[ccp4bb] Workshop announcement @ Inst Pasteur Montevideo - Uruguay : Modern Approaches in Drug Discovery for Neglected Infectious Diseases

[Alejandro Buschiazzo]

Dear Colleagues:

We are pleased to announce the Workshop: "Modern Approaches in Drug 
Discovery for Neglected Infectious Diseases" at the Institut Pasteur de 
Montevideo (Uruguay).


*Dates:* November 3rd - 8th, 2014

*Venue**: *Institut Pasteur de Montevideo (Montevideo, Uruguay)

*Invited speakers:* Wim Hol (University of Washington, Seattle, USA), 
Paul Michels (University of Edinburgh, Edinburgh, UK), Celerino 
Abad-Zapatero (University of Illinois at Chicago, Chicago, USA), Hugo 
Cerecetto (UdelaR), Marcelo Comini (IP Montevideo), Sergio Pantano (IP 
Montevideo), Alejandro Buschiazzo (IP Montevideo)*

*
*Aim:*
The general aim of this International Workshop is to train students in 
state-of-the-art approaches for drug discovery and rational design, with 
special emphasis on target-based methods. The course will provide with a 
multidisciplinary view, with invited professors covering a diverse set 
of subjects : protein crystallography, in silico methods for molecular 
simulations, medicinal chemistry and biology of neglected infectious 
diseases.** For details of the activity please see the preliminary 
program. 



The course will be in English.

This activity is supported by the /Center for Structural Biology of the 
MERCOSUR /(CeBEM ), jointly with the /United 
Nations University Biotechnology Programme for Latin America and the 
Caribbean/ (UNU - BIOLAC ).


*
**Applicants:*

Graduate students and young research scientists are encouraged to apply. 
24 students will be selected among the applications. The Course will 
provide financial support for the students, covering registration fees, 
and for the case of those coming from abroad, all local expenses 
(lodging, per diem and local transportation).

/*
The application deadline is September 8th, 2014. The results will be 
announced by September 30th.*/


The application form, activity program, contact information and other 
details can be found at the web site of the course 



Please address further inquiries tosbdd_cou...@pasteur.edu.uy 


Looking forward to welcoming you in Montevideo!

--
Alejandro Buschiazzo, PhD
Research Scientist
Unit of Protein Crystallography
Institut Pasteur de Montevideo
Mataojo 2020
Montevideo 11400
URUGUAY
Phone: +598 25220910 int. 120
Fax:   +598 25224185
http://www.pasteur.edu.uy/pxf

[ccp4bb] Research Scientist - Protein Purification [off topic, job posting]

[Artem Evdokimov]

Friends,

Sorry for the off-topic post :) our sister group has an opening for a
research scientist in protein expression and purification (actual job
posting below, or apply through the web site with a job code 00TZZ):

http://jobs.monsanto.com/missouri/research-and-development/jobid5442876-research-scientist-protein-sciences-jobs

Thank you,

Artem

St. Louis, Missouri

Monsanto is seeking a talented and self-motivated individual to become part
of the Biotechnology organization. The *Research Scientist* will join the
Protein Expression and Purification group to support protein production
needs in Biotechnology and other sectors in the company. The candidate will
primarily be engaged in optimizing existing methods, trouble-shooting, and
developing new strategies for challenging protein production using E. coli
and other heterologous expression systems. The work involves dealing with
complex, novel and diverse proteins and requires comprehensive knowledge of
protein biochemistry, and extensive hands-on experiences in protein
production area.
The team is fast-paced and timeline driven. The successful candidate is
expected to interact effectively with multiple project teams across
Biotechnology and other sectors of Monsanto. We seek individuals with
diverse backgrounds, excellent people/communication skills and who can
contribute at both the individual level as well as on a team level.



*Responsibilities include: *• Develop methods for recombinant protein
expression and purification
• Manage the design, execution, analysis and summarization of research
experiments
• Evaluate new technologies to meet evolving project needs on protein
production
• Interface with project teams to understand project needs and provide
inputs and deliver results in a timely fashion





*Required Education and Skills: *• Minimum of a PhD in Biochemistry or
other biological science area
• Minimum of three or more years of relevant work experience
• Hands-on experience in protein chromatography and molecular cloning
• Extensive experience on recombinant protein expression in multiple
expression systems such as E.coli, insect or yeast
• Ability to work collaboratively with internal and external team members
• Excellent oral and written communication, data documentation, and
presentation skills
• Proficient in Microsoft Office suite
• Flexibility and capability to accomplish multi-task assignments



*Desired Education and Skills: *• Experience with membrane protein
purification
• Familiar with automated liquid handling systems

Monsanto is an equal opportunity employer. We value a diverse combination
of ideas, perspectives and cultures. EEO Employer
Minorities/Females/Protected Veterans/Disabled

[ccp4bb] Imaging Facilities Manager - Research Assistant Professor

[Reza Khayat]

Hi,

The Advanced Science Research Center is seeking applicants for 
a faculty position. 

Research faculty engage in, are responsible for, manage, 
and/or execute significant areas of research or scholarship.  
They may serve as principal or co-principal investigators on 
grants or contracts, manage postdoctoral fellows and their 
research projects or supervise graduate or undergraduate 
student research.  Research Faculty hold full-time, non-tenure 
track positions.   While they may participate in instructional 
programs, such as lectures or demonstrations, they are not 
assigned regular teaching duties.

Campus Specific Information:

The City University of New York's newest facility, the 
Advanced Science Research Center (ASRC) builds on the success 
of the University's rich past, and the determination to become 
a national leader in visionary scientific research in the 
future.  With a focus in the fields of Nanotechnology, 
Photonics, Structural Biology, Neuroscience, and Environmental 
Sciences, the ASRC will operate as a nucleus of a University-
wide science enterprise, fostering the development of an 
integrated research network that brings together faculty, 
students, and post-doctoral fellows from CUNY's colleges 
across the five boroughs.  This state-of-the-art, world class 
facility will house a staff of elite scientists and leaders 
who will seek to break down the walls between disparate but 
increasingly inter-related disciplines of applied science.

The new facility's equipment will house two premier FEI Titan 
(S)TEM's.  One being a new generation 300kV Titan Themis 
optimized for CryoTEM using a side-entry cryo holder.  The 
second being a new materials science image corrected 200kV 
(S)TEM Titan Themis with a superX EDS detector.  In addition, 
the facility will also be equipped with a 120kV LaB6 Tecnai 
Spirit for training and sample screening, as well as a latest 
generation Helios 660 dualbeam for sample preparation and 3D 
visualization.  All of these instruments will enable cutting-
edge research across a wide range of scientific disciplines.

Reporting to the Scientific Director of the Nanoscience 
Initiative at the ASRC, the Imaging Facility Manager will take 
responsibility for the day-to-day operation, maintenance and 
management of a new, state-of-the-art imaging facility. Duties 
include the development and provision of training in addition 
to assisting internal and external users. The successful 
candidate will have the opportunity to be involved in 
collaborative research in the scientific areas supported at 
the ASRC, and will be encouraged to develop and drive an 
independent research program in electron microscopy and its 
uses in modern scientific research. 
To learn more about the ASRC visit www.asrc.cuny.edu.

Key responsibilities include, but are not limited to:
- Advises and trains internal and external users with varying 
degrees of experience in experimental design, sample 
preparation, imaging and data interpretation. Includes 
production of training manuals.
- Performs microscopy and data analysis for external users; 
including reporting of results.
- Maintenance of laboratory, instruments and computers. 
- Planning and management of booking, access and finances to 
the facility; includes organizing regular users meetings. 
- Contributes to planning of extensions or updates of the 
facility. 
- Assists with preparation of grant proposals, presentations 
and publications.
- Actively seeks new collaborative projects within the CUNY 
system and externally.
- Contributes to dissemination of results through seminars and 
publications.
- Actively participates in collaborative research within the 
ASRC. Drives innovative research in area of imaging. 
- Performs other duties as required.

QUALIFICATIONS

Ph.D. and postdoctoral experience in a relevant area of 
physics, materials science, nanotechnology, biosciences or 
engineering.  Also required are success in carrying out 
research and ability to advise and/or oversee the direct work 
of others.

Other qualifications include:

- Excellent publication track record in the area of applied 
electron microscopy.  
- Extensive laboratory research experience using electron 
microscopes, including experimental design of TEM and SEM 
experiments.
- Experience in cryogenic-temperature transmission electron 
microscopy for direct-imaging of biological/soft matter.
- Experienced in equipment installation, implementation of 
relevant upgrades and improvements and liaising with 
suppliers.
- Excellent problem solving skills and a proven ability to 
learn and teach in a multidisciplinary environment. 
- Highly motivated with an ability to work independently or in 
teams.
- Demonstrated ability to prioritize and work to meet tight 
deadlines.
- Strong attention to detail.
- Excellent verbal and written communication skills.

COMPENSATION

CUNY offers faculty a competitive compensation and benefits 

Re: [ccp4bb] C2/I2 space groups

[Antonio L. Llamas-Saiz]

There is a good description of this situation in the paper:
"Conventional Cells—The Last Step Toward General Acceptance of Standard 
Conventional Cells for the Reporting of Crystallographic Data" 
published in J. Res. Natl. Inst. Stand. Technol. 107, 373–377 (2002).

The conclusion and recommendation quoted from this paper is "...In all cases 
then, the practice for the monoclinic system would be to select a conventional 
cell based on the shortest vectors in the ac plane (b-axis unique) for 
primitive as well as centered cells."

Hope this helps.

Antonio
-
Dr. Antonio L. Llamas-Saiz
Unidade de Raios X. RIAIDT
Edificio CACTUS. Campus Vida
Universidade de Santiago de Compostela
E-15782 Santiago de Compostela
SPAIN
Tel.: +34 881 816 223
Fax.: +34 881 816 203
E-mail: antonio.lla...@usc.es
-



-Original Message-
From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of Phil Evans
Sent: Wednesday, May 21, 2014 9:07 PM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] C2/I2 space groups

I2 and C2 are different settings of the same group. The official IUCr 
convention is to use the one which gives the beta angle closer to 90 degrees. 
As far as I know all programs should now be able to use the I2 setting, but if 
it worries you, you can reindex to C2

Phil

On 21 May 2014, at 17:54, Roberto Battistutta  
wrote:

> Dear All,
> a question about C2 and I2 space groups.
> Processing a dataset, XDS output says C2, with dimensions 122.8, 56,9 81,5 
> and beta 125.1°.
> Aimless reindexes to I2 with 81.6, 56.9, 101.1 and 96.2°.
> Phenix (refine) returns a warning "NOTE: non-standard setting used: I 1 2 1".
> In the PDB there are indeed several examples of I2 choices.
> 
> The two space groups are equivalent as indicated in the International Tables 
> (all with number 5), but why different programs use different conventions? Is 
> there any rationale? By the way, the volumes of the two unit cells are very 
> similar.
> 
> Thanks,
> Roberto.
> 
> 
> Roberto Battistutta
> Associate Professor
> Department of Chemistry
> University of Padua
> via Marzolo 1, 35131 Padova - ITALY
> tel. +39.049.827.5262
> fax. +39.049.827.5829
> roberto.battistu...@unipd.it
> www.chimica.unipd.it/roberto.battistutta/
> VIMM (Venetian Institute of Molecular Medicine) via Orus 2, 35129 
> Padova - ITALY tel. +39.049.7923.236 fax +39.049.7923.250 www.vimm.it

Re: [ccp4bb] Potentially serious if unusual bug in handling symmetry

[Phil Evans]

OK I guess Pointless is accepting the number as given in the reference file, 
rather than changing it.

If Pointless is just determining the space group it does give the "correct" 
(i.e. weird CCP4 convention) number

* Space group = 'P 2 21 21' (number 3018)

I'm not sure how to test this as I don't know how to make an mtz file with P 2 
21 21 /sgn 18, but I will look into it

Phil

On 23 May 2014, at 12:34, Eleanor Dodson  wrote:

> 
>  Someone here has seen his Rfactors leap from 18% to 42% and was naturally 
> distressed! 
> We have tracked down the problem to this:
> 
> Steps he took were:
> 
> 1)  Integrate with XDS and feed output through pointless/aimless etc.
> He used a phenix refined mtz to "Match Laue and indexing" 
> 
> The space group there is given by PHENIX 
> as "P 2 21 21 " but the spacegroup NUMBER is given as 18 (ie P21 21 2 in CCP4 
> symmetry library) .
> 
> pointless then output an mtz file with SPACEGROUP number as 18 and SG name as 
> P 2 21 21.
> The symmetry operators are correctly listed for P 2 21 21
>  This is the version number: CCP4 6.4: POINTLESS  version 1.9.8 : 
> 02/05/14
> 
> 2) When the refinement was repeated with REFMAC  the spacegroup was taken as 
> P21 21 2 - ie the SG number 18 overrode the listed symmetry operators in the 
> mtz file, and the SG name P 2 21 21 given on the CRYST1 card was ignored.
> 
> The refmac version used is  CCP4 6.4: Refmac_5.8.0071 version 5.8.0071 : 
> 04/04/14
> 
> 
> The user thinks that in REFMAC 5.8.0033 this problem did not occur, but I 
> havent checked that..
> 
> 
> Anyway - it does emphasise the importance of checking symmetry operators for 
> consistency with both the SG name and number (Yes, George, I know you have 
> always said this is the only correct policy!) Maybe an extra subroutine could 
> be added to the symmetry library and called from other programs..
> 
> And ideally checking all sources of symmetry information for consistency and 
> stopping if there is a serious disagreement. 
> 
> 
> In the short term we simply took the processed mtz file and ran
> mtzutils hklin1 corrupted.mtz hklout fixed.mtz
> SYMM 3018   (or symm "P2 21 21" ) 
> and the fixed file was OK
> 
> Eleanor Dodson
> 
> 
> 

Re: [ccp4bb] Potentially serious if unusual bug in handling symmetry

[Phil Evans]

Surely Refmac or any other program should honour the symmetry operators in the 
MTZ file - that's why they are there!

Phil

On 23 May 2014, at 12:34, Eleanor Dodson  wrote:

> 
>  Someone here has seen his Rfactors leap from 18% to 42% and was naturally 
> distressed! 
> We have tracked down the problem to this:
> 
> Steps he took were:
> 
> 1)  Integrate with XDS and feed output through pointless/aimless etc.
> He used a phenix refined mtz to "Match Laue and indexing" 
> 
> The space group there is given by PHENIX 
> as "P 2 21 21 " but the spacegroup NUMBER is given as 18 (ie P21 21 2 in CCP4 
> symmetry library) .
> 
> pointless then output an mtz file with SPACEGROUP number as 18 and SG name as 
> P 2 21 21.
> The symmetry operators are correctly listed for P 2 21 21
>  This is the version number: CCP4 6.4: POINTLESS  version 1.9.8 : 
> 02/05/14
> 
> 2) When the refinement was repeated with REFMAC  the spacegroup was taken as 
> P21 21 2 - ie the SG number 18 overrode the listed symmetry operators in the 
> mtz file, and the SG name P 2 21 21 given on the CRYST1 card was ignored.
> 
> The refmac version used is  CCP4 6.4: Refmac_5.8.0071 version 5.8.0071 : 
> 04/04/14
> 
> 
> The user thinks that in REFMAC 5.8.0033 this problem did not occur, but I 
> havent checked that..
> 
> 
> Anyway - it does emphasise the importance of checking symmetry operators for 
> consistency with both the SG name and number (Yes, George, I know you have 
> always said this is the only correct policy!) Maybe an extra subroutine could 
> be added to the symmetry library and called from other programs..
> 
> And ideally checking all sources of symmetry information for consistency and 
> stopping if there is a serious disagreement. 
> 
> 
> In the short term we simply took the processed mtz file and ran
> mtzutils hklin1 corrupted.mtz hklout fixed.mtz
> SYMM 3018   (or symm "P2 21 21" ) 
> and the fixed file was OK
> 
> Eleanor Dodson
> 
> 
> 

Re: [ccp4bb] Potentially serious if unusual bug in handling symmetry

[Ian Tickle]

Eleanor

Clearly the space group name when given should always override the number,
since whereas there is universal agreement on what the names should be
(allowing for variants such as P21 and P1211 and +/- redundant spaces),
there is no universal agreement on what the numbers should be (in fact the
numbers mean completely different things, here one number refers to the
standard setting and the other to the actual setting).

Cheers

-- Ian


On 23 May 2014 12:34, Eleanor Dodson  wrote:

>
>  Someone here has seen his Rfactors leap from 18% to 42% and was naturally
> distressed!
> We have tracked down the problem to this:
>
> Steps he took were:
>
> 1)  Integrate with XDS and feed output through pointless/aimless etc.
> He used a phenix refined mtz to "Match Laue and indexing"
>
> The space group there is given by PHENIX
> as "P 2 21 21 " but the spacegroup NUMBER is given as 18 (ie P21 21 2 in
> CCP4 symmetry library) .
>
> pointless then output an mtz file with SPACEGROUP number as 18 and SG name
> as P 2 21 21.
> The symmetry operators are correctly listed for P 2 21 21
>  This is the version number: CCP4 6.4: POINTLESS  version
> 1.9.8 : 02/05/14
>
> 2) When the refinement was repeated with REFMAC  the spacegroup was taken
> as P21 21 2 - ie the SG number 18 overrode the listed symmetry operators in
> the mtz file, and the SG name P 2 21 21 given on the CRYST1 card was
> ignored.
>
> The refmac version used is  CCP4 6.4: Refmac_5.8.0071 version 5.8.0071
> : 04/04/14
>
>
> The user thinks that in REFMAC 5.8.0033 this problem did not occur, but I
> havent checked that..
>
>
> Anyway - it does emphasise the importance of checking symmetry operators
> for consistency with both the SG name and number (Yes, George, I know you
> have always said this is the only correct policy!) Maybe an extra
> subroutine could be added to the symmetry library and called from other
> programs..
>
> And ideally checking all sources of symmetry information for consistency
> and stopping if there is a serious disagreement.
>
>
> In the short term we simply took the processed mtz file and ran
> mtzutils hklin1 corrupted.mtz hklout fixed.mtz
> SYMM 3018   (or symm "P2 21 21" )
> and the fixed file was OK
>
> Eleanor Dodson
>
>
>
>

[ccp4bb] Potentially serious if unusual bug in handling symmetry

[Eleanor Dodson]

 Someone here has seen his Rfactors leap from 18% to 42% and was naturally
distressed!
We have tracked down the problem to this:

Steps he took were:

1)  Integrate with XDS and feed output through pointless/aimless etc.
He used a phenix refined mtz to "Match Laue and indexing"

The space group there is given by PHENIX
as "P 2 21 21 " but the spacegroup NUMBER is given as 18 (ie P21 21 2 in
CCP4 symmetry library) .

pointless then output an mtz file with SPACEGROUP number as 18 and SG name
as P 2 21 21.
The symmetry operators are correctly listed for P 2 21 21
 This is the version number: CCP4 6.4: POINTLESS  version 1.9.8
: 02/05/14

2) When the refinement was repeated with REFMAC  the spacegroup was taken
as P21 21 2 - ie the SG number 18 overrode the listed symmetry operators in
the mtz file, and the SG name P 2 21 21 given on the CRYST1 card was
ignored.

The refmac version used is  CCP4 6.4: Refmac_5.8.0071 version 5.8.0071
: 04/04/14


The user thinks that in REFMAC 5.8.0033 this problem did not occur, but I
havent checked that..


Anyway - it does emphasise the importance of checking symmetry operators
for consistency with both the SG name and number (Yes, George, I know you
have always said this is the only correct policy!) Maybe an extra
subroutine could be added to the symmetry library and called from other
programs..

And ideally checking all sources of symmetry information for consistency
and stopping if there is a serious disagreement.


In the short term we simply took the processed mtz file and ran
mtzutils hklin1 corrupted.mtz hklout fixed.mtz
SYMM 3018   (or symm "P2 21 21" )
and the fixed file was OK

Eleanor Dodson

[ccp4bb] Position available at Syngenta - Team Leader Protein Crystallography

[Daniel Kloer]

*Team Leader Protein Crystallography*


Jealott's Hill, Bracknell, Berkshire, UK

We are seeking a highly talented and motivated crystallographer who is
enthusiastic about working across the range of protein crystallography
activities covering a wide variety of biological systems. The successful
candidate will have a strong background in protein production and
crystallization as well as x-ray data collection, structure refinement and
validation. Computational and molecular modelling skills are a plus.

The successful candidate will need to demonstrate flexible teamworking and
a tenacious approach to delivering structural solution outputs to projects.
Excellent oral and written communication skills and the ability to
translate structural knowledge to a meaningful output for multidisciplinary
project teams are highly desirable qualities for this position.

*Responsibilities*

• Lead the protein crystallography team and provide protein crystallography
support for research projects
• Maintain a strategic overview of projects requiring structural biology
support; engage and communicate effectively with stakeholders to ensure
optimal use of resources
• Guide molecular biology and protein purification for crystallography
• Carry out crystallization, x-ray data collection, structure determination
and refinement of proteins and protein-ligand complexes
• Communicate results to chemists, computational chemists and
cross-disciplinary project teams so that results make an impact in
structure-based design and understanding of SAR of new leads
• Develop and maintain high quality standards for in-house structure data
and crystallographic computing procedures
• Responsible for organization of own and team's laboratory work including
ordering laboratory supplies and equipment
• Formal and informal teaching and coaching of other lab staff and trainees

*Experience required*


• PhD in macromolecular crystallography/structural biology plus 5 years
industry experience or equivalent
• Demonstrated experience in protein crystallization, structure
determination, refinement and validation

• Knowledge of chemistry, molecular structure and protein-ligand
interactions
• Knowledge of software for protein structure solution and refinement
• Knowledge of protein production



*About Syngenta*



Syngenta is one of the world’s leading companies with more than 27.000
employees in over 90 countries dedicated to our purpose: Bringing plant
potential to life. Through world-class science, global reach and commitment
to our customers we help to increase crop productivity, protect the
environment and improve health and quality of life. For more information
about us please go to http://www.syngenta.com/.



For a full job profile and to apply to this position, please visit



http://www.syngentajobs.com/Taleo_apply.html?CountryCode=2gb&lang=en&location=23236270036668&portal=101430233
- job number 14006122


Application deadline is 16th June.


I am happy to answer informal questions about the position (please use the
e-mail address below), but if you wish to apply you must go through the
Syngenta Jobs website linked above.



Thanks,



Daniel Kloer



Head of Protein Analysis and Computational Chemistry

Syngenta

daniel.kl...@syngenta.com

[ccp4bb] 2nd International Workshop on Pontin/RUVBL1 & Reptin/RUVBL2 - 2nd Announcement

[Pedro M. Matias]

Dear CCP4ers,

It is our great pleasure to announce that the registration for this 
workshop, that will take place in very nice surroundings in Oeiras 
(Portugal) next October 10-12, is now open.


The Workshop will divided into 5 sessions covering the following topics:

- Structural Biology
- Chromatin remodeling and pre-rRNA processing
- Regulation of gene expression
- Transcription
- Pathophysiology

Each session will be structured as follows:

- Invited lecture 35 minutes
- Invited lecture 35 minutes
- Coffee/Tea break 50 minutes
- Selected talks from Abstracts

Poster sessions will be held during coffee/tea and lunch breaks.

Please visit http://pontinreptin2014.itqb.unl.pt where you will find 
regularly updated information on this meeting.


A lot has happened since the exciting First Workshop in 2012 that 
gathered people from 15 countries in Bordeaux in 2012. For those of 
you who did not attend, you can get a flavor of it by reading its 
Proceedings (Sci. Signal. 2013; 6, mr1).


Whether Pontin/RUVBL1 & Reptin/RUVBL2 are at the core of your 
studies, or whether you recently fell upon them in the course of your 
research, this Workshop will allow you to meet all the specialists in 
this complex field and find collaborations.


Register early to benefit from a reduced rate and to make sure that 
you will be in. There are still many open slots for oral 
communications besides invited speakers.


Important dates:

Early registration deadline - June 30 (150 Eur PhD students / 200 Eur 
PhD holders)

Registration deadline - July 31 (200 Eur PhD students / 250 Eur PhD holders)
Registration fee & accomodation payment deadline - August 15
Abstract submission deadline - August 31

We have secured a special single room rate of 50 Eur/night at nearby 
Hotel Riviera () - this rate is good until August 15.


We look forward to meeting you soon in Portugal!

The local organizing committee,

Pedro Matias
Tiago Bandeiras
Sara Silva


Industry and Medicine Applied Crystallography
Macromolecular Crystallography Unit
___
Phones : (351-21) 446-9100 Ext. 1669
  (351-21) 446-9669 (direct)
Fax   : (351-21) 441-1277 or 443-3644

email : mat...@itqb.unl.pt

http://www.itqb.unl.pt/research/biological-chemistry/industry-and-medicine-applied-crystallography
http://www.itqb.unl.pt/labs/macromolecular-crystallography-unit

Mailing address :
Instituto de Tecnologia Quimica e Biologica
Apartado 127
2781-901 OEIRAS
Portugal

[ccp4bb] Position at Diamond Light Source

[David Hall]

This Sunday is the close date for applications for a software position at 
Diamond Light Source - please follow the link below for details:

http://www.diamond.ac.uk/Careers/Vacancies/All/DIA0919_CH.html

Best regards

Dave Hall

I04 PBS & MX Village Coordinator | Diamond Light 
Source
t: 01235 778926  |  e: david.h...@diamond.ac.uk
http://www.diamond.ac.uk/mx





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