GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuG in Stenotrophomonas chelatiphaga DSM 21508

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_042615044.1 ABB28_RS00970 carbohydrate ABC transporter permease

Query= TCDB::Q72H66
         (280 letters)



>NCBI__GCF_001431535.1:WP_042615044.1
          Length = 278

 Score =  140 bits (352), Expect = 4e-38
 Identities = 84/266 (31%), Positives = 143/266 (53%), Gaps = 6/266 (2%)

Query: 15  LLVVFVVVYSVFPFYWAVISSFKPSDALFSPDPSFLPVPFTLEHYENVFLQANFGRNLLN 74
           LLV+ +V  S+ P  W V  S  P+    +  P   P   T  +Y  +F +   G N  N
Sbjct: 19  LLVLALV--SLAPLLWMVSVSVMPAGEATTFPPPLTPSHVTFANYHELFARTGMGVNFAN 76

Query: 75  SLIVAGGATLLSLVLGVLAAYALGRLPFPPKNAVMYIVLSMTMFPQIAVLGGLFLLLRQT 134
           SL+V+   TL SL+L  +A YA  +L F  ++ +  ++++  + P    +  LFLL++Q 
Sbjct: 77  SLLVSVAITLGSLLLNTMAGYAFAKLRFVGRDRLFQVLMAALVIPAQVAMLPLFLLMKQL 136

Query: 135 GLFNTHLGLILTYLLFTLPFTVWVLVGYFRGLPRELEEAAYVDGATPLQTLLKVMLPLTG 194
           GL N+  G+I+  L     F ++++  Y R +P EL EAA +DGA  ++   +++LP+  
Sbjct: 137 GLVNSFGGVIVPALATV--FGIFLVRQYARSIPDELLEAARMDGAGEMRIFFQIVLPMLK 194

Query: 195 PGLVTTGLLAFIAAWNEYLFALTFTVGDSVKTVPPAIASFGGATPFEIPWGSIMAASVVV 254
           P LVT  +  F+ AWN++++ L         T+P A+A+       ++    +MA +VV 
Sbjct: 195 PVLVTLSIFTFMGAWNDFMWPLIVLTDQEHYTLPVALATLSREHIMDVE--MMMAGAVVT 252

Query: 255 TVPLVVLVLVFQQRIVAGLTAGAVKG 280
            +P++ L L+ Q+  + GL  G+VKG
Sbjct: 253 VIPVLALFLLLQRYYIQGLMLGSVKG 278


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: 137
Number of extensions: 3
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: 278
Length adjustment: 26
Effective length of query: 254
Effective length of database: 252
Effective search space:    64008
Effective search space used:    64008
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.

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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