Alignments for a candidate for nagEIIA in Psychromonas ossibalaenae JAMM 0738

GapMind for catabolism of small carbon sources

Alignments for a candidate for nagEIIA in Psychromonas ossibalaenae JAMM 0738

Align PTS system glucose-specific EIICBA component; EC 2.7.1.-; EC 2.7.1.69 (characterized)
to candidate WP_019612846.1 G327_RS0100730 PTS transporter subunit EIIC

Query= CharProtDB::CH_001857
         (699 letters)



>NCBI__GCF_000381745.1:WP_019612846.1
          Length = 486

 Score =  318 bits (816), Expect = 3e-91
 Identities = 189/517 (36%), Positives = 288/517 (55%), Gaps = 40/517 (7%)

Query: 4   ALFGVLQKIGRALMLPVAILPAAGILLAIGNAMQNKDMIQVLHFLSNDNVQLVAGVMESA 63
           ++ G +QK+G+ALM+PVA LPAA IL+ +G  M           +   +  ++A  +  +
Sbjct: 2   SVLGYMQKVGKALMVPVATLPAAAILMGVGYWMDP---------VGWGSESILAAFLIKS 52

Query: 64  GQIVFDNLPLLFAVGVAIGLANG-DGVAGIAAIIGYLVMNVSMSAVLLANGTIPSDSVER 122
           G  + DN+ LLFA+GVA GL+    G A ++  + ++V+   +S   +A       S   
Sbjct: 53  GGAIIDNMALLFAIGVAFGLSKDKSGNAALSGFVAFMVLTTLLSPASVAQLEGIDISEVP 112

Query: 123 AKFFTENHPAYVNMLGIPTLATGVFGGIIVGVLAALLFNRFYTIELPQYLGFFAGKRFVP 182
           A F   N+                F GI+VG+++A ++N++  +ELP+ L FF+GKR VP
Sbjct: 113 AAFGRINNQ---------------FVGILVGIISAEIYNKYSAVELPKALAFFSGKRLVP 157

Query: 183 IVTSISALILGLIMLVIWPPIQHGLNAFSTGLVEANPTLAAFIFGVIERSLIPFGLHHIF 242
           I+TS++ ++L  + L IWP +  GL+ F   L ++   + A +FG   R ++  G+HH  
Sbjct: 158 ILTSVAGMLLAFVFLYIWPLVFEGLSVFGQYL-QSLDAVGAGLFGFFNRLMLSVGMHHAL 216

Query: 243 YSPFWYEFFSYKSAAGEIIRGDQRIFMAQIKDGVQLTA--GTFMTGKYPFMMFGLPAAAL 300
           Y  FW++           + G Q      I DG  +    G +  G +P MMFGLP AAL
Sbjct: 217 YPVFWFDVVGINDIPN-FLGGAQ-----SIADGTAVIGKTGMYQAGFFPIMMFGLPGAAL 270

Query: 301 AIYHEAKPQNKKLVAGIMGSAALTSFLTGITEPLEFSFLFVAPVLFAIHCLFAGLSFMVM 360
           A+YH A+P+NK  V  IM +AA+ SF TGITEPLEFSF+F+APVL+ +H +  G+S  + 
Sbjct: 271 AMYHCAEPRNKDKVFSIMIAAAMASFFTGITEPLEFSFMFLAPVLYLLHAVLTGISLYIA 330

Query: 361 QLLNVKIGMTFSGGLIDYFLFGILPNRTAWWLVIPVGLGLAVIYYFGFRFAIRKFNLKTP 420
             +    G  FS G +D+ L    P  T W+++I  GL    +YY  FRFAI KF+ KTP
Sbjct: 331 ASMEWMAGFGFSAGFVDFVLSSQNPLATKWYMLIAQGLVFFALYYTLFRFAITKFDFKTP 390

Query: 421 GR-EDAAEETAAPGKTGEAGDLPYEILQAMGDQENIKHLDACITRLRVTVNDQKKVDKDR 479
           GR ED   +    GK     +L +  +  +G  +NI  +D CITRLR+TV D  K D   
Sbjct: 391 GRGEDMNNDN---GKEVNINELTHAYIAGIGGADNILEVDNCITRLRLTVKDSSKADAAA 447

Query: 480 LKQLGASGVLEVG-NNIQAIFG-PRSDGLKTQMQDII 514
           LK +GA+GV+ +G + +Q I G  + D +  +M++I+
Sbjct: 448 LKAIGAAGVVVMGKDGLQVIIGLGKVDKVAAEMKNIL 484


Lambda     K      H
   0.323    0.141    0.412 

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: 885
Number of extensions: 42
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 699
Length of database: 486
Length adjustment: 36
Effective length of query: 663
Effective length of database: 450
Effective search space:   298350
Effective search space used:   298350
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 53 (25.0 bits)

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

Downloads

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

Related tools

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