会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 61. 发明申请
    • UNIFIED SIMD PROCESSOR
    • 统一SIMD处理器
    • WO2005037326A2
    • 2005-04-28
    • PCT/GB2004004377
    • 2004-10-13
    • CLEARSPEED TECHNOLOGY PLCSTUTTARD DAVIDWILLIAMS DAVIDPACKER JAMESDAVIDSON COLINHICKEY NEILDAY TIMOTHY
    • STUTTARD DAVIDWILLIAMS DAVIDPACKER JAMESDAVIDSON COLINHICKEY NEILDAY TIMOTHY
    • G06F15/80A61K51/04A61K31/16A61P35/00
    • G06F9/3887G06F9/3885
    • A data processor comprises a single control unit and an integral execution unit adapted to operate on both parallel and scalar data under the same instruction set. The execution unit comprises a SMO part comprising an array of processing elements adapted to operate on the parallel data and a scalar part adapted to operate on the scalar data. Substantially all the instructions are operable on the parallel and/or the scalar data. Preferably, both the scalar part and the SIMD part have a complete range of addressing modes that allow them to support: scalar variables pointing to data in scalar memory; scalar variables pointing to data in memory in the SIMD part of the execution unit; SHVM variables pointing to memory in the SIMD part of the execution unit; and SIMD variables pointing to data in scalar memory. The scalar part, the SIMD part, and I/O means are adapted to be operated in parallel by the same instruction stream.
    • 数据处理器包括单个控制单元和适于在相同指令集下的并行和标量数据上操作的整体执行单元。 执行单元包括SMO部分,其包括适于对并行数据进行操作的处理元件阵列和适于对标量数据进行操作的标量部分。 基本上所有的指令都可以在并行和/或标量数据上操作。 优选地,标量部分和SIMD部分都具有允许它们支持的完整范围的寻址模式:指向标量存储器中的数据的标量变量; 标量变量指向执行单元的SIMD部分中的存储器中的数据; SHVM变量指向执行单元的SIMD部分中的存储器; 和SIMD变量指向标量存储器中的数据。 标量部分,SIMD部分和I / O装置适于由相同的指令流并行操作。
    • 64. 发明申请
    • A METHOD FOR MAPPING THE ACTIVE SITES BOUND BY ENZYMES THAT COVALENTLY MODIFY SUBSTRATE MOLECULES
    • 一种通过酶促共价修饰底物分子来定位有活性位点的方法
    • WO9923109A3
    • 1999-07-08
    • PCT/GB9803259
    • 1998-10-30
    • PEPTIDE THERAPEUTICS LTDCLARK JONATHANLAMONT ALANWILLIAMS DAVID
    • CLARK JONATHANLAMONT ALANWILLIAMS DAVID
    • C12Q1/48A61K38/00A61K38/55A61K45/00A61P43/00C07B61/00C07K1/04C12Q1/42A61K38/08G01N33/68
    • C07K1/047A61K38/00
    • This invention provides for the active site mapping of enzymes which catalyse covalent modification including, but not limited to phosphorylation, acylation, dephosphorylation in which a fixed residue (known as the catalytic residue) such as a tyrosine, serine, threonine, histidine, aspartic acid residue or any other residue containing an appropriate side chain is modified. Mapping of protein kinases is exemplified. The method of the invention has an additional level of complexity over and above that of the self-deconvoluting libraries described in WO97/42216. This involves making a library of smaller libraries (referred to as subsets) where a fixed residue is moved stepwise through the sequence of amino acids or other groups (such as peptidomimetics). Using 5 subsets of libraries of peptides of 5 amino acids allows the mapping of a sequence of 9 amino acids. In general one could carry out the invention using n subsets of n-mer peptides so as to provide mapping data for the residues from -(n-1) to +(n-1) either side of the active site. Thus in general the length of the mapped sequence would be (2n)-1. In this invention there is no need to separate modified from unmodified sequences because of the self deconvoluting nature of the library. The assay screen produces a series of hits, the patterns of which reveal the unique sequences in each well. This enables a pattern of substrate preferences to be determined for any enzyme. The unique sequences obtained using this invention can be used to provide substrates for high throughput assays and provide detailed information about the active site to aid rational drug design. This invention can also be used as an inhibitor library to screen against known modifying enzymes where a known substrate exists and can be set up in an assay format.
    • 本发明提供催化共价修饰的酶的活性位点作图,包括但不限于磷酸化,酰化,去磷酸化,其中固定的残基(称为催化残基)如酪氨酸,丝氨酸,苏氨酸,组氨酸,天冬氨酸 残基或含有适当侧链的任何其他残基被修饰。 蛋白激酶的图谱是示例性的。 本发明的方法比WO97 / 42216中描述的自去卷积文库具有更高的复杂程度。 这涉及制作一个较小的文库(称为亚组)的库,其中固定的残基逐步移动通过氨基酸或其他基团(例如肽模拟物)的序列。 使用5个氨基酸的肽库的5个亚组允许绘制9个氨基酸的序列。 通常可以使用n个n聚体肽亚组来实施本发明,从而为从活性位点两侧的 - (n-1)至+(n-1)的残基提供映射数据。 因此,通常映射序列的长度将是(2n)-1。 在本发明中,由于文库的自去卷积性质,不需要将修饰与未修饰的序列分开。 化验屏幕产生一系列命中,其中的模式显示每个孔中的独特序列。 这使得可以为任何酶确定底物偏好的模式。 使用本发明获得的独特序列可以用于提供用于高通量测定的底物并且提供关于活性位点的详细信息以帮助合理的药物设计。 本发明也可以用作抑制剂文库筛选已知的修饰酶,其中已知的底物存在并且可以以测定形式建立。