GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuF in Cupriavidus basilensis 4G11

Align Maltose transport system permease protein malF aka TT_C1628, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized)
to candidate RR42_RS22880 RR42_RS22880 ABC transporter permease

Query= TCDB::Q72H67
         (291 letters)



>FitnessBrowser__Cup4G11:RR42_RS22880
          Length = 301

 Score =  167 bits (424), Expect = 2e-46
 Identities = 95/278 (34%), Positives = 156/278 (56%), Gaps = 5/278 (1%)

Query: 9   LAWILVLPTLLVVVLVAGYPLAQVFYWSFFKADIAFVEPPEFVGLENYAYLFQDPDFRQA 68
           L  +++ P L+ + L+ G P     Y+S     +       FVGL N+  + Q+P F ++
Sbjct: 16  LGALMLAPALIYIALLLGIPFLLSIYYSLSDITVG-TRAMHFVGLANFQRIVQNPTFWRS 74

Query: 69  LWNTLKFTVVSVSLETVLGLAIALIIHSNFRGRGLVRTAILIPWAIPTVVSAKMWQWMLN 128
           L N L FT+VS +L  VL   +AL +  +FRG+ LVR  IL+PW  P  + +  W W+ +
Sbjct: 75  LGNALVFTLVSQALVVVLAKILALALLRDFRGKWLVRLLILLPWVAPISLGSIGWLWIFD 134

Query: 129 DVYGVINVLGVKLGLLSQKV--AFLARPELLLPSIIAVDVWKTTPFMALLLLAGLQMIPE 186
            VY +IN     LGL   +    +L +P+L + S+I VDVW+  P   +++LAGL  IP+
Sbjct: 135 PVYSIINWTLRALGLFGPQTWPVWLGQPDLAMASVILVDVWRLLPLATVIILAGLHGIPQ 194

Query: 187 ELYEAASIDGASRWQQFWSITLPLLTPALVVALIFRTLDALRVFDVVFVMSGVNP--ATR 244
           ++++AA++DGA  W+    I +PL+ P ++VAL+F  +  L    ++FV++   P   T+
Sbjct: 195 DIHDAAAMDGAGFWRHLLRINIPLVMPIMLVALLFGIVFTLTDMIIIFVLTRGGPYDTTQ 254

Query: 245 TLAVYNRQTLVDFQDLGYGSAISVAILVIIFAFVLLYM 282
            LA     T +   DL  G+AIS+ +  ++ A V L +
Sbjct: 255 VLASLAFFTGIQGGDLAEGAAISLFLFPLLVAVVALLL 292


Lambda     K      H
   0.329    0.142    0.433 

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: 240
Number of extensions: 13
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: 291
Length of database: 301
Length adjustment: 26
Effective length of query: 265
Effective length of database: 275
Effective search space:    72875
Effective search space used:    72875
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: 48 (23.1 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