GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuG in Sinorhizobium meliloti 1021

Align ABC-type transporter, integral membrane subunit, component of Trehalose porter. Also binds sucrose (Boucher and Noll, 2011). Induced by glucose and trehalose. Directly regulated by trehalose-responsive regulator TreR (characterized)
to candidate SMc01979 SMc01979 sugar transport system permease ABC transporter protein

Query= TCDB::G4FGN6
         (278 letters)



>FitnessBrowser__Smeli:SMc01979
          Length = 277

 Score =  206 bits (523), Expect = 6e-58
 Identities = 101/266 (37%), Positives = 169/266 (63%), Gaps = 2/266 (0%)

Query: 13  IAVVLILIWCVFPLYWAFISSIKPDRDLFEKNPSLFPKRITFENYVKVFKERPFHINIKN 72
           +AV+  + + +FPL+W    ++ P+  L+ +   L+P R + E++  V +   F +  +N
Sbjct: 14  LAVLAYIAFALFPLFWLLKVAVTPNDLLYSEGIRLWPSRASLEHFDFVLRHSAFPVFFRN 73

Query: 73  SIIVAGITTVLALVVGSLAGYAIARLKFRGKVIVMSLILAVSMFPQVSILGSLFLILRGL 132
           S+IV+G T V+  ++ SL+GYA++R +FRGK  +++L+L   MFP V ++  +F IL  L
Sbjct: 74  SLIVSGSTAVIVTILASLSGYALSRFRFRGKYWLVTLMLLTQMFPLVMLVAPIFKILSPL 133

Query: 133 KLINTYTGLIIPYTAMNLPLTVWVLQSFFRELPKEVEESAFIDGASKLRTLWSIVLPMSA 192
            L N+ TGL++ YTA N+P   +++QSFF  +PK++EE+A IDGA++      I+LP++ 
Sbjct: 134 GLTNSLTGLVVVYTAFNVPFATFLMQSFFDGIPKDLEEAAMIDGATQFVAFRQIILPLTL 193

Query: 193 PGLVATGLLTFIAAWNEFLFALTFMQKPSLYTVPVAVALFKGASQYEIPWGQLMAAAVIV 252
           PG+ AT    F AAW+E LF+L  +   +  T PV +  F   S++ + +GQ+MAA V+ 
Sbjct: 194 PGIAATLGFVFTAAWSELLFSLMLISGNAQATFPVGLLSF--VSKFSVDFGQMMAAGVLA 251

Query: 253 TLPLVILVLVFQNRIIAGLSAGAVKG 278
            +P  +  L+ Q  ++ GL+AGAVKG
Sbjct: 252 LIPACLFFLLIQRYLVQGLTAGAVKG 277


Lambda     K      H
   0.329    0.142    0.424 

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: 207
Number of extensions: 9
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: 278
Length of database: 277
Length adjustment: 25
Effective length of query: 253
Effective length of database: 252
Effective search space:    63756
Effective search space used:    63756
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: 47 (22.7 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