GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglF' in Marinomonas arctica 328

Align Inner membrane ABC transporter permease protein (characterized, see rationale)
to candidate WP_111605924.1 DK187_RS03325 sugar ABC transporter permease

Query= uniprot:A8LLL5
         (334 letters)



>NCBI__GCF_003259225.1:WP_111605924.1
          Length = 336

 Score =  408 bits (1048), Expect = e-118
 Identities = 203/330 (61%), Positives = 255/330 (77%), Gaps = 8/330 (2%)

Query: 8   LITIIIGVGGCVGYFYFANQFLDKVLYPAKGPKAGR---NINRANQIRPWIFLFPALFVL 64
           L+T+I+GV GC  YFY +N  LDK+ +P K   A +   N+  AN IRPW+FL PA+ +L
Sbjct: 8   LVTMILGVLGCAVYFYGSNILLDKI-FPTKNRPAQQVASNLRIANSIRPWLFLGPAVLLL 66

Query: 65  LLYLGYPVVETLRLSLLERVPGGGYQWVGLDNYAQMASEPKFWEAMRNNMFWLIVVPALS 124
             YL YPV++++RLS  +R    G ++VGL NY  +    +F+E+ RNNM WLIVVP  +
Sbjct: 67  TFYLFYPVIDSIRLSFFDR---SGEEFVGLSNYVWLFGSDEFFESFRNNMLWLIVVPTAA 123

Query: 125 TAFGLLAAQLTDRIKWGNVAKSIIFMPMAISFVGASVIWKLVYDGRPIEQEQIGILNAII 184
           T FGL+ A +TDRI WGN+AKS+IFMPMAISF+GASVIWK +YD R     QIG+LNA++
Sbjct: 124 TFFGLIIATMTDRIWWGNIAKSLIFMPMAISFIGASVIWKFIYDFRSGGDAQIGLLNAVV 183

Query: 185 VGLGGDPVTFLTIPFWNNFFLMIVLVWVQTGFAMVILSAALRGIPEETIEAAIIDGASPL 244
           V  GG+P  ++TIPFWNNFFLMI+LVW+QTGFAMVILSAALRGIP+ETIEAA++DGA+ L
Sbjct: 184 VFFGGEPQNWITIPFWNNFFLMIILVWIQTGFAMVILSAALRGIPDETIEAAVLDGANGL 243

Query: 245 QIFFKIKVPQIMPTVVVVWTTITLVVLKVFDIVFAMTNGQWETQVLANYMFDKLFR-AND 303
           QIFFKI VPQI  T+ VVWTTIT++VLKVFDIV AMTNGQW+TQVLAN MFD +FR   D
Sbjct: 244 QIFFKIMVPQIWGTIAVVWTTITILVLKVFDIVLAMTNGQWDTQVLANQMFDWMFRGGGD 303

Query: 304 WGVGSASAMVIMLLVTPILIWNIHSARKEM 333
           +G G+  A+VIM+LV PI++WNI  A  EM
Sbjct: 304 FGRGAVVAIVIMVLVIPIMVWNIKRANAEM 333


Lambda     K      H
   0.329    0.143    0.455 

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: 416
Number of extensions: 16
Number of successful extensions: 4
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: 334
Length of database: 336
Length adjustment: 28
Effective length of query: 306
Effective length of database: 308
Effective search space:    94248
Effective search space used:    94248
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: 49 (23.5 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