GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PfGW456L13_1897 in Desulfovibrio vulgaris Miyazaki F

Align ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized)
to candidate 8500851 DvMF_1589 ABC transporter related (RefSeq)

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1897
         (386 letters)



>FitnessBrowser__Miya:8500851
          Length = 354

 Score =  204 bits (518), Expect = 4e-57
 Identities = 122/313 (38%), Positives = 175/313 (55%), Gaps = 14/313 (4%)

Query: 1   MATLELRNVNKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGG 60
           M+ + L NV K +G      + ++ L+I  GE   ++GPSGCGK+T +  +AG E +  G
Sbjct: 1   MSYVRLVNVTKRFGG--VTAVDSLNLEIGRGECFSMLGPSGCGKTTTLRMVAGFEDLDDG 58

Query: 61  AILVDDADISG------MSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDE 114
            I V D  +S       + P+ RD  MVFQ++A++P +SV +N+AF L+IR++  AEID 
Sbjct: 59  EIHVGDRLLSARRNNYYLPPEKRDFGMVFQAFAVWPHLSVYENVAFPLRIRRLSAAEIDR 118

Query: 115 EVARVSKLLQIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEM 174
                     +  +  + P  LSGG +QRVA+ RALA  P + L DEPLS+LD  LR EM
Sbjct: 119 RTREALHHTSLADVAQKSPDDLSGGGKQRVALARALAINPDVMLLDEPLSSLDPHLREEM 178

Query: 175 RTEMKLMHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVAS 234
           R E+K + +    + +YVTHDQ EAM L D++ VM++G++QQ GTP D+Y NPAN FV  
Sbjct: 179 RFEIKDLQRTFGFSILYVTHDQSEAMALSDRIMVMRNGVVQQVGTPLDVYTNPANSFVFG 238

Query: 235 FIGSPPMNFIPLRLQRKDGRLLALLDSGQARCELPLGMQDAGLEDREVILGIRPEQI-IL 293
           FIG    NF+ + L  +    L  ++ G AR           +      L  RP +I   
Sbjct: 239 FIGL--SNFLDVNLTPEG---LVRVNGGDARVTPATPPSARLVSAGRAALASRPSEIDFT 293

Query: 294 ANGEANGLPTIRA 306
           A G   G+   RA
Sbjct: 294 AEGGLRGVVRRRA 306


Lambda     K      H
   0.319    0.138    0.393 

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: 334
Number of extensions: 12
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: 386
Length of database: 354
Length adjustment: 30
Effective length of query: 356
Effective length of database: 324
Effective search space:   115344
Effective search space used:   115344
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 (21.7 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