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.