Evidence map›Paper›PMID 32140737›Full record

ReviewThe Journal of membrane biology2020

PX Domain-Containing Kinesin KIF16B and Microtubule-Dependent Intracellular Movements.

Bo-Jie Li, Hao Chen, Su-Su Jiang, Chu-Yao Wang, Qin-Hui Tuo, Shi-Yin Long, Cai-Ping Zhang, Duan-Fang Liao

Abstract readReview
PubMed Publisher
In one paragraph

Review in The Journal of membrane biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 39% of its field
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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Bo-Jie LiDepartment of Biochemistry & Molecular Biology, Medical College, University of South China, Hengyang, 421001, Hunan, China.ORCID 0000-0002-3243-6840
Hao ChenDepartment of Clinical Laboratory, The First Affiliated Hospital, University of South China, Hengyang, 421001, Hunan, China.
Su-Su JiangDepartment of Biochemistry & Molecular Biology, Medical College, University of South China, Hengyang, 421001, Hunan, China.
Chu-Yao WangDepartment of Biochemistry & Molecular Biology, Medical College, University of South China, Hengyang, 421001, Hunan, China.
Qin-Hui TuoDivision of Stem Cell Regulation and Application, State Key Laboratory of Chinese Medicine Powder and Medicine Innovation in Hunan (incubation), Hunan University of Chinese Medicine, Changsha, 410208, Hunan, China.
Shi-Yin LongDepartment of Biochemistry & Molecular Biology, Medical College, University of South China, Hengyang, 421001, Hunan, China. longshiyin@126.com.ORCID 0000-0002-9957-4703
Cai-Ping ZhangDepartment of Biochemistry & Molecular Biology, Medical College, University of South China, Hengyang, 421001, Hunan, China. zhangcpin@163.com.
Duan-Fang LiaoState Key Laboratory of Chinese Medicine Powder and Medicine Innovation in Hunan (Incubation), Hunan University of Chinese Medicine, Hanpu Science & Education District, Changsha, 410208, Hunan, China.
University of South China · CNHunan University of Traditional Chinese Medicine · CNFirst Affiliated Hospital of University of South China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a member of the kinesin-3 family, kinesin family member 16B (KIF16B) has a characteristic PhoX homology (PX) domain that binds to membranes containing phosphatidylinositol-3-phosphate (PI(3)P) and moves along microtubule filaments to the plus end via a process regulated by coiled coils in the stalk region in various cell types. The physiological function of KIF16B supports the transport of intracellular cargo and the formation of endosomal tubules. Ras-related protein (Rab) coordinates many steps of membrane transport and are involved in the regulation of KIF16B-mediated vesicle trafficking. Data obtained from clinical research suggest that KIF16B has a potential effect on the disease processes in intellectual disability, abnormal lipid metabolism, and tumor brain metastasis. In this review, we summarize recent advances in the structural and physiological characteristics of KIF16B as well as diseases associated with KIF16B disorders, and speculating its role as a potential adaptor for intracellular cholesterol trafficking.

Indexed as

Protein Interaction Domains and MotifsAnimalsCarrier ProteinsCell MembraneDisease SusceptibilityHumansIntracellular SpaceKinesinsMicrotubulesProtein BindingProtein TransportStructure-Activity RelationshipCarrier ProteinsKIF16B protein, humanKinesinsCholesterol transportEndocytic traffickingKIF16BKinesin

Identifiers

PMID32140737
OpenAlexW3009291130

What OpenQuestion holds

Textmetadata
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.