 | Authors: Amine Heddad, Andrea Krings, Markus Brameier and Bob MacCallum, Stockholm Bioinformatics Center, Stockholm University, Sweden. |
NucPred
Fetching P11075 from www.uniprot.org...
The NucPred score for your sequence is 0.78 (see score help below)
1 MSEQNSVVNAEKGDGEISSNVETASSVNPSVKPQNAIKEEAKETNGEDQK 50
51 CKGPENAGSTAETKETSNDATNGMKTPEETEDTNDKRHDDEGEDGDEDED 100
101 EDEDEDEDNGDEDDEDVDSSSSETSSEDGEDSESVSGESTESSSGEDEES 150
151 DESDGNTSNSSSGDESGSEEEEEEEEEEEEEENAGEPAIAHQDSVPTNDS 200
201 TAPRSTHTRNISLSSNGSNTNSTIILVKTTLETILNDKDIKKNSNAQKAI 250
251 ERTLQKFKEFDPQTTNNPHYVDSILVFEALRASCRTKSSKVQSLALDCLS 300
301 KLFSFRSLDETLLVNPPDSLASNDQRQDAADGITPPPKQKIIDAAIDTIS 350
351 DCFQGEGTDDRVELQIVRALSSCILEEDSSSLCHGASLLKAIRTIYNVFV 400
401 FSLNPSNQGIAQATLTQIISSVYDKIDLKQSTSSAVSLSTKNHQQQSAIE 450
451 LSEASENAETPAPLTLENMDKLNDDEERLMDAQQPDSIAITNQDLAVKDA 500
501 FLVFRVMAKICAKPLETELDMRSHAVRSKLLSLHIIYSIIKDHIDVFLSH 550
551 NIFLPGKERVCFIDSIRQYLRLVLSRNAASPLAPVFEVTLEIMWLLIANL 600
601 RADFVKEIPVFLTEIYFPISELTTSTSQQKRYFLSVIQRICNDPRTLVEF 650
651 YLNYDCNPGMPNVMEITVDYLTRLALTRVEITQTQRSYYDEQISKSLSTY 700
701 NFSQLPLLTSSNLSSSPDVGQVNLLFPLDFALKMVSLNCIVSVLRSLSSW 750
751 AHKALNPNTHTANKVLLNTTSSARQESRSSLSNDVRSSIMTSNDDFKPTY 800
801 EDEESRSLSSQNIDADDPTQFENLKLRKTALSECIAIFNNKPKKAIPVLI 850
851 KKGFLKDDSPISIAKWLLETEGLDMAAVGDYLGEGDDKNIAIMHAFVDEF 900
901 DFTGMSIVDALRSFLQSFRLPGEGQKIDRFMLKFAERFVDQNPGVFSKAD 950
951 TAYVLSYSLIMLNTDLHSSQIKNKMSLQEFLENNEGIDNGRDLPRDFLEG 1000
1001 LFNEIANNEIKLISEQHQAMLSGDTNLVQQQQSAFNFFNSRDLTREAYNQ 1050
1051 VSKEISSKTELVFKNLNKNKGGPDVYYAASHVEHVKSIFETLWMSFLAAL 1100
1101 TPPFKDYDDIDTTNKCLEGLKISIKIASTFRINDARTSFVGALVQFCNLQ 1150
1151 NLEEIKVKNVNAMVILLEVALSEGNYLEGSWKDILLVVSQMERLQLISKG 1200
1201 IDRDTVPDVAQARVANPRVSYESSRSNNTSFFDVWGKKATPTELAQEKHH 1250
1251 NQTLSPEISKFISSSELVVLMDNIFTKSSELSGNAIVDFIKALTAVSLEE 1300
1301 IESSENASTPRMFSLQKMVDVCYYNMDRIKLEWTPLWAVMGKAFNKIATN 1350
1351 SNLAVVFFAIDSLRQLSMRFLDIEELSGFEFQHDFLKPFEYTVQNSGNTE 1400
1401 VQEMIIECFRNFILTKSESIKSGWKPILESLQYTARSSTESIVLKTQLLV 1450
1451 SNDIVTNHFENVFSQEDAFSELVGVFREITKNKRFQKLSLHALESLRKMT 1500
1501 QNVADICFYNENKTEEERKHNDALLRGKDIFQDVWFPMLFCFNDTIMTAE 1550
1551 DLEVRSRALNYMFDALVAYGGKFNDDFWEKICKKLLFPIFGVLSKHWEVN 1600
1601 QFNSHDDLSVWLSTTLIQALRNLIALFTHYFESLNRMLDGFLGLLVSCIC 1650
1651 QENDTIARIGRSCLQQLILQNVSKFNEYHWNQIGDVFDKLFDLTTANELF 1700
1701 DYDPLQQGRKSSVSHHQTTNDTSQHSDDDSNDRRENDSNISETVERAHQE 1750
1751 ESSEDVGGDMVETLNGQTKLNNGNSVPTVKDELNPKPASLSIPKKTKHMK 1800
1801 RNESNEDIRRRINIKNSIVVKCVLQLLMIELLNELFENEDFAHCIPYKEA 1850
1851 IRITRLLEKSYEFSRDFNEDYGLRTRLVEARVVDKIPNLLKQETSAAAVL 1900
1901 LDIMFQLYLNDDEKKADLITRLITICIQVVEGYVSLDDRTMERSINAWRS 1950
1951 VIVEILQGYYEFDDEDFRLYCPAMYALVIQILDKSVPTELRHAIKQFLSR 2000
2001 VGELYLSTD 2009
Positively and negatively influencing subsequences are coloured according to the following scale:
(non-nuclear) negative ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||| positive (nuclear)
What does the NucPred score mean?
| You have to decide on a NucPred score threshold. Sequences which score greater than or equal to this threshold are predicted to spend some time in the nucleus. Higher thresholds yield fewer predicted nuclear proteins, but these predictions are more accurate (you can have higher confidence in them). The table below gives more details of the performance of NucPred estimated using the sequences it was trained on (by cross-validation). Another benchmark is available in the Bioinformatics 2007 paper. |
| NucPred score threshold | Specificity | Sensitivity |
| see above | fraction of proteins predicted to be nuclear that actually are nuclear | fraction of true nuclear proteins that are predicted (coverage) |
| 0.10 | 0.45 | 0.88 |
| 0.20 | 0.52 | 0.83 |
| 0.30 | 0.57 | 0.77 |
| 0.40 | 0.63 | 0.69 |
| 0.50 | 0.70 | 0.62 |
| 0.60 | 0.71 | 0.53 |
| 0.70 | 0.81 | 0.44 |
| 0.80 | 0.84 | 0.32 |
| 0.90 | 0.88 | 0.21 |
| 1.00 | 1.00 | 0.02 |
| Sequences which score >= 0.8 with NucPred and which
are predicted by PredictNLS to contain an NLS have been shown to be 93% correct with a coverage of 16%. (PredictNLS by itself is 87% correct with 26% coverage on the same data.) |
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