Published June 1982
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Structure of bound water and refinement of acid metmyoglobin
Description
The structure of myoglobin has been determined by x-ray diffraction for the acidmet, deoxy, and the oxy forms. Neutron diffraction work, done in this laboratory, has demonstrated that hydrogen and deuterium positions can be located. In addition to the localization of H and D, neutron diffraction provides a unique method for studying the water structure because of the strong scattering ability of D2O. The scattering factor of deuterium is nearly twice as large as that of hydrogen, and it increases the visibility of water molecules in Fourier maps, so that in a neutron map a water molecule appears about three times as strong as in an equivalent electron-density map. (DT)
Availability note (English)
MF available from INIS under the Report Number; Available from NTIS, PC A02/MF A01 as DE84006541.Files
15049024.pdf
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Additional details
Publishing Information
- Imprint Pagination
- 14 p.
- Report number
- BNL--34098
Conference
- Title
- Brookhaven symposium biology 32.
- Dates
- 1-4 Jun 1982.
- Place
- Upton, NY (USA).
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 15049024
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- FOURIER ANALYSIS; MOLECULAR STRUCTURE; MYOGLOBIN; NEUTRON DIFFRACTION; WATER
- Descriptors DEC
- CARBOXYLIC ACIDS; COHERENT SCATTERING; DIFFRACTION; GLOBINS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; HYDROGEN COMPOUNDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; OXYGEN COMPOUNDS; PIGMENTS; PORPHYRINS; PROTEINS; SCATTERING
Optional Information
- Secondary number(s)
- CONF-8206240--3.