Published June 1982 | Version v1
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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.

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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.