    2: ...CDK2 complexed with the triazolopyrimidine inhibitor==
    3: ...de='right'caption='[[2c6i]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
    5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C6I FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
    7: ...,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-YL]AMINO}BENZENESULFONAMIDE'>DT1</scene></td></tr>
17. 2c6k (6,480 bytes)
    2: ...CDK2 complexed with the triazolopyrimidine inhibitor==
    3: ...de='right'caption='[[2c6k]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
    5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C6K FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 1.9&#8491;</td></tr>
    7: ...,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-YL]AMINO}BENZENESULFONAMIDE'>DT2</scene></td></tr>
18. 2c68 (6,508 bytes)
    2: ...CDK2 complexed with the triazolopyrimidine inhibitor==
    3: ...de='right'caption='[[2c68]], [[Resolution|resolution]] 1.95&Aring;' scene=''>
    5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C68 FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 1.95&#8491;</td></tr>
    7: ...YLIDENE)-N-(PYRIDIN-4-YLMETHYL)-1,5-DIHYDROPYRAZOLO[1,5-A]PYRIMIDIN-7-AMINE'>CT6</scene></td></tr>
19. 2c6o (6,447 bytes)
    2: ...CDK2 complexed with the triazolopyrimidine inhibitor==
    3: ...de='right'caption='[[2c6o]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
    5: ...> use [https://proteopedia.org/fgij/fg.htm?mol=2C6O FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.1&#8491;</td></tr>
    7: ...and=4SP:O6-CYCLOHEXYLMETHOXY-2-(4-SULPHAMOYLANILINO)+PURINE'>4SP</scene></td></tr>
20. 2c6t (6,584 bytes)
    2: ...CDK2 complexed with the triazolopyrimidine inhibitor==
    3: ...de='right'caption='[[2c6t]], [[Resolution|resolution]] 2.61&Aring;' scene=''>
    5: ...nts</b> use [https://proteopedia.org/fgij/fg.htm?mol=2C6T FirstGlance]. <br>
    6: ...ethodDat&quot;>X-ray diffraction, [[Resolution|Resolution]] 2.61&#8491;</td></tr>
    7: ...>, <scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene></td></tr>

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