GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuF in Luteipulveratus mongoliensis MN07-A0370

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_052594639.1 VV02_RS20690 sugar ABC transporter permease

Query= TCDB::Q72H67
         (291 letters)



>NCBI__GCF_001190945.1:WP_052594639.1
          Length = 323

 Score =  174 bits (441), Expect = 2e-48
 Identities = 102/277 (36%), Positives = 156/277 (56%), Gaps = 2/277 (0%)

Query: 9   LAWILVLPTLLVVVLVAGYPLAQVFYWSFFKADIAFVEPPEFVGLENYAYLFQDPDFRQA 68
           L W L  P  ++++LV  YP+A   Y S F   +   +   FV L+NY     DP F QA
Sbjct: 36  LGWRLAGPAFIIMLLVTLYPIAYAIYLSLFSYRLTDPDARRFVFLQNYVTSLTDPLFWQA 95

Query: 69  LWNTLKFTVVSVSLETVLGLAIALIIHSNFRGRGLVRTAILIPWAIPTVVSAKMWQWMLN 128
              T    VV++ +E VLG+AIA++++     R  +RT +LIP+AI TVVSA  W +  +
Sbjct: 96  FITTFVIVVVTLVIELVLGMAIAMLMNKIVIPRRTLRTIVLIPYAIITVVSAFSWLFAAS 155

Query: 129 DVYGVIN--VLGVKLGLLSQKVAFLARPELLLPSIIAVDVWKTTPFMALLLLAGLQMIPE 186
              G  N  +     G       +       L  I   ++WKTTPFM+LLLLAGL  +  
Sbjct: 156 VDTGFFNHWLHAFTFGGFPLDYDWFGGRWSSLTIISLSEIWKTTPFMSLLLLAGLAQVDG 215

Query: 187 ELYEAASIDGASRWQQFWSITLPLLTPALVVALIFRTLDALRVFDVVFVMSGVNPATRTL 246
            + EAA +DGA+ WQ+F+ + LP +  AL+VA++FRTLDA+R++D   VM+G    T TL
Sbjct: 216 AMEEAAKVDGATWWQRFYKVILPNMKAALMVAVLFRTLDAVRIYDNPQVMTGGANKTMTL 275

Query: 247 AVYNRQTLVDFQDLGYGSAISVAILVIIFAFVLLYMR 283
           ++      ++  ++G GSA++V + +I+     L++R
Sbjct: 276 SMLVSNETINRVEIGMGSALAVILFIIVLIIAALFVR 312


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: 241
Number of extensions: 9
Number of successful extensions: 2
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: 323
Length adjustment: 27
Effective length of query: 264
Effective length of database: 296
Effective search space:    78144
Effective search space used:    78144
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