GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03645 in Dyella japonica UNC79MFTsu3.2

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate N515DRAFT_2414 N515DRAFT_2414 simple sugar transport system permease protein

Query= uniprot:D8IZC8
         (344 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2414
          Length = 358

 Score =  142 bits (359), Expect = 1e-38
 Identities = 114/330 (34%), Positives = 173/330 (52%), Gaps = 21/330 (6%)

Query: 20  SSSTTAQW-------LLHRLGMLPVLVVLYLLFYGLTLYLSGDGTSNFASAE---NTMNI 69
           SS+ +++W       L H L  L  L+ L LL  G  L+  G     +       N ++I
Sbjct: 11  SSAISSRWGRGLRRCLAHPL--LWPLLTLILLLAGNGLFNPGFLALQWRDGHLYGNLIDI 68

Query: 70  LRQVAINLVLAAGMTFVILTAGIDLSVGSVLAVSAV-----LGMQVSLGAAPGW-AIPMF 123
             + A   +++ GMT VI   G+D+SVG+VLA++A      +G   + G  P W AI   
Sbjct: 69  AHRAAPLALVSLGMTLVIALRGLDISVGAVLAIAATVAAWTIGHVSNDGLLPLWLAIAAA 128

Query: 124 IFSGLVMGMVNGAMVALLNINAFVVTLGTMTAFRGAAYLLADGTTVLNNDIPSFEWIGNG 183
           + +G + G+ NG +V    +   V TL  M A RG A  ++ G  +L      + ++GNG
Sbjct: 129 LAAGALCGLWNGWLVVGAGMQPIVATLILMVAGRGIAQSISGGQ-ILTLYYAPYSFLGNG 187

Query: 184 DFLHVPWLIWVAVAVVLLSWVILRKTVLGMHIYAIGGNLQAARLTGIRVGLVLLFVYSIS 243
             L +P+ ++V  AV  L  + LRKT LG+ + AIG N QAA + G+R   + L  Y   
Sbjct: 188 FVLGLPFSLFVVAAVFALLQLALRKTALGLFVRAIGHNPQAAHVAGVRARAITLGAYVFC 247

Query: 244 GLFSGLAGAMSASRLYGAN-GNWGSGYELDAIAAVVLGGTSLMGGVGSIWGTVVGALIIG 302
           G+ + LAG + +S +  A+  N G   ELDAI AV LGG+ L GG  S+ G+++GALII 
Sbjct: 248 GIAAALAGLLVSSNVNSADANNAGLLLELDAILAVALGGSLLGGGRFSLAGSLLGALIIQ 307

Query: 303 VMNNGLTILGLSSFWQYVAKGAVIVLAVIL 332
            +   +  +G+        K AV+V AV+L
Sbjct: 308 ALTTTIYAIGVPPQVNLAVK-AVLVFAVML 336


Lambda     K      H
   0.324    0.138    0.417 

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: 312
Number of extensions: 16
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 344
Length of database: 358
Length adjustment: 29
Effective length of query: 315
Effective length of database: 329
Effective search space:   103635
Effective search space used:   103635
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 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