 |
1FMO |
CRYSTAL STRUCTURE OF A POLYHISTIDINE-TAGGED RECOMBINANT CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH THE PEPTIDE INHIBITOR PKI(5-24) AND ADENOSINE |
I |
E |
Protein kinase-like (PK-like) |
|
 |
1FYN |
PHOSPHOTRANSFERASE |
B |
A |
SH3-like barrel |
|
 |
1GWQ |
HUMAN OESTROGEN RECEPTOR ALPHA LIGAND-BINDING DOMAIN IN COMPLEX WITH RALOXIFENE CORE AND TIF2 NRBOX2 PEPTIDE |
C |
A |
Nuclear receptor ligand-binding domain |
|
 |
1GWR |
HUMAN OESTROGEN RECEPTOR ALPHA LIGAND-BINDING DOMAIN IN COMPLEX WITH 17BETA-OESTRADIOL AND TIF2 NRBOX3 PEPTIDE |
C |
A |
Nuclear receptor ligand-binding domain |
|
 |
1H24 |
CDK2/CYCLIN A IN COMPLEX WITH A 9 RESIDUE RECRUITMENT PEPTIDE FROM E2F |
E |
B |
Cyclin-like |
|
 |
1H27 |
CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P27 |
E |
B |
Cyclin-like |
|
 |
1MFL |
The Structure of ERBIN PDZ domain bound to the Carboxy-terminal tail of the ErbB2 Receptor |
B |
A |
PDZ domain-like |
|
 |
1O9U |
GLYCOGEN SYNTHASE KINASE 3 BETA COMPLEXED WITH AXIN PEPTIDE |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1Q1S |
Mouse Importin alpha- phosphorylated SV40 CN peptide complex |
A |
C |
alpha-alpha superhelix |
|
 |
1Q1T |
Mouse Importin alpha: non-phosphorylated SV40 CN peptide complex |
A |
C |
alpha-alpha superhelix |
|
 |
1Q8T |
The Catalytic Subunit of cAMP-dependent Protein Kinase (PKA) in Complex with Rho-kinase Inhibitor Y-27632 |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1Q8U |
The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor H-1152P |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1Q8W |
The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor Fasudil (HA-1077) |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1QMZ |
PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX |
E |
C |
Protein kinase-like (PK-like) |
|
 |
1STC |
CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH STAUROSPORINE |
I |
E |
Protein kinase-like (PK-like) |
|
 |
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 |
|
|
 |
1YCQ |
XENOPUS LAEVIS MDM2 BOUND TO THE TRANSACTIVATION DOMAIN OF HUMAN P53 |
B |
A |
SWIB/MDM2 domain |
|
 |
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) |
|
 |
2B1J |
Crystal Structure of Unphosphorylated CheY Bound to the N-Terminus of FliM |
C |
A |
Flavodoxin-like |
|
 |
2BZK |
CRYSTAL STRUCTURE OF THE HUMAN PIM1 IN COMPLEX WITH AMPPNP AND PIMTIDE |
A |
B |
|
|
 |
2BZW |
THE CRYSTAL STRUCTURE OF BCL-XL IN COMPLEX WITH FULL-LENGTH BAD |
B |
A |
|
|
 |
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 |
|
|
 |
2C5I |
N-TERMINAL DOMAIN OF TLG1 COMPLEXED WITH N-TERMINUS OF VPS51 IN DISTORTED CONFORMATION |
P |
T |
|
|
 |
2C5K |
N-TERMINAL DOMAIN OF TLG1 COMPLEXED WITH N-TERMINUS OF VPS51 |
P |
T |
|
|
 |
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 |
|
 |
2CE8 |
AN EH1 PEPTIDE BOUND TO THE GROUCHO-TLE WD40 DOMAIN. |
X |
A |
7-bladed beta-propeller |
|
 |
2CE9 |
A WRPW PEPTIDE BOUND TO THE GROUCHO-TLE WD40 DOMAIN. |
X |
A |
7-bladed beta-propeller |
|
 |
2IV9 |
B2-APPENDAGE FROM AP2 IN COMPLEX WITH EPS15 PEPTIDE |
P |
BA |
Subdomain of clathrin and coatomer appendage domain |
|
 |
2IZX |
MOLECULAR BASIS OF AKAP SPECIFICITY FOR PKA REGULATORY SUBUNITS |
C |
AB |
|
|
 |
2J6F |
N-TERMINAL SH3 DOMAIN OF CMS (CD2AP HUMAN HOMOLOG) BOUND TO CBL-B PEPTIDE |
C |
A |
|
|
 |
2J6O |
ATYPICAL POLYPROLINE RECOGNITION BY THE CMS N-TERMINAL SH3 DOMAIN. CMS:CD2 HETEROTRIMER |
C |
A |
|
|
 |
2J7X |
STRUCTURE OF ESTRADIOL-BOUND ESTROGEN RECEPTOR BETA LBD IN COMPLEX WITH LXXLL MOTIF FROM NCOA5 |
B |
A |
Nuclear receptor ligand-binding domain |
|
 |
2J7Y |
STRUCTURE OF 17-EPIESTRIOL-BOUND ESTROGEN RECEPTOR BETA LBD IN COMPLEX WITH LXXLL MOTIF FROM NCOA5 |
B |
A |
Nuclear receptor ligand-binding domain |
|
 |
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) |
|
 |
2JDS |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH A-443654 |
I |
A |
Protein kinase-like (PK-like) |
|
 |
2JDT |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE |
I |
A |
|
|
 |
2JDV |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH A-443654 |
I |
A |
|
|
 |
2JF1 |
CRYSTAL STRUCTURE OF THE FILAMIN A REPEAT 21 COMPLEXED WITH THE INTEGRIN BETA2 CYTOPLASMIC TAIL PEPTIDE |
T |
A |
Immunoglobulin-like beta-sandwich |
|
 |
2JF9 |
ESTROGEN RECEPTOR ALPHA LBD IN COMPLEX WITH A TAMOXIFEN-SPECIFIC PEPTIDE ANTAGONIST |
P |
AC |
|
|
 |
2JGB |
STRUCTURE OF HUMAN EIF4E HOMOLOGOUS PROTEIN 4EHP WITH M7GTP |
B |
A |
|
|
 |
2JGC |
STRUCTURE OF THE HUMAN EIF4E HOMOLOGOUS PROTEIN, 4EHP WITHOUT LIGAND BOUND |
B |
A |
|
|
 |
2Q0N |
Structure of human p21 activating kinase 4 (PAK4) in complex with a consensus peptide |
B |
A |
|
|
 |
2QIY |
yeast Deubiquitinase Ubp3 and Bre5 cofactor complex |
C |
AB |
Cystatin-like |
|