GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuF in Jannaschia aquimarina GSW-M26

Align Maltose transport system permease protein malF aka TT_C1628, 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_043919942.1 jaqu_RS15665 sugar ABC transporter permease

Query= TCDB::Q72H67
         (291 letters)



>NCBI__GCF_000877395.1:WP_043919942.1
          Length = 305

 Score =  182 bits (463), Expect = 6e-51
 Identities = 97/287 (33%), Positives = 164/287 (57%), Gaps = 8/287 (2%)

Query: 11  WILVLPTLLVVVLVAGYPLAQVFYWSFFKADIAF-VEPPEFVGLENYAYLFQDPDFRQAL 69
           ++ + P +LV+ +   YP+  + + SF   + +  +   EFVGL NY YL  D  FR++ 
Sbjct: 11  YLFLAPAVLVMAVALLYPIGYMIWASFLDWNPSQRIGEAEFVGLRNYIYLLGDAAFRESF 70

Query: 70  WNTLKFTVVSVSLETVLGLAIALIIHSNFRGRGLVRTAILIPWAIPTVVSAKMWQWMLND 129
           W T++F  + V++E VLG+ +AL++    RG  ++RT  ++P  I  +V   MW++M + 
Sbjct: 71  WVTIRFAAIVVTVEMVLGVGLALLLDRKLRGMTVLRTIFILPMMIAPIVVGLMWRYMYHP 130

Query: 130 VYGVINVLGVKLGLLSQKVAFLARPELLLPSIIAVDVWKTTPFMALLLLAGLQMIPEELY 189
             G +N +   +GL S    +L+       SI+  D+W+ TPF+ +L LA LQ +P+   
Sbjct: 131 TVGTLNRMLESVGLPS--APWLSDGTWAFASIVIADIWQWTPFIFILALAALQSLPQSAM 188

Query: 190 EAASIDGASRWQQFWSITLPLLTPALVVALIFRTLDALRVFDVVFVMSGVNP--ATRTLA 247
           EAA IDGAS WQ  W + LPL+ P L+V  + R +DA +V +V+ V++   P  +T  +A
Sbjct: 189 EAARIDGASGWQLIWHVKLPLMLPVLIVTALLRLIDAFKVLEVILVLTNGGPGLSTEIVA 248

Query: 248 VYNRQTLVDFQDLGYGSAISVAILVIIFAFVLL---YMRTVGKEALK 291
           +   +T  +FQDLG  +A+S  +L+++    +L   Y R   + A +
Sbjct: 249 LRIARTAQEFQDLGTAAAMSNLLLILLLVLTILMFGYTRLTERRAAR 295


Lambda     K      H
   0.329    0.142    0.433 

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: 240
Number of extensions: 13
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: 291
Length of database: 305
Length adjustment: 26
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 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