Proteinbase brings together protein designs, experimental results, and design methods in one place to share, compare, and learn.
id: golden-cobra-iron
IFNAR2
Strong
3.9e-8 M
True
11.1 kDa
92
id: bright-otter-reed
Multiple (2)
Weak (2), Strong (2)
True
9.3 kDa
80
id: brisk-boar-cloud
MDM2
Strong
4.4e-8 M
True
12.1 kDa
102
id: shy-shark-cypress
EGFR
Strong
1.4e-9 M
True
25.8 kDa
241
Cradle • 4 days ago
12 EGFR binders designed by Cradle for the Adaptyv 2024 protein design competition, generated through Cradle's zero-shot diversification pipeline.
+7
EPFL-LPDI • 20 days ago
Designs from the original BindCraft1 publication re-validated at Adaptyv
+91
Microsoft Research • 19 days ago
Validating proteins designed with Microsoft Research’s EvoDiff to block the cancer-linked MDM2–p53 interaction
+22
Protein binder design pipeline that can be used to design miniprotein and peptide binders
A flexible de novo binder design workflow using RFdiffusion for backbone generation
Fine-tuning pipeline combining reinforcement learning algorithms (GRPO, DPO) with the ZymCTRL protein language model.
protein
833
Proteins validated
134
Binders
EGFR is a cell-surface receptor that turns growth factor signals into instructions for cells to divide and survive. Extra copies or mutations drive many tumors, so EGFR is a top target for cancer medicines.
protein
62
Proteins validated
51
Binders
IL-7Rα is the alpha chain that pairs with the common gamma chain to deliver IL-7 survival cues to lymphocytes. Surface levels of IL-7Rα forecast immune fitness and highlight intervention points in autoimmunity and leukemia.
protein
40
Proteins validated
31
Binders
PD-L1 is an immune checkpoint ligand that binds PD-1 to quiet T-cell signals and cytokine release. Tumors and immune cells boost PD-L1 under stress, so blocking it can restart anti-tumor immunity.
protein
27
Proteins validated
12
Binders
MDM2 is an E3 ligase that binds p53 and marks it for degradation to keep stress responses in check. Tumors that overproduce MDM2 silence p53, so inhibitors aim to restore the tumor suppressor.