| Link type | Probability | Chain A piercings | Chain B piercings | Chain E piercings | Chain F piercings | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
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Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
| view details |
|
Other | 30% | -282E -282E -100F -243F | -282A -6B | ||||||||||
Chain A Sequence |
EVKKIPTMIEGFDDISHGGLPQGATTLVSGTSGTGKTLFAVQFLYNGITIFNEPGIFVTFEESPQDIIKNALSFGWNLQSLIDQGKLFILDASPDPDGQEVAGDFDLSALIERIQYAIRKYKATRVSIDSVTAVFQQYDAASVVRREIFRLAFRLAQLGVTTIMTTERVDEYGPVARFGVEEFVSDNVVILRNVL--ERRRRTVEILKLRGTTHMKGEYPFTINNGINIFDYK |
Chain A Sequence |
KTAVLKLYVAGNTPNSVRALKTLNNILEKEFKGVYALKVIDVLKNPQLAEEDKILATPTLAKVLPPPVRRIIGDLSNREKVLIALRLLA |
Chain A Sequence |
DPQHRLSQKLKERLGYLGVYYKRDTAFFFRRMSPADKRKLLDELRSIYRTIVLEYFNTDAKVNERIDEFVSKAFFADISVSQVLEIHVELMDTFSKQLKLEGRSEDILLDYRLTLIDVIAHLSEMYRRSIPR |
Chain A Sequence |
VDPQHRLSQKLKERLGYLGVYYKRDTAFFFRRMSPADKRKLLDELRSIYRTIVLEYFNTDAKVNERIDEFVSKAFFADISVSQVLEIHVELMDTFSKQLKLEGRSEDILLDYRLTLIDVIAHLSEMYRRSIPRE |
| sequence length | 233,89,132,134 |
| structure length | 231,89,132,134 |
| publication title |
Structural basis of the day-night transition in a bacterial circadian clock.
pubmed doi rcsb |
| molecule tags | Transcription regulator |
| molecule keywords | Circadian clock protein kinase KaiC |
| source organism | Thermosynechococcus elongatus |
| missing residues | A: 212-215 |
| pdb deposition date | 2016-05-12 |
| LinkProt deposition date | 2017-04-01 |
Image from the rcsb pdb (www.rcsb.org)#similar chains in the LinkProt database (?% sequence similarity) ...loading similar chains, please wait... #similar chains, but unlinked ...loading similar chains, please wait... #similar chains in the pdb database (?% sequence similarity) ...loading similar chains, please wait...