GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuG in Streptacidiphilus oryzae TH49

Align Maltose transport system permease protein malG aka TT_C1629, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized)
to candidate WP_037572995.1 BS73_RS15830 carbohydrate ABC transporter permease

Query= TCDB::Q72H66
         (280 letters)



>NCBI__GCF_000744815.1:WP_037572995.1
          Length = 295

 Score =  194 bits (492), Expect = 2e-54
 Identities = 99/276 (35%), Positives = 162/276 (58%), Gaps = 1/276 (0%)

Query: 5   SRLLGRLFFYLLVVFVVVYSVFPFYWAVISSFKPSDALFSPDPSFLPVPFTLEHYENVFL 64
           SR +  ++  + +VF  V + FP YW ++++ +P   L S  P F P       +  VF 
Sbjct: 21  SRAMTGVWNTVALVFAAVMA-FPLYWLLLTAVQPGRDLLSAYPKFWPTGIQFGSFRTVFA 79

Query: 65  QANFGRNLLNSLIVAGGATLLSLVLGVLAAYALGRLPFPPKNAVMYIVLSMTMFPQIAVL 124
            +NF  +LLN+ I+  GA +L L +G +AA  + R  F  +N  +  +L + M P +A++
Sbjct: 80  DSNFATDLLNTAIITVGAIVLGLAVGFMAAVGVARFRFAGRNPFVVAMLIVQMVPLVALV 139

Query: 125 GGLFLLLRQTGLFNTHLGLILTYLLFTLPFTVWVLVGYFRGLPRELEEAAYVDGATPLQT 184
             LF++L + GL++   G++L YL+FT+P+ VW L  +   +PREL+EAA VDG T    
Sbjct: 140 IPLFIVLDRVGLYDQLFGVVLAYLVFTIPYVVWTLRTFIVNIPRELDEAAMVDGCTQWGA 199

Query: 185 LLKVMLPLTGPGLVTTGLLAFIAAWNEYLFALTFTVGDSVKTVPPAIASFGGATPFEIPW 244
             +V+LPLT PGL+TTG+  +I AWNE+  A T       +T    +  +  +      +
Sbjct: 200 FFRVVLPLTVPGLITTGVYCWIQAWNEFAIANTLLTSAGKQTSMVWLTGWSASQTHGADY 259

Query: 245 GSIMAASVVVTVPLVVLVLVFQQRIVAGLTAGAVKG 280
           G+ MA S+++++P+++L  + Q+R+  GLTAGAVKG
Sbjct: 260 GAQMAGSLLISLPVIILFTLLQKRLAGGLTAGAVKG 295


Lambda     K      H
   0.329    0.145    0.439 

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: 164
Number of extensions: 4
Number of successful extensions: 1
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: 280
Length of database: 295
Length adjustment: 26
Effective length of query: 254
Effective length of database: 269
Effective search space:    68326
Effective search space used:    68326
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 24 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