Evidence map›Paper›PMID 33167861›Full record

ArticleBMC bioinformatics2020

A sequence embedding method for enzyme optimal condition analysis.

Xiangjun Li, Zhixin Dou, Yuqing Sun, Lushan Wang, Bin Gong, Lin Wan

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

6 authors.

Xiangjun LiSchool of Software, Shandong University, Shunhua Road, Jinan, 250101, China.
Zhixin DouState Key Laboratory of Microbial Technology, Shandong University, Binhai Road, Qingdao, 266237, China.
Yuqing SunSchool of Software, Shandong University, Shunhua Road, Jinan, 250101, China. sun_yuqing@sdu.edu.cn.
Lushan WangState Key Laboratory of Microbial Technology, Shandong University, Binhai Road, Qingdao, 266237, China.
Bin GongSchool of Software, Shandong University, Shunhua Road, Jinan, 250101, China.
Lin WanSchool of Software, Shandong University, Shunhua Road, Jinan, 250101, China.

Funding

Key Research and Development Program of Shandong Province 2017GGX10114Key Research and Development Program of Shandong Province 2019JZZY010107Major Project of NSF Shandong Province ZR2018ZB0420National Key R&D Program of China 2016YFB0201700National Key R&D Program of China 2018YFB0204000National Key R&D Program of China 2018YFC0831401National Natural Science Foundation of China 31770054National Natural Science Foundation of China 91646119
6 · The paper itself

Abstract

backgroundAn enzyme activity is influenced by the external environment. It is important to have an enzyme remain high activity in a specific condition. A usual way is to first determine the optimal condition of an enzyme by either the gradient test or by tertiary structure, and then to use protein engineering to mutate a wild type enzyme for a higher activity in an expected condition.

resultsIn this paper, we investigate the optimal condition of an enzyme by directly analyzing the sequence. We propose an embedding method to represent the amino acids and the structural information as vectors in the latent space. These vectors contain information about the correlations between amino acids and sites in the aligned amino acid sequences, as well as the correlation with the optimal condition. We crawled and processed the amino acid sequences in the glycoside hydrolase GH11 family, and got 125 amino acid sequences with optimal pH condition. We used probabilistic approximation method to implement the embedding learning method on these samples. Based on these embedding vectors, we design a computational score to determine which one has a better optimal condition for two given amino acid sequences and achieves the accuracy 80% on the test proteins in the same family. We also give the mutation suggestion such that it has a higher activity in an expected environment, which is consistent with the previously professional wet experiments and analysis.

conclusionA new computational method is proposed for the sequence based on the enzyme optimal condition analysis. Compared with the traditional process that involves a lot of wet experiments and requires multiple mutations, this method can give recommendations on the direction and location of amino acid substitution with reference significance for an expected condition in an efficient and effective way.

Indexed as

Amino Acid SequenceComputational BiologyGlycoside HydrolasesHydrogen-Ion ConcentrationNeural Networks, ComputerGlycoside HydrolasesBioinformaticsEmbeddingProtein sequence analysis

Identifiers

PMID33167861
PMCPMC7653822

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.