GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuF in Sinorhizobium meliloti 1021

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 SMa0710 SMa0710 ABC transporter permease

Query= TCDB::Q72H67
         (291 letters)



>FitnessBrowser__Smeli:SMa0710
          Length = 337

 Score =  189 bits (479), Expect = 1e-52
 Identities = 101/281 (35%), Positives = 161/281 (57%), Gaps = 3/281 (1%)

Query: 5   RQVRLAWILVLPTLLVVVLVAGYPLAQVFYWSFFKADIAFVEPPEF-VGLENYAYLFQDP 63
           RQ  L ++L+LP + +V L+  YPL      SF K  +A +  P     LENY  LF  P
Sbjct: 49  RQHWLGYLLLLPAVALVALIIVYPLFVSLDLSFQKIGMATLSAPRKPFTLENYHKLFASP 108

Query: 64  DFRQALWNTLKFTVVSVSLETVLGLAIALIIHSNFRGRGLVRTAILIPWAIPTVVSAKMW 123
           DF  + W T+K  VV  +    +GL  AL++++ F+GR L R  + +PWA+P V++  ++
Sbjct: 109 DFWNSCWVTIKLVVVVSAACFAVGLGTALLVNNRFKGRTLARLFVALPWAVPEVIAVVIF 168

Query: 124 QWMLNDVYGVINVLGVKLGLLSQKVAFLARPELLLPSIIAVDVWKTTPFMALLLLAGLQM 183
            W+ +  +G++N L +KLG+ SQ + + + P      +    +WK  PF++++ LAGLQ 
Sbjct: 169 AWIFDSSFGLMNWLFIKLGITSQMINWFSEPTAAFWVVAITMIWKGYPFVSIMTLAGLQS 228

Query: 184 IPEELYEAASIDGASRWQQFWSITLPLLTPALVVALIFRTLDALRVFDVVFVMSGVNP-- 241
           IPE+ Y AA +DGA+ +Q+FW IT+P+L P L V  +   L   R F ++ V++   P  
Sbjct: 229 IPEDFYNAAKVDGANAFQRFWYITIPVLMPVLGVTSVLVVLWVFRDFSIIKVLTDGGPLK 288

Query: 242 ATRTLAVYNRQTLVDFQDLGYGSAISVAILVIIFAFVLLYM 282
           AT+TL++        F ++GY SAI +  LV+     LL +
Sbjct: 289 ATQTLSIMTYDQAFGFFNMGYASAIGIVTLVLCVVASLLML 329


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: 266
Number of extensions: 10
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: 291
Length of database: 337
Length adjustment: 27
Effective length of query: 264
Effective length of database: 310
Effective search space:    81840
Effective search space used:    81840
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 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