GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Desulfovibrio vulgaris Miyazaki F

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate 8500849 DvMF_1587 ABC transporter related (RefSeq)

Query= reanno::Dino:3607124
         (338 letters)



>FitnessBrowser__Miya:8500849
          Length = 366

 Score =  204 bits (520), Expect = 2e-57
 Identities = 133/363 (36%), Positives = 189/363 (52%), Gaps = 37/363 (10%)

Query: 1   MAGIKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRI 60
           MA I +  I K YG    L  ++L +  GE    +GPSGCGK+ LLR +AG E   +G I
Sbjct: 1   MADITLAGIGKAYGAHAVLDGLSLTVNHGECFTLLGPSGCGKTVLLRLIAGFETPDAGTI 60

Query: 61  EIGGRDVTT------VEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERI 114
            IGG  V+       V P  RDL +VFQ YA++PHM+V +N+ + +K+ G     R  ++
Sbjct: 61  SIGGEPVSDAVTGDCVPPDARDLGVVFQDYAVWPHMSVADNIGYPLKLAGLPAAERTRQV 120

Query: 115 AEAARVLQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRV 174
            E   ++ L    +R P QLSGGQ+QRVA+ RA+V  PS+ L DEPL NLDA LR +MR 
Sbjct: 121 LETVEMVNLTGLENRMPSQLSGGQQQRVALARALVGRPSLMLLDEPLCNLDANLREEMRF 180

Query: 175 ELEGLHKQLGATMIYVTHDQVEAMTMADKIVVLNR-GRIEQVGSPMDLYHKPNSRFVAEF 233
           E++ L + LG T++YVTHDQ  A+ ++D++ +++  G I QVG+P +++ +P   FV  F
Sbjct: 181 EIKELQRTLGITILYVTHDQEIALAISDRLAIMDHAGAIRQVGTPWEIFERPADEFVFRF 240

Query: 234 IG----------SPAMNVFSSDV----GLQDISLDASAAFVGCRPEHIEIVPDGDGHIAA 279
           +G            AM     +     GL D   DA     G RP  + +   GDG +  
Sbjct: 241 MGVANFLPARRRGMAMLAAGGEQPVPWGLPD--GDAEHWMAGFRPSDVRLARQGDG-LRG 297

Query: 280 TVHVKERLGGESLLYLGLKGGGQIVARVGGDDETKVGAAVSLRFSR--------HRLHQF 331
           TV     LG  +   + + G     A      +T    A  L F+         H LH F
Sbjct: 298 TVRRASFLGAMTDYLIEVDG-----ASFRTQLDTHEALARGLMFAEGEPCVVGFHDLHWF 352

Query: 332 DEA 334
           D A
Sbjct: 353 DAA 355


Lambda     K      H
   0.320    0.139    0.396 

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: 312
Number of extensions: 15
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: 338
Length of database: 366
Length adjustment: 29
Effective length of query: 309
Effective length of database: 337
Effective search space:   104133
Effective search space used:   104133
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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