Alignments for a candidate for SMIT1 in Echinicola vietnamensis KMM 6221, DSM 17526

GapMind for catabolism of small carbon sources

Alignments for a candidate for SMIT1 in Echinicola vietnamensis KMM 6221, DSM 17526

Align Sodium/myo-inositol cotransporter 2; Na(+)/myo-inositol cotransporter 2; Sodium-dependent glucose cotransporter; Sodium/glucose cotransporter KST1; rKST1; Sodium/myo-inositol transporter 2; SMIT2; Solute carrier family 5 member 11 (characterized)
to candidate Echvi_1880 Echvi_1880 transporter, SSS family

Query= SwissProt::Q28728
         (674 letters)



>FitnessBrowser__Cola:Echvi_1880
          Length = 624

 Score =  284 bits (726), Expect = 1e-80
 Identities = 165/487 (33%), Positives = 268/487 (55%), Gaps = 36/487 (7%)

Query: 28  DIAVLVLYFLFVLAVGLW--STVKTKRDTVKGYFLAGGDMVWWPVGASLFASNVGSGHFV 85
           D  + ++Y L +++VGLW   T K    T + YFLA   + WW VGASL A+N+ + HF+
Sbjct: 9   DYVIFIVYALAIVSVGLWVSRTKKGLEKTAQEYFLADKSLTWWAVGASLLAANISAEHFI 68

Query: 86  GLAGSGAATGISVAAYEFNGMFSVLMLAWIFLPIYIAGQVTTMPEYLRRRFGGSRIAITL 145
           G +GSG A G+ ++AYE+    +++++A  FLPI++   V TMP++L  RF    ++   
Sbjct: 69  GTSGSGFAIGLGISAYEWIAAIALIIVAKYFLPIFLKHGVYTMPQFLSERF-NKGVSTAF 127

Query: 146 AVLYLFIYIFTKISVDMYAGAIFIQQSLHLDLYLSVVGLLAVTALYTVAGGLAAVIYTDA 205
           AV +L +Y+F  ++   Y GA+ + + + + L   ++GLL  + +Y++ GGL AV +TD 
Sbjct: 128 AVFWLLVYVFVNLTSVSYLGALALDKIMGIPLQYGIIGLLIFSGIYSIYGGLEAVAWTDV 187

Query: 206 LQTLIMLVGALTLMGYSFAAVGGMEGL-----------QEKYFLALPSNRSENSSCGLPR 254
           +Q +I++ G L     +  AVG  +G+           ++ + + +P  R          
Sbjct: 188 VQVIILVAGGLITTFLALDAVGMGDGIFAGMSNLYNDAKDHFVMIMPQGRVMVPDGLGGS 247

Query: 255 EDAFHLFRDPLTSDLPWPG-ILFGMSIPSLWYWCTDQVIVQRSLAAKNLSHAKGGSLMAA 313
            DAF         DLP    IL GM + +L YW  +Q I+Q+ LAAK++  AK G L A 
Sbjct: 248 RDAF--------QDLPGLAVILGGMWLTNLGYWGFNQYIIQKGLAAKSIEEAKKGLLFAG 299

Query: 314 YLKVLPLFIMVFPGMVSRILFPDQVACADPETCQRVCNNP------SGCSDIAYPKLVLE 367
           YLK+L   I+V PG+ + +L  D      PE    + N P         SD AYP L+  
Sbjct: 300 YLKLLMPIIVVIPGIAAYVLINDY----SPEQLAAILNMPVEHIGTIQKSDEAYPWLLRN 355

Query: 368 LLPTGLRGLMMAVMVAALMSSLTSIFNSASTIFTMDLWN-HVRPRASEKELMIVGRVFVL 426
            +P G+RGL  A + AA++SSL S+ NS STIFTMD++  + +P A+  +L+  GR+  +
Sbjct: 356 FIPNGIRGLAFAALAAAIVSSLASMINSTSTIFTMDIYKVYFKPNANNHQLVRTGRIVAV 415

Query: 427 LLVLVSVLWIPVVQASQGGQLFVYIQAISSYLQPPVAMVFVLGCFWKRANEKGAFWGLVL 486
           + + ++++  P  Q +   Q+F YIQ  + Y+ P V +VF +G  W++A    A W  + 
Sbjct: 416 VALAIAMIVAP--QLASLDQVFQYIQEYTGYIYPGVVVVFGMGLIWRQATASAALWTAIA 473

Query: 487 GLLLGFI 493
            +  G +
Sbjct: 474 TIPAGIV 480


Lambda     K      H
   0.325    0.138    0.426 

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: 886
Number of extensions: 51
Number of successful extensions: 6
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: 674
Length of database: 624
Length adjustment: 38
Effective length of query: 636
Effective length of database: 586
Effective search space:   372696
Effective search space used:   372696
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 54 (25.4 bits)

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

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Protein sequences (fasta format)
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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 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