메뉴 건너뛰기




Volumn 132, Issue 25, 2010, Pages 8610-8617

Evolution of metal selectivity in templated protein interfaces

Author keywords

[No Author keywords available]

Indexed keywords

CONFORMATIONAL CHANGE; DIVALENT METALS; ELECTRON TRANSFER PROTEINS; FUNCTIONAL DIVERSITY; HIGH-AFFINITY SITES; METAL BINDING PROPERTIES; METAL SELECTIVITY; METALLO-PROTEINS; PROTEIN ARCHITECTURES; PROTEIN INTERFACES; RATIONAL DESIGN; SELECTIVE BINDING; SIGNALING PROTEINS; TEMPLATED; TEMPLATING;

EID: 77955443867     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja910844n     Document Type: Article
Times cited : (54)

References (41)
  • 12
    • 77955437028 scopus 로고    scopus 로고
    • 2+ were determined separately using EGTA as a competing ligand. See Experimental Section for more details
    • 2+ were determined separately using EGTA as a competing ligand. See Experimental Section for more details.
  • 14
    • 77955443602 scopus 로고    scopus 로고
    • 4 scaffold
    • 4 scaffold.
  • 21
    • 77955452021 scopus 로고    scopus 로고
    • 4. If they are bound to the core in a fashion that would compete with Zn binding, their average dissociation constants would have to be ∼40 μM each to compensate for the free energy difference between the four-Zn-bound and two-Cu-bound. species listed in Table 1
    • 4. If they are bound to the core in a fashion that would compete with Zn binding, their average dissociation constants would have to be ∼40 μM each to compensate for the free energy difference between the four-Zn-bound and two-Cu-bound. species listed in Table 1.
  • 31
    • 0028103275 scopus 로고
    • Collaborative Computational Project, Number 4. 1994.
    • Collaborative Computational Project, Number 4. 1994. Acta Crystallogr. 1994, D50, 760-763.
    • (1994) Acta Crystallogr. , vol.D50 , pp. 760-763


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.