Alignments for a candidate for fruI in Megamonas funiformis YIT 11815

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruI in Megamonas funiformis YIT 11815

Align Phosphoenolpyruvate--protein phosphotransferase (EC 2.7.3.9) (characterized)
to candidate WP_008539428.1 HMPREF9454_RS09390 phosphoenolpyruvate--protein phosphotransferase

Query= reanno::pseudo5_N2C3_1:AO356_07335
         (954 letters)



>NCBI__GCF_000245775.1:WP_008539428.1
          Length = 568

 Score =  342 bits (878), Expect = 3e-98
 Identities = 197/530 (37%), Positives = 313/530 (59%), Gaps = 19/530 (3%)

Query: 432 ESAAIERERLQNALNQVRSDIQGLIERAKAKAIREIFITHQEMLDDPELTDEVDTRLKLG 491
           E+ A   E LQ  +  +R   +G++E+A       I   H+ M+ DP L +    +L   
Sbjct: 47  EALAYAAEVLQTNIKTLRD--KGMLEQAG------IMEAHRMMVQDPMLEENAMLKLGAC 98

Query: 492 ESAQAAWMGVIEAAAKEQEALQDALLAERAADLRDVGRRVLAQLCGVETPNEPDQPYILV 551
            SA  A +   E  A   E + D    ERA D+RDVG+RV  ++ G++         IL 
Sbjct: 99  GSAPKAVLEASEENASIFEQMDDTYFRERAVDIRDVGKRVTRRILGLKEKTVDGGAVILC 158

Query: 552 MDEVGPSDVARLDPTRVAGILTARGGATAHSAIVARALGIPALVGAGAAVLLLAPGTSLL 611
            +E+ PS +A +   ++AG++   G  T H+ I+A+A  IP + G G  +  +     ++
Sbjct: 159 GEEIEPSVIANIPTEKIAGVILGNGSTTCHAVIIAKARAIPTVAGLGDKIKDIPDNAEVI 218

Query: 612 LDGQRGRLHVDPDAATLQRAKEERDTREQRLKVAAEQRHEPALTRDGHAVEVFANIGESA 671
           L+G+ G + V+P    +   + + + + +  +  A+    P +T+DG  V++ ANI    
Sbjct: 219 LNGETGEIFVEPTEDLIASYQVKLEEQRRLKEHYAQLSKLPTVTKDGVEVDLMANISTHL 278

Query: 672 GVASAVEQGAEGIGLLRTELIFMAHSQAPDEATQEAEYRKVLDGLAGRPLVVRTLDVGGD 731
            V +A++ GA+G+GL R+E +FM     PDE TQ   Y++ ++   G   V+RT+D+GGD
Sbjct: 279 DVEAAMKFGAKGVGLFRSEFLFMGRDTIPDEETQFKAYKEAIEKCNGHLCVIRTMDIGGD 338

Query: 732 KPLPYWPIAKEENPFLGVRGIRLTLQRPQVMEAQLRALLRSADSRPLRIMFPMVGSVDEW 791
           KPLPY  I +EENPFLG R IR+ L R +V   Q++A+LR+       +M PMV +V+E 
Sbjct: 339 KPLPYLNIPEEENPFLGYRAIRICLNRREVFMPQVKAILRAGLYGKAAMMLPMVINVEEV 398

Query: 792 RQARAMTERLRLEI-----PVA-DLQLGIMIEVPSAALLAPVLAKEVDFFSVGTNDLTQY 845
           +Q RA+ E  + ++     P + ++QLGIM+E P+AA++ PVLAK +DFFS+GTNDL QY
Sbjct: 399 KQVRAIIEEAKSQLAHEEKPFSNNVQLGIMVETPAAAVMTPVLAKYLDFFSIGTNDLVQY 458

Query: 846 TLAIDRGHPTLSAQADGLHPAVLQLIDITVRAAHAHGKWVGVCGELAADPLAVPVLVGLG 905
           TLA+DR +  +S   +  +PAVL+LI +T+ +A  +  WVG+CGE+A+DP A  +L+ +G
Sbjct: 459 TLAVDRVNTNVSYLYNHFNPAVLRLIKLTIESARNNNIWVGMCGEMASDPNAAAILMAMG 518

Query: 906 VDELSVSARSIAEVKARVRELSLAQVQTLAQAAL-AVGSADDVRALVEAL 954
           ++ELS+SA SI  VK ++R ++ AQ    A+AAL  V + +D  A+ E L
Sbjct: 519 INELSMSAPSIPRVKEKIRSITSAQ----AKAALDTVMTMEDGNAIKEYL 564


Lambda     K      H
   0.318    0.135    0.381 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 849
Number of extensions: 39
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 954
Length of database: 568
Length adjustment: 40
Effective length of query: 914
Effective length of database: 528
Effective search space:   482592
Effective search space used:   482592
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 55 (25.8 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources