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_157063392.1 VV02_RS12555 ABC transporter permease subunit

Query= TCDB::Q72H67
         (291 letters)



>NCBI__GCF_001190945.1:WP_157063392.1
          Length = 315

 Score =  154 bits (388), Expect = 3e-42
 Identities = 93/281 (33%), Positives = 153/281 (54%), Gaps = 13/281 (4%)

Query: 5   RQVRLAWILVLPTLLVVVLVAGYPLAQVFYWSFFKADIAFVEPPEFVGLENYAYLFQDPD 64
           R+    W+ + P  + ++L    P+      + F+ D       +F+GL+N+  +F DP 
Sbjct: 26  RENLAGWLFLAPDAIGLLLFVAIPMVLALGIALFEVDS--FGHYDFIGLDNFQRMFGDPM 83

Query: 65  FRQALWNTLKFTVVSVSLETVLGLAIALIIHSNFRGRGLVRTAILIPWAIPTVVSAKMWQ 124
              ++W T+K+ V+ V L  V GL +AL++   F G  +VRT + +P A+  VV   +WQ
Sbjct: 84  LWSSIWVTVKYVVLFVPLSFVAGLGLALLVRDYFPGVAIVRTLLFLPNAVSLVVVGLLWQ 143

Query: 125 WMLNDVYGVINVLGVKLGLLSQKVAFLARPELLLPSIIAVDVWKTTPFMALLLLAGLQMI 184
           ++L D  GV++  G K+GL    +++L  P+  L S + + VW T  +  LL +AGL+ I
Sbjct: 144 FLLVDKQGVLSKAGDKVGL--DGISWLGDPKYALISYVLISVWFTMGYQMLLFMAGLKDI 201

Query: 185 PEELYEAASIDGASRWQQFWSITLPLLTPA---LVVALIFRTLDALRVFDVVFVMSGVNP 241
             E  +AA IDGA+ WQ+F  +  PLL P    +++  +  ++  L+ FD+VFV++   P
Sbjct: 202 NPEYLDAAKIDGATPWQRFRHVIWPLLQPTSFFVLITSLVASVTGLQAFDLVFVLTKGGP 261

Query: 242 ATRTLAV--YNRQTLVDFQDLGYGSAISVAILVIIFAFVLL 280
             RT  V  Y  Q    F   GY +AI+    VI+ AF++L
Sbjct: 262 DNRTSTVVFYVYQQAFTFGHYGYAAAIT----VILVAFLML 298


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: 266
Number of extensions: 18
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: 315
Length adjustment: 27
Effective length of query: 264
Effective length of database: 288
Effective search space:    76032
Effective search space used:    76032
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