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Article title matches

  1. Category:Transcriptionally active conformation in absence of ligand (89 bytes)
    1: ... keyword Transcriptionally active conformation in absence of ligand
  2. Category:Homodimer in the absence of ligand (65 bytes)
    1: List of pages with the keyword Homodimer in the absence of ligand
  3. Category:Absence of ligand (48 bytes)
    1: List of pages with the keyword Absence of ligand
  4. Category:Gt-b fold absence of c-terminal alpha-helix (74 bytes)
    1: List of pages with the keyword Gt-b fold absence of c-terminal alpha-helix
  5. Category:Absence of c-terminal alpha-helix (64 bytes)
    1: List of pages with the keyword Absence of c-terminal alpha-helix
  6. Category:Absence of hydrogen bonding (58 bytes)
    1: List of pages with the keyword Absence of hydrogen bonding
  7. Category:Protein in the absence of substrate (66 bytes)
    1: List of pages with the keyword Protein in the absence of substrate
  8. Category:Absence (38 bytes)
    1: List of pages with the keyword Absence

Page text matches

  1. Hemoglobin (19,396 bytes)
    113: ...emoglobin: Structure of bovine deoxyhaemoglobin, absence of specific chloride binding sites, and origin of...
  2. 2boq (5,896 bytes)
    24: ...al. The H2O2-activated VP was self-reduced in the absence of reducing substrates. Trp164 is also involved i...
  3. 2cn5 (7,986 bytes)
    13: ...ic spindle assembly by phosphorylating BRCA1. Its absence may be a cause of the chromosomal instability obs...
  4. 2cn7 (4,592 bytes)
    24: ...and L, which differ mainly by the presence (H) or absence (L) of active ferroxidase centres. We report the ...
  5. 2cn8 (7,949 bytes)
    13: ...ic spindle assembly by phosphorylating BRCA1. Its absence may be a cause of the chromosomal instability obs...
  6. 2cn6 (4,654 bytes)
    24: ...and L, which differ mainly by the presence (H) or absence (L) of active ferroxidase centres. We report the ...
  7. 2wc2 (4,802 bytes)
    22: ...nding. Here we report the structure of CAP in the absence of cAMP, which, together with structures of CAP i...
  8. 1wcb (4,834 bytes)
    22: ...pha proton only from D-alanine. Together with the absence of any residue capable of deprotonating C alpha o...
  9. 1qrz (5,533 bytes)
    10: ...y normal, or slightly reduced antigen levels, and absence of clinical manifestations. Plasminogen deficienc...
  10. 7hhl (5,508 bytes)
    14: ...inity compounds have been developed recently. The absence of this subpocket in LEDGF PWWP limits the attain...
  11. 7hhm (5,505 bytes)
    14: ...inity compounds have been developed recently. The absence of this subpocket in LEDGF PWWP limits the attain...
  12. 7hhn (5,503 bytes)
    14: ...inity compounds have been developed recently. The absence of this subpocket in LEDGF PWWP limits the attain...
  13. 7hho (5,493 bytes)
    14: ...inity compounds have been developed recently. The absence of this subpocket in LEDGF PWWP limits the attain...
  14. 7hhp (5,479 bytes)
    14: ...inity compounds have been developed recently. The absence of this subpocket in LEDGF PWWP limits the attain...
  15. 7hhq (5,492 bytes)
    14: ...inity compounds have been developed recently. The absence of this subpocket in LEDGF PWWP limits the attain...
  16. 7hhr (5,482 bytes)
    14: ...inity compounds have been developed recently. The absence of this subpocket in LEDGF PWWP limits the attain...
  17. 2adr (3,773 bytes)
    24: ...-terminal (non-finger) PAR is unstructured in the absence of DNA and undergoes a folding transition on bind...
  18. 2cfi (4,487 bytes)
    24: ...drogenase has been determined in the presence and absence of a substrate analogue. The structures reveal co...
  19. 1cfp (5,102 bytes)
    23: ...e structure of the reduced S100B homodimer in the absence of calcium. Each monomer consists of a four-helix...
  20. 2cfq (3,668 bytes)
    24: ...ocation. No sugar-binding site is observed in the absence of ligand, and deprotonation of the key residue G...

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