GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctM in Desulfovibrio vulgaris Hildenborough

Align Putative TRAP dicarboxylate transporter, DctM subunit (characterized, see rationale)
to candidate 208936 DVU0009 DedA family protein

Query= uniprot:Q88NP0
         (426 letters)



>MicrobesOnline__882:208936
          Length = 426

 Score =  283 bits (725), Expect = 5e-81
 Identities = 158/419 (37%), Positives = 252/419 (60%), Gaps = 10/419 (2%)

Query: 1   MEAFILLGSFIVLILIGMPVAYALGLSALIGAWWIDIPLQAMMI--QVASGVNKFSLLAI 58
           M A +L G   +L     P+  A+G SA   A  I   +  M+   ++ +G + F LLA+
Sbjct: 1   MTALVLFGMLGLLFACNAPIMLAVGASAF-AALLIKGGMDPMVAVQRLYAGADSFPLLAV 59

Query: 59  PFFVLAGAIMAEGGMSRRLVAFAGVLVGFVRGGLSLVNIMASTFFGAISGSSVADTASVG 118
           P F+ AG +M+ GG+S+R+V  A  LVG + GGL++V++++S FF  +SGS+ ADTA+VG
Sbjct: 60  PLFMTAGQLMSAGGISQRIVRLADTLVGHLPGGLAVVSVVSSMFFAGVSGSAAADTAAVG 119

Query: 119 SVLIPEMERKGYPREFSTAVTVSGSVQALLTPPSHNSVLYSLAAGGTVSIASLFMAGIMP 178
           S+LIP M  +GY   F+ AV  +     ++ PPS   +++    G   SI  LF  G+MP
Sbjct: 120 SILIPSMVARGYSPAFAGAVQAAAGSIGVVIPPSIPMIVFGALTGA--SIGKLFAGGVMP 177

Query: 179 GLLLSAVMMGLCLIFAKK--RNYPKGEVIPLREALKIAGEALWGLMAMVIILGGILSGVF 236
           GLL+   +   C+    +  R   + E   +  AL  AG   W L A  IILGGI+SGV 
Sbjct: 178 GLLMGITLSAWCVHEGLRSGRETRRFEPAAVWPALLRAG---WSLGAPAIILGGIISGVC 234

Query: 237 TATESAAVAVVWSFFVTMFIYRDYKWRDLPKLMHRTVRTISIVMILIGFAASFGYVMTLM 296
           TATE+AAVAVV++F V +F +R+   R LP L+     T  +VM +I  A+ FG+VM + 
Sbjct: 235 TATEAAAVAVVYAFLVGLFAHRELDLRRLPALLLDAAVTSGVVMSIIAAASLFGWVMAIE 294

Query: 297 QIPSKITTAFLTLSDNRYVILMCINFMLMLLGTVMDMAPLILILTPILLPVITGIGVDPV 356
           +IP+ +  A L +    +++L+ +N +L+L GT+++    +++L P+L+ ++  +G+D +
Sbjct: 295 RIPAALADAILAVGGEGWMLLLAVNILLLLAGTMLETTAALILLVPVLVQLLPRMGIDLI 354

Query: 357 HFGMIMLVNLGIGLITPPVGAVLFVGSAIGKVSIESTVKALMPFYLALFLVLMAVTYIP 415
           H G+I+++NL IG++TPP+G  L V   I +V + +  +A++P    L + LM VTYIP
Sbjct: 355 HLGVIVVMNLSIGMLTPPLGVCLMVSCGIARVPLATLARAVLPLLAVLVVDLMLVTYIP 413


Lambda     K      H
   0.329    0.142    0.418 

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: 545
Number of extensions: 33
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: 426
Length of database: 426
Length adjustment: 32
Effective length of query: 394
Effective length of database: 394
Effective search space:   155236
Effective search space used:   155236
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 (21.8 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