1eiw
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Solution structure of hypothetical protein MTH538 from Methanobacterium thermoautotrophicum
OverviewOverview
The structure of MTH538, a previously uncharacterized hypothetical protein, from Methanobacterium thermoautotrophicum, has been determined by NMR, spectroscopy. MTH538 is one of numerous structural genomics targets, selected in a genome-wide survey of uncharacterized sequences from this, organism. MTH538 is a so-called singleton, a sequence not closely related, to any other (known) sequences. The structure of MTH538 closely resembles, the known structures of receiver domains from two component response, regulator systems, such as CheY, and is similar to the structures of, flavodoxins and GTP-binding proteins. Tests on MTH538 for characteristic, activities of CheY and flavodoxin were negative. MTH538 did not become, phosphorylated in the presence of acetyl phosphate and Mg(2+), although it, appeared to bind Mg(2+). MTH538 also did not bind flavin mononucleotide, (FMN) or coenzyme F(420). Nevertheless, sequence and structure parallels, between MTH538/CheY and two families of ATPase/phosphatase proteins, suggest that MTH538 may have a role in a phosphorylation-independent, two-component response regulator system.
About this StructureAbout this Structure
1EIW is a Single protein structure of sequence from Methanothermobacter thermautotrophicus. Full crystallographic information is available from OCA.
ReferenceReference
Structure-based functional classification of hypothetical protein MTH538 from Methanobacterium thermoautotrophicum., Cort JR, Yee A, Edwards AM, Arrowsmith CH, Kennedy MA, J Mol Biol. 2000 Sep 8;302(1):189-203. PMID:10964569
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OCA- Pages with broken file links
- Methanothermobacter thermautotrophicus
- Single protein
- Arrowsmith, C.H.
- Cort, J.R.
- Kennedy, M.A.
- NESG, Northeast.Structural.Genomics.Consortium.
- (a/b)5 doubly wound fold
- Chey-like fold
- Flavodoxin-like fold
- Nesg
- Northeast structural genomics consortium
- Parallel beta sheet
- Protein structure initiative
- Psi
- Structural genomics