kinome poster

1
MYT1 Wee1 Wee1B PIK3R4 SgK493 VRK1 VRK2 Bub1 BubR1 CK1g2 CK1a CK1a2 CK1d CK1e CK1g1 CK1g3 PRPK Haspin SCYL2 SCYL1 SCYL3 SgK196 SgK396 Slob VRK3 MSK1 p70S6K p70S6Kb RSK3 PKCi PKCz PKN3 RSK4 PKCd PKCu RSK1/p90RSK RSK2 PKCg PKCh PKCe PKCa PKCb GRK4 GRK5 TLK2 PLK1 PLK4 PLK3 PLK2 MRCKb MRCKa GRK6 RHODK/GRK1 AurA/Aur2 TLK1 AurB/Aur1 AurC/Aur3 DMPK ROCK1 ROCK2 NDR1 NDR2 DMPK2 YANK2 YANK3 YANK1 SgK494 PDK1 BARK1/GRK2 BARK2/GRK3 GRK7 MAST3 MASTL MAST2 MAST4 MAST1 PKN1/PRK1 PKN2/PRK2 MSK2 LATS1 LATS2 Akt3/PKBg SGK2 Akt1/PKBa Akt2/PKBb SGK1 SGK3 CRIK PKAa PKAb PRKY PRKX PKG2 PKG1 PKAg CAMKK1 CAMKK2 ULK1 ULK2 BIKE AAK1 SBK RSKL2 RSKL1 IKKa IKKb IKKe TBK1 SgK069 SgK110 GAK MPSK1 MAP2K5 MAP2K7 OSR1 STLK3 STLK5 STLK6 MKK3/MAP2K3 MKK6/MAP2K6 SEK1/MAP2K4 TAO3 PAK3 PAK6 MEK1/MAP2K1 MEK2/MAP2K2 LOK SLK COT NIK GCN2~b TAO2 TAO1 PAK1 PAK2 PAK4 PAK5 PBK CDK8 CDK11 ERK7 ERK3 ERK4 CDKL5 GSK3a GSK3b ICK MAK CCRK CDK9 CDK7 NLK CDKL1 CDKL4 CDKL2 CDKL3 CHED CRK7 CDK4 CDK6 CDK10 PITSLRE ERK5 JNK2 CDK5 ERK1 ERK2 JNK1 JNK3 p38a p38b p38d p38g CDC2/CDK1 PCTAIRE3 PFTAIRE1 PFTAIRE2 CDK2 CDK3 PCTAIRE1 PCTAIRE2 CK2a2 CK2a1 MOK SgK071 RNAseL CLIK1L CLIK1 TTK KIS IRE1 IRE2 TBCK HRI GCN2 PKR PERK/PEK CDC7 MAP3K4 KHS1 KHS2 NRK/ZC4 MYO3A MYO3B MST1 MST2 MST4 TNIK/ZC2 HGK/ZC1 MINK/ZC3 MAP3K8 MEKK6/MAP3K6 RIPK3 LIMK1 LIMK2 TESK1 TESK2 ALK1 ALK2 TGFbR2 MISR2 BMPR2 RIPK2 HH498 TAK1 ILK ARAF KSR KSR2 BMPR1A BMPR1B ALK7 ActR2 ActR2B ANKRD3 SgK288 ZAK BRAF RAF1 ALK4 TGFbR1 DLK LZK MLK2 MLK4 MLK1 MLK3 LRRK1 LRRK2 SgK496 RIPK1 WNK3 WNK1 WNK2 NRBP1 NRBP2 WNK4 MEKK1/MAP3K1 MEKK2/MAP3K2 MEKK3/MAP3K3 ASK/MAP3K5 MAP3K7 MLKL SgK307 SgK424 IRAK4 HSER CYGD CYGF IRAK2 ANPa ANPb IRAK1 IRAK3 ULK3 ULK4 Fused MELK NIM1 SNRK SSTK TSSK3 TSSK1 AMPKa1 AMPKa2 BRSK1 BRSK2 NuaK1 NuaK2 MARK4 QSK MARK3 QIK SIK MARK1 MARK2 CaMK1b CaMK1g RSK3~b CHK2 PKD2 HUNK DCAMKL3 CASK MAPKAPK5 VACAMKL PSKH1 PSKH2 MAPKAPK2 MAPKAPK3 MSK1~b MSK2~b RSK4~b TSSK2 TSSK4 Nek6 Nek7 Nek2 Nek8 Nek9 Nek11 Nek4 Nek3 Nek1 Nek5 Nek10 STK33 MNK1 MNK2 PhKg1 PhKg2 PKD3 DCAMKL1 DCAMKL2 CaMK4 CaMK2a CaMK2d CaMK2b CaMK2g RSK1~b RSK2~b PKD1 Trb1 Trb3 Trb2 SgK495 DRAK1 DAPK1 DAPK2 caMLCK SgK085 DAPK3 DRAK2 skMLCK smMLCK TTN Trad Trio Obscn SPEG Obscn~b SPEG~b Pim1 Pim3 Pim2 CHK1 PASK Lkb1 SuRTK106 JAK1~b Tyk2~b JAK2~b JAK3~b MOS Lmr1 Lmr2 Lmr3 EphA2 Etk/BMX BTK ITK BLK Fgr EphA8 TEC TXK Lck Fyn HCK Lyn Src Yes EphA7 EphB4 EphA6 EphB3 EphA4 EphB1 EphB2 EphA3 EphA5 EphA10 EphB6 Fer FRK Brk Srm EphA1 Abl Arg CSK CTK FLT4 CCK4/PTK7 PDGFRa PDGFRb Axl Mer FGFR1 FGFR4 FLT1 KDR Fms/CSFR Kit ALK LTK IGF1R InsR DDR1 DDR2 MuSK TRKA FGFR2 FGFR3 TRKB TRKC EGFR HER2 Tyro3/ Sky Met Ron Ret FLT3 Ros IRR ROR1 ROR2 Tnk1 HER3 JAK3 PYK2 ZAP70 RYK TIE1 HER4 Ack JAK1 Tyk2 JAK2 Syk TIE2 FAK Fes HPK1 GCK MST3 YSK1 SgK223 SgK269 PINK1 TTBK1 TTBK2 CaMK1a CaMK1d PRP4 SRPK2 HIPK4 CLK3 CLK4 CLK2 CLK1 MSSK1 SRPK1 DYRK1A DYRK1B DYRK4 HIPK3 DYRK2 DYRK3 HIPK1 HIPK2 TKL TK STE CK1 CMGC AGC CAMK THE Kinome Kinome Human Authors Gerard Manning, David B. Whyte, Ricardo Martinez, Sucha Sudarsanam, Sugen Inc., South San Francisco, CA, USA; Tony Hunter, Salk Institute, La Jolla, CA, USA. This poster accompanies the paper “The Protein Kinase Complement of the Human Genome” (Manning et al., Science, 6 December 2002). Science coordinator L. Bryan Ray Design and production Anne Ashley, David Comb, Michael Melnick, C. Faber Smith, J. White, David M. Tompkins, Marcus Spiegler Copyeditor Harry Jach Sponsored by Cell Signaling Technology, Inc. and Sugen, Inc. © 2002 Science, a publication of the American Association for the Advancement of Science ABC1 Alpha Brd PDHK PIKK RIO AlphaK1 AlphaK2 ChaK2 ChaK1 EEF2K AlphaK3 Brd2 Brd3 Brd4 BrdT PDHK2 PDHK3 PDHK1 PDHK4 BCKDK RIOK3 RIOK1 RIOK2 ATM ATR SMG1 FRAP DNAPK TRRAP TIF1 TIF1b TIF1g TIF1a ADCK1 ADCK5 ADCK3 ADCK4 ADCK2 ATYPICAL PROTEIN KINASES his phylogenetic tree depicts the relationships between members of the complete superfamily of human protein kinases. Protein kinases constitute one of the largest human gene families and are key regulators of cell function. The 518 human protein kinases control protein activity by catalyzing the addition of a negatively charged phosphate group to other proteins. Protein kinases modulate a wide variety of biological processes, especially those that carry signals from the cell membrane to intracellular targets and coordinate complex biological functions. Most protein kinases belong to a single superfamily of enzymes whose catalytic domains are related in sequence and structure. The main diagram illustrates the similarity between the protein sequences of these catalytic domains. Each kinase is at the tip of a branch, and the similarity between various kinases is inversely related to the distance between their positions on the tree diagram. Most kinases fall into small families of highly related sequences, and most families are part of larger groups. The seven major groups are labeled and colored distinctly. Other kinases are shown in the center of the tree, colored gray. The relationships shown on the tree can be used to predict protein substrates and biological function for many of the over 100 uncharacterized kinases presented here. The inset diagram shows trees for seven atypical protein kinase families. These proteins have verified or strongly predicted kinase activity, but have little or no sequence similarity to members of the protein kinase superfamily. A further eight atypical protein kinases in small families of one or two genes are not shown. T Mapping Procedures The main dendrogram shows the sequence similarity between protein kinase domains, derived from public sequences and gene-prediction methods detailed in Manning et al. (Science, 6 December 2002). Domains were defined by hidden Markov model profile analysis and multiple sequence alignment. The initial branching pattern was built from a neighbor-joining tree derived from a ClustalW protein sequence alignment of the domains. This was extensively modified by reference to other alignment and tree-building methods (hmmalign and parsimony trees) and by extensive pairwise sequence alignment of kinase domains. The curved layout was created manually. Many branch lengths are semiquantitative, but the branching pattern is more informative than any single automatic method. The atypical kinase trees were generated automatically by ClustalW alignment of full- length protein sequences followed by neighbor-joining tree building. Unpublished kinases are named where possible according to family nomenclature. Some divergent kinases retain a numerical SgK (Sugen kinase) accession number. The second domains of dual-domain kinases are named with a “~b” suffix. Detailed subtrees and sequence alignments of individual groups and families, and comparative genomic trees are available at http://www.kinase.com. Information on regulation and substrates of many of these kinases is available at http://www.cellsignal.com. Group names AGC Containing PKA, PKG, PKC families; CAMK Calcium/calmodulin-dependent protein kinase; CK1 Casein kinase 1; CMGC Containing CDK, MAPK, GSK3, CLK families; STE Homologs of yeast Sterile 7, Sterile 11, Sterile 20 kinases; TK Tyrosine kinase; TKL Tyrosine kinase–like. Kinase names (A selective list includes those cases in which the full name is more informative than the abbreviation or acronym shown on the tree. Other full names and synonyms are available at http://www.kinase.com.) ActR Activin receptor; ALK (TK group) Anaplastic lymphoma kinase; ALK (TKL group) Activin-like receptor kinase; AMPK Adenosine monophosphate–activated protein kinase; Aur Aurora; BARK β-adrenergic receptor kinase; BLK B lymphocyte tyrosine kinase; BMPR Bone morphogeneic protein receptor; BMX Bone marrow tyrosine kinase gene in chromosome X; BRD Bromodomain kinase; BRSK Brain-selective kinase; CaMK Calcium/calmodulin-dependent protein kinase; CAMKK CaMK kinase; CCK-4 Colon carcinoma kinase–4; CDK Cyclin-dependent kinase; CDKL Cyclin-dependent kinase–like; CK Casein kinase; CLK Cdc2-like kinase; CSFR Colony- stimulating factor receptor; DAPK Death-associated protein kinase; DCAMKL Doublecortin- and CaMK-like; DDR Discoidin domain receptor; DMPK Dystrophia myotonica protein kinase; DNAPK DNA-activated protein kinase; DRAK DAPK-related apoptosis-inducing kinase; DYRK Dual- specificity tyrosine phosphorylation–regulated kinase; EEF2K Eukaryotic elongation factor–2 kinase; EGFR Epidermal growth factor receptor; Eph Ephrin receptor; ERK Extracellular signal–regulated kinase; FAK Focal adhesion kinase; FGFR Fibroblast growth factor receptor; FRK Fos-regulatory kinase; GRK G protein–coupled receptor kinase; GSK Glycogen synthase kinase; HIPK Homeodomain-interacting protein kinase; IKK I-κB kinase; ILK Integrin-linked kinase; InsR Insulin receptor; IRAK Interleukin-1 receptor–associated kinase; IRE Inositol- requiring; IRR Insulin receptor–related; JAK Janus kinase; JNK c-Jun NH 2 -terminal kinase; KSR Kinase suppressor of Ras; LATS Large tumor suppressor; LIMK Lim domain–containing kinase; LMR Lemur kinase; LRRK Leucine rich–repeat kinase; MAP2K Mitogen-activated protein kinase kinase; MAP3K Mitogen-activated protein kinase kinase kinase; MAPK Mitogen-activated protein kinase; MAPKAPK MAPK–activated protein kinase; MARK Microtubule-associated protein/microtubule affinity–regulating kinase; MAST Microtubule-associated serine-threonine kinase; MLCK Myosin light chain kinase; MLK Mixed lineage kinase; MNK MAPK-interacting kinase; MRCK Myotonic dystrophy–related CDC42-binding kinase; MSK Mitogen- and stress- activated protein kinase; MuSK Muscle-specific kinase; NDR Nuclear, Dbf2-related kinase; NIK Nuclear factor κB–inducing kinase; PAK p21-activated kinase; PDGFR Platelet-derived growth factor receptor; PDHK Pyruvate dehydrogenase kinase; PDK Phosphoinositide-dependent kinase; PhK Phosphorylase kinase; PIKK Phosphatidylinositol 3-kinase–related kinase; PKA Protein kinase A; PKB Protein kinase B; PKC Protein kinase C; PKD Protein kinase D; PKG Protein kinase G; PKN Protein kinase N; PKR Protein kinase, double-stranded RNA–dependent; PRK Protein kinase C–related kinase; PSKH Protein serine kinase H; RIPK Receptor-interacting protein kinase; ROCK Rho-associated, coiled-coil–containing kinase; ROR Regeneron orphan receptor; RSK Ribosomal protein S6 kinase; RSKL RSK-like; SgK Sugen kinase; SGK Serum- and glucocorticoid-regulated kinase; SRPK Serine-arginine splicing factor protein kinase; SYK Spleen tyrosine kinase; TAK Transforming growth factor–β–activated kinase; TEC Tyrosine kinase expressed in hepatocellular carcinoma; TESK Testis-specific kinase; TGFbR Transforming growth factor–β receptor; TIE Tyrosine kinase with immunoglobulin and EGF repeats; TIF1 Transcriptional intermediary factor 1; TLK Tousled-like kinase; TSSK Testis-specific serine SIGNAL TRANSDUCTION KNOWLEDGE ENVIRONMENT WWW.STKE.ORG SIGNAL TRANSDUCTION KNOWLEDGE ENVIRONMENT WWW.STKE.ORG

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The human kinome (kinase map) in one easy graphic

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Page 1: Kinome Poster

MYT1Wee1Wee1B

PIK3R4

SgK493

VRK1VRK2

Bub1BubR1

CK1g2

CK1a

CK1a2

CK1d

CK1e

CK1g1CK1g3

PRPKHaspin

SCYL2SCYL1SCYL3

SgK196

SgK396Slob

VRK3

MSK1

p70S6Kp70S6Kb

RSK3

PKCiPKCz

PKN3

RSK4

PKCdPKCu

RSK1/p90RSKRSK2

PKCg

PKChPKCe

PKCaPKCb

GRK4

GRK5

TLK2

PLK1

PLK4

PLK3

PLK2

MRCKb

MRCKa

GRK6

RHODK/GRK1

AurA/Aur2

TLK1

AurB/Aur1AurC/Aur3

DMPK

ROCK1ROCK2

NDR1NDR2

DMPK2

YANK2YANK3

YANK1

SgK494

PDK1

BARK1/GRK2BARK2/GRK3

GRK7

MAST3MASTL

MAST2

MAST4 MAST1

PKN1/PRK1PKN2/PRK2

MSK2

LATS1LATS2

Akt3/PKBg

SGK2

Akt1/PKBaAkt2/PKBb

SGK1SGK3

CRIK

PKAaPKAb

PRKYPRKX

PKG2PKG1

PKAg

CAMKK1CAMKK2

ULK1

ULK2

BIKE

AAK1

SBK

RSKL2RSKL1

IKKa

IKKbIKKe

TBK1

SgK069SgK110

GAK

MPSK1

MAP2K5

MAP2K7

OSR1STLK3

STLK5STLK6

MKK3/MAP2K3MKK6/MAP2K6SEK1/MAP2K4

TAO3

PAK3

PAK6MEK1/MAP2K1

MEK2/MAP2K2

LOKSLK

COTNIK

GCN2~b

TAO2TAO1

PAK1

PAK2 PAK4PAK5

PBK

CDK8 CDK11

ERK7

ERK3ERK4

CDKL5

GSK3a

GSK3b ICKMAK

CCRK

CDK9

CDK7

NLK

CDKL1CDKL4

CDKL2CDKL3

CHEDCRK7

CDK4CDK6

CDK10

PITSLRE

ERK5

JNK2

CDK5

ERK1

ERK2

JNK1JNK3

p38ap38b

p38dp38g

CDC2/CDK1

PCTAIRE3

PFTAIRE1PFTAIRE2

CDK2 CDK3

PCTAIRE1

PCTAIRE2

CK2a2CK2a1

MOK

SgK071

RNAseL

CLIK1LCLIK1

TTKKIS

IRE1IRE2 TBCK

HRI

GCN2PKRPERK/PEK

CDC7

MAP3K4

KHS1KHS2

NRK/ZC4

MYO3A

MYO3B

MST1MST2

MST4

TNIK/ZC2

HGK/ZC1MINK/ZC3

MAP3K8

MEKK6/MAP3K6

RIPK3

LIMK1LIMK2

TESK1TESK2

ALK1ALK2

TGFbR2

MISR2BMPR2

RIPK2

HH498TAK1ILK

ARAF

KSR KSR2

BMPR1ABMPR1B

ALK7

ActR2ActR2B

ANKRD3 SgK288

ZAK BRAFRAF1

ALK4TGFbR1

DLKLZK

MLK2

MLK4

MLK1

MLK3

LRRK1LRRK2

SgK496

RIPK1

WNK3WNK1

WNK2NRBP1NRBP2

WNK4MEKK1/MAP3K1

MEKK2/MAP3K2MEKK3/MAP3K3

ASK/MAP3K5MAP3K7

MLKL

SgK307SgK424

IRAK4

HSER

CYGD

CYGF

IRAK2

ANPa

ANPb

IRAK1IRAK3

ULK3

ULK4Fused

MELK

NIM1SNRK

SSTK

TSSK3

TSSK1

AMPKa1AMPKa2

BRSK1BRSK2

NuaK1NuaK2

MARK4

QSK

MARK3

QIKSIK

MARK1MARK2

CaMK1b

CaMK1g

RSK3~b

CHK2

PKD2

HUNK

DCAMKL3

CASK

MAPKAPK5VACAMKL

PSKH1PSKH2

MAPKAPK2MAPKAPK3

MSK1~bMSK2~b

RSK4~b

TSSK2

TSSK4

Nek6Nek7

Nek2

Nek8Nek9

Nek11

Nek4

Nek3

Nek1

Nek5

Nek10

STK33

MNK1MNK2PhKg1

PhKg2

PKD3 DCAMKL1DCAMKL2

CaMK4

CaMK2aCaMK2d

CaMK2bCaMK2g

RSK1~b

RSK2~b

PKD1

Trb1

Trb3

Trb2

SgK495

DRAK1

DAPK1DAPK2

caMLCK

SgK085

DAPK3

DRAK2skMLCK

smMLCK

TTN

TradTrio

Obscn

SPEG

Obscn~bSPEG~b

Pim1

Pim3Pim2

CHK1

PASKLkb1

SuRTK106JAK1~bTyk2~b

JAK2~bJAK3~b

MOS

Lmr1Lmr2

Lmr3

EphA2

Etk/BMXBTK

ITK

BLK

Fgr

EphA8

TECTXK

Lck

FynHCKLyn

Src

Yes

EphA7

EphB4

EphA6

EphB3

EphA4

EphB1

EphB2

EphA3

EphA5

EphA10

EphB6

Fer

FRK

BrkSrm

EphA1

AblArg

CSKCTK

FLT4

CCK4/PTK7

PDGFRa

PDGFRb

AxlMer

FGFR1FGFR4

FLT1KDR Fms/CSFR

Kit

ALKLTK

IGF1RInsR

DDR1DDR2

MuSK

TRKA

FGFR2 FGFR3

TRKB

TRKC

EGFR HER2

Tyro3/Sky

MetRon

Ret

FLT3

Ros

IRR

ROR1ROR2

Tnk1HER3 JAK3

PYK2ZAP70

RYKTIE1 HER4

Ack JAK1Tyk2

JAK2

Syk

TIE2

FAK

Fes

HPK1

GCKMST3

YSK1

SgK223SgK269

PINK1

TTBK1TTBK2

CaMK1aCaMK1d

PRP4

SRPK2

HIPK4

CLK3

CLK4

CLK2CLK1

MSSK1

SRPK1

DYRK1ADYRK1B

DYRK4

HIPK3

DYRK2DYRK3

HIPK1HIPK2

TKLTK

STE

CK1

CMGC

AGC

CAMK

THE

KinomeKinomeHuman

Authors Gerard Manning, David B. Whyte, Ricardo Martinez, Sucha Sudarsanam, Sugen Inc., South San Francisco, CA, USA; Tony Hunter, Salk Institute, La Jolla, CA, USA. This poster accompanies the paper “The Protein Kinase Complement of the Human Genome” (Manning et al., Science, 6 December 2002).Science coordinator L. Bryan RayDesign and production Anne Ashley, David Comb, Michael Melnick, C. Faber Smith, J. White, David M. Tompkins, Marcus SpieglerCopyeditor Harry Jach Sponsored by Cell Signaling Technology, Inc. and Sugen, Inc.

© 2002 Science, a publication of the American Association for the Advancement of Science

ABC1

Alpha

Brd

PDHK

PIKK

RIO

AlphaK1AlphaK2

ChaK2ChaK1

EEF2KAlphaK3

Brd2Brd3

Brd4BrdT

PDHK2PDHK3PDHK1

PDHK4BCKDK

RIOK3RIOK1

RIOK2

ATMATR

SMG1

FRAPDNAPK

TRRAP

TIF1TIF1b

TIF1gTIF1a

ADCK1ADCK5

ADCK3ADCK4ADCK2

ATYPICAL PROTEIN KINASES

his phylogenetic tree depicts the relationships between members of the complete superfamily of human protein kinases. Protein kinases constitute one of the largest human gene families and are key regulators of cell function. The 518 human protein kinases control protein activity by catalyzing the addition of a negatively charged phosphate group to other proteins. Protein kinases modulate a wide variety of biological processes, especially those that carry signals from the cell membrane to intracellular targets and coordinate complex biological functions. Most protein kinases belong to a single superfamily of enzymes whose catalytic domains are related in sequence and structure. The main diagram illustrates the similarity between the protein sequences of these catalytic domains. Each kinase is at the tip of a branch, and the similarity between various kinases is inversely related to the distance between their positions on the tree diagram. Most kinases fall into small families of highly related sequences, and most

families are part of larger groups. The seven major groups are labeled and colored distinctly. Other kinases are shown in the center of the tree, colored gray. The relationships shown on the tree can be used to predict protein substrates and biological function for many of the over 100 uncharacterized kinases presented here. The inset diagram shows trees for seven atypical protein kinase families. These proteins have verified or strongly predicted kinase activity, but have little or no sequence similarity to members of the protein kinase superfamily. A further eight atypical protein kinases in small families of one or two genes are not shown.

T

Mapping Procedures

The main dendrogram shows the sequence similarity between protein kinase

domains, derived from public sequences and gene-prediction methods detailed in

Manning et al. (Science, 6 December 2002). Domains were defined by hidden

Markov model profile analysis and multiple sequence alignment. The initial

branching pattern was built from a neighbor-joining tree derived from a ClustalW

protein sequence alignment of the domains. This was extensively modified by

reference to other alignment and tree-building methods (hmmalign and parsimony

trees) and by extensive pairwise sequence alignment of kinase domains. The

curved layout was created manually. Many branch lengths are semiquantitative, but

the branching pattern is more informative than any single automatic method. The

atypical kinase trees were generated automatically by ClustalW alignment of full-

length protein sequences followed by neighbor-joining tree building. Unpublished

kinases are named where possible according to family nomenclature. Some

divergent kinases retain a numerical SgK (Sugen kinase) accession number. The

second domains of dual-domain kinases are named with a “~b” suffix. Detailed

subtrees and sequence alignments of individual groups and families, and

comparative genomic trees are available at http://www.kinase.com. Information on

regulation and substrates of many of these kinases is available at

http://www.cellsignal.com.

Group namesAGC Containing PKA, PKG, PKC families; CAMK Calcium/calmodulin-dependent protein kinase; CK1 Casein kinase 1; CMGC Containing CDK, MAPK, GSK3, CLK families; STE Homologs of yeast Sterile 7, Sterile 11, Sterile 20 kinases; TK Tyrosine kinase; TKL Tyrosine kinase–like.

Kinase names(A selective list includes those cases in which the full name is more informative than the abbreviation or acronym shown on the tree. Other full names and synonyms are available at http://www.kinase.com.) ActR Activin receptor; ALK (TK group) Anaplastic lymphoma kinase; ALK (TKL group) Activin-like receptor kinase; AMPK Adenosine monophosphate–activated protein kinase; Aur Aurora; BARK β-adrenergic receptor kinase; BLK B lymphocyte tyrosine kinase; BMPR Bone morphogeneic protein receptor; BMX Bone marrow tyrosine kinase gene in chromosome X; BRD Bromodomain kinase; BRSK Brain-selective kinase; CaMK Calcium/calmodulin-dependent protein kinase; CAMKK CaMK kinase; CCK-4 Colon carcinoma kinase–4; CDK Cyclin-dependent kinase; CDKL Cyclin-dependent kinase–like; CK Casein kinase; CLK Cdc2-like kinase; CSFR Colony-stimulating factor receptor; DAPK Death-associated protein kinase; DCAMKL Doublecortin- and CaMK-like; DDR Discoidin domain receptor; DMPK Dystrophia myotonica protein kinase; DNAPK DNA-activated protein kinase; DRAK DAPK-related apoptosis-inducing kinase; DYRK Dual-specificity tyrosine phosphorylation–regulated kinase; EEF2K Eukaryotic elongation factor–2 kinase; EGFR Epidermal growth factor receptor; Eph Ephrin receptor; ERK Extracellular signal–regulated kinase; FAK Focal adhesion kinase; FGFR Fibroblast growth factor receptor; FRK Fos-regulatory kinase; GRK G protein–coupled receptor kinase; GSK Glycogen synthase kinase; HIPK Homeodomain-interacting protein kinase; IKK I-κB kinase; ILK Integrin-linked kinase; InsR Insulin receptor; IRAK Interleukin-1 receptor–associated kinase; IRE Inositol-requiring; IRR Insulin receptor–related; JAK Janus kinase; JNK c-Jun NH2-terminal kinase; KSR Kinase suppressor of Ras; LATS Large tumor suppressor; LIMK Lim domain–containing kinase; LMR Lemur kinase; LRRK Leucine rich–repeat kinase; MAP2K Mitogen-activated protein kinase kinase; MAP3K Mitogen-activated protein kinase kinase kinase; MAPK Mitogen-activated protein kinase; MAPKAPK MAPK–activated protein kinase; MARK Microtubule-associated protein/microtubule affinity–regulating kinase; MAST Microtubule-associated serine-threonine kinase; MLCK Myosin light chain kinase; MLK Mixed lineage kinase; MNK MAPK-interacting kinase; MRCK Myotonic dystrophy–related CDC42-binding kinase; MSK Mitogen- and stress-activated protein kinase; MuSK Muscle-specific kinase; NDR Nuclear, Dbf2-related kinase; NIK Nuclear factor κB–inducing kinase; PAK p21-activated kinase; PDGFR Platelet-derived growth factor receptor; PDHK Pyruvate dehydrogenase kinase; PDK Phosphoinositide-dependent kinase; PhK Phosphorylase kinase; PIKK Phosphatidylinositol 3-kinase–related kinase; PKA Protein kinase A; PKB Protein kinase B; PKC Protein kinase C; PKD Protein kinase D; PKG Protein kinase G; PKN Protein kinase N; PKR Protein kinase, double-stranded RNA–dependent; PRK Protein kinase C–related kinase; PSKH Protein serine kinase H; RIPK Receptor-interacting protein kinase; ROCK Rho-associated, coiled-coil–containing kinase; ROR Regeneron orphan receptor; RSK Ribosomal protein S6 kinase; RSKL RSK-like; SgK Sugen kinase; SGK Serum- and glucocorticoid-regulated kinase; SRPK Serine-arginine splicing factor protein kinase; SYK Spleen tyrosine kinase; TAK Transforming growth factor–β–activated kinase; TEC Tyrosine kinase expressed in hepatocellular carcinoma; TESK Testis-specific kinase; TGFbR Transforming growth factor–β receptor; TIE Tyrosine kinase with immunoglobulin and EGF repeats; TIF1 Transcriptional intermediary factor 1; TLK Tousled-like kinase; TSSK Testis-specific serine

SIGNAL TRANSDUCTIONKNOWLEDGE ENVIRONMENT

WWW.STKE.ORG

SIGNAL TRANSDUCTIONKNOWLEDGE ENVIRONMENT

WWW.STKE.ORG