GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16925 in Sinorhizobium meliloti 1021

Align Monosaccharide-transporting ATPase; EC 3.6.3.17 (characterized, see rationale)
to candidate SM_b21375 SM_b21375 sugar uptake ABC transporter permease

Query= uniprot:B2SYR4
         (338 letters)



>FitnessBrowser__Smeli:SM_b21375
          Length = 320

 Score =  203 bits (516), Expect = 5e-57
 Identities = 112/314 (35%), Positives = 188/314 (59%), Gaps = 3/314 (0%)

Query: 26  KAKWWQQITEYSLIVIFVVMFATM-SLTVDHFFSIENMLGLALSISQIGMVSCTMMFCLA 84
           KA   + + +Y  I + +VM   + S     F ++ N + +   ++ + + +  M + + 
Sbjct: 8   KAALVRALKQYGGIFLSLVMLCIVFSFFNPRFMTVVNFMNILQQVAVVAIAAFGMTWVIL 67

Query: 85  SRDFDLSVGSTVAFAGVLCAMVLNATGNTFI-AIVAAVAAGGVIGFVNGAVIAYLRINAL 143
             + DLSVGS +A AG++ A    A G  F  AI   +AAG ++G +NG + A L + + 
Sbjct: 68  LGEIDLSVGSIIAVAGMVGAQCF-AFGMGFAPAIALTLAAGALMGMLNGVLTAKLLLPSF 126

Query: 144 ITTLATMEIVRGLGFIVSHGQAVGVSSDTFIALGGLSFFGVSLPIWVTLLCFIVFGVMLN 203
           I T+ATM I RG+  + ++G    + ++T+ A+G  SF G+ + IWV  + F++  ++L+
Sbjct: 127 IVTVATMGIYRGMVSLPTNGAPAMIENETWTAIGTESFLGLPIIIWVVAVLFVINQIVLS 186

Query: 204 QTVYGRNTLAIGGNPEASRLAGINVERTRVYIFLIQGAVTALAGVILASRITSGQPNAAQ 263
           +T +GR     GGN EA+  +GI V+R ++ IF+I G + A++GV+L+SR+ S Q NA  
Sbjct: 187 KTSFGRRAYLTGGNREAAVYSGIKVDRLKILIFMISGVMAAISGVLLSSRLFSAQTNAGM 246

Query: 264 GFELNVISACVLGGVSLLGGRATISGVVIGVLIMGTVENVMNLMNIDAFYQYLVRGAILL 323
            +EL+ I+A VLGG SL GG  T+ G +IG LI+G + N MN++++  FYQ +V+G ++L
Sbjct: 247 SYELDAIAAAVLGGTSLAGGVGTMVGTLIGALIIGVMNNGMNMLSVPYFYQLIVKGLVIL 306

Query: 324 AAVLLDQLKNRGSR 337
            AV LD    +  R
Sbjct: 307 VAVWLDVRAKQAKR 320


Lambda     K      H
   0.326    0.139    0.396 

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: 307
Number of extensions: 15
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: 338
Length of database: 320
Length adjustment: 28
Effective length of query: 310
Effective length of database: 292
Effective search space:    90520
Effective search space used:    90520
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 (21.7 bits)
S2: 49 (23.5 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