GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctM in Sinorhizobium meliloti 1021

Align C4-dicarboxylate TRAP transporter large permease protein DctM (characterized)
to candidate SM_b20297 SM_b20297 permease

Query= SwissProt::Q9HU16
         (427 letters)



>FitnessBrowser__Smeli:SM_b20297
          Length = 426

 Score =  309 bits (791), Expect = 1e-88
 Identities = 156/412 (37%), Positives = 246/412 (59%), Gaps = 1/412 (0%)

Query: 11  FLLMFIGVPIAVSLGLSGALTILLFSPDSVRSLAIKLFETSEHYTLLAIPFFLLSGAFMT 70
           F L+  G+P+  +L +  AL  +L+    +     ++      + LLA+PFF+L+   M 
Sbjct: 9   FALLIAGMPVGFTL-IVAALAYMLWQGTGLNFAGQRMIAGLNSFPLLAVPFFILTAQLMN 67

Query: 71  TGGVARRLIDFANACVGHIRGGLAIAAVLACMLFAALSGSSPATVAAVGSIAIAGMVRSG 130
             GV  R+ DFA A VGHIRGGL    ++A +LF+ +SGS+ A  A +G + I  M  +G
Sbjct: 68  LSGVTERIFDFAKALVGHIRGGLGHVNIMASVLFSGMSGSAVADAAGLGQLEIKAMRDAG 127

Query: 131 YPQAFGAGIVCNAGTLGILIPPSIVMVVYAAATETSVGKLFIAGVVPGLLLGLILMVVIY 190
           Y + F   I   +  +G LIPPSI +VVY     TS+G LF+ G+VPGLL    LM+++Y
Sbjct: 128 YDEQFSGSITAASAIIGPLIPPSIPLVVYGVIANTSIGGLFLGGIVPGLLCAASLMIMVY 187

Query: 191 IVARVKKLPAMPRVSLREWLASARKALWGLLLMVIILGGIYSGAFTPTEAAAVAAVYSAF 250
           ++A  +      R   R   ++   AL  L+   II+GGI++G F+PTEAA VAA Y+ F
Sbjct: 188 VIAWRRNYATAQRAGFRRVWSTFWHALLPLITPFIIIGGIFAGVFSPTEAAVVAASYALF 247

Query: 251 VALFVYRDMRLSECPKVLLESGKLTIMLMFIIANAMLFAHVLTTEQIPQSIASWVTELGL 310
           + + VYR++  ++   VL E+   T  +  +I    LF +V+  EQ+PQ +A++      
Sbjct: 248 LGVVVYREITFAKLVTVLRETVSHTAAVGLLIMGVSLFGYVIAREQVPQHVATFFLTYAE 307

Query: 311 SPWMFLLVVNIVLLIAGNFMEPSAIILILAPIFFPIAMELGIDPIHLGIIMVVNMEIGLI 370
            P  FL++VN++LL  G F+E  AI+L++ P+  P A++ G+DP+H G+++V N+ IG++
Sbjct: 308 DPLTFLILVNLMLLALGTFIEALAILLLIVPVLVPTALQFGVDPVHFGVMVVFNLMIGIL 367

Query: 371 TPPVGLNLFVTSAVTGMPLGATIRAALPWLMILLVFLIIVTYIPAVSLALPN 422
           TPP+G+ LFV S V  +P G   R  LP L+ L+V L+++T  PA+   +P+
Sbjct: 368 TPPMGVALFVVSKVADIPFGVLARGILPLLIPLVVVLVLITIFPALVTFIPD 419


Lambda     K      H
   0.330    0.144    0.425 

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: 453
Number of extensions: 27
Number of successful extensions: 1
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: 427
Length of database: 426
Length adjustment: 32
Effective length of query: 395
Effective length of database: 394
Effective search space:   155630
Effective search space used:   155630
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 (21.9 bits)
S2: 51 (24.3 bits)

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:

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