I have 2 protein crystal structures and I would like to align their origins so I can then generate the crystal packing of each and compare them.
Hi Engi, is your purpose to align the cells of the structures? I'm not aware of such a program. It will also depend on the lattice type of the two if they are similar or not.
Hi Tjaard Pijning thanks for your reply. My purpose is to align the assymetric unit cell, yes.
Some papers report performing a "STD self intensity" test to check the aggregation of compounds in STD NMR. Can anyone please elaborate how such a test is performed?
07 August 2019 6,949 2 View
I read in the attached paper the equation for HSQC spectra (equation 8). What about HMQC? I cannot find a reference online. Thanks!
04 May 2019 9,901 2 View
I am purifying a protein with a his tag. The TEV cleavage site I read is composed of ENLYFQG, and this G remains after cleavage. What I found to also remain is an 'am'. It is before the first...
09 October 2017 1,565 2 View
I have lysed my e. coli cells (after adding protease inhibitors to the lysis buffer) and freezed the lysate. I then unfroze with the intent of purifying my protein , however due to column...
06 July 2017 4,494 7 View
I express using BL21 DE3 e-coli cells and use the ZYM 5052 media. Some colleagues who also use this media have suggested adding IPTG to increase the protein expression. Would that make any sense...
06 July 2017 6,416 3 View
I usually add 100ug/ml of kanamycin to my ZYM culture media. I accidently in a moment of fatigue added the entire 100mg/ml stock to one of my batches! What effect will this have on the cell growth...
07 August 2016 5,051 3 View
After following the exact protocol of the NucleoSpin Plasmid purification kit, I measured the concentration to find the 260/280 ratio 2.15! Any idea what could have gone wrong and how can I fix this?
04 May 2016 2,957 4 View
I was expressing protein in E coli cells at 37 degrees and the OD was 1. I had to store the culture over 3 nights, so I stored it at 4 degrees to prevent over expression. After the 3 nights I...
04 May 2016 3,401 4 View
I have reverse sequences (AB1 format), can I base on reverse DNA sequences to perform nucleotide alignment, convert nucleotides to amino acids and deposit the sequence in GenBank database?
11 August 2024 5,138 1 View
Hello experts, Does anyone know any free software about retention index prediction ?
08 August 2024 7,403 2 View
Hi! So i attempted to understand a novel protein behavior towards heat application by analyzing its secondary structure change. I subjected the protein to a thermal denaturation analysis using...
06 August 2024 1,989 3 View
During low-temperature testing, new diffraction peaks that appear could be indicative of several phenomena. In one of our tests, we observed notable new peaks around 40° and 45° in a specific...
06 August 2024 726 3 View
Molecular docking software/ websites?
02 August 2024 8,704 7 View
Dear All, I am trying to transfect a pCDNA3.1 vector containing my gene of interest. The purpose is to figure out the localization of the protein of interest. I have fused the protein with GFP on...
31 July 2024 9,892 4 View
What information we can get from PXRD analysis other than from SCXRD analysis of a crystal ?
30 July 2024 6,261 4 View
Hello , I established a stable cell line expressing GFP tagged to a centrosomal gene having G418 drug selection marker. I validated the stable line by IFA and Western blotting, results are fine....
29 July 2024 5,007 0 View
How to apply magnetic field parallel to b axis of any crystal
29 July 2024 4,083 2 View
I created a file with my outgroup and ingroup species using Beauti, ran it in BEAST, viewed it in Tracer, and then used TreeAnnotator to create a file that I imported into RASP. Could someone...
28 July 2024 2,979 1 View