4n6v

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'''Unreleased structure'''
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{{STRUCTURE_4n6v| PDB=4n6v | SCENE= }}
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===Partial rotational order disorder structure of human stefin B===
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The entry 4n6v is ON HOLD until Paper Publication
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==Disease==
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[[http://www.uniprot.org/uniprot/CYTB_HUMAN CYTB_HUMAN]] Defects in CSTB are the cause of progressive myoclonic epilepsy type 1 (EPM1) [MIM:[http://omim.org/entry/254800 254800]]. EPM1 is an autosomal recessive disorder characterized by severe, stimulus-sensitive myoclonus and tonic-clonic seizures. The onset, occurring between 6 and 13 years of age, is characterized by convulsions. Myoclonus begins 1 to 5 years later. The twitchings occur predominantly in the proximal muscles of the extremities and are bilaterally symmetrical, although asynchronous. At first small, they become late in the clinical course so violent that the victim is thrown to the floor. Mental deterioration and eventually dementia develop.<ref>PMID:9012407</ref>
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Authors: Renko, M., Taler-Vercic, A., Mihelic, M., Zerovnik, E., Turk, D.
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==Function==
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[[http://www.uniprot.org/uniprot/CYTB_HUMAN CYTB_HUMAN]] This is an intracellular thiol proteinase inhibitor. Tightly binding reversible inhibitor of cathepsins L, H and B.
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Description: Partial rotational order disorder structure of human stefin B
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==About this Structure==
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[[4n6v]] is a 10 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4N6V OCA].
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==Reference==
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<references group="xtra"/><references/>
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[[Category: Mihelic, M.]]
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[[Category: Renko, M.]]
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[[Category: Taler-Vercic, A.]]
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[[Category: Turk, D.]]
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[[Category: Zerovnik, E.]]
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[[Category: Crystal disorder]]
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[[Category: Cystatin b]]
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[[Category: Hydrolase inhibitor]]
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[[Category: Partial rotational order disorder]]
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[[Category: Stefin b]]

Revision as of 06:44, 9 April 2014

Template:STRUCTURE 4n6v

Contents

Partial rotational order disorder structure of human stefin B

Disease

[CYTB_HUMAN] Defects in CSTB are the cause of progressive myoclonic epilepsy type 1 (EPM1) [MIM:254800]. EPM1 is an autosomal recessive disorder characterized by severe, stimulus-sensitive myoclonus and tonic-clonic seizures. The onset, occurring between 6 and 13 years of age, is characterized by convulsions. Myoclonus begins 1 to 5 years later. The twitchings occur predominantly in the proximal muscles of the extremities and are bilaterally symmetrical, although asynchronous. At first small, they become late in the clinical course so violent that the victim is thrown to the floor. Mental deterioration and eventually dementia develop.[1]

Function

[CYTB_HUMAN] This is an intracellular thiol proteinase inhibitor. Tightly binding reversible inhibitor of cathepsins L, H and B.

About this Structure

4n6v is a 10 chain structure. Full crystallographic information is available from OCA.

Reference

  1. ↑ Lalioti MD, Mirotsou M, Buresi C, Peitsch MC, Rossier C, Ouazzani R, Baldy-Moulinier M, Bottani A, Malafosse A, Antonarakis SE. Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1). Am J Hum Genet. 1997 Feb;60(2):342-51. PMID:9012407

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