 |
2J6F |
N-TERMINAL SH3 DOMAIN OF CMS (CD2AP HUMAN HOMOLOG) BOUND TO CBL-B PEPTIDE |
C |
A |
|
|
 |
2JCC |
AH3 RECOGNITION OF MUTANT HLA-A2 W167A |
C |
EFA |
Immunoglobulin-like beta-sandwich |
|
 |
2QPY |
AR LBD with small molecule |
B |
A |
Nuclear receptor ligand-binding domain |
|
 |
2R28 |
The complex Structure of Calmodulin Bound to a Calcineurin Peptide |
C |
AB |
EF Hand-like |
|
 |
2RFX |
Crystal Structure of HLA-B*5701, presenting the self peptide, LSSPVTKSF |
C |
A |
MHC antigen-recognition domain |
|
 |
2UWE |
LARGE CDR3A LOOP ALTERATION AS A FUNCTION OF MHC MUTATION |
C |
EFA |
Immunoglobulin-like beta-sandwich |
|
 |
2V2W |
T CELL CROSS-REACTIVITY AND CONFORMATIONAL CHANGES DURING TCR ENGAGEMENT |
C |
A |
MHC antigen-recognition domain |
|
 |
2V2X |
T CELL CROSS-REACTIVITY AND CONFORMATIONAL CHANGES DURING TCR ENGAGEMENT. |
C |
A |
MHC antigen-recognition domain |
|
 |
2VAY |
CALMODULIN COMPLEXED WITH CAV1.1 IQ PEPTIDE |
B |
A |
EF Hand-like |
|
 |
2VLJ |
THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN |
C |
DEA |
Immunoglobulin-like beta-sandwich |
|
 |
2VLK |
THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN |
C |
DEA |
Immunoglobulin-like beta-sandwich |
|
 |
2VLL |
THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN |
C |
A |
MHC antigen-recognition domain |
|
 |
2VLR |
THE STRUCTURAL DYNAMICS AND ENERGETICS OF AN IMMUNODOMINANT T-CELL RECEPTOR ARE PROGRAMMED BY ITS VBETA DOMAIN |
C |
DEA |
Immunoglobulin-like beta-sandwich |
|
 |
2W73 |
HIGH-RESOLUTION STRUCTURE OF THE COMPLEX BETWEEN CALMODULIN AND A PEPTIDE FROM CALCINEURIN A |
K |
ABF |
|
|
 |
2Z32 |
Crystal structure of Keap1 complexed with Prothymosin alpha |
B |
A |
6-bladed beta-propeller |
|
 |
3BEJ |
Structure of human FXR in complex with MFA-1 and co-activator peptide |
E |
A |
Nuclear receptor ligand-binding domain |
|
 |
3BO8 |
The High Resolution Crystal Structure of HLA-A1 Complexed with the MAGE-A1 Peptide |
C |
A |
|
|
 |
3BP4 |
The high resolution crystal structure of HLA-B*2705 in complex with a Cathepsin A signal sequence peptide pCatA |
C |
A |
|
|
 |
3BP7 |
The high resolution crystal structure of HLA-B*2709 in complex with a Cathepsin A signal sequence peptide, pCatA |
C |
A |
|
|
 |
3BQD |
Doubling the Size of the Glucocorticoid Receptor Ligand Binding Pocket by Deacylcortivazol |
B |
A |
Nuclear receptor ligand-binding domain |
|
 |
3BW9 |
Crystal Structure of HLA B*3508 in complex with a HCMV 12-mer peptide from the pp65 protein |
C |
A |
MHC antigen-recognition domain |
|
 |
3BWA |
Crystal Structure of HLA B*3508 in complex with a HCMV 8-mer peptide from the pp65 protein |
C |
A |
MHC antigen-recognition domain |
|
 |
3BXL |
Crystal structure of the R-type calcium channeL (CaV2.3) IQ domain and CA2+calmodulin complex |
B |
A |
EF Hand-like |
|
 |
3BYA |
Structure of a Calmodulin Complex |
B |
A |
|
|
 |
3BZF |
The human non-classical major histocompatibility complex molecule HLA-E |
P |
A |
MHC antigen-recognition domain |
|
 |
3C9N |
Crystal Structure of a SARS Corona Virus Derived Peptide Bound to the Human Major Histocompatibility Complex Class I molecule HLA-B*1501 |
C |
A |
MHC antigen-recognition domain |
|
 |
3D18 |
Crystal structure of HLA-B*2709 complexed with a variant of the latent membrane protein 2 peptide (LMP2(L)) of epstein-barr virus |
C |
A |
|
|
 |
3D7V |
Crystal structure of Mcl-1 in complex with an Mcl-1 selective BH3 ligand |
B |
A |
|
|
 |
3DCG |
Crystal Structure of the HIV Vif BC-box in Complex with Human ElonginB and ElonginC |
F |
B |
POZ domain |
|
 |
3DCT |
FXR with SRC1 and GW4064 |
B |
A |
Nuclear receptor ligand-binding domain |
|
 |
3DX6 |
Crystal Structure of B*4402 presenting a 10mer EBV epitope |
C |
A |
|
|
 |
3DX7 |
Crystal Structure of HLA-B*4403 presenting 10mer EBV antigen |
C |
A |
|
|
 |
3DX8 |
Crystal Structure of B*4405 presenting a 10mer EBV epitope |
C |
A |
|
|
 |
3E7C |
Glucocorticoid Receptor LBD bound to GSK866 |
D |
B |
|
|
 |
3E94 |
Crystal structure of RXRalpha ligand binding domain in complex with tributyltin and a coactivator fragment |
B |
A |
|
|
 |
3EQS |
Crystal structure of human MDM2 in complex with a 12-mer peptide inhibitor |
B |
A |
|
|
 |
3ET1 |
Structure of PPARalpha with 3-[5-Methoxy-1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-propionic acid |
P |
A |
|
|
 |
3ET3 |
Structure of PPARgamma with 3-[5-Methoxy-1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-propionic acid |
P |
A |
|
|
 |
3FQT |
Phosphorylation of self-peptides alters Human Leukocyte Antigen Class I-restricted antigen presentation and generates tumor specific epitopes |
C |
A |
|
|
 |
3FQW |
Phosphorylation of self-peptides alters Human Leukocyte Antigen Class I-restricted antigen presentation and generates tumor specific epitopes |
C |
A |
|
|
 |
3FUG |
Crystal Structure of the Retinoid X Receptor Ligand Binding Domain Bound to the Synthetic Agonist 3-[4-Hydroxy-3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-phenyl]acrylic Acid |
B |
A |
|
|
 |
3FXV |
Identification of an N-oxide pyridine GW4064 analogue as a potent FXR agonist |
B |
A |
|
|
 |
3G03 |
Structure of human MDM2 in complex with high affinity peptide |
B |
ACD |
|
|
 |
3G8I |
Aleglitazar, a new, potent, and balanced PPAR alpha/gamma agonist for the treatment of type II diabetes |
Z |
A |
|
|
 |
3G9E |
Aleglitaar. a new. potent, and balanced dual ppara/g agonist for the treatment of type II diabetes |
B |
A |
|
|
 |
3GIV |
Antigen processing influences HIV-specific cytotoxic T lymphocyte immunodominance |
C |
A |
|
|
 |
3GJF |
Rational development of high-affinity T-cell receptor-like antibodies |
C |
LHA |
|
|
 |
3H0A |
Crystal Structure of Peroxisome Proliferator-Activated Receptor Gamma (PPARg) and Retinoic Acid Receptor Alpha (RXRa) in Complex with 9-cis Retinoic Acid, Co-activator Peptide, and a Partial Agonist |
B |
A |
|
|