Vaccinia virus complement control protein is monomeric, and retains structural and functional integrity after exposure to adverse conditions

SA Smith; G Krishnasamy; KHM Murthy; A Cooper; K Bromek; PN Barlow; GJ Kotwal

Vaccinia virus complement control protein is monomeric, and retains structural and functional integrity after exposure to adverse conditions

SA Smith
, G Krishnasamy
, KHM Murthy
, A Cooper
, K Bromek
, PN Barlow
, GJ Kotwal

School of Biological Sciences

Research output: Contribution to journal › Article › peer-review

Original language	Undefined/Unknown
Pages (from-to)	55-64
Number of pages	10
Journal	BBA - Proteins and Proteomics
Volume	1598
Issue number	1-2
Publication status	Published - 2002

Structural basis for regulation of the complement cascade by complement receptor type 1
Barlow, P. (Principal Investigator)
Biotechnology and Biological Sciences Research Council
11/01/99 → 10/01/02
Project: Research

Cite this

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title = "Vaccinia virus complement control protein is monomeric, and retains structural and functional integrity after exposure to adverse conditions",

author = "SA Smith and G Krishnasamy and KHM Murthy and A Cooper and K Bromek and PN Barlow and GJ Kotwal",

year = "2002",

language = "Undefined/Unknown",

volume = "1598",

pages = "55--64",

journal = "BBA - Proteins and Proteomics",

publisher = "Elsevier",

number = "1-2",

}

TY - JOUR

T1 - Vaccinia virus complement control protein is monomeric, and retains structural and functional integrity after exposure to adverse conditions

AU - Smith, SA

AU - Krishnasamy, G

AU - Murthy, KHM

AU - Cooper, A

AU - Bromek, K

AU - Barlow, PN

AU - Kotwal, GJ

PY - 2002

Y1 - 2002

M3 - Article

VL - 1598

SP - 55

EP - 64

JO - BBA - Proteins and Proteomics

JF - BBA - Proteins and Proteomics

IS - 1-2

ER -

Vaccinia virus complement control protein is monomeric, and retains structural and functional integrity after exposure to adverse conditions

Projects

Structural basis for regulation of the complement cascade by complement receptor type 1

Cite this