 |
1FYN |
PHOSPHOTRANSFERASE |
B |
A |
SH3-like barrel |
|
 |
1H24 |
CDK2/CYCLIN A IN COMPLEX WITH A 9 RESIDUE RECRUITMENT PEPTIDE FROM E2F |
E |
B |
Cyclin-like |
|
 |
1H25 |
CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM RETINOBLASTOMA-ASSOCIATED PROTEIN |
E |
B |
Cyclin-like |
|
 |
1IID |
Crystal Structure of Saccharomyces cerevisiae N-myristoyltransferase with Bound S-(2-oxo)pentadecylCoA and the Octapeptide GLYASKLA |
O |
A |
Acyl-CoA N-acyltransferases (Nat) |
|
 |
1JBP |
Crystal Structure of the Catalytic Subunit of cAMP-dependent Protein Kinase Complexed with a Substrate Peptide, ADP and Detergent |
S |
A |
|
|
 |
1K3A |
Structure of the Insulin-like Growth Factor 1 Receptor Kinase |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1L3R |
Crystal Structure of a Transition State Mimic of the Catalytic Subunit of cAMP-dependent Protein Kinase |
I |
A |
|
|
 |
1LEW |
CRYSTAL STRUCTURE OF MAP KINASE P38 COMPLEXED TO THE DOCKING SITE ON ITS NUCLEAR SUBSTRATE MEF2A |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1LEZ |
CRYSTAL STRUCTURE OF MAP KINASE P38 COMPLEXED TO THE DOCKING SITE ON ITS ACTIVATOR MKK3B |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1M27 |
Crystal structure of SAP/FynSH3/SLAM ternary complex |
B |
A |
SH2-like |
|
 |
1NVQ |
The Complex Structure Of Checkpoint Kinase Chk1/UCN-01 |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1NVR |
The Complex Structure Of Checkpoint Kinase Chk1/Staurosporine |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1NVS |
The Complex Structure Of Checkpoint Kinase Chk1/SB218078 |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1O6K |
STRUCTURE OF ACTIVATED FORM OF PKB KINASE DOMAIN S474D WITH GSK3 PEPTIDE AND AMP-PNP |
C |
A |
Protein kinase-like (PK-like) |
|
 |
1O6L |
CRYSTAL STRUCTURE OF AN ACTIVATED AKT/PROTEIN KINASE B (PKB-PIF CHIMERA) TERNARY COMPLEX WITH AMP-PNP AND GSK3 PEPTIDE |
C |
A |
Protein kinase-like (PK-like) |
|
 |
1O9U |
GLYCOGEN SYNTHASE KINASE 3 BETA COMPLEXED WITH AXIN PEPTIDE |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1OW6 |
Paxillin LD4 motif bound to the Focal Adhesion Targeting (FAT) domain of the Focal Adhesion Kinase |
D |
A |
Four-helical up-and-down bundle |
|
 |
1SVE |
Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 1 |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1SVG |
Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 4 |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1SVH |
Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 8 |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1UEF |
Crystal Structure of Dok1 PTB Domain Complex |
D |
B |
PH domain-like barrel |
|
 |
1UKH |
Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125 |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1WBP |
SRPK1 BOUND TO 9MER DOCKING MOTIF PEPTIDE |
B |
C |
|
|
 |
1YDR |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H7 PROTEIN KINASE INHIBITOR 1-(5-ISOQUINOLINESULFONYL)-2-METHYLPIPERAZINE |
I |
E |
Protein kinase-like (PK-like) |
|
 |
1YDS |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H8 PROTEIN KINASE INHIBITOR [N-(2-METHYLAMINO)ETHYL]-5-ISOQUINOLINESULFONAMIDE |
I |
E |
Protein kinase-like (PK-like) |
|
 |
1YDT |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H89 PROTEIN KINASE INHIBITOR N-[2-(4-BROMOCINNAMYLAMINO)ETHYL]-5-ISOQUINOLINE |
I |
E |
Protein kinase-like (PK-like) |
|
 |
1ZKK |
Crystal structure of hSET8 in ternary complex with H4 peptide (16-24) and AdoHcy |
E |
AB |
|
|
 |
1ZYS |
Co-crystal structure of Checkpoint Kinase Chk1 with a pyrrolo-pyridine inhibitor |
B |
A |
|
|
 |
2A3I |
Structural and Biochemical Mechanisms for the Specificity of Hormone Binding and Coactivator Assembly by Mineralocorticoid Receptor |
B |
A |
|
|
 |
2B9H |
Crystal structure of Fus3 with a docking motif from Ste7 |
C |
B |
|
|
 |
2B9I |
Crystal structure of Fus3 with a docking motif from Msg5 |
C |
B |
|
|
 |
2B9J |
Crystal structure of Fus3 with a docking motif from Far1 |
C |
B |
|
|
 |
2BFY |
COMPLEX OF AURORA-B WITH INCENP AND HESPERIDIN. |
D |
A |
|
|
 |
2BZK |
CRYSTAL STRUCTURE OF THE HUMAN PIM1 IN COMPLEX WITH AMPPNP AND PIMTIDE |
A |
B |
|
|
 |
2C1A |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL)AMIDE |
I |
A |
Protein kinase-like (PK-like) |
|
 |
2C1B |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH (4R,2S)-5\'-(4-(4-CHLOROBENZYLOXY)PYRROLIDIN-2-YLMETHANESULFONYL)ISOQUINOLINE |
I |
A |
Protein kinase-like (PK-like) |
|
 |
2C3I |
CRYSTAL STRUCTURE OF HUMAN PIM1 IN COMPLEX WITH IMIDAZOPYRIDAZIN I |
A |
B |
|
|
 |
2CCH |
THE CRYSTAL STRUCTURE OF CDK2 CYCLIN A IN COMPLEX WITH A SUBSTRATE PEPTIDE DERIVED FROM CDC MODIFIED WITH A GAMMA-LINKED ATP ANALOGUE |
E |
B |
Cyclin-like |
|
 |
2ERZ |
Crystal Structure of c-AMP Dependent Kinase (PKA) bound to hydroxyfasudil |
I |
E |
Protein kinase-like (PK-like) |
|
 |
2F7E |
PKA complexed with (S)-2-(1H-Indol-3-yl)-1-(5-isoquinolin-6-yl-pyridin-3-yloxymethyl-etylamine |
I |
E |
Protein kinase-like (PK-like) |
|
 |
2F7X |
Protein Kinase A bound to (S)-2-(1H-Indol-3-yl)-1-[5-((E)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamine |
I |
E |
Protein kinase-like (PK-like) |
|
 |
2FFF |
Open Form of a Class A Transpeptidase Domain |
A |
B |
beta-lactamase/transpeptidase-like |
|
 |
2FYS |
Crystal structure of Erk2 complex with KIM peptide derived from MKP3 |
D |
BA |
Protein kinase-like (PK-like) |
|
 |
2G1T |
A Src-like Inactive Conformation in the Abl Tyrosine Kinase Domain |
G |
C |
|
|
 |
2GFC |
cAMP-dependent protein kinase PKA catalytic subunit with PKI-5-24 |
I |
A |
Protein kinase-like (PK-like) |
|
 |
2GPH |
Docking motif interactions in the MAP kinase ERK2 |
B |
A |
|
|
 |
2HWN |
Crystal Structure of RII alpha Dimerization/Docking domain of PKA bound to the D-AKAP2 peptide |
E |
AB |
Dimerization-anchoring domain of cAMP-dependent PK regulatory subunit |
|
 |
2JAM |
CRYSTAL STRUCTURE OF HUMAN CALMODULIN-DEPENDENT PROTEIN KINASE I G |
D |
A |
|
|
 |
2JDO |
STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE |
C |
A |
Protein kinase-like (PK-like) |
|
 |
2JDR |
STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH THE INHIBITOR A-443654 |
C |
A |
Protein kinase-like (PK-like) |
|