GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuF in Ochrobactrum thiophenivorans DSM 7216

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 WP_094506566.1 CEV31_RS07130 sugar ABC transporter permease

Query= TCDB::Q72H67
         (291 letters)



>NCBI__GCF_002252445.1:WP_094506566.1
          Length = 317

 Score =  175 bits (444), Expect = 1e-48
 Identities = 105/269 (39%), Positives = 152/269 (56%), Gaps = 6/269 (2%)

Query: 16  PTLLVVVLVAGYPLAQVFYWSFFKADIAFVEPPE--FVGLENYAYLFQDPDFRQALWNTL 73
           P L+++  +   PL     ++F   DI  + P    FVGLE++  L  D  F ++L NTL
Sbjct: 39  PALILIGAIMLVPLILGVSYAF--RDIQLLNPFSGGFVGLEHFRELATDQAFYRSLKNTL 96

Query: 74  KFTVVSVSLETVLGLAIALIIHSNFRGRGLVRTAILIPWAIPTVVSAKMWQWMLNDVYGV 133
            +T  SV L+ V GL +AL++   F GRGL +  I +PWA+PT ++   W W+ N V G 
Sbjct: 97  WWTGCSVLLQFVFGLILALLLDKPFAGRGLAQALIFLPWAVPTFLTGLNWAWLFNPVIGP 156

Query: 134 INVLGVKLGLLSQKVAFLARPELLLPSIIAVDVWKTTPFMALLLLAGLQMIPEELYEAAS 193
           +      +GLLS     L+ P L +  II   VW   PF A+ +LA LQ IP +LYEAAS
Sbjct: 157 LPHWLHAIGLLSAPDNILSDPNLAMWGIITAGVWWGIPFFAITMLAALQAIPRDLYEAAS 216

Query: 194 IDGASRWQQFWSITLPLLTPALVVALIFRTLDALRVFDVVFVMSGVNPATRTLAVYNRQT 253
           IDGA   Q+F SITLP L P + + ++ RT+      D++ VM+G  PA RT  V +   
Sbjct: 217 IDGAGPAQRFLSITLPYLAPTMAITILLRTVWIANSADLIVVMTGGGPADRTQIVASYIF 276

Query: 254 LVDFQ--DLGYGSAISVAILVIIFAFVLL 280
              F+  D GY SAI++ +LV++  + +L
Sbjct: 277 TQAFKRLDFGYASAIAMVLLVLLMVYSML 305


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: 235
Number of extensions: 10
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: 317
Length adjustment: 27
Effective length of query: 264
Effective length of database: 290
Effective search space:    76560
Effective search space used:    76560
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 24 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