Protein Pf6N2E2_3339 in Pseudomonas fluorescens FW300-N2E2
Annotation: FitnessBrowser__pseudo6_N2E2:Pf6N2E2_3339
Length: 954 amino acids
Source: pseudo6_N2E2 in FitnessBrowser
Candidate for 9 steps in catabolism of small carbon sources
Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
D-fructose catabolism | fruI | hi | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) (characterized) | 99% | 100% | 1814.3 | trehalose-specific PTS system, I, HPr, and IIA components | 46% | 518.1 |
sucrose catabolism | fruI | hi | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) (characterized) | 99% | 100% | 1814.3 | trehalose-specific PTS system, I, HPr, and IIA components | 46% | 518.1 |
trehalose catabolism | treEIIA | med | trehalose-specific PTS system, I, HPr, and IIA components (characterized) | 46% | 78% | 518.1 | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) | 99% | 1814.3 |
N-acetyl-D-glucosamine catabolism | nagF | med | N-acetylglucosamine-specific PTS system, I, HPr, and IIA components (nagF) (characterized) | 42% | 78% | 465.3 | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) | 99% | 1814.3 |
D-glucosamine (chitosamine) catabolism | nagF | med | N-acetylglucosamine-specific PTS system, I, HPr, and IIA components (nagF) (characterized) | 42% | 78% | 465.3 | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) | 99% | 1814.3 |
D-fructose catabolism | fruB | lo | Multiphosphoryl transfer protein; MTP; Diphosphoryl transfer protein; DTP; Phosphotransferase FPr protein; Pseudo-HPr (characterized) | 40% | 99% | 240.7 | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) | 99% | 1814.3 |
sucrose catabolism | fruB | lo | Multiphosphoryl transfer protein; MTP; Diphosphoryl transfer protein; DTP; Phosphotransferase FPr protein; Pseudo-HPr (characterized) | 40% | 99% | 240.7 | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) | 99% | 1814.3 |
glycerol catabolism | dhaM | lo | PEP-dependent dihydroxyacetone kinase, phosphoryl donor subunit DhaM; Dihydroxyacetone kinase subunit M; EC 2.7.1.121 (characterized) | 31% | 68% | 114 | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) | 99% | 1814.3 |
D-mannitol catabolism | cmtB | lo | Mannitol-specific phosphotransferase enzyme IIA component (characterized, see rationale) | 37% | 94% | 97.8 | Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) | 99% | 1814.3 |
Sequence Analysis Tools
View Pf6N2E2_3339 at FitnessBrowser
Find papers: PaperBLAST
Find functional residues: SitesBLAST
Search for conserved domains
Find the best match in UniProt
Compare to protein structures
Predict transmenbrane helices: Phobius
Predict protein localization: PSORTb
Find homologs in fast.genomics
Fitness BLAST: loading...
Sequence
MLELTLEQISMAQTAVDKDAALQLLADKLVADGLVAEGYLAGLQAREAQGSTFLGQGIAI
PHGTPQTRDLVHSTGVRLLQFPEGVDWGDGQIVYLAIGIAAKSDEHLRLLQLLTRALGET
DLGQALRRAGSAEALLKLLQGAPQELALDAQMIGLGVSADDFEELVWRGARLLRQADCVS
NGFAGVLQQVDALPLGDGLWWLHSEQTVKRPGLAFVTPDKPIRYLGQPLSGLFCLASLGE
AHQALLERLCALLIEGRGHELGRATSSRKVLEVLGGELPADWPSARIGLANAHGLHARPA
KILAQLAKSFEGEIRVRIVDGQDSAVSAKSLSKLLSLGARRGQVLEFIAEPSIANDALPA
LLAAIEEGLGEEVEPLPPPSAPRETVMAEVATVMLAPESGSLIQAVAAAPGIAIGPAHIQ
VLQAIDYPLRGESAAIERERLQNALNQVRRDIQGLIERAKAKAIREIFITHQEMLDDPEL
SDEVDTRLKLGESAQAAWMGVVEAAAKEQEALQDALLAERAADLRDVGRRVLAQLCGVET
PNEPDQPYILVMDEVGPSDVARLDPTRVAGILTARGGATAHSAIVARALGIPALVGAGAA
VLLLAPGTSLLLDGQRGRLHVDPDAATLQRAKEERDTREQRLKVAAEQRHEPALTRDGHA
VEVFANIGESAGVAGAVEQGAEGIGLLRTELIFMAHSQAPDEATQEAEYRKVLDGLAGRP
LVVRTLDVGGDKPLPYWPIAKEENPFLGVRGIRLTLQRPQVMEAQLRALLRSADNRPLRI
MFPMVGSVDEWRQARAMTERLRQEIPVADLQLGIMIEVPSAALLAPVLAKEVDFFSVGTN
DLTQYTLAIDRGHPTLSAQADGLHPAVLQLIDITVRAAHAHGKWVGVCGELAADPLAVPV
LVGLGVDELSVSARSIAEVKARVRELSLAQVQTLAQEALAVGSADDVRALVEAL
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
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About GapMind
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using
ublast (a fast alternative to protein BLAST)
against a database of manually-curated proteins (most of which are experimentally characterized) or by using
HMMer with enzyme models (usually from
TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
- ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
- HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.
where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").
Otherwise, a candidate is "medium confidence" if either:
- ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
- ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
- HMMer finds a hit (regardless of coverage or other bits).
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps."
For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways.
For diverse bacteria and archaea that can utilize a carbon source, there is a complete
high-confidence catabolic pathway (including a transporter) just 38% of the time, and
there is a complete medium-confidence pathway 63% of the time.
Gaps may be due to:
- our ignorance of proteins' functions,
- omissions in the gene models,
- frame-shift errors in the genome sequence, or
- the organism lacks the pathway.
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory