2fhi

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[[Category: tumor suppressor]]
[[Category: tumor suppressor]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 12:59:48 2007''
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 17:14:46 2007''

Revision as of 15:10, 30 October 2007


2fhi, resolution 2.60Å

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SUBSTRATE ANALOG (IB2) COMPLEX WITH THE HIS 96 ASN SUBSTITUTION OF THE FRAGILE HISTIDINE TRIAD PROTEIN, FHIT

Overview

Alterations in the FHIT gene at 3p14.2 occur as early and frequent events, in the development of several common human cancers. The ability of human, Fhit-negative cells to form tumors in nude mice is suppressed by stable, reexpression of Fhit protein. Fhit protein is a diadenosine, P1,P3-triphosphate (ApppA) hydrolase whose fungal and animal homologs form, a branch of the histidine triad (HIT) superfamily of nucleotide-binding, proteins. Because the His-96 --> Asn substitution of Fhit, which retards, ApppA hydrolase activity by seven orders of magnitude, did not block, tumor-suppressor activity in vivo, we determined whether this mutation, affected ApppA binding or particular steps in the ApppA catalytic cycle., Evidence is presented that His-96 --> Asn protein binds ApppA well and, ... [(full description)]

About this Structure

2FHI is a [Single protein] structure of sequence from [Homo sapiens] with IB2 as [ligand]. Active as [Bis(5'-adenosyl)-triphosphatase], with EC number [3.6.1.29]. Structure known Active Site: HIT. Full crystallographic information is available from [OCA].

Reference

Genetic, biochemical, and crystallographic characterization of Fhit-substrate complexes as the active signaling form of Fhit., Pace HC, Garrison PN, Robinson AK, Barnes LD, Draganescu A, Rosler A, Blackburn GM, Siprashvili Z, Croce CM, Huebner K, Brenner C, Proc Natl Acad Sci U S A. 1998 May 12;95(10):5484-9. PMID:9576908

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