GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcC in Sinorhizobium meliloti 1021

Align Fructose import permease protein FrcC (characterized)
to candidate SMc02031 SMc02031 permease

Query= SwissProt::Q9F9B1
         (360 letters)



>FitnessBrowser__Smeli:SMc02031
          Length = 349

 Score =  188 bits (478), Expect = 2e-52
 Identities = 117/323 (36%), Positives = 177/323 (54%), Gaps = 22/323 (6%)

Query: 49  AVPLIVLVLSLIAFGVILGGKFFSAFTMTLILQQVAIVGIVGAAQTLVILTAGIDLSVGA 108
           A PLI LVL L+A+       F +   ++ + +Q A V I+   QT VILT GIDLSV A
Sbjct: 30  AGPLIALVL-LMAYLAFATSNFLTLDNLSNVARQSAFVAILAVGQTFVILTGGIDLSVAA 88

Query: 109 IMVLSS----VIMGQ----FTFRYGF-PPALSVICGLGVGALCGYINGTLVARMKLPPFI 159
           I  LS+    V++ Q    F   +GF PP ++++ G+ +G   G +NG L+++ K+P FI
Sbjct: 89  IAALSASITAVLLTQPLVLFGIDFGFVPPPVAILIGILIGMAAGALNGWLISKFKIPDFI 148

Query: 160 VTLGMWQIVLASNFLYSANETIRAQDISANASI---LQFFGQNFRIGNAVFTYGVVVMVL 216
            TLG       +  L +  + +     +A   +   L + G     G  +F   V  ++ 
Sbjct: 149 ATLGTMTAFRGAALLVT--DGLPVPSFNAGRQLPESLIWVG-----GGQLFGVPVSALIA 201

Query: 217 LVCLL--WYVLNRTAWGRYVYAVGDDPEAAKLAGVNVTRMLISIYTLSGLICALAGWALI 274
           L+C    WYVL  TA GR +YAVG +  AA  +G++++R  I  Y +SGL+ A+AG  L+
Sbjct: 202 LLCAAAGWYVLRYTALGRAIYAVGGNRAAAHSSGISISRTKIMTYAISGLLAAIAGIILV 261

Query: 275 GRIGSVSPTAGQFANIESITAVVIGGISLFGGRGSIMGMLFGALIVGVFSLGLRLMGTDP 334
           GR+ S +        + SI +VVIGG +LFGG G + G + GA I+GV   GL L+   P
Sbjct: 262 GRLNSANALMADGEELRSIASVVIGGTNLFGGEGGVWGSIIGAAIIGVLGNGLNLLDVSP 321

Query: 335 QWTYLLIGLLIIIAVAIDQWIRK 357
            W  +  G++I++ V  DQW R+
Sbjct: 322 FWQRIAQGVVIVVVVIFDQWRRR 344


Lambda     K      H
   0.327    0.141    0.420 

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: 370
Number of extensions: 26
Number of successful extensions: 4
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: 360
Length of database: 349
Length adjustment: 29
Effective length of query: 331
Effective length of database: 320
Effective search space:   105920
Effective search space used:   105920
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 bits)

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

Links

Downloads

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:

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:

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:

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