Structure analysis

Crystal Structure of the HpcC from Thermus Thermophilus HB8

X-ray diffraction
2.1Å resolution
Source organism: Thermus thermophilus HB8
Assembly composition:
homo tetramer (preferred)
Entry contents: 1 distinct polypeptide molecule

Assemblies

Assembly 1 (preferred)
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Multimeric state: homo tetramer
Accessible surface area: 63692.4 Å2
Buried surface area: 26497.85 Å2
Dissociation area: 4,029.3 Å2
Dissociation energy (ΔGdiss): 41 kcal/mol
Dissociation entropy (TΔSdiss): 16.65 kcal/mol
Symmetry number: 4
PDBe Complex ID: PDB-CPX-178033
    Assembly 1
Confidence : 98%
No. subunits : 4
Symmetry : D2
3DComplex & QSbio predictionx
No. subunits : 4
Symmetry : D2

Macromolecules

PDBe-KB: UniProt Coverage View: Q5SJP9  
151550100150200250300350400450500
 
200400MRYADRVAGISWETIEEVRRRLKERPALHFIAGEFVPSESGETFPSLDPATNEVLGVAARGGEREVDRAAKAAHEAFQRWSRTKAKERKRYLLRIAELIEKHADELAVMECLDAGQVLRIVRAQVARAAENFAFYAEYAEHAMEDRTFPVDRDWLYYTVRVPAGPVGIITPWNAPLMLSTWRIAPALAFGNTVVLKPAEWSPFTATKLAEILKEADLPPGVFNLVQGFGEEAGAALVAHPLVPLLTLTGETETGKIVMRNAADHLKRLSPELGGKSPALVFADADLERALDAVVFQIFSFNGERCTASSRLLVEEKIFEDFVGKVVERARAIRVGHPLDPETEVGPLIHPEHLQRVLGYVEAGKREGARLLVGGERAKTSFRGEDLSRGNYLLPTVFVGENHMKIAQEEIFGPVLVAIPFKDEEEALRKANDTKYGLAAYVFTRDLERAHRLALELEAGMVYLNSHNVRHLPTPFGGVKGSGDRREGGTYALDFYTDLKTIALPLRPPHVPKFGK
UniProt
Q5SJP9
Chains
Domains
Secondary structure
Flexibility predictions
Early folding residue predictions
Ligand binding sites
Interaction interfaces
Sequence conservation

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