1. Basic Information
| Name: | JAK2_HUMAN |
| Accession#: | O60674 |
| Description: | Tyrosine-protein kinase JAK2 |
| AA Number: | 1140 |
| Sequence: |
1 51 101 151 201 251 301 351 401 451 501 551 601 651 701 751 801 851 901 951 1001 1051 1101
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SEQUENCEMG MACLTMTEME GTSTSSIYQN GDISGNANSM KQIDPVLQVY LYHSLGKSEA DYLTFPSGEY VAEEICIAAS KACGITPVYH NMFALMSETE RIWYPPNHVF HIDESTRHNV LYRIRFYFPR WYCSGSNRAY RHGISRGAEA PLLDDFVMSY LFAQWRHDFV HGWIKVPVTH ETQEECLGMA VLDMMRIAKE NDQTPLAIYN SISYKTFLPK CIRAKIQDYH ILTRKRIRYR FRRFIQQFSQ CKATARNLKL KYLINLETLQ SAFYTEKFEV KEPGSGPSGE EIFATIIITG NGGIQWSRGK HKESETLTEQ DLQLYCDFPN IIDVSIKQAN QEGSNESRVV TIHKQDGKNL EIELSSLREA LSFVSLIDGY YRLTADAHHY LCKEVAPPAV LENIQSNCHG PISMDFAISK LKKAGNQTGL YVLRCSPKDF NKYFLTFAVE RENVIEYKHC LITKNENEEY NLSGTKKNFS SLKDLLNCYQ METVRSDNII FQFTKCCPPK PKDKSNLLVF RTNGVSDVPT SPTLQRPTHM NQMVFHKIRN EDLIFNESLG QGTFTKIFKG VRREVGDYGQ LHETEVLLKV LDKAHRNYSE SFFEAASMMS KLSHKHLVLN YGVCVCGDEN ILVQEFVKFG SLDTYLKKNK NCINILWKLE VAKQLAWAMH FLEENTLIHG NVCAKNILLI REEDRKTGNP PFIKLSDPGI SITVLPKDIL QERIPWVPPE CIENPKNLNL ATDKWSFGTT LWEICSGGDK PLSALDSQRK LQFYEDRHQL PAPKWAELAN LINNCMDYEP DFRPSFRAII RDLNSLFTPD YELLTENDML PNMRIGALGF SGAFEDRDPT QFEERHLKFL QQLGKGNFGS VEMCRYDPLQ DNTGEVVAVK KLQHSTEEHL RDFEREIEIL KSLQHDNIVK YKGVCYSAGR RNLKLIMEYL PYGSLRDYLQ KHKERIDHIK LLQYTSQICK GMEYLGTKRY IHRDLATRNI LVENENRVKI GDFGLTKVLP QDKEYYKVKE PGESPIFWYA PESLTESKFS VASDVWSFGV VLYELFTYIE KSKSPPAEFM RMIGNDKQGQ MIVFHLIELL KNNGRLPRPD GCPDEIYMIM TECWNNNVNQ RPSFRDLALR VDQIRDNMAG |
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*Highlighted peptides (with yellow background) have developed assays.
*Green background amino acids are PTMs.
2. Protein Separation
Sample Preparation: 1 million cells from cell line K526 were lysed in an immuno-precipitation buffer containing 20 mM Tris-HCL (pH 7.6), 150 mM NaCl, 1mN EDTA, 0.1% NP-40, 100ug/ml PMSF, and 1mM sodium vanadate. Cell lysates were vortexed on ice for 30 minutes and spun to clear. The Supernatant was then incubated with protein A, and then with JAK2 specific antibody that has already been bound to protein A. Samples were incubated overnight, washed and then the beads were boiled in gel loading buffer and run for 1 hour on an SDS page gel (12% Bis-Tris). Resulting gel bands were then excised, reduced, alkylated and digested overnight with trypsin.
3. LC-MS/MS Data
NILVENENR
No LC-MS/MS for this peptide.
FGSLDTYLK
No LC-MS/MS for this peptide.
SNLLVFR
No LC-MS/MS for this peptide.
LSDPGISITVLPK
No LC-MS/MS for this peptide.
SDNIIFQFTK
No LC-MS/MS for this peptide.
IQDYHILTR
No LC-MS/MS for this peptide.
4. LC-MRM Screening
Peptides screening: Peptides and transitions for analysis were selected from previous LC-MS/MS experiments. The results were screened for those with the highest specificity and the most intense transitions.