GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braE in Desulfovibrio vulgaris Miyazaki F

Align Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale)
to candidate 8502039 DvMF_2752 inner-membrane translocator (RefSeq)

Query= uniprot:Q1MCU1
         (463 letters)



>FitnessBrowser__Miya:8502039
          Length = 330

 Score =  191 bits (485), Expect = 3e-53
 Identities = 115/300 (38%), Positives = 168/300 (56%), Gaps = 33/300 (11%)

Query: 140 IQILIYVMLAWGLNIVVGLAGLLDLGYVAFYAVGAYSYALLSSYFGLSFWVLLPLSGIFA 199
           + I +Y +LA  LNI++G AGL  +G+ AFYAVGAY  A+ ++ +G+     +P +G+ A
Sbjct: 32  VSIGLYSVLALSLNIILGQAGLFHMGHAAFYAVGAYVTAIANTMWGVPVLWAMPFAGLAA 91

Query: 200 ALWGVILGFPVLRLRGDYLAIVTLAFGEIIRLVLINWT-DVTKGTFGISSIPKATLFGIP 258
           AL+ +++  P++ LRGDYL IVT+   EI+R+ LIN    +T G  GI  I +  LFG  
Sbjct: 92  ALFAMVVARPIIHLRGDYLLIVTIGIVEIVRIALINNVFGLTGGANGIFGISRPMLFGFK 151

Query: 259 FDATAGGFAKLFHLPISSAYYKIFLFYLILALCMLTAYVTIRLRRMPIGRAWEALREDEI 318
                   AK  H            +YL+ A    +  +  RL     GRA   ++ED+ 
Sbjct: 152 -------IAKPVH-----------FYYLVWAYVACSILLFRRLENSRFGRALNYIKEDDT 193

Query: 319 ACRSLGINTVTTKLTAFATGAMFAGFAGSFFAARQGFVSPESFVFLESAVILAIVVLGGM 378
           A    G+N  + KL AF  GA +AG  G+ +AA+   +SPESF F ES V+ AIV+LGG 
Sbjct: 194 AAEGSGVNIASYKLWAFVLGAFWAGMTGTIYAAKMTIISPESFSFWESVVLFAIVILGG- 252

Query: 379 GSLTGIAIAAIVMVGGTELLREMSFLKLIFGPDFTPELYRMLIFGLAMVVVMLFKPRGFV 438
           GS  G+ + A +++G  E  RE +               RML FGLAMVV+M+F+P+G +
Sbjct: 253 GSNRGVLLGAFLLIGLPEFFREFASA-------------RMLAFGLAMVVMMIFRPQGML 299


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: 503
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: 330
Length adjustment: 31
Effective length of query: 432
Effective length of database: 299
Effective search space:   129168
Effective search space used:   129168
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.

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