The CRISPR-Cpf1 nuclease is the best alternative to the commonly used Cas9 for genome editing. Cpf1 recognizes a protospacer adjacent motif (PAM) sequence of TTTV, which differs from the Cas9 PAM sequence, NGG. Having Cpf1 as a second option increases the likelihood of editing as close as possible to your desired target site. In this presentation, Dr Rolf Turk introduces the optimized Alt-R™ CRISPR-Cpf1 System and explains how it can be used as a powerful new tool for your genome editing research. Dr Turk presents the basics of the system, as well as protocols for getting started in genome editing.
The CRISPR-Cpf1 nuclease is the best alternative to the commonly used Cas9 for genome editing. Cpf1 recognizes a protospacer adjacent motif (PAM) sequence of TTTV, which differs from the Cas9 PAM sequence, NGG. Having Cpf1 as a second option increases the likelihood of editing as close as possible to your desired target site. In this presentation, Dr Rolf Turk introduces the optimized Alt-R™ CRISPR-Cpf1 System and explains how it can be used as a powerful new tool for your genome editing research. Dr Turk presents the basics of the system, as well as protocols for getting started in genome editing.
Genome editing by CRISPR systems has proven to be groundbreaking for basic biomedical research with significant implications for the treatment of human diseases. While the CRISPR-Cas9 and CRISPR-Cas12a (Cpf1) systems enable genome editing in a broad range of host species and cell types, both can exhibit poor editing efficiencies at specific target sites or in systems where delivery of CRISPR reagents is difficult. There are concerns about target specificity of the CRISPR-Cas9 system and, in many cases, typical remedies such as modified guide RNAs or mutant Cas9 proteins cause loss of genome editing efficiency. Many of these solutions for improving specificity were developed for delivery of the Cas9-gRNA complex via plasmid DNA vectors rather than delivery as ribonucleoproteins (RNPs). However, RNP delivery of CRISPR reagents is being increasingly used because of the risk of unwanted stimulation of the immune system by plasmid delivery.
In this webinar, Dr Vakulskas discusses improved Cas9 and Cas12a (Cpf1) nucleases that have been optimized to significantly increase editing efficiency in living cells. He also presents data showing that IDT’s latest high-fidelity Cas9, Alt-R HiFi S.p. Cas9 V3, increases on-target editing efficiency and dramatically reduces off-target editing.
The CRISPR/Cas9 system has emerged as one of the leading tools for modifying genomes of organisms ranging from E. coli to humans. In a recent webinar, "New RNA Tools for Optimized CRISPR/Cas 9 Genome Editing", we presented how we developed the Alt-R™ CRISPR-Cas9 System for genome editing. Here, we take a look at designing your target sequences and ordering them as Alt-R CRISPR crRNA. We review the other components of the system and walk through the experimental process step by step, from design to evaluation of editing potency. We also discuss challenges and potential pitfalls and provide tips and guidance towards successful genome editing experiments. Learn more: http://www.idtdna.com/crispr
The CRISPR-Cas9 system demonstrates unparalleled genome editing efficiency in a broad range of species and cell types, but it suffers from concerns related to target specificity. Modified guide RNAs and mutant Cas9 proteins have been developed to reduce off-target editing but, in many cases, the alterations also significantly reduce on-target editing performance. In this presentation, Dr Chris Vakulskas discusses a novel, high-fidelity Cas9 protein that reduces off-target gene editing, while maintaining high on-target activity. Dr Vakulskas presents data from the development of the new Alt-R® S.p. HiFi Cas9 Nuclease 3NLS and describes its usefulness in mitigating unwanted off-target gene editing, without the issues associated with transfection of plasmid DNA.
Presentation by Tina Graves-Lindsay at GRC/GIAB ASHG 2017 workshop "Getting the most from the reference assembly and reference materials" on production of reference grade assemblies for various human populations.
#SEJThinkTank Webinar: Social Marketing Hacks To Crush It in 2015Search Engine Journal
Looking for ways to rock your social marketing? The data is in, and savvy marketers are using it to turn readily available social data into attributable conversions. Join Daniel Morrison of aimClear as he covers selling with first-touch social psychographic data: disciplined, high intent, active targeting, including owned-audience cookie pools for performance marketers to exploit.
Amy Vernon of The Daily Dot #SEJSummit: Lessons from the NewsroomSearch Engine Journal
Amy Vernon of The Daily Dot looks at search and social through the lens of a journalist and explains how key strategies for success in the newsroom can be applied to digital marketing. She will also share how and why SEOs should be concerned with audience engagement in 2016.
Genome editing by CRISPR systems has proven to be groundbreaking for basic biomedical research with significant implications for the treatment of human diseases. While the CRISPR-Cas9 and CRISPR-Cas12a (Cpf1) systems enable genome editing in a broad range of host species and cell types, both can exhibit poor editing efficiencies at specific target sites or in systems where delivery of CRISPR reagents is difficult. There are concerns about target specificity of the CRISPR-Cas9 system and, in many cases, typical remedies such as modified guide RNAs or mutant Cas9 proteins cause loss of genome editing efficiency. Many of these solutions for improving specificity were developed for delivery of the Cas9-gRNA complex via plasmid DNA vectors rather than delivery as ribonucleoproteins (RNPs). However, RNP delivery of CRISPR reagents is being increasingly used because of the risk of unwanted stimulation of the immune system by plasmid delivery.
In this webinar, Dr Vakulskas discusses improved Cas9 and Cas12a (Cpf1) nucleases that have been optimized to significantly increase editing efficiency in living cells. He also presents data showing that IDT’s latest high-fidelity Cas9, Alt-R HiFi S.p. Cas9 V3, increases on-target editing efficiency and dramatically reduces off-target editing.
The CRISPR/Cas9 system has emerged as one of the leading tools for modifying genomes of organisms ranging from E. coli to humans. In a recent webinar, "New RNA Tools for Optimized CRISPR/Cas 9 Genome Editing", we presented how we developed the Alt-R™ CRISPR-Cas9 System for genome editing. Here, we take a look at designing your target sequences and ordering them as Alt-R CRISPR crRNA. We review the other components of the system and walk through the experimental process step by step, from design to evaluation of editing potency. We also discuss challenges and potential pitfalls and provide tips and guidance towards successful genome editing experiments. Learn more: http://www.idtdna.com/crispr
The CRISPR-Cas9 system demonstrates unparalleled genome editing efficiency in a broad range of species and cell types, but it suffers from concerns related to target specificity. Modified guide RNAs and mutant Cas9 proteins have been developed to reduce off-target editing but, in many cases, the alterations also significantly reduce on-target editing performance. In this presentation, Dr Chris Vakulskas discusses a novel, high-fidelity Cas9 protein that reduces off-target gene editing, while maintaining high on-target activity. Dr Vakulskas presents data from the development of the new Alt-R® S.p. HiFi Cas9 Nuclease 3NLS and describes its usefulness in mitigating unwanted off-target gene editing, without the issues associated with transfection of plasmid DNA.
Presentation by Tina Graves-Lindsay at GRC/GIAB ASHG 2017 workshop "Getting the most from the reference assembly and reference materials" on production of reference grade assemblies for various human populations.
#SEJThinkTank Webinar: Social Marketing Hacks To Crush It in 2015Search Engine Journal
Looking for ways to rock your social marketing? The data is in, and savvy marketers are using it to turn readily available social data into attributable conversions. Join Daniel Morrison of aimClear as he covers selling with first-touch social psychographic data: disciplined, high intent, active targeting, including owned-audience cookie pools for performance marketers to exploit.
Amy Vernon of The Daily Dot #SEJSummit: Lessons from the NewsroomSearch Engine Journal
Amy Vernon of The Daily Dot looks at search and social through the lens of a journalist and explains how key strategies for success in the newsroom can be applied to digital marketing. She will also share how and why SEOs should be concerned with audience engagement in 2016.
Are you seeking to convert an excel spreadsheet into a native iPhone or iPad app? We can help.
Not only we help you in converting an excel sheet into iOS application but we also walk you through the benefits of having such an app so that you can make the most out of it. For more Contact us (650) 666-3071 @ Spaceotechnologies.com or Email us : Spaceo.Inquiry@gmail.com .
#SEJThinkTank: Harnessing the Networks of Your Podcast Guests & Audiences Search Engine Journal
Did you know you can raise more awareness for your podcast by leveraging the networks of your guests and audiences?
In managing any content, you need to continuously build your audience. Join Kelsey Jones, Executive Editor at SEJ for presentation about looking at the resources you already have.
Steal from the Startups: Entrepreneur Style Growth Tactics for Big Brands by ...Search Engine Journal
Steal from the Startups: Entrepreneur Style Growth Tactics for Big Brands
By Kevin Henrikson Partner Group Engineering Manager, Microsoft
Accelerated growth and agile marketing tactics aren't just for startups. Kevin will review examples and how-tos on startup techniques that he's deployed successfully with enterprise level marketing teams, focusing on funnel improvement and paid advertising.
Link Building Metrics: Managing Projects and SEOs with Page One PowerSearch Engine Journal
Link building is a challenge for all brands. Your strategy will vary depending on your goals, industry, and competition level, not to mention the skills of the individual link builder.
In this webinar, produced in partnership with Page One Power, Project Manager Cody Cahill, has the link building solutions you’ve been looking for.
15 thought leaders presenting at the Authority Rainmaker conference share integrated marketing advice on Design, Content, Traffic and Conversion.
Authority Rainmaker conference is May 13-15 in Denver, CO featuring nationally known experts including Daniel Pink, Sally Hogshead, Chris Brogan and Henry Rollins. Marketing experts include Brian Clark, Ann Handley, Joe Pulizzi, Danny Sullivan, and many others.
This eBook was produced for Copyblogger Media by TopRank Online Marketing.
Los días 20 y 21 de octubre de 2016, la Fundacion Ramón Areces organizó un simposio internacional para analizar las 'Enfermedades raras de la piel: de la clínica al gen y viceversa'. El doctor Fernando Larcher Laguzzi, del CIEMAT-Universidad Carlos III de Madrid-IIS Fundación Jiménez Díaz, ejerció de coordinador.
Identifying candidate targets for Cancer Therapy with Integrated Text Mining ...Ann-Marie Roche
In this 60 minute webinar, Philip L. Lorenzi Ph.D. talked to us about autophagy, a programmed process in which cell contents are delivered to lysosomes for degradation and which appears to have both tumor-suppressive and tumor-promoting functions. Phillip and his colleagues have compiled a comprehensive, curated inventory of autophagy modulators by integrating information from published siRNA screens, multiple pathway analysis algorithms, and extensive text-mining of the literature and he will provide extensive analysis of their sources of information and their complex relationships with each other.
Stratégies orthogonales pour la caractérisation de glycoprotéines thérapeutiq...Quality Assistance s.a.
Stratégies orthogonales pour la caractérisation de glycoprotéines thérapeutiques par LC/MS par Arnaud Delobel, R&D Director
Visit www.quality-assistance.com for more information
Presentation of Fridtof Lund-Johansen in 1st International Antibody Validatio...St John's Laboratory Ltd
Fridtjof Lund-Johansen is an MDPhD who has worked for 30 years with antibodies and flow cytometry. He took his degree at the University of Bergen in Norway. He then did post-docs in California, first at Becton Dickinson in San Jose and then at DNAX instiute of Immunology in Palo Alto. He is now a PI at the Institute of Immunology at Oslo University Hospital where he leads an effort to develop antibody-based proteomics. His technology is called MAP for microsphere affinity proteomics. He will talk about how MAP can be used to test thousands of antibodies in parallel.
For more details about 1st international antibody validation forum please check on http://www.stjohnslabs.com/ac_cms/blog
BIOC 405 Assignment 1 Dr Moore Due Friday March 1st, .docxtangyechloe
BIOC 405 Assignment 1: Dr Moore
Due Friday March 1st, 2019 before 16:00 in Room 3D30.8 HSc
1. (a)In your handout for protein kinase A, there is a table of known substrate
sequences, in other words sequences of peptides phosphorylated by PKA. Please do your
best to align the substrate sequences provided, and from the alignment, predict what a good
consensus substrate for PKA will be. To present your alignment, please use an equal width
font for the protein sequences (Courier or Courier New work well). Highlight the P(0)
residue, P(-1) etc.
(b)The regulatory subunit (R) of protein kinase A has a short sequence
(RRRRGAISA that is critical for inhibiting the activity of the kinase catalytic subunit. This
short sequence of the R-subunit actually sits in the active site cleft of PKA in the
crystallographically-determined structure of the inhibited RC complex. Can you deduce
what the function of this sequence is? Using the answer to part (a) as a guide, please align
the inhibitory sequence with the known substrate sequences to deduce how this sequence
likely functions to inhibit PKA. Furthermore, using your class notes, can you make a guess
at which residues on PKA might interact with specific residues from the R-inhibitory
peptide?
2. For a regularly spaced 1-Dimensional array of atoms (spacing =13 Å) calculate the
total number of diffraction maxima and their scattering angles (for perfect in phase
scattering from the atoms in the 1-D array) between scattering angles of zero and ninety
degrees Use a wavelength of d=1.25 Å. Please include a drawing to explain the diffraction
condition and show your calculations.
3. Using site specific mutagenesis to change residues in the substrate binding cleft of
PKA (not residues involved in catalytic roles), how would you alter PKA’s substrate
specificity at P-3, and P-2 to Glu and P+1 to Asn? By this, I mean how would you
specifically make mutations in the PKA enzyme amino acid sequence (not the substrate
sequence) that would select for binding and phosphorylation of a peptide sequence that
would clearly differ from the known substrate sequence preferred by PKA as outlined
above. Be sure to clearly highlight exactly what residues in the PKA sequence you would
have to change (and to what amino acid) to achieve this.
4. The following lines of data describe the atomic coordinates for an arginine residue in
a protein molecule in PDB (protein data bank) format. Since proteins are three-dimensional
objects, the position of each atom is specified in space by its X, Y and Z coordinates. On each
line of a PDB formatted file, the atom number is given, the atom type is next (e.g. N-
backbone nitrogen, backbone carbonyl oxygen etc), the residue name (here ARG 431 in chain
D; in this instance the protein crystal contains four independent copies of the polypeptide
chain, labelled A through D), then the X-coordinate for that atom, the Y-coordinate for that
atom and the Z-coo.
Struggling with low editing efficiency or delivery problems in primary or difficult-to-transfect cells? In this presentation, learn about the advantages of using a Cas9:crRNA:tracrRNA ribonucleoprotein (RNP) complex for genome editing. We show the benefits of using RNP complexes, including ease of use, limiting off-target effects, and stability. We also present data showing how genome editing efficiency rates are improved by our Cas9 electroporation enhancer. Furthermore, we provide advice on how to optimize transfection using the Alt-R™ CRISPR-Cas9 System in combination with different electroporation methodologies.
Two-Tailed PCR - New Ultrasensitive and Ultraspecific Technique for the Quant...Kate Barlow
Mikael Kubista, Department of Biotechnology, CAS and TATAA Biocenter
We present a highly specific, sensitive and cost-effective system to quantify miRNA expression based on novel chemistry called Two-tailed RT-qPCR. It takes advantage of target-specific primers for reverse transcription composed of two hemiprobes complementary to two different parts of the targeted miRNA, connected by a hairpin structure. The introduction of a second probe ensures high sensitivity and enables discrimination of highly homologous miRNAs irrespectively of the position of the mismatched nucleotide. Two-tailed RT-qPCR has a dynamic range of 7 logs and a sensitivity sufficient to detect less than ten target miRNA molecules. The reverse transcription step can be multiplexed and it allows for rapid testing with a total analysis time of less than 2.5 hours.
Data Integration: What I Haven't Yet AchievedNeil Saunders
Data integration is a hot topic in bioinformatics, but the term means different things to different people. What do we think it means? Talk given at CSIRO Bioinformatics & Biostatistics group meeting, November 21 2012.
What can science networking online do for youNeil Saunders
A talk on networking and blogging for life scientists. Part of a science communication seminar series, Diamantina Institute, Princess Alexandra hospital, Brisbane.
The Viking labelled release experiment: life on Mars?Neil Saunders
This is a very old talk from around 1999 that I gave to my department at the Free University of Amsterdam. It\'s very out of date now, but still interesting.
How to get verified on Coinbase Account?_.docxBuy bitget
t's important to note that buying verified Coinbase accounts is not recommended and may violate Coinbase's terms of service. Instead of searching to "buy verified Coinbase accounts," follow the proper steps to verify your own account to ensure compliance and security.
where can I find a legit pi merchant onlineDOT TECH
Yes. This is very easy what you need is a recommendation from someone who has successfully traded pi coins before with a merchant.
Who is a pi merchant?
A pi merchant is someone who buys pi network coins and resell them to Investors looking forward to hold thousands of pi coins before the open mainnet.
I will leave the what'sapp contact of my personal pi merchant to trade with
+12349014282
Financial Assets: Debit vs Equity Securities.pptxWrito-Finance
financial assets represent claim for future benefit or cash. Financial assets are formed by establishing contracts between participants. These financial assets are used for collection of huge amounts of money for business purposes.
Two major Types: Debt Securities and Equity Securities.
Debt Securities are Also known as fixed-income securities or instruments. The type of assets is formed by establishing contracts between investor and issuer of the asset.
• The first type of Debit securities is BONDS. Bonds are issued by corporations and government (both local and national government).
• The second important type of Debit security is NOTES. Apart from similarities associated with notes and bonds, notes have shorter term maturity.
• The 3rd important type of Debit security is TRESURY BILLS. These securities have short-term ranging from three months, six months, and one year. Issuer of such securities are governments.
• Above discussed debit securities are mostly issued by governments and corporations. CERTIFICATE OF DEPOSITS CDs are issued by Banks and Financial Institutions. Risk factor associated with CDs gets reduced when issued by reputable institutions or Banks.
Following are the risk attached with debt securities: Credit risk, interest rate risk and currency risk
There are no fixed maturity dates in such securities, and asset’s value is determined by company’s performance. There are two major types of equity securities: common stock and preferred stock.
Common Stock: These are simple equity securities and bear no complexities which the preferred stock bears. Holders of such securities or instrument have the voting rights when it comes to select the company’s board of director or the business decisions to be made.
Preferred Stock: Preferred stocks are sometime referred to as hybrid securities, because it contains elements of both debit security and equity security. Preferred stock confers ownership rights to security holder that is why it is equity instrument
<a href="https://www.writofinance.com/equity-securities-features-types-risk/" >Equity securities </a> as a whole is used for capital funding for companies. Companies have multiple expenses to cover. Potential growth of company is required in competitive market. So, these securities are used for capital generation, and then uses it for company’s growth.
Concluding remarks
Both are employed in business. Businesses are often established through debit securities, then what is the need for equity securities. Companies have to cover multiple expenses and expansion of business. They can also use equity instruments for repayment of debits. So, there are multiple uses for securities. As an investor, you need tools for analysis. Investment decisions are made by carefully analyzing the market. For better analysis of the stock market, investors often employ financial analysis of companies.
how to swap pi coins to foreign currency withdrawable.DOT TECH
As of my last update, Pi is still in the testing phase and is not tradable on any exchanges.
However, Pi Network has announced plans to launch its Testnet and Mainnet in the future, which may include listing Pi on exchanges.
The current method for selling pi coins involves exchanging them with a pi vendor who purchases pi coins for investment reasons.
If you want to sell your pi coins, reach out to a pi vendor and sell them to anyone looking to sell pi coins from any country around the globe.
Below is the what'sapp information for my personal pi vendor.
+12349014282
What website can I sell pi coins securely.DOT TECH
Currently there are no website or exchange that allow buying or selling of pi coins..
But you can still easily sell pi coins, by reselling it to exchanges/crypto whales interested in holding thousands of pi coins before the mainnet launch.
Who is a pi merchant?
A pi merchant is someone who buys pi coins from miners and resell to these crypto whales and holders of pi..
This is because pi network is not doing any pre-sale. The only way exchanges can get pi is by buying from miners and pi merchants stands in between the miners and the exchanges.
How can I sell my pi coins?
Selling pi coins is really easy, but first you need to migrate to mainnet wallet before you can do that. I will leave the what'sapp contact of my personal pi merchant to trade with.
+12349014282
1. Elemental Economics - Introduction to mining.pdfNeal Brewster
After this first you should: Understand the nature of mining; have an awareness of the industry’s boundaries, corporate structure and size; appreciation the complex motivations and objectives of the industries’ various participants; know how mineral reserves are defined and estimated, and how they evolve over time.
Yes of course, you can easily start mining pi network coin today and sell to legit pi vendors in the United States.
Here the what'sapp contact of my personal vendor.
+12349014282
#pi network #pi coins #legit #passive income
#US
Abhay Bhutada Leads Poonawalla Fincorp To Record Low NPA And Unprecedented Gr...Vighnesh Shashtri
Under the leadership of Abhay Bhutada, Poonawalla Fincorp has achieved record-low Non-Performing Assets (NPA) and witnessed unprecedented growth. Bhutada's strategic vision and effective management have significantly enhanced the company's financial health, showcasing a robust performance in the financial sector. This achievement underscores the company's resilience and ability to thrive in a competitive market, setting a new benchmark for operational excellence in the industry.
Turin Startup Ecosystem 2024 - Ricerca sulle Startup e il Sistema dell'Innov...Quotidiano Piemontese
Turin Startup Ecosystem 2024
Una ricerca de il Club degli Investitori, in collaborazione con ToTeM Torino Tech Map e con il supporto della ESCP Business School e di Growth Capital
What price will pi network be listed on exchangesDOT TECH
The rate at which pi will be listed is practically unknown. But due to speculations surrounding it the predicted rate is tends to be from 30$ — 50$.
So if you are interested in selling your pi network coins at a high rate tho. Or you can't wait till the mainnet launch in 2026. You can easily trade your pi coins with a merchant.
A merchant is someone who buys pi coins from miners and resell them to Investors looking forward to hold massive quantities till mainnet launch.
I will leave the what's app number of my personal pi vendor to trade with.
+12349014282
5. Kinase specificity - peptide specificity Amino acid frequency in substrate sequences at X{7}[ST]X{7} sites CK-2 PKA MAPK
6. Structural basis for peptide specificity Substrate heptapeptide binding to protein kinase A PKA surface + heptapeptide RRASIHD Schematic of heptapeptide + PKA SDRs
7. Accurate location of key residues using HMMER *->Yellkkl GkG aFGkVylardkktgrlv AiK vik..........eril Y+++k+lG+G+FGkV+la+++ tg++vA+K+i+++ +++ + ri+ snf1p 55 YQIVKTL GE GS F GKVKLAYHTTTGQKV ALK IINkkvl aks dmqGRIE 101 rEikiLkk.dHPNIVkLydvfed.dklylVmEyceGdl GdL fdllkkrgr rEi+ L+ +HP+I+kLydv+ ++d++ +V Ey+++ +Lfd++++r + snf1p 102 REISYLRLlRHPHIIKLYDVIKSkDEIIMVIEYAGN-- - E L FD YIVQRDK 148 rglrkvlsE.earfyfrQilsaLeYLHsqgIiHRDLKPeNiLLds..hvK +sE+ear++f+Qi+sa+eY+H+++I+HRDLKPeN+LLd++ +vK snf1p 149 ------MSEqEARRFFQQIISAVEYCHRHKIVHRDLKPENLLLDEhlNVK 192 la DFG lArql......ttfvGTpeYm APE vl...gYgkpavDiWSlGcil +aDFGl+ ++++++ +t +G+p+Y APEv++++ Y +p+vD+WS+G+il snf1p 193 IA DFG L SNIMtdgnflK TS CG S P NY A APE VIsgkLYAGPEVDVWSCGVIL 242 yElltGkpPFp..qldlifkkig..........SpeakdLikklLvkdPe y +l+++ PF+++ + ++fk+i ++ ++ ++ Sp a Lik++L ++P snf1p 243 YVMLCRRLPFDdeSIPVLFKNISngvytlpkflSPGAAGLIKRMLIVNPL 292 kRlta.eaLedeldikaHPff<-* +R++++e+++ + +f snf1p 293 NRISIhEIMQ-------DDWF 306 GkG, AiK, GdL, DFG, APE anchor positions -3 +3 Substrate heptapeptide X X X [ST] X X X
8.
9.
10. PredikinDB construction Substrate UniProt entry ID IF2A_MOUSE AC Q6ZWX6 ; Q3TIQ0; OS Mus musculus (Mouse) . FT MOD_RES 49 49 Phospho serine (by HRI ) ( By similarity ). FT MOD_RES 52 52 Phospho serine (by EIF2AK3 , GCN2 , HRI and PKR ). Entries in table_kinases that match kinase name and species Q9Z2R9 EIF2AK1 Eif2ak1; Hri Q9Z2B5 EIF2AK3 Eif2ak3;Pek;Perk Q9QZ05 EIF2AK4 Eif2ak4; Gcn2 ;Kiaa1338 Q03963 EIF2AK2 Eif2ak2; Pkr ;Prkr;Tik Entry in table_psites substrate_ac residue posn hepta conf kinase_name kinase_ac Q6ZWX6 S 49 ILLSELS 2 HRI Q9Z2R9 Q6ZWX6 S 52 SELSRRR 1 EIF2AK3 Q9Z2B5 Q6ZWX6 S 52 SELSRRR 1 GCN2 Q9QZ05 Q6ZWX6 S 52 SELSRRR 1 HRI Q9Z2R9 Q6ZWX6 S 52 SELSRRR 1 PKR Q03963 PredikinDB links phosphorylation sites to their specific kinase sequences
13. Scoring matrices: SDR method Query kinase: GEL+1 = E GEL+3 = F GEL+4 = S Type = Ser/Thr SQL query for heptapeptide position -3: select hepta from psites, kinases where kinase_type = 'Ser/Thr' and psites.kinase_ac = kinases.kinase_ac and GELp1 rlike '[ D E N ] ' and GELp3 rlike '[ F WY ] ' and GELp4 rlike '[ AN S T ]' Heptapeptides : Q FSTVKG E QFSTVK R SVSEAA R SGSSPN R HDSGLD R RMSDEF A RGSFDA Repeat for positions -2 to +3 and corresponding SDRs Frequency matrix PWM (weights) matrix score substrates
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19. The Predikin webserver: implementation http://predikin.biosci.uq.edu.au perl.so MySQL PredikinDB PHP Predikin.pm Apache Server DisEMBL TMHMM BLAST pantherScore HMMER Client (browser)