GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Pseudovibrio axinellae Ad2

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate WP_068009667.1 PsAD2_RS19325 ribose ABC transporter permease

Query= uniprot:B2T9V8
         (351 letters)



>NCBI__GCF_001623255.1:WP_068009667.1
          Length = 314

 Score =  166 bits (419), Expect = 1e-45
 Identities = 98/302 (32%), Positives = 162/302 (53%), Gaps = 12/302 (3%)

Query: 44  LPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLAESLIVLTGKFDLSLESTVGI 103
           L  L +L+   +F + +FL   N++++L  ++  A++ +  + ++LT   DLS+ S +  
Sbjct: 13  LIGLIILMAAVSFANANFLGVDNMLNILRQTSINAVIAMGMTFVILTSGIDLSVGSILAF 72

Query: 104 APAVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGFINGFLVVRLRLNAFIVTLAML 163
           A A+ A L+        GM  P    L A ++VGA +G  +G ++    +  FI TL  +
Sbjct: 73  AGAICASLI--------GMDTPLVVALFATIMVGAGLGATSGVIISYFNVQPFIATLVGM 124

Query: 164 IVLRGMLVGATKGGTL----FDMPTSFFALATTIVLGLPLSVWLAAAAFAIAAFMLRYHR 219
            ++RG  +  T+G  +     D+  SF+      + G+P  V L    FAI  F+L   R
Sbjct: 125 TMIRGATLVYTQGRPVSTGSHDVAESFYQFGAGYIFGIPHPVILMIVIFAICWFILSQTR 184

Query: 220 LGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGYVGAINANQGNGMI 279
            GR +YAIGGN   AR +GI V+++   V+ L   LA++ G+I+T  + +     G G  
Sbjct: 185 FGRYVYAIGGNENVARLSGINVKKVKILVYALSGALAALAGIILTARLESAQPTAGLGYE 244

Query: 280 FTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFWIQAIYGAIILGSL 339
               AA V+GG SL GGKG +FG + G L++GV+ N L +  V S++     GA+IL ++
Sbjct: 245 LDAIAAVVLGGTSLAGGKGRVFGTIIGALIIGVLNNALNIMDVSSYYQMIAKGAVILLAV 304

Query: 340 MV 341
           +V
Sbjct: 305 VV 306


Lambda     K      H
   0.326    0.140    0.397 

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: 263
Number of extensions: 14
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: 351
Length of database: 314
Length adjustment: 28
Effective length of query: 323
Effective length of database: 286
Effective search space:    92378
Effective search space used:    92378
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 (21.6 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