GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0029 in Cupriavidus basilensis 4G11

Align TM0029, 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 RR42_RS27420 RR42_RS27420 ABC transporter permease

Query= TCDB::Q9WXN6
         (280 letters)



>FitnessBrowser__Cup4G11:RR42_RS27420
          Length = 280

 Score =  147 bits (372), Expect = 2e-40
 Identities = 85/283 (30%), Positives = 144/283 (50%), Gaps = 14/283 (4%)

Query: 1   MFRTMIRPLFKNKKFIIGFSIFLFFLFLGIFGPMFYRVDPTEMTWDYEQPP------SSA 54
           M  T  R   +NK  ++G  +   F  L +FGP     DP    WD  Q P         
Sbjct: 1   MKNTFWRRFCRNKAAVLGMVVLAGFAVLALFGPWMAGHDP----WDMVQQPFLQPMQEPG 56

Query: 55  HPLGTDTYGRDVLAQLLHGIRSSLYIGFLAAIISLVIGTIIGSFSAVKRGIVDDVLMGIT 114
             +GTDT GRD+LA ++HG R SL IG ++ ++SL+IG  +G+ S    G +D  LM  T
Sbjct: 57  FAMGTDTMGRDILAGVIHGARISLLIGVVSTVVSLLIGVTLGAISGYFGGWIDAALMRFT 116

Query: 115 NIVLTTPSILIAILIASYLKVRSVEMVAVILGLFQWPWFARAIRAQLMSVMSREYVYLSV 174
            +    PS  +A+++ +  +  S+  +   + +  WP  AR +R++ +++  R++V  + 
Sbjct: 117 ELFQAVPSFALALVLVAIFE-PSIGSIVAAIAIVSWPPVARLVRSEFLTLRQRDFVQAAK 175

Query: 175 MAGYSDLRLVIEDLIPTIATYAFMSFVLFINGGIMGEAGLSLIGLGPTQGISLGIMLQWA 234
           +AG S  R+++  ++P  ++   +   L +   I+ E+ LS +GLG    +S G M+  A
Sbjct: 176 LAGQSTPRIILSQILPNASSPIVVMASLMVATAILLESSLSFLGLGDPNHMSWGYMVGSA 235

Query: 235 VLMEAVRRGLWWWFVPPGLAIVAVTASLLVISTAMDEVFNPRL 277
                V R  WW  V PG AI+    +L ++   +++  N RL
Sbjct: 236 ---RTVLRQAWWMAVFPGTAILLTVLALNMVGEGLNDALNARL 275


Lambda     K      H
   0.330    0.144    0.441 

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: 197
Number of extensions: 15
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: 280
Length of database: 280
Length adjustment: 26
Effective length of query: 254
Effective length of database: 254
Effective search space:    64516
Effective search space used:    64516
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: 47 (22.7 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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