Robust zero-watermarking is a protection of copyright approach that is both effective and distortion-free, and it has grown into a core of research on the subject of digital watermarking. This paper proposes a revolutionary zero-watermarking approach for color images using convolutional neural networks (CNN) and a 2D logistic-adjusted Chebyshev map (2D-LACM). In this algorithm, we first extracted deep feature maps from an original color image using the pre-trained VGG19. These feature maps were then fused into a featured image, and the owner's watermark sequence was incorporated using an XOR operation. Finally, 2D-LACM encrypts the copyright watermark and scrambles the binary feature matrix to ensure security. The experimental results show that the proposed algorithm performs well in terms of imperceptibility and robustness. The BER values of the extracted watermarks were below 0.0044 and the …

The tertiary structures of proteins play a critical role in determining their functions, interactions, and bonding in molecular chemistry. Proteins are known to demonstrate natural dynamism under various physiological conditions, which enables them to adjust their tertiary structures and effectively interact with the surrounding molecules. The present study utilized the remarkable progress made in Generative Adversarial Networks (GANs) to generate tertiary structures that accurately mimic the inherent attributes of actual proteins, which includes the backbone conformation as well as the local and distal characteristics of proteins. The current study has introduced a robust model, ROD-WGAN hybrid, that is able to generate large-scale tertiary protein structures that greatly mimic those found in nature. We have made several noteworthy contributions in pursuit of this objective by integrating the ROD-WGAN model with 

Revealing the tertiary structure of proteins holds huge significance as it unveils their vital properties and functions. These intricate three-dimensional configurations comprise diverse interactions including ionic, hydrophobic, and disulfide forces. In certain instances, these structures exhibit missing regions, necessitating the reconstruction of specific segments, thereby resulting in challenges in protein design, which encompasses loop modeling, circular permutation, and interface prediction. To address this problem, we present two pioneering models: pix2pix generative adversarial network (GAN) and PLM-GAN. The pix2pix GAN model is adept at generating and inpainting distance matrices of protein structures, whereas the PLM-GAN model incorporates residual blocks into the U-Net network of the GAN, building upon the foundation of the pix2pix GAN model. To bolster the models’ performance, we introduce a novel loss function named the “missing to real regions loss” (L_MTR) within the GAN framework. Additionally, we introduce a distinctive approach of pairing two different distance matrices: one representing the native protein structure and the other representing the same structure with a missing region that undergoes changes in each successive epoch. Moreover, we extend the reconstruction of missing regions, encompassing up to 30 amino acids and increase the protein length by 128 amino acids. The evaluation of our pix2pix GAN and PLM-GAN models on a random selection of natural proteins (4ZCB, 3FJB, and 2REZ) demonstrated promising experimental results. Our models constitute significant contributions to addressing intricate challenges in protein structure design. These contributions hold immense potential to propel advancements in protein–protein interactions, drug design, and further innovations in protein engineering. Data, code, trained models, examples, and measurements are available on https://github.com/mena01/PLM-GAN-A-Large-Scale-Protein-Loop-Modeling-Using-pix2pix-GAN_.