3.6.4.B1: kinesin K16
This is an abbreviated version!
For detailed information about kinesin K16, go to the full flat file.
Word Map on EC 3.6.4.B1
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3.6.4.B1
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microtubule
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cargo
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testis-specific
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crem
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microtubule-dependent
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plant-specific
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kinesin-related
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phragmoplast
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phosphorylation-independent
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male-specific
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analysis
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medicine
- 3.6.4.B1
- microtubule
-
cargo
-
testis-specific
- crem
-
microtubule-dependent
-
plant-specific
-
kinesin-related
- phragmoplast
-
phosphorylation-independent
-
male-specific
- analysis
- medicine
Reaction
Synonyms
AtPAKRP1, AtPAKRP1L, GhKCH1, K16MD, KCBP, KIF 14, KIF18A, KIF4, KIF5, KIF5B, KIF5C, KIFC5A, kinesin K-16, kinesin K16, kinesin K16MD, kinesin KIF17b, kinesin kif5c, kinesin superfamily protein 5B, kinesin-1 motor protein, kinesin-like calmodulin-binding protein, KLP-6 kinesin, MS-KIF18A
ECTree
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Engineering
Engineering on EC 3.6.4.B1 - kinesin K16
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Q101C
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modification in loop L5 and labeling of mutant Cys residue with 2-(4'-(2''-iodoacetamido)phenyl)aminonaphthalene-6-sulfonic acid. In the absence of nucleotides, label is incorporated at almost equimolar ratio into loop L5. In the presence of ATP and ADP, the incorporated amount is reduced to 0.62 and 0.32 mol label per mol of motor domain, respectively
additional information
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in KIF14 depleted cells, citron kinase but not other components of the central spindle and cleavage furrow fail to localize. Localization of KIF14 and citron kinase to the central spindle and midbody is codependent, they form a complex depending on the activation state of citron kinase
additional information
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overexpression of KIFC5A in mouse cells causes the formation of aberrant, non-separated microtubule asters and mitotic arrest in a prometaphase-like state. KIFC5A knockdown partly rescues the phenotype caused by inhibition of plus-end directed motor Eg5 by monastrol on the mitotic spindle. Silencing also results in centrosome amplification detectable throughout the cell cycle. KIFC5A interacts with nucleotide-binding proteins 1 and 2. Knockdown of nucleotide-binding protein 1 or double knockdown of nucleotide-binding proteins 1 and 2 both phenocopy the KIFC5A silencing effect