Evidence map›Paper›PMID 40060652›Full record

ArticlebioRxiv : the preprint server for biology2025

CYCLICCAE: A CONFORMATIONAL AUTOENCODER FOR EFFICIENT HETEROCHIRAL MACROCYCLIC BACKBONE SAMPLING.

Andrew C Powers, P Douglas Renfrew, Parisa Hosseinzadeh, Vikram Khipple Mulligan

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Andrew C PowersDepartment of Bioengineering, University of Oregon, Eugene, Oregon.ORCID 0009-0002-0935-6444
P Douglas RenfrewCenter for Computational Biology, Flatiron Institute, New York, New York.ORCID 0000-0003-4267-2932
Parisa HosseinzadehDepartment of Bioengineering, University of Oregon, Eugene, Oregon.ORCID 0000-0002-3128-7433
Vikram Khipple MulliganCenter for Computational Biology, Flatiron Institute, New York, New York.ORCID 0000-0001-6038-8922

Funding

A data-driven approach towards generation of permeable peptide therapeuticsDP2GM146249 · NIGMS · UNIVERSITY OF OREGON · PI HOSSEINZADEH, PARISA · 2021 to 2024
$2.2M
NIGMS NIH HHS DP2 GM146249
6 · The paper itself

Abstract

Macrocycles are a promising therapeutic class. The incorporation of heterochiral and non-natural chemical building-blocks presents challenges for rational design, however. With no existing machine learning methods tailored for heterochiral macrocycle design, we developed a novel convolutional autoencoder model to rapidly generate energetically favorable macrocycle backbones for heterochiral design and structure prediction. Our approach surpasses the current state-of-the-art method, Generalized Kinematic loop closure (GenKIC) in the Rosetta software suite. Given the absence of large, available macrocycle datasets, we created a custom dataset in-house and

Indexed as

autoencoderdrug designheterochiralmachine learningmacrocyclepeptidepeptoidRosetta

Identifiers

PMID40060652
PMCPMC11888347

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.