GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuF in Nocardioides dokdonensis FR1436

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_068109004.1 I601_RS10140 sugar ABC transporter permease

Query= TCDB::Q72H67
         (291 letters)



>NCBI__GCF_001653335.1:WP_068109004.1
          Length = 316

 Score =  190 bits (483), Expect = 3e-53
 Identities = 104/278 (37%), Positives = 168/278 (60%), Gaps = 7/278 (2%)

Query: 8   RLAWILVLPTLLVVVLVAGYPLAQVFYWSFFKADIAFVEPPEFVGLENYAYLFQDPDFRQ 67
           RL   LV P ++V+++V  +P+ +  Y S +   +      EF+GL NY     D  F +
Sbjct: 32  RLGQRLVAPAIVVMLIVTAFPILRALYLSLYNYSLTAPADREFIGLSNYVTALTDSLFWR 91

Query: 68  ALWNTLKFTVVSVSLETVLGLAIALIIHSNFRGRGLVRTAILIPWAIPTVVSAKMWQWML 127
            +  T+ + VV+V++E V+G A AL++H     RGL+RT+ILIP+ I TVVS   WQ+  
Sbjct: 92  DIGVTVLYMVVTVAIELVIGFAFALVMHRVIFARGLIRTSILIPYGIITVVSGFAWQFAF 151

Query: 128 NDVYGVINVLGVKLGLLSQKVAFLARPELLLPSIIAVDVWKTTPFMALLLLAGLQMIPEE 187
               G +N     L  ++    +   P   + +I+  ++WKTTPFM+LLLLAGL  + E+
Sbjct: 152 TYQNGFVNGW---LPFIADDFNWFGSPPPAIIAIMVSEIWKTTPFMSLLLLAGLAQVSED 208

Query: 188 LYEAASIDGASRWQQFWSITLPLLTPALVVALIFRTLDALRVFDVVFVMSGVNPATRTLA 247
           + EAA +DGA+ WQ+ W + LP +  A++VA++FR LDA R+FD +FVM+     T +++
Sbjct: 209 MVEAAKVDGATWWQRMWKVVLPNMKAAIMVAVLFRALDAYRIFDNIFVMTAGAQGTESIS 268

Query: 248 VYN-RQTLVDFQDLGYGSAISVAIL--VIIFAFVLLYM 282
               RQ++  FQ LG GSA++V +   V++ A++++ M
Sbjct: 269 FLTYRQSIEQFQ-LGMGSALAVLLFLSVLLVAWLIVKM 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: 247
Number of extensions: 13
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: 316
Length adjustment: 27
Effective length of query: 264
Effective length of database: 289
Effective search space:    76296
Effective search space used:    76296
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