GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braE in Desulfovibrio vulgaris Hildenborough

Align Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale)
to candidate 206139 DVU0714 branched-chain amino acid ABC transporter, permease protein

Query= uniprot:Q1MCU1
         (463 letters)



>MicrobesOnline__882:206139
          Length = 317

 Score =  197 bits (502), Expect = 3e-55
 Identities = 114/300 (38%), Positives = 173/300 (57%), Gaps = 33/300 (11%)

Query: 140 IQILIYVMLAWGLNIVVGLAGLLDLGYVAFYAVGAYSYALLSSYFGLSFWVLLPLSGIFA 199
           + I +Y +LA  LN+++G AGL  +G+ AFYAVGAY+ A+L++ + +     +P++G+ A
Sbjct: 31  VSIGLYAVLALSLNLILGQAGLFHMGHAAFYAVGAYTAAILNTVYHVPVLWTMPVAGLLA 90

Query: 200 ALWGVILGFPVLRLRGDYLAIVTLAFGEIIRLVLINWT-DVTKGTFGISSIPKATLFGIP 258
           AL+ +++  P++ LRGDYL IVT+   EI+R+ LIN    +T G  GI  I +  LFG  
Sbjct: 91  ALFALVVARPIIHLRGDYLLIVTIGIVEIVRIALINNVFGITGGANGIFGISRPMLFGYK 150

Query: 259 FDATAGGFAKLFHLPISSAYYKIFLFYLILALCMLTAYVTIRLRRMPIGRAWEALREDEI 318
                                 I  +YLI     ++  +  RL     GRA   ++ED++
Sbjct: 151 ISK------------------PIQFYYLIWTWVAISILLFRRLECSRFGRALNYIKEDDV 192

Query: 319 ACRSLGINTVTTKLTAFATGAMFAGFAGSFFAARQGFVSPESFVFLESAVILAIVVLGGM 378
           A    G++T   KL AF  GA++AG  G+F+AA+   +SPESF F ES V+ AIV+LGG 
Sbjct: 193 AAEGSGVDTAYYKLAAFVLGALWAGMTGTFYAAKMTIISPESFSFWESVVLFAIVILGG- 251

Query: 379 GSLTGIAIAAIVMVGGTELLREMSFLKLIFGPDFTPELYRMLIFGLAMVVVMLFKPRGFV 438
           GS  G+ + A +++G  EL R+ +               RMLIFGLAMVV+M+F+P+G +
Sbjct: 252 GSNRGVLLGAFLLIGLPELFRDFASA-------------RMLIFGLAMVVMMIFRPQGML 298


Lambda     K      H
   0.330    0.145    0.432 

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: 457
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: 463
Length of database: 317
Length adjustment: 30
Effective length of query: 433
Effective length of database: 287
Effective search space:   124271
Effective search space used:   124271
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: 50 (23.9 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