GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Desulfacinum hydrothermale DSM 13146

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 WP_170920437.1 B9A12_RS07750 ABC transporter permease

Query= TCDB::Q9WXN7
         (338 letters)



>NCBI__GCF_900176285.1:WP_170920437.1
          Length = 334

 Score =  169 bits (427), Expect = 1e-46
 Identities = 105/343 (30%), Positives = 173/343 (50%), Gaps = 24/343 (6%)

Query: 6   MFKYLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRVAQANPEAIRAAERTL 65
           M  ++LRR + L+ T    + +VF +   +PG+P   +L            A   A + +
Sbjct: 1   MLSFILRRTLALIPTVFGISVLVFFMIHLVPGDPAEMMLG---------ERASEQALKEV 51

Query: 66  MEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIVAW 125
            E+ GL KP YVQY  F+ +  +GDLG ++     K+   I    P T+ L + A I A 
Sbjct: 52  REQLGLDKPLYVQYGRFLARLAKGDLGRALRTN-EKITTEIADRFPATVELSIAAMIFAV 110

Query: 126 ILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLP------- 178
            LG   G L+A ++ +  D   +  SL+   +P +WLG+I + +F V LGWLP       
Sbjct: 111 TLGMLAGILSATRQYSVFDYSSMIFSLVGVSMPIFWLGLILMIIFSVHLGWLPLSGRLSY 170

Query: 179 ------VQGAYSQGTIPNLSWSFFVDVLKHYIMPFASIVVSAMGGWAIGMRLMVIYELGS 232
                 + G Y   ++  L+W    D + H IMP  ++    M   A   R  ++  L  
Sbjct: 171 HIHIESITGLYILDSLLTLNWPALKDAVWHIIMPAFTLSTIPMAIIARITRSSMLEVLRQ 230

Query: 233 DYAMFSEYLGMKDKRI-FKYVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGYLL 291
           DY   ++  G+  + + +K+  +N+L+P IT + L  G +LGGA++TE +F +PG G  L
Sbjct: 231 DYIRTAKAKGLAPRVVHYKHALKNALIPVITVIGLQFGILLGGAILTETIFAWPGIGLWL 290

Query: 292 FRALTTLDYPLIQGIFVILIASIYLANFIVDFLYALIDPRIRL 334
             A+   D+  +QG  +++  +    N +VD LYA I+PRI++
Sbjct: 291 LNAVYARDFNAVQGGTMLIATTFVTINMLVDILYAWINPRIKV 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: 295
Number of extensions: 18
Number of successful extensions: 5
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: 334
Length adjustment: 28
Effective length of query: 310
Effective length of database: 306
Effective search space:    94860
Effective search space used:    94860
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 Apr 09 2024. 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