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2H6R

Crystal Structure of triosephosphate isomerase (TIM) from Methanocaldococcus jannaschii

Summary for 2H6R
Entry DOI10.2210/pdb2h6r/pdb
DescriptorTriosephosphate isomerase (2 entities in total)
Functional Keywordsbeta-alpha barrel, isomerase
Biological sourceMethanocaldococcus jannaschii
Cellular locationCytoplasm (By similarity): Q58923
Total number of polymer chains8
Total formula weight186175.97
Authors
Gayathri, P.,Banerjee, M.,Vijayalakshmi, A.,Balaram, H.,Balaram, P.,Murthy, M.R.N. (deposition date: 2006-06-01, release date: 2007-02-06, Last modification date: 2023-10-25)
Primary citationGayathri, P.,Banerjee, M.,Vijayalakshmi, A.,Azeez, S.,Balaram, H.,Balaram, P.,Murthy, M.R.N.
Structure of triosephosphate isomerase (TIM) from Methanocaldococcus jannaschii
Acta Crystallogr.,Sect.D, 63:206-220, 2007
Cited by
PubMed Abstract: The crystal structure of a recombinant triosephosphate isomerase (TIM) from the archaeabacterium Methanocaldococcus jannaschii has been determined at a resolution of 2.3 A using X-ray diffraction data from a tetartohedrally twinned crystal. M. jannaschii TIM (MjTIM) is tetrameric, as suggested by solution studies and from the crystal structure, as is the case for two other structurally characterized archaeal TIMs. The archaeabacterial TIMs are shorter compared with the dimeric TIMs; the insertions in the dimeric TIMs occur in the vicinity of the tetramer interface, resulting in a hindrance to tetramerization in the dimeric TIMs. The charge distribution on the surface of the archaeal TIMs also facilitates tetramerization. Analysis of the barrel interactions in TIMs suggests that these interactions are unlikely to account for the thermal stability of the archaeal TIMs. A novelty of the unliganded structure of MjTIM is the complete absence of electron density for the loop 6 residues. The disorder of this loop could be ascribed to a missing salt bridge between residues at the N- and C-terminal ends of the loop in MjTIM.
PubMed: 17242514
DOI: 10.1107/S0907444906046488
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

226707

數據於2024-10-30公開中

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