BMRB Entry 6480
Chem Shift validation: AVS_anomalous, AVS_full
BMRB Entry DOI: doi:10.13018/BMR6480
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Title: The loss of stability of a naturally occurring ATP7A mutant is the cause of Menkes disease PubMed: 16083905
Deposition date: 2005-02-02 Original release date: 2005-11-14
Authors: Banci, L.; Bertini, I.; Cantini, F.; Migliardi, M.; Rosato, A.; Wang, S.
Citation: Banci, L.; Bertini, I.; Cantini, F.; Migliardi, M.; Rosato, A.; Wang, S.. "An Atomic-level Investigation of the Disease-causing A629P Mutant of the Menkes Protein, ATP7A." J. Mol. Biol. 352, 409-417 (2005).
Assembly members:
Copper-transporting ATPase 1(E.C.3.6.3.4), polymer, 75 residues, Formula weight is not available
CU1, non-polymer, 63.546 Da.
Natural source: Common Name: Human Taxonomy ID: 9606 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Homo sapiens
Experimental source: Production method: recombinant technology
Entity Sequences (FASTA):
Copper-transporting ATPase 1(E.C.3.6.3.4): MGDGVLELVVRGMTCASCVH
KIESSLTKHRGILYCSVALA
TNKAHIKYDPEIIGPRDIIH
TIESLGFEASLVKIE
- assigned_chemical_shifts
| Data type | Count |
| 15N chemical shifts | 70 |
| 1H chemical shifts | 469 |
Additional metadata:
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