Evidence map›Paper›PMID 39707457›Full record

ArticleJournal of cheminformatics2024

Interface-aware molecular generative framework for protein-protein interaction modulators.

Jianmin Wang, Jiashun Mao, Chunyan Li, Hongxin Xiang, Xun Wang, Shuang Wang, Zixu Wang, Yangyang Chen, Yuquan Li, Kyoung Tai No and 2 more

Abstract read
In one paragraph

Article in Journal of cheminformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Hot-Spot-Guided Generative Deep Learning for Drug-Like PPI Inhibitor Design.Interdisciplinary sciences, computational life sciences · 2026
    Article
  3. Review
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jianmin WangDepartment of Integrative Biotechnology, Yonsei University, Incheon, 21983, Republic of Korea.
Jiashun MaoDepartment of Integrative Biotechnology, Yonsei University, Incheon, 21983, Republic of Korea.
Chunyan LiSchool of Informatics, Yunnan Normal University, Kunming, China.
Hongxin XiangCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, 410082, Hunan, China.
Xun WangSchool of Computer Science and Technology, China University of Petroleum, Qingdao, 266580, Shandong, China.
Shuang WangSchool of Computer Science and Technology, China University of Petroleum, Qingdao, 266580, Shandong, China.
Zixu WangDepartment of Computer Science, University of Tsukuba, Tsukuba, 3058577, Japan.
Yangyang ChenDepartment of Computer Science, University of Tsukuba, Tsukuba, 3058577, Japan.
Yuquan LiCollege of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.
Kyoung Tai NoDepartment of Integrative Biotechnology, Yonsei University, Incheon, 21983, Republic of Korea. ktno@yonsei.ac.kr.
Tao SongSchool of Computer Science and Technology, China University of Petroleum, Qingdao, 266580, Shandong, China. tsong@upc.edu.cn.
Xiangxiang ZengCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, 410082, Hunan, China. xzeng@hnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein-protein interactions (PPIs) play a crucial role in numerous biochemical and biological processes. Although several structure-based molecular generative models have been developed, PPI interfaces and compounds targeting PPIs exhibit distinct physicochemical properties compared to traditional binding pockets and small-molecule drugs. As a result, generating compounds that effectively target PPIs, particularly by considering PPI complexes or interface hotspot residues, remains a significant challenge. In this work, we constructed a comprehensive dataset of PPI interfaces with active and inactive compound pairs. Based on this, we propose a novel molecular generative framework tailored to PPI interfaces, named GENiPPI. Our evaluation demonstrates that GENiPPI captures the implicit relationships between the PPI interfaces and the active molecules, and can generate novel compounds that target these interfaces. Moreover, GENiPPI can generate structurally diverse novel compounds with limited PPI interface modulators. To the best of our knowledge, this is the first exploration of a structure-based molecular generative model focused on PPI interfaces, which could facilitate the design of PPI modulators. The PPI interface-based molecular generative model enriches the existing landscape of structure-based (pocket/interface) molecular generative model. SCIENTIFIC CONTRIBUTION: This study introduces GENiPPI, a protein-protein interaction (PPI) interface-aware molecular generative framework. The framework first employs Graph Attention Networks to capture atomic-level interaction features at the protein complex interface. Subsequently, Convolutional Neural Networks extract compound representations in voxel and electron density spaces. These features are integrated into a Conditional Wasserstein Generative Adversarial Network, which trains the model to generate compound representations targeting PPI interfaces. GENiPPI effectively captures the relationship between PPI interfaces and active/inactive compounds. Furthermore, in fewshot molecular generation, GENiPPI successfully generates compounds comparable to known disruptors. GENiPPI provides an efficient tool for structure-based design of PPI modulators.

Indexed as

Conditional WGANGATGeometric deep learningMolecular generative modelProtein–protein interaction modulators

Identifiers

PMID39707457
PMCPMC11662471

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.