GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Phaeobacter inhibens BS107

Align ABC transporter membrane-spanning permease-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized)
to candidate GFF1633 PGA1_c16550 putative branched-chain amino acid transport system, permease component

Query= TCDB::Q8DQI0
         (292 letters)



>FitnessBrowser__Phaeo:GFF1633
          Length = 306

 Score =  150 bits (380), Expect = 3e-41
 Identities = 96/306 (31%), Positives = 166/306 (54%), Gaps = 30/306 (9%)

Query: 3   LMLQQLVNGLILGSVYALLALGYTMVYGIIKLINFAHGDIYMMGAFIGYFLINSFQMNFF 62
           L+L+Q++NGL  G +  L+A G T+V+G++ LIN AHG +YM+GAF    ++ ++  +F 
Sbjct: 5   LILEQILNGLQFGVMLFLMAAGLTLVFGVMGLINLAHGALYMVGAFAA-AVVAAWTGSFV 63

Query: 63  VALIVAMLATAILGVVIEFLAYRPLRHSTRIAVLITAIGVSFLLEYGMVYLVGANTRAFP 122
           +AL+ ++ A A  G ++EFL  R L     +  ++    +  +   G  ++ G    +FP
Sbjct: 64  LALMASLAAAAAAGALVEFLVIRKLYDRDHLDQVLATFALILIFSEGTRWVFG----SFP 119

Query: 123 QAIQTVRYDLGPISLTN------VQLMILGISLILMILLQVIVQKTKMGKAMRAVSVDSD 176
             +    Y  GPISL         +L I+ I L++   L  ++ +T++G  +RA   D +
Sbjct: 120 LFLDVPSYLSGPISLPGGIEYPLYRLTIIAIGLVVAAGLFWLIARTRIGIQIRAGESDRE 179

Query: 177 AAQLMGINVNRTISFTFALGSALAGAAGVLIALYYNSLEPLMGVTPGLKSFVAAVLGGIG 236
               +G+++++  +  FALG+ALAG AG L+     S++  MG    + +FV  V+GGIG
Sbjct: 180 MIAALGVDISKLYTLVFALGAALAGLAGALVGA-IQSVQVGMGEPVLILAFVVIVIGGIG 238

Query: 237 IIPGAALGGFVIGLLETF-----------------ATAFGMSDFRDAIVYGILLLILIVR 279
            I GA +G  ++GL +T                  AT+ G S     ++Y ++ +IL+VR
Sbjct: 239 SIKGAMVGALLVGLTDTLGGVFLPQMFALFMEPASATSVGAS-LASMLIYILMAVILLVR 297

Query: 280 PAGILG 285
           P+G+ G
Sbjct: 298 PSGLYG 303


Lambda     K      H
   0.330    0.146    0.407 

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: 198
Number of extensions: 10
Number of successful extensions: 2
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: 292
Length of database: 306
Length adjustment: 27
Effective length of query: 265
Effective length of database: 279
Effective search space:    73935
Effective search space used:    73935
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: 48 (23.1 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