(Q33490081)

English

Purification, crystallization and preliminary crystallographic analysis of protein MJ1225 from Methanocaldococcus jannaschii, a putative archaeal homologue of gamma-AMPK

scientific article published on 30 July 2009

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scholarly article

1 reference

Europe PubMed Central

27 July 2017

Purification, crystallization and preliminary crystallographic analysis of protein MJ1225 from Methanocaldococcus jannaschii, a putative archaeal homologue of gamma-AMPK (English)

1 reference

Europe PubMed Central

27 July 2017

object named as

Iker Oyenarte

3

0 references

Luis Alfonso Martínez-Cruz

object named as

Luis Alfonso Martínez-Cruz

6

0 references

author name string

Inmaculada Gómez García

1

1 reference

Europe PubMed Central

27 July 2017

Danel Kortázar

2

1 reference

Europe PubMed Central

27 July 2017

José María Mato

4

1 reference

Europe PubMed Central

27 July 2017

María Luz Martínez-Chantar

5

1 reference

Europe PubMed Central

27 July 2017

language of work or name

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publication date

30 July 2009

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Europe PubMed Central

27 July 2017

Acta Crystallographica Section F: Structural Biology Communications

1 reference

Europe PubMed Central

27 July 2017

65

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Europe PubMed Central

27 July 2017

Pt 8

1 reference

Europe PubMed Central

27 July 2017

813-817

1 reference

Europe PubMed Central

27 July 2017

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1 reference

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1 reference

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1 reference

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Structural insight into AMPK regulation: ADP comes into play

1 reference

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1 reference

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Structural basis for AMP binding to mammalian AMP-activated protein kinase

1 reference

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1 reference

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Structure of a CBS-domain pair from the regulatory gamma1 subunit of human AMPK in complex with AMP and ZMP

1 reference

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1 reference

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Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

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Myotonia caused by mutations in the muscle chloride channel gene CLCN1.

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Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

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Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene

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Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

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Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome

1 reference

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Characterization of AMP-activated protein kinase gamma-subunit isoforms and their role in AMP binding

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Characteristics and crystal structure of bacterial inosine-5'-monophosphate dehydrogenase

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1107/S1744309109026475

1 reference

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

27 July 2017

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