HMI-PRED
HMI-PRED predicts structural protein-protein interactions between host proteins and microbial proteins (bacteria, viruses, fungi, and protozoa) by detecting interface mimicry to reveal how microbial proteins may exploit host binding surfaces.
Key Features:
- Interface mimicry-based prediction: Uses structural information to detect mimicry of host protein interfaces by microbial proteins to infer potential interactions.
- Structural modeling of HMI complexes: Generates structural models of potential host-microbe interaction (HMI) complexes based on predicted interface compatibility.
- Identification of disrupted endogenous and exogenous PPIs: Identifies host endogenous and exogenous protein-protein interactions that could be perturbed by microbial proteins.
- Support for homology models: Accepts and utilizes uploaded homology models of microbial proteins when experimental structures are unavailable.
- Tissue expression annotation: Associates targeted host proteins with tissue expression profiles to provide biological context for predicted interactions.
Scientific Applications:
- Molecular mechanism elucidation: Elucidates molecular bases of host-microbe interactions by revealing structural mimicry and binding interfaces.
- Target identification: Aids identification and prioritization of host proteins that may serve as therapeutic or experimental targets.
- Pathogenesis investigation: Supports investigation of pathogenic mechanisms by showing how microbial proteins can modulate host signaling and immune processes.
Methodology:
Structural bioinformatics techniques focused on interface mimicry and structural compatibility between microbial and host proteins to predict protein-protein interactions.
Topics
Details
- Tool Type:
- api
- Added:
- 1/18/2021
- Last Updated:
- 1/30/2021
Operations
Publications
Guven-Maiorov E, Hakouz A, Valjevac S, Keskin O, Tsai C, Gursoy A, Nussinov R. HMI-PRED: A Web Server for Structural Prediction of Host-Microbe Interactions Based on Interface Mimicry. Journal of Molecular Biology. 2020;432(11):3395-3403. doi:10.1016/j.jmb.2020.01.025. PMID:32061934. PMCID:PMC7261632.