Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

SInCRe

General information

URL: http://proline.biochem.iisc.ernet.in/sincre/
Full name: Structural Interactome Computational Resource
Description: Structural Interactome Computational Resource is a Open Source Integrated Computational Resource for the Analysis of the Structural Interactome of Mycobacterium tuberculosis to predict Off-Site Interactions of Drug Candidates
Year founded: 2015
Last update: 2015-06-30
Version: v1.0
Accessibility:
Accessible
Country/Region: India

Classification & Tag

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Contact information

University/Institution: Indian Institute of Science
Address: Molecular Biophysics Unit, Indian Institute of Science, Bangalore, India
City:
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Country/Region: India
Contact name (PI/Team): Narayanaswamy Srinivasan
Contact email (PI/Helpdesk): ns@mbu.iisc.ernet.in

Publications

26130660
SInCRe-structural interactome computational resource for Mycobacterium tuberculosis. [PMID: 26130660]
Metri R, Hariharaputran S, Ramakrishnan G, Anand P, Raghavender US, Ochoa-Montaño B, Higueruelo AP, Sowdhamini R, Chandra NR, Blundell TL, Srinivasan N.

We have developed an integrated database for Mycobacterium tuberculosis H37Rv (Mtb) that collates information on protein sequences, domain assignments, functional annotation and 3D structural information along with protein-protein and protein-small molecule interactions. SInCRe (Structural Interactome Computational Resource) is developed out of CamBan (Cambridge and Bangalore) collaboration. The motivation for development of this database is to provide an integrated platform to allow easily access and interpretation of data and results obtained by all the groups in CamBan in the field of Mtb informatics. In-house algorithms and databases developed independently by various academic groups in CamBan are used to generate Mtb-specific datasets and are integrated in this database to provide a structural dimension to studies on tuberculosis. The SInCRe database readily provides information on identification of functional domains, genome-scale modelling of structures of Mtb proteins and characterization of the small-molecule binding sites within Mtb. The resource also provides structure-based function annotation, information on small-molecule binders including FDA (Food and Drug Administration)-approved drugs, protein-protein interactions (PPIs) and natural compounds that bind to pathogen proteins potentially and result in weakening or elimination of host-pathogen protein-protein interactions. Together they provide prerequisites for identification of off-target binding. © The Author(s) 2015. Published by Oxford University Press.

Database (Oxford). 2015:2015() | 6 Citations (from Europe PMC, 2025-12-27)

Ranking

All databases:
5920/6895 (14.155%)
Health and medicine:
1499/1738 (13.809%)
Interaction:
1064/1194 (10.972%)
5920
Total Rank
6
Citations
0.6
z-index

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Record metadata

Created on: 2016-01-14
Curated by:
Pei Liu [2022-08-28]
Lin Xia [2016-03-28]
Mengwei Li [2016-01-14]