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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Integrated unsupervised–supervised modeling and prediction of protein–peptide affinities at structural level
Peng Zhou, Wen Li, Jing Lin, et al.
Briefings in Bioinformatics (2022) Vol. 23, Iss. 3
Closed Access | Times Cited: 51

Showing 1-25 of 51 citing articles:

Targeting peptide‐mediated interactions in omics
Jing Lin, Shaozhou Wang, Li Wen, et al.
PROTEOMICS (2022) Vol. 23, Iss. 6
Closed Access | Times Cited: 30
PepQSAR: a comprehensive data source and information platform for peptide quantitative structure–activity relationships
Jing Lin, Li Wen, Yuwei Zhou, et al.
Amino Acids (2022) Vol. 55, Iss. 2, pp. 235-242
Closed Access | Times Cited: 27
Systematic analysis and comparison of peptide specificity and selectivity between their cognate receptors and noncognate decoys
Jianping Shu, Juelin Li, Shaozhou Wang, et al.
Journal of Molecular Recognition (2022) Vol. 36, Iss. 3
Closed Access | Times Cited: 23
Machine annealing‐guided navigation of antihypertensive food peptide selectivity between human ACE N‐ and C‐domains in structurally interacting diversity space
Li Mei, Shuyong Shang, Shaozhou Wang, et al.
Journal of Molecular Recognition (2023) Vol. 36, Iss. 6
Closed Access | Times Cited: 15
Systematic molecular profiling of non-native N6-substitution effects on m6A binding to the YTH domains of human RNA m6A readers in diabetes
Yuting Li, Peng Tan, Q. Liu, et al.
Biophysical Chemistry (2025) Vol. 320-321, pp. 107417-107417
Closed Access
A Structure-based Data Set of Protein-peptide Affinities and its Nonredundant Benchmark: Potential Applications in Computational Peptidology
Shaozhou Wang, Haiyang Ye, Shuyong Shang, et al.
Current Medicinal Chemistry (2023) Vol. 31, Iss. 26, pp. 4127-4137
Closed Access | Times Cited: 12
Competitive Disruption of the Intermolecular Interaction Between Anesthetic PKC Isozyme ζ and its Cognate Substrates using Halogenated Peptidic Inhibitors with Affinity Improved by a Designer Halogen(X)/Hydrogen(H)-Bonding (dgr[XHB]) System
Fang Lian, Zhong Wang, Zhidong Zhou, et al.
International Journal of Peptide Research and Therapeutics (2025) Vol. 31, Iss. 3
Closed Access
Rational design and exploitation of the molecular diversity space of PRX1‐derived SRX1 peptidic inhibitors containing proteinogenic and nonproteinogenic amino acids
Haijin Yang, Ping Li, Yi Wan, et al.
Journal of the Chinese Chemical Society (2025)
Closed Access
Profiling prediction of nuclear receptor modulators with multi-task deep learning methods: toward the virtual screening
Jiye Wang, Chaofeng Lou, Guixia Liu, et al.
Briefings in Bioinformatics (2022) Vol. 23, Iss. 5
Closed Access | Times Cited: 15
Systematic Profiling of Mitogen-Inducible Gene 6 and Its Derived Peptides Binding to Receptor Tyrosine Kinases in Bone Cancers at Molecular and Cellular Levels
Jinping Ni, Zhidong Zhong, Weikang Lu, et al.
International Journal of Peptide Research and Therapeutics (2024) Vol. 30, Iss. 1
Closed Access | Times Cited: 2
A deep attention model for wide-genome protein-peptide binding affinity prediction at a sequence level
Xiaohan Sun, Zhixiang Wu, Jingjie Su, et al.
International Journal of Biological Macromolecules (2024) Vol. 276, pp. 133811-133811
Closed Access | Times Cited: 2
Research on Bitter Peptides in the Field of Bioinformatics: A Comprehensive Review
Shanghua Liu, Tianyu Shi, Junwen Yu, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 18, pp. 9844-9844
Open Access | Times Cited: 2
Exploiting the chemical diversity space of phosphopeptide binding to nasopharyngeal carcinoma PLK1 PBD domain with unnatural amino acid building blocks by using QSAR-based genetic optimization
Ruiyan Ma, Jun Yang, Jing Wu, et al.
SAR and QSAR in environmental research (2024) Vol. 35, Iss. 10, pp. 899-918
Closed Access | Times Cited: 2
Structural modeling, energetic analysis and molecular design of a π-stacking system at the complex interface of pediatric respiratory syncytial virus nucleocapsid with the C-terminal peptide of phosphoprotein
Haiyan Liu, Lili Shen, Chunhua Pan, et al.
Biophysical Chemistry (2022) Vol. 292, pp. 106916-106916
Closed Access | Times Cited: 10
π-Stacking Interactions Involved in Gynecologic Tankyrase-1/Inhibitor Recognition and Association: Implications for Rational Design of Aromatic Pentapeptide Ligands
Yu Du, Lin Xu
International Journal of Peptide Research and Therapeutics (2024) Vol. 30, Iss. 2
Closed Access | Times Cited: 1
Computational Design and Experimental Validation of an Orthogonal X-bond/H-bond System to Improve the Binding Affinity and Recognition Specificity between Anesthetic Protein Kinase Ci and Its Pseudosubstrate Peptide
R. P. Kuang, Yamin Li, Chonghui Zhang, et al.
Journal of Computational Biophysics and Chemistry (2024) Vol. 23, Iss. 07, pp. 971-982
Closed Access | Times Cited: 1
Computational design and experimental confirmation of a disulfide-stapled YAP helixα1-trap derived from TEAD4 helical hairpin to selectively capture YAP α1-helix with potent antitumor activity
Kaipeng Li, Lijun Liu
Journal of Computer-Aided Molecular Design (2024) Vol. 38, Iss. 1
Closed Access | Times Cited: 1
Targeting peptide‐mediated interaction between the N‐protein and P‐protein of human pediatric respiratory syncytial virus by molecular design of chemically stapled helical peptides
Tingting Yan, Yixian Zhang, Lu Liu, et al.
Journal of the Chinese Chemical Society (2023) Vol. 70, Iss. 9, pp. 1835-1846
Open Access | Times Cited: 3
Molecular insight into the π‐stacking interactions of human ovarian cancer PARP‐1 with its small‐molecule inhibitors and rational design of aromatic amino acid‐rich peptides to target PARP‐1 based on the π‐stacking network
Chunxia Pan, Lei Chen, Xinxin Zhang, et al.
Journal of the Chinese Chemical Society (2022) Vol. 69, Iss. 5, pp. 775-785
Closed Access | Times Cited: 5
Orthogonal threading‐through‐β‐sheet design of lung cancer EGFR extracellular domain‐derived peptidic mimotopes binding to anti‐EGFR antibody
X Zhang, Na Chang, Xian‐Qi Zhang
Chemical Biology & Drug Design (2022) Vol. 101, Iss. 4, pp. 848-854
Closed Access | Times Cited: 5
Molecular Stapling of Human Pediatric RSV Phosphoprotein’s C-terminal Tail-Derived Peptides to Target the Coupled Folding-Upon-Binding Event Between Phosphoprotein and Nucleocapsid
Leling Zhang, Gong Yong, Lili Shen
International Journal of Peptide Research and Therapeutics (2022) Vol. 29, Iss. 1
Closed Access | Times Cited: 5
Integrated in silico–in vitro rational design of oncogenic EGFR-derived specific monoclonal antibody-binding peptide mimotopes
Ke Chen, Lili Ge, Guorui Liu
Journal of Bioinformatics and Computational Biology (2023) Vol. 21, Iss. 02
Closed Access | Times Cited: 2
Computational Analysis and Rational Design of N-Substituting Perturbation on the Affinity and Specificity of Pediatric Fyn SH3–Peptoid Interaction
Qin Liu, Jie Wang, Lin Shi, et al.
Journal of Computational Biophysics and Chemistry (2023) Vol. 22, Iss. 07, pp. 765-776
Closed Access | Times Cited: 2
Dynamics simulation, energetics calculation and experimental analysis of the intermolecular interaction between human neonatal ABL SH3 domain and its N -substituted peptoid ligands
Shijian Zhao, Lili Shen, Qiuqin Wang, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 22, pp. 12637-12644
Closed Access | Times Cited: 2
Molecular design and systematic optimization of a halogen‐bonding system between the asthma interleukin‐5 receptor and its cyclic peptide ligand
Quan He, Shuanglan Xu, Xiaomei Ma, et al.
Chemical Biology & Drug Design (2023) Vol. 103, Iss. 1
Open Access | Times Cited: 2
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