GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araH in Sinorhizobium meliloti 1021

Align L-arabinose ABC transporter, permease protein AraH (characterized)
to candidate SM_b21375 SM_b21375 sugar uptake ABC transporter permease

Query= CharProtDB::CH_014278
         (328 letters)



>FitnessBrowser__Smeli:SM_b21375
          Length = 320

 Score =  215 bits (548), Expect = 1e-60
 Identities = 118/308 (38%), Positives = 185/308 (60%), Gaps = 1/308 (0%)

Query: 20  RIWDQYG-MLVVFAVLFIACAIFVPNFATFINMKGLGLAISMSGMVACGMLFCLASGDFD 78
           R   QYG + +   +L I  + F P F T +N   +   +++  + A GM + +  G+ D
Sbjct: 13  RALKQYGGIFLSLVMLCIVFSFFNPRFMTVVNFMNILQQVAVVAIAAFGMTWVILLGEID 72

Query: 79  LSVASVIACAGVTTAVVINLTESLWIGVAAGLLLGVLCGLVNGFVIAKLKINALITTLAT 138
           LSV S+IA AG+  A            +A  L  G L G++NG + AKL + + I T+AT
Sbjct: 73  LSVGSIIAVAGMVGAQCFAFGMGFAPAIALTLAAGALMGMLNGVLTAKLLLPSFIVTVAT 132

Query: 139 MQIVRGLAYIISDGKAVGIEDESFFALGYANWFGLPAPIWLTVACLIIFGLLLNKTTFGR 198
           M I RG+  + ++G    IE+E++ A+G  ++ GLP  IW+     +I  ++L+KT+FGR
Sbjct: 133 MGIYRGMVSLPTNGAPAMIENETWTAIGTESFLGLPIIIWVVAVLFVINQIVLSKTSFGR 192

Query: 199 NTLAIGGNEEAARLAGVPVVRTKIIIFVLSGLVSAIAGIILASRMTSGQPMTSIGYELIV 258
                GGN EAA  +G+ V R KI+IF++SG+++AI+G++L+SR+ S Q    + YEL  
Sbjct: 193 RAYLTGGNREAAVYSGIKVDRLKILIFMISGVMAAISGVLLSSRLFSAQTNAGMSYELDA 252

Query: 259 ISACVLGGVSLKGGIGKISYVVAGILILGTVENAMNLLNISPFAQYVVRGLILLAAVIFD 318
           I+A VLGG SL GG+G +   + G LI+G + N MN+L++  F Q +V+GL++L AV  D
Sbjct: 253 IAAAVLGGTSLAGGVGTMVGTLIGALIIGVMNNGMNMLSVPYFYQLIVKGLVILVAVWLD 312

Query: 319 RYKQKAKR 326
              ++AKR
Sbjct: 313 VRAKQAKR 320


Lambda     K      H
   0.327    0.141    0.414 

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: 329
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: 328
Length of database: 320
Length adjustment: 28
Effective length of query: 300
Effective length of database: 292
Effective search space:    87600
Effective search space used:    87600
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: 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