View & Compare Final Processed Spectrum For CD0003897000

Human DUTPase (dutp pyrophosphatase)


Citation: No citation information currently associated with this entry.


Citation: The PCDDB (protein circular dichroism data bank): A bioinformatics resource for protein characterisations and methods development.
Ramalli SG, Miles AJ, Janes RW, Wallace BA., J Mol Biol (2022)


Validation report compiled by Validichro v1.4.0, 2015-04-01, 3:55pm. - FLAG

Depositors Notes: Uniprot sequence does not match the protein sequence used because it is a cloned protein identical to the pdb structure. It does not contain the mitochondrial signal sequence, this is the 112-252 residues fragment of the Uniprot sequence. Standard deviation was not subject to a Flag using Validichro instead this protein demonstrates a flag for max magnitude. We suggest: the spectrum under analysis is perfectly valid, but novel and be worth inclusion in the reference set.

Missing Wavelengths PASS ?
Maximum Delta Epsilon PASS ?
Minimal Level of Maximum Delta Epsilon PASS ?
Peak Locations PASS ?
Feature Width PASS ?
Experimental Temperature PASS ?
UniProt sequence FLAG ?
Molecular Weight PASS ?
Number of Residues PASS ?
Mean Residue Weight value PASS ?
Concentration and Pathlength PASS ?
CSA / ACS peak ratio PASS ?
CSA / ACS Temperature PASS ?
Peak Shift test PASS ?
Standard Deviation FLAG ?
Noise: 260-270nm PASS ?
Flat topped peaks PASS ?
Wavelength range PASS ?
Interval resolution PASS ?
High Tension Voltage 240-260nm PASS ?
Projection Test PASS ?
Standard Deviation At Peak PASS ?
Depositor Note Uniprot sequence does not match the protein sequence used because it is a cloned protein identical to the pdb structure. It does not contain the mitochondrial signal sequence, this is the 112-252 residues fragment of the Uniprot sequence. Standard deviation was not subject to a Flag using Validichro instead this protein demonstrates a flag for max magnitude. We suggest: the spectrum under analysis is perfectly valid, but novel and be worth inclusion in the reference set. ?

The PCDDB is a development of the Department of Biological Sciences, Institute of Structural and Molecular Biology, Birkbeck College, University of London and the School of Biological and Chemical Sciences, Queen Mary University of London, UK. It is supported by a grant from the BBSRC. Copyright of the design and implementation of this site are retained by the schools and the authors.