GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Acidovorax sp. GW101-3H11

Align TM0030, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate Ac3H11_2047 Dipeptide transport system permease protein DppB (TC 3.A.1.5.2)

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2047
          Length = 326

 Score =  163 bits (412), Expect = 6e-45
 Identities = 110/338 (32%), Positives = 182/338 (53%), Gaps = 23/338 (6%)

Query: 6   MFKYLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRVAQANPEAIRAAERTL 65
           M  ++LRR I  ++  I    I F+L + + G+P+  +L        A PE IR    +L
Sbjct: 1   MLAFILRRLIQAVIVMITVAFISFMLFQYV-GDPVVFLLG-----QDATPEQIRELRASL 54

Query: 66  MEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIVAW 125
               GL KP++VQ+  F+  A +G+ G S+     KV  LI    P TL L L A  +A 
Sbjct: 55  ----GLDKPFFVQFGHFLVNAAQGEFGLSLR-QGAKVSRLIAERFPATLELALVAAFLAL 109

Query: 126 ILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLPVQGAYSQ 185
            +G  +G  AA KR T+  +  +T SL+   +P + +G++ I +F V LGW P   ++ +
Sbjct: 110 AIGVPMGVYAALKRGTFTSQLFMTLSLLGVSLPTFLIGILLILVFAVTLGWFP---SFGR 166

Query: 186 GTIPNLSWSFFVDVLK-----HYIMPFASIVVSAMGGWAIGMRLMVIYELGSDYAMFSEY 240
           G +  + W +   +LK     H I+P  ++ +  +      +R  ++  L +DY  F+  
Sbjct: 167 GEVVQMGW-WSTGLLKAKGWHHIILPAVTLAIFQLTLIMRLVRAEMLEVLRTDYIKFARA 225

Query: 241 LGMKDKRI-FKYVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGYLLFRALTTLD 299
            G+ ++ I F +  +N+L+P +T   L LGG++  A+ITE VF +PG G L  +A+T  D
Sbjct: 226 RGLSNRAIHFGHALKNTLVPVMTITGLQLGGLIAFAIITETVFQWPGMGLLFIQAVTFAD 285

Query: 300 YPLIQGIFVILIASIYLA-NFIVDFLYALIDPRIRLGQ 336
            P +   ++ LIA I++  N +VD LY  +DPR+R+G+
Sbjct: 286 IP-VMAAYLCLIALIFVVINLVVDLLYFAVDPRLRVGK 322


Lambda     K      H
   0.329    0.146    0.449 

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: 283
Number of extensions: 17
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: 338
Length of database: 326
Length adjustment: 28
Effective length of query: 310
Effective length of database: 298
Effective search space:    92380
Effective search space used:    92380
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 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