GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16925 in Rhodobacter viridis JA737

Align Arabinose ABC transporter permease (characterized, see rationale)
to candidate WP_110805878.1 C8J30_RS10880 ABC transporter permease

Query= uniprot:A0A161GM94
         (322 letters)



>NCBI__GCF_003217355.1:WP_110805878.1
          Length = 352

 Score =  174 bits (441), Expect = 3e-48
 Identities = 108/312 (34%), Positives = 165/312 (52%), Gaps = 17/312 (5%)

Query: 28  LAAIGIFVLCTLMIDNFLSPLNMRGLGLAISTTGIAACTMLYCLASGHFDLSVGSVIA-C 86
           LA I +F     M  NFLS  N   +    + T   A  M + + +G  DLSVGS +  C
Sbjct: 26  LALILVFGFFAFMAPNFLSVANSVIVAKHAALTAFLAIGMTFVIITGGIDLSVGSTVGLC 85

Query: 87  AGVVAAVVMRDTNSVFLGIS-------AALVM--GLIVGLINGIVIAKLRVNALITTLAT 137
           A V   +++   +   +G         A LVM  G+ VG +NGI+I KL V   I TL T
Sbjct: 86  AMVSGWLILYGIDLGAMGTMQFNTLEIALLVMCVGVFVGFVNGILITKLNVAPFIATLGT 145

Query: 138 MQIVRGLAYIFANGKA-------VGVSQESFFVFGNGQMFGVPVPILITIVCFLFFGWLL 190
           + I RG A + + G+              SF   G G   G+PV I + I   L   ++ 
Sbjct: 146 LYIARGAALLSSGGRTFPNLSGNADYGSASFPGIGAGTFLGLPVQIWMLIAVGLVAAYIA 205

Query: 191 NYTTYGRNTMAIGGNQEAALLAGVNVDRTKIIIFAVHGVIGALAGVILASRMTSGQPMIG 250
             T  GR+  A+GGN+  A L+GV V+R K+ ++   G   A+ G+I+AS++ +  P  G
Sbjct: 206 KRTPLGRHIYAVGGNERGAALSGVKVNRVKLFVYMFSGFCAAIVGLIIASQLQAAHPATG 265

Query: 251 QGFELTVISACVLGGVSLSGGIGMIRHVIAGVLILAIIENAMNLKNIDTFYQYVIRGSIL 310
           + FEL  I+A VLGG SLSGG G I   I G  +++I+ + + + ++ +F+Q VI+G ++
Sbjct: 266 ETFELNAIAAAVLGGTSLSGGRGKIGGTIVGAFVISILSDGLVMMSVSSFWQTVIKGLVI 325

Query: 311 LLAVVIDRLKQR 322
           + AVVID+ + +
Sbjct: 326 VAAVVIDQAQSK 337


Lambda     K      H
   0.330    0.144    0.420 

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: 255
Number of extensions: 12
Number of successful extensions: 1
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: 322
Length of database: 352
Length adjustment: 28
Effective length of query: 294
Effective length of database: 324
Effective search space:    95256
Effective search space used:    95256
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: 49 (23.5 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