GapMind for catabolism of small carbon sources

 

Alignments for a candidate for deoxyribonate-transport in Burkholderia phytofirmans PsJN

Align 2-deoxy-D-ribonate transporter 1 (characterized)
to candidate BPHYT_RS28245 BPHYT_RS28245 MFS transporter

Query= reanno::WCS417:GFF1429
         (438 letters)



>FitnessBrowser__BFirm:BPHYT_RS28245
          Length = 442

 Score =  324 bits (830), Expect = 4e-93
 Identities = 167/409 (40%), Positives = 243/409 (59%), Gaps = 5/409 (1%)

Query: 11  QALNKLMFVKLMPLLIIAYILSFLDRTNIALAKHHLDVDLGISAAAYGLGAGLFFLTYAL 70
           +A+N  +  +L+P L++ Y+L+FLDR NI  A+  L  D G+S AA+  GAG+FF+ YAL
Sbjct: 10  EAINSKVMRRLLPFLLLMYVLAFLDRANIGFAQKALQHDTGLSNAAFAFGAGVFFIGYAL 69

Query: 71  SEIPSNLIMHKVGARFWIARIMVTWGLISAAMAFVQGETSFYVLRLLLGIAEAGLFPGVM 130
            E+PSNL++H+VGAR W+ RIMVTWGL+SAAM      T+FY LR LLG+AEAG FPGV+
Sbjct: 70  FEVPSNLLLHRVGARVWMCRIMVTWGLVSAAMCLAHTPTAFYTLRFLLGVAEAGFFPGVI 129

Query: 131 LYLTYWFNREQRARATGYFLLGVCFANIIGGPVGAALMRMDGMLGWHGWQWMFMLEG-LP 189
            YLT+WF +  RARA G F  G   A I G P+  +L+ + G LG  GWQW+F++EG L 
Sbjct: 130 YYLTHWFPQSARARAVGVFYFGAPLAFIFGSPLSGSLLELHGALGLTGWQWLFLVEGALA 189

Query: 190 AVAFAWVVWRKLPDRPSKAPWLSAEEARGIEQRIAQETEEGAGEGGHSLKNWLTP-QILL 248
           +    W  W  L +RP  A WL  +E   +   + ++    +  G H +   L   ++LL
Sbjct: 190 SAVGVWAFW-YLDNRPEDARWLEPQERASLRAALDEDALLASAHGPHRILAALVDRRVLL 248

Query: 249 AIFVYFCHQITIYTVIFFLPSIISKY-GELSTMSVGLLTSLPWIAAALGALLIPRFATTP 307
              +Y   Q+++Y VIF+LP  ++ + G    + VGL+ +LPW+ A      +PR A   
Sbjct: 249 LSAIYLLIQMSVYGVIFYLPQQVAAFLGTTVGLRVGLVAALPWLCALAVTWYVPRRADRT 308

Query: 308 GRCRRLLVTGLLTMALGLGIAS-VSGPVFSLLGFCLSAVMFFVVQSIIFLYPASRLKGVA 366
           G  RR  V  L+   LG+G++  V  P+F LL  C +A  F   Q + + +P   L G A
Sbjct: 309 GEHRRWAVVLLIVAGLGIGVSGLVHSPLFGLLALCCAASGFIAAQPLFWTFPTRYLTGAA 368

Query: 367 LAGGLGFVNACGLLGGFVGPSVMGVIEQSTGNAMNGLKVIALVLVVAAL 415
            AGG+  +N+ G LGGF+ PS+    E +  +   GL V+ +  ++AAL
Sbjct: 369 AAGGIALINSLGGLGGFIAPSLRTAAEHAFASTSAGLVVLGVSSLLAAL 417


Lambda     K      H
   0.327    0.141    0.438 

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: 581
Number of extensions: 33
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: 438
Length of database: 442
Length adjustment: 32
Effective length of query: 406
Effective length of database: 410
Effective search space:   166460
Effective search space used:   166460
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 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 17 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