GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Desulfovibrio oxyclinae DSM 11498

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate WP_018123488.1 B149_RS0102020 ABC transporter ATP-binding protein

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



>NCBI__GCF_000375485.1:WP_018123488.1
          Length = 311

 Score =  167 bits (422), Expect = 4e-46
 Identities = 110/327 (33%), Positives = 160/327 (48%), Gaps = 35/327 (10%)

Query: 6   IDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRIEIGGR 65
           ++ + K Y     L D+   +E GE V  +GPSG GK+TLL+ +AGL+  +SGR+     
Sbjct: 5   VEGLTKTYEAAPVLEDVTFGMEKGEMVSIIGPSGAGKTTLLKLVAGLDRPTSGRV----- 59

Query: 66  DVTTVEPA-DRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARVLQLE 124
            +   EP+ +  + MVFQ Y L+P MTV EN+ FG++      D  + R+ E      L 
Sbjct: 60  -IFQNEPSRENPVIMVFQDYVLFPSMTVCENVAFGLRARRLSGDEVRRRVMEVLDYFGLV 118

Query: 125 DYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLHKQLG 184
              D  P  LSGGQRQRVAI R +V NP + L DEP +NLD  L++Q    +    +  G
Sbjct: 119 SKADAYPEHLSGGQRQRVAIARGLVVNPMMLLLDEPFANLDRNLKLQTAEFIRETQRNFG 178

Query: 185 ATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMNVFSS 244
            T + VTHD  EA  M+D+I ++  GR+ Q G   D+Y  P     A F+G   +NV   
Sbjct: 179 VTTLSVTHDLEEAFVMSDRIGLVMDGRLVQFGEARDVYFNPVHEDAARFLG--PLNVLEG 236

Query: 245 DVGLQDISLDASAAFVGC--------RPEHIEIVP--DGDGHIAATVHVKERLGGESLLY 294
           +V             +GC        RPE + + P  DG G +           G    Y
Sbjct: 237 EV----------LTLMGCEGTQRRAVRPESLLLHPREDGAGRVLCA-----DFAGHFTKY 281

Query: 295 LGLKGGGQIVARVGGDDETKVGAAVSL 321
           L ++ G  ++   G D   + G  V++
Sbjct: 282 L-VEVGDTVITVYGTDSALRHGDRVAI 307


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: 282
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: 338
Length of database: 311
Length adjustment: 28
Effective length of query: 310
Effective length of database: 283
Effective search space:    87730
Effective search space used:    87730
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: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. 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