GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0029 in Acidovorax sp. GW101-3H11

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 Ac3H11_4826 Dipeptide transport system permease protein DppC (TC 3.A.1.5.2)

Query= TCDB::Q9WXN6
         (280 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4826
          Length = 290

 Score =  130 bits (328), Expect = 3e-35
 Identities = 88/272 (32%), Positives = 140/272 (51%), Gaps = 12/272 (4%)

Query: 11  KNKKFIIGFSIFLFFLFLGIFGPMFYRVDPTEMTWDYEQP-PSSAHPLGTDTYGRDVLAQ 69
           +++ F+IG  + L  +       ++    P EM    +   PS  H LGTD +GRDV + 
Sbjct: 22  RHRSFVIGAVLSLLLILAAALSLVWTPWSPYEMDLANKLAGPSGTHWLGTDAFGRDVASL 81

Query: 70  LLHGIRSSLYIGFLAAIISLVIGTIIGSFSAVKRGIVDDVLMGITNIVLTTPSILIAILI 129
           LL G R+S+ +G +A  I L IGT +G  +A KRG V++++M + +     P+IL AI++
Sbjct: 82  LLVGARNSILVGVIAVGIGLTIGTALGLLAAAKRGWVEELIMRLADFTFAFPAILSAIMM 141

Query: 130 ASYLKVRSVEMVAVILGLFQWPWFARAIRAQLMSVMSREYVYLSVMAGYSDLRLVIEDLI 189
            +      V  + + +G+F  P FAR  RA   +V SREY+  S   G    R+ IE ++
Sbjct: 142 TAVFGAGIVNSI-IAIGIFNIPTFARVTRASANAVWSREYIMASRACGKGSWRITIEHVL 200

Query: 190 PTIATYAFMSFVLFINGGIMGEAGLSLIGLG--PTQGISLGIMLQWA--VLMEAVRRGLW 245
           P I +   +   +     I+ EA LS +GLG  P Q  S G ML  A  ++ +A    +W
Sbjct: 201 PNILSVLIVQATIQFAIAILAEAALSYLGLGTQPPQP-SWGRMLSEAQTLMFQAPLLAVW 259

Query: 246 WWFVPPGLAIVAVTASLLVISTAMDEVFNPRL 277
                PG+AI      L ++   + ++ +PRL
Sbjct: 260 -----PGVAIALAVLGLNLLGDGLRDLLDPRL 286


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: 179
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: 290
Length adjustment: 26
Effective length of query: 254
Effective length of database: 264
Effective search space:    67056
Effective search space used:    67056
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.

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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