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Protein Page:
KRas (human)
p Phosphorylation
ac Acetylation
me Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
ub Ubiquitylation
sm Sumoylation
ne Neddylation
gl O-GlcNAc
ga O-GalNAc
pa Palmitoylation
ad Adenylation
sn S-Nitrosylation
ca Caspase cleavage
sc Succinylation

Overview
KRas Ras proteins bind GDP/GTP and possess intrinsic GTPase activity. Interacts with PHLPP. Interacts (active GTP-bound form preferentially) with RGS14. Alternate between an inactive form bound to GDP and an active form bound to GTP. Activated by a guanine nucleotide-exchange factor (GEF) and inactivated by a GTPase- activating protein (GAP). Belongs to the small GTPase superfamily. Ras family. 2 isoforms of the human protein are produced by alternative splicing. Note: This description may include information from UniProtKB.
Protein type: Motility/polarity/chemotaxis; G protein, monomeric; Oncoprotein; G protein; G protein, monomeric, Ras
Chromosomal Location of Human Ortholog: 12p12.1
Cellular Component: cytoplasm; cytosol; extrinsic to internal side of plasma membrane; focal adhesion; lipid raft; membrane; mitochondrion; plasma membrane
Molecular Function: GDP binding; GMP binding; GTP binding; GTPase activity; LRR domain binding; protein binding; protein complex binding
Biological Process: actin cytoskeleton organization and biogenesis; activation of NF-kappaB transcription factor; axon guidance; cytokine and chemokine mediated signaling pathway; epidermal growth factor receptor signaling pathway; forebrain astrocyte development; homeostasis of number of cells within a tissue; intracellular protein transport; leukocyte migration; MAPKKK cascade; negative regulation of cell differentiation; negative regulation of neuron apoptosis; nucleocytoplasmic transport; positive regulation of cell proliferation; positive regulation of MAP kinase activity; positive regulation of nitric-oxide synthase activity; positive regulation of protein amino acid phosphorylation; positive regulation of Rac protein signal transduction; Ras protein signal transduction; regulation of long-term neuronal synaptic plasticity; regulation of protein stability; regulation of synaptic transmission, GABAergic; response to glucocorticoid stimulus; response to mineralocorticoid stimulus; social behavior; stimulatory C-type lectin receptor signaling pathway; striated muscle cell differentiation; visual learning
Disease: Bladder Cancer; Breast Cancer; Cardiofaciocutaneous Syndrome 2; Gastric Cancer, Hereditary Diffuse; Leukemia, Acute Myeloid; Lung Cancer; Noonan Syndrome 3; Pancreatic Cancer; Schimmelpenning-feuerstein-mims Syndrome
Reference #:  P01116 (UniProtKB)
Gene Symbols: KRAS
Molecular weight: 21,656 Da
Basal Isoelectric point: 6.33  Predict pI for various phosphorylation states
CST Pathways:  Actin Dynamics  |  Angiogenesis  |  B Cell Receptor Signaling  |  ErbB/HER Signaling  |  ESC Pluripotency and Differentiation  |  GPCR Signaling to MAPKs  |  Growth And Differentiation Control by MAPKs  |  IL6 Signaling  |  Inhibition of Apoptosis  |  Insulin Receptor Signaling  |  NF-kB Signaling  |  SAPK/JNK Signaling Cascades  |  T Cell Receptor Signaling  |  TGF-ß Signaling  |  Warburg Effect
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
Select Structure to View Below

KRas

Protein Structure Not Found.
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Sites Implicated In
cell growth, induced: Y64‑p
molecular association, regulation: Y64‑p

Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

Show Multiple Sequence Alignment


 LTP 

LTP: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 HTP 

HTP: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

► Hide Isoforms
 
0 1 T2‑p ______MtEyKLVVV
0 1 Y4‑p ____MtEyKLVVVGA
0 10 S39‑p YDPTIEDsyRKQVVI
0 3 Y40‑p DPTIEDsyRKQVVID
1 1 R41 PTIEDsyRKQVVIDG
1 1 K42 TIEDsyRKQVVIDGE
1 5 Y64‑p DTAGQEEySAMRDQY
0 1 S89‑p FAINNTKsFEDIHHy
0 1 Y96‑p sFEDIHHyREQIKRV
2 0 K104‑ac REQIKRVkDsEDVPM
1 0 K104‑ub REQIKRVkDsEDVPM
0 1 S106‑p QIKRVkDsEDVPMVL
0 3 K117‑ub PMVLVGNkCDLPSRT
0 34 K128‑ub PSRTVDTkQAQDLAR
2 5 K147‑ub PFIETSAkTRQRVED
0 1 T148 FIETSAkTRQRVEDA
0 17 Y157‑p QRVEDAFyTLVREIR
0 1 T158 RVEDAFyTLVREIRQ
0 1 - gap
6 0 - gap
  KRas iso2  
T2 ______MTEYKLVVV
Y4 ____MTEYKLVVVGA
S39 YDPTIEDSYRKQVVI
Y40 DPTIEDSYRKQVVID
R41 PTIEDSYRKQVVIDG
K42 TIEDSYRKQVVIDGE
Y64 DTAGQEEYSAMRDQY
S89 FAINNTKSFEDIHHY
Y96 SFEDIHHYREQIKRV
K104 REQIKRVKDSEDVPM
K104 REQIKRVKDSEDVPM
S106 QIKRVKDSEDVPMVL
K117 PMVLVGNKCDLPSRT
K128 PSRTVDTKQAQDLAR
K147 PFIETSAKtRQGVDD
T148‑p FIETSAKtRQGVDDA
Y157‑p QGVDDAFytLVREIR
T158‑p GVDDAFytLVREIRK
K179‑ac KDGKKKKkKsKTKCV
S181‑p GKKKKkKsKTKCVIM
  mouse

► Hide Isoforms
 
T2 ______MTEYKLVVV
Y4 ____MTEYKLVVVGA
S39‑p YDPTIEDsYRKQVVI
Y40 DPTIEDsYRKQVVID
R41 PTIEDsYRKQVVIDG
K42 TIEDsYRKQVVIDGE
Y64 DTAGQEEYSAMRDQY
S89 FAINNTKSFEDIHHY
Y96 SFEDIHHYREQIKRV
K104 REQIKRVKDSEDVPM
K104 REQIKRVKDSEDVPM
S106 QIKRVKDSEDVPMVL
K117‑ub PMVLVGNkCDLPSRT
K128‑ub PSRTVDTkQAQELAR
K147‑ub PFIETSAkTRQRVED
T148 FIETSAkTRQRVEDA
Y157 QRVEDAFYTLVREIR
T158 RVEDAFYTLVREIRQ
- gap
- gap
  KRas iso2  
T2 ______MTEYKLVVV
Y4 ____MTEYKLVVVGA
S39 YDPTIEDSYRKQVVI
Y40 DPTIEDSYRKQVVID
R41 PTIEDSYRKQVVIDG
K42 TIEDSYRKQVVIDGE
Y64 DTAGQEEYSAMRDQY
S89 FAINNTKSFEDIHHY
Y96 SFEDIHHYREQIKRV
K104 REQIKRVKDSEDVPM
K104 REQIKRVKDSEDVPM
S106 QIKRVKDSEDVPMVL
K117 PMVLVGNKCDLPSRT
K128 PSRTVDTKQAQELAR
K147 PFIETSAKTRQGVDD
T148 FIETSAKTRQGVDDA
Y157 QGVDDAFYTLVREIR
T158 GVDDAFYTLVREIRK
K179 KDGKKKKKKsRTRCT
S181‑p GKKKKKKsRTRCTVM
  rat

 
T2 ______MTEYKLVVV
Y4 ____MTEYKLVVVGA
S39 YDPTIEDSYrkQVVI
Y40 DPTIEDSYrkQVVID
R41‑m2 PTIEDSYrkQVVIDG
K42‑m2 TIEDSYrkQVVIDGE
Y64 DTAGQEEYSAMRDQY
S89 FAINNTKSFEDIHHY
Y96 SFEDIHHYREQIKRV
K104 REQIKRVKDSEDVPM
K104 REQIKRVKDSEDVPM
S106 QIKRVKDSEDVPMVL
K117 PMVLVGNKCDLPSRT
K128‑ub PSRTVDTkQAQELAR
K147 PFIETSAKTRQRVED
T148 FIETSAKTRQRVEDA
Y157 QRVEDAFYTLVREIR
T158 RVEDAFYTLVREIRQ
- gap
- gap
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