Traditionally, proteins are described in a single static state (a picture). It is now increasingly recognised that many proteins can adopt multiple states and move between these conformational states dynamically (a movie). Even more, not every protein has a well-defined three-dimensional structure, many are partly or fully disordered. These predictions describe backbone and side-chain dynamics, disorder, early folding events, beta-sheet aggregation and phase separation.
In this atlas
Entries here
Genes
Chromosomes
Reviewed in UniProt
Last updated 36 minutes ago.
About this proteome
Extracted from UniProtKB
Escherichia coli is a Gram-negative straight rod, which either uses peritrichous flagella for mobility or is nonmotile. It is a facultatively anaerobic chemoorganotroph capable of both respiratory and fermentative metabolism. E.coli serves a useful function in the body by suppressing the growth of harmful bacterial species and by synthesising appreciable amounts of vitamins. It is an important component of the biosphere. It colonizes the lower gut of animals and survives when released to the natural environment, allowing widespread dissemination to new hosts. Pathogenic E.coli strains are responsible for infection of the enteric, urinary, pulmonary and nervous systems. Comparison of 20 E.coli/Shigella strains shows the core genome to be about 2000 genes while the pan-genome has over 18,000 genes. There are multiple, striking integration hotspots that are conserved across the genomes, corresponding to regions of abundant and parallel insertions and deletions of genetic material. As of 2006, highly accurate sequences are available for K-12 / MG1655 and K-12 / W3110, strains that have been separate since the mid 1950s. Sequencing of PCR products indicates that there are only eight true insertion/deletion or base differences between the two strains, in addition to 13 sites where differences are due to insertion sequences, defective prophages and two sites due to the W3110 inversion between the ribosomal RNA genes rrnD and rrnE. The K-12 strains belong to phylogenetic group A. Historically UniProtKB/Swiss-Prot considered the F plasmid to be part of the genetic makeup of strain K-12 / MG1655, whereas in fact the F plasmid was lost in a precursor strain following UV treatment and passage over blood agar. Thus we have removed the F plasmid from this genome. It can however be retrieved by searching in UniProtKB with the accession number AP001918.
What is included
This atlas covers the reviewed entries of this proteome — the manually curated Swiss-Prot section of UniProtKB. Every entry in this proteome is reviewed, so nothing is left out.
- UniProt proteome
- UP000000625
- Taxonomy
- 83333 · ECOLI
- Proteome type
- Reference proteome
- Strain
- K12 / MG1655 / ATCC 47076
- Superkingdom
- bacteria
- Genome assembly
- GCA_000005845.2 · ENA/EMBL
- Completeness (BUSCO)
- 100% · 440/440
Source: UniProt proteome UP000000625, last modified 5 Dec 2025. Retrieved 19 Aug 2026 (3 days, 4 hours ago) and cached for a week.
What do we provide?
Sequence-based predictions that help explain the behaviour of the proteins in the escherichia coli (strain k12) proteome. Not all of these proteins, or regions of them, have a well-defined three-dimensional structure as available from the PDB; many are dynamic or ambiguous. These predictions give clues as to how such regions behave.
- DynaMine
- backbone and side-chain dynamics
- DisoMine
- disorder
- EFoldMine
- early folding
- AgMata
- beta-sheet aggregation
- PSPer
- phase separation
How do I proceed?
Open the entry list and click a UniProt accession. Each entry page carries:
- Overview — every prediction on one plot.
- Interpretation — disorder classified as order, transition or disorder.
- Values and Statistics — the numbers behind the plots.
- Sequence — residues coloured by prediction.
- PSP — phase-separation propensity.
- Visualization 1D-3D — a 3D model coloured by prediction.
- Downloads — sequence, predictions and structures.
Prefer code? Everything is available through the REST API.