GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Pseudomonas putida KT2440

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 PP_0881 PP_0881 dipeptide ABC transporter - putative membrane subunit

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__Putida:PP_0881
          Length = 336

 Score =  174 bits (441), Expect = 3e-48
 Identities = 113/342 (33%), Positives = 171/342 (50%), Gaps = 23/342 (6%)

Query: 6   MFKYLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRVAQANPEAIRAAERTL 65
           M  ++ RR   L+ T+   T + F L R IPG+P+ +++ G  RV   +PE    A    
Sbjct: 1   MLSFIARRLGLLIPTFFGITLLTFALIRLIPGDPV-EVMMGERRV---DPEMHAQA---- 52

Query: 66  MEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIVAW 125
           ME  GL KP  VQY +++ K  +GDLG S+      V    + + P TL L   A + A 
Sbjct: 53  MERLGLNKPLPVQYLDYVGKLAQGDLGESLRTR-ESVWREFLTLFPATLELAFAALLFAG 111

Query: 126 ILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLPVQGAYSQ 185
           ++G   G +AA KR +  D GV+  SL    +P +W G+I I  F V LGW PV G    
Sbjct: 112 VVGLLAGVIAALKRGSLFDHGVMGISLAGYSMPIFWWGLILIMFFSVSLGWTPVSGRIDL 171

Query: 186 -------------GTIPNLSWSFFVDVLKHYIMPFASIVVSAMGGWAIGMRLMVIYELGS 232
                         T+ +     F D + H I+P   +    +   A   R  ++  L  
Sbjct: 172 LYDIEPKTGFMLIDTLLSDEEGAFKDAVMHLILPAIVLGTIPLAVIARMTRSSMLEVLRE 231

Query: 233 DYAMFSEYLGMKDKRI-FKYVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGYLL 291
           DY   +   G+   R+ F +  RN+L+P +T   L +G +L GA++TE +F++PG G  L
Sbjct: 232 DYIRTARAKGLSPARVVFVHGLRNALIPVLTVFGLQVGTLLAGAVLTETIFSWPGIGKWL 291

Query: 292 FRALTTLDYPLIQGIFVILIASIYLANFIVDFLYALIDPRIR 333
             A+   DYP++Q   +++   + L NF+VD LY L +PRIR
Sbjct: 292 IEAIGARDYPVVQNGILLIACLVILVNFVVDILYGLANPRIR 333


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: 311
Number of extensions: 19
Number of successful extensions: 3
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: 336
Length adjustment: 28
Effective length of query: 310
Effective length of database: 308
Effective search space:    95480
Effective search space used:    95480
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