GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuG in Paraburkholderia bryophila 376MFSha3.1

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 H281DRAFT_04157 H281DRAFT_04157 sorbitol ABC transporter membrane protein /mannitol ABC transporter membrane protein

Query= TCDB::Q72H66
         (280 letters)



>FitnessBrowser__Burk376:H281DRAFT_04157
          Length = 291

 Score =  163 bits (412), Expect = 5e-45
 Identities = 87/265 (32%), Positives = 147/265 (55%), Gaps = 6/265 (2%)

Query: 15  LLVVFVVVYSVFPFYWAVISSFKPSDALFSPDPSFLPVPFTLEHYENVFLQANFGRNLLN 74
           +L  FV +   FP +W  I++FK     +S    F P   T + +  VF ++N+     N
Sbjct: 33  VLAWFVALLLFFPIFWMTITAFKTEQQAYSSSLFFTP---TFDSFREVFARSNYFSFAWN 89

Query: 75  SLIVAGGATLLSLVLGVLAAYALGRLPFPPKNAVMYIVLSMTMFPQIAVLGGLFLLLRQT 134
           S++++ G T+L L+L V AAYA+   P      V+  +LS  M P + VL  ++LL + +
Sbjct: 90  SILISVGVTVLCLILAVPAAYAMAFFPTRRTQKVLLWMLSTKMMPSVGVLVPIYLLWKNS 149

Query: 135 GLFNTHLGLILTYLLFTLPFTVWVLVGYFRGLPRELEEAAYVDGATPLQTLLKVMLPLTG 194
           GL +T  GL++ Y L  LP  VW+   YF  +PR++ EA  +DGA   Q ++ +++P+  
Sbjct: 150 GLLDTVSGLVIVYTLINLPIAVWMSFTYFAEIPRDILEAGRIDGAATWQEIVYLLMPMAL 209

Query: 195 PGLVTTGLLAFIAAWNEYLFALTFTVGDSVKTVPPAIASFGGATPFEIPWGSIMAASVVV 254
           PGL +T LL  I +WNE  +++  +   S    P  +     ++P  + W  + AAS++ 
Sbjct: 210 PGLASTALLLVILSWNEAFWSINLS---SSNAAPLTVFIASYSSPEGLFWAKLSAASLLA 266

Query: 255 TVPLVVLVLVFQQRIVAGLTAGAVK 279
             P++++  + Q+++V GLT GAVK
Sbjct: 267 VAPILIVGWLSQKQLVRGLTFGAVK 291


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: 160
Number of extensions: 8
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: 280
Length of database: 291
Length adjustment: 26
Effective length of query: 254
Effective length of database: 265
Effective search space:    67310
Effective search space used:    67310
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