GapMind for catabolism of small carbon sources

 

Aligments for a candidate for deoxyribonate-transport in Dyella japonica UNC79MFTsu3.2

Align 2-deoxy-D-ribonate transporter 1 (characterized)
to candidate N515DRAFT_2085 N515DRAFT_2085 Sugar phosphate permease

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



>FitnessBrowser__Dyella79:N515DRAFT_2085
          Length = 434

 Score =  291 bits (744), Expect = 4e-83
 Identities = 158/413 (38%), Positives = 237/413 (57%), Gaps = 5/413 (1%)

Query: 19  VKLMPLLIIAYILSFLDRTNIALAKHHLDVDLGISAAAYGLGAGLFFLTYALSEIPSNLI 78
           ++L+P L I Y+ ++LDR NI  AK  +  DL  S A YGLGAG+FF+ Y L E+PSN++
Sbjct: 21  LRLLPFLFICYVAAYLDRVNIGFAKLQMLSDLHFSEAVYGLGAGVFFIGYFLFEVPSNML 80

Query: 79  MHKVGARFWIARIMVTWGLISAAMAFVQGETSFYVLRLLLGIAEAGLFPGVMLYLTYWFN 138
           +H++GAR WI+RIMV+W L+SAA   V   T+FYVLR LLG+AEAG FPG++LYLTYW+ 
Sbjct: 81  LHRLGARLWISRIMVSWALVSAATMLVTTPTAFYVLRFLLGVAEAGFFPGIVLYLTYWYP 140

Query: 139 REQRARATGYFLLGVCFANIIGGPVGAALMR-MDGMLGWHGWQWMFMLEGLPAVAFAWVV 197
             +R R    F+ G+  A ++GGP+   +M    G+ G   WQW+F+LE LP++A     
Sbjct: 141 SARRGRMNALFMTGIPIAGVLGGPLSGWIMHAFGGVHGLANWQWLFLLEALPSLALGIAT 200

Query: 198 WRKLPDRPSKAPWLSAEEARGIEQRIAQETEEGAGEGGHSLKNWLTPQILLAIFVYFCHQ 257
              LP+    A WL A E + +E R+A + + G+     S+   +    L AI  YFC  
Sbjct: 201 PFVLPNGIRSASWLDAREKQLLEDRLAGDPQAGSEASLRSVMADVRVWRLAAI--YFCCM 258

Query: 258 ITIYTVIFFLPSIISKYGELSTMSVGLLTSLPWIAAALGALLIPRFATTPGRCRRLLVTG 317
           + +Y V F+LP++I+  G    + VGLLT++P+  A +  +L+ R +      R  L   
Sbjct: 259 MGLYGVSFYLPTLIAAAGVDDALDVGLLTAIPYAVAVVSMILLARSSDRHNERRWHLAAA 318

Query: 318 LLTMALGLGIASVSGP--VFSLLGFCLSAVMFFVVQSIIFLYPASRLKGVALAGGLGFVN 375
            +  A GL  +++ G   V  L+   L          + + +P+S L G A A G+  +N
Sbjct: 319 SIAGAAGLYASTLCGSELVLGLIALSLGTAGVLSTMPVFWTWPSSVLAGTAAAAGIAMIN 378

Query: 376 ACGLLGGFVGPSVMGVIEQSTGNAMNGLKVIALVLVVAALAALRLRMGHEPER 428
           + G L GFV PS++G ++  T +   GL V+A+ L++ A  AL       P R
Sbjct: 379 SIGNLAGFVSPSIIGWMKDLTHSTNAGLWVVAVALLLGAALALLGSAAKAPAR 431


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: 559
Number of extensions: 28
Number of successful extensions: 6
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: 434
Length adjustment: 32
Effective length of query: 406
Effective length of database: 402
Effective search space:   163212
Effective search space used:   163212
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 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