GapMind for catabolism of small carbon sources

 

Aligments for a candidate for deoxyribonate-transport in Herbaspirillum seropedicae SmR1

Align 2-deoxy-D-ribonate transporter 1 (characterized)
to candidate HSERO_RS11250 HSERO_RS11250 MFS transporter

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



>FitnessBrowser__HerbieS:HSERO_RS11250
          Length = 435

 Score =  296 bits (758), Expect = 9e-85
 Identities = 160/404 (39%), Positives = 235/404 (58%), Gaps = 5/404 (1%)

Query: 20  KLMPLLIIAYILSFLDRTNIALAKHHLDVDLGISAAAYGLGAGLFFLTYALSEIPSNLIM 79
           +L+PLL + Y+ S+LDR N+  AK  +  DL  S   YGLGAG+FFL Y + E+PSN+I+
Sbjct: 27  RLLPLLFLCYVASYLDRVNVGFAKLQMLQDLKFSDTVYGLGAGIFFLGYFVFEVPSNMIL 86

Query: 80  HKVGARFWIARIMVTWGLISAAMAFVQGETSFYVLRLLLGIAEAGLFPGVMLYLTYWFNR 139
           HKVGAR WIARIM+TWG+IS AMA+V     FY++R LLG+AEAG FPGV+LYLTYW+  
Sbjct: 87  HKVGARLWIARIMITWGIISGAMAYVTTPEMFYIMRFLLGVAEAGFFPGVILYLTYWYPA 146

Query: 140 EQRARATGYFLLGVCFANIIGGPVGAALMR-MDGMLGWHGWQWMFMLEGLPAVAFAWVVW 198
            +R + T  F+ G+  + +IGGP+   +M  M G+ G  GWQWMF+LE +P++    +V 
Sbjct: 147 ARRGKITALFMTGIALSGVIGGPLSGWIMHAMPGVWGHTGWQWMFILEAIPSLILGVMVI 206

Query: 199 RKLPDRPSKAPWLSAEEARGIEQRIAQETEEGAGEGGHSLKNWLTPQILLAIFVYFCHQI 258
             + DR   A WLS EE R +E  I+   EE   E       +   ++ L   +YFC  +
Sbjct: 207 LYMKDRIRDADWLSEEEKRLLEANISH--EESQKEHLSLGAMFANGRVWLGALIYFCFVM 264

Query: 259 TIYTVIFFLPSIISKYGELSTMSVGLLTSLPWIAAALGALLIPRFATTPGRCRRLLVTGL 318
            +Y V F+LP+II   G    ++VGLLT++P+  AA   +LI R A      R  +    
Sbjct: 265 GLYGVSFWLPTIIKATGVSDPLNVGLLTAIPYAFAAAAMVLIGRSADARRERRWHVAIPA 324

Query: 319 LTMALGLGIASVSG--PVFSLLGFCLSAVMFFVVQSIIFLYPASRLKGVALAGGLGFVNA 376
               +GL +++  G     ++    L++V       + +  P + L G A A G+  +N+
Sbjct: 325 FIGCIGLLLSTQYGHNTTLAMASLTLASVGILTTLPLFWSLPTAFLSGTAAAAGIALINS 384

Query: 377 CGLLGGFVGPSVMGVIEQSTGNAMNGLKVIALVLVVAALAALRL 420
            G L GFV P ++G ++ +T +   G+ V+A  LV+  L  L L
Sbjct: 385 LGNLAGFVSPFLVGWLKDATQSTNAGMYVLAASLVIGGLLTLTL 428


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: 597
Number of extensions: 23
Number of successful extensions: 5
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: 435
Length adjustment: 32
Effective length of query: 406
Effective length of database: 403
Effective search space:   163618
Effective search space used:   163618
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.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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