GapMind for catabolism of small carbon sources

 

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

Align Galactofuranose-binding protein YtfQ (characterized)
to candidate N515DRAFT_2412 N515DRAFT_2412 simple sugar transport system substrate-binding protein

Query= SwissProt::P39325
         (318 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2412
          Length = 319

 Score =  281 bits (720), Expect = 1e-80
 Identities = 154/312 (49%), Positives = 203/312 (65%), Gaps = 5/312 (1%)

Query: 5   LLIVSAVSAAMSSMALAAPLTVGFSQVGSESGWRAAETNVAKSEAEKRGITLKIADGQQK 64
           +L ++    +  +      +TVGFSQVG+ES WR A T   KS     G  LK +D QQK
Sbjct: 10  MLAIALAGCSRDAGKQVGQVTVGFSQVGAESEWRTANTASVKSALVAPGFDLKFSDAQQK 69

Query: 65  QENQIKAVRSFVAQGVDAIFIAPVVATGWEPVLKEAKDAEIPVFLLDRSIDVKDKSLYMT 124
           QENQIKA+RSF+AQ VD I  +PVV +GWEPVL+EAK A IPV L DR++ V D SLY +
Sbjct: 70  QENQIKALRSFIAQRVDVIAFSPVVESGWEPVLREAKAAGIPVVLTDRAVKVSDASLYAS 129

Query: 125 TVTADNILEGKLIGDWLVKEVNGK--PCNVVELQGTVGASVAIDRKKGFAEAIKNAPNIK 182
            + +D I EG+  G WL+++  GK  P  VVELQGTVG++ AIDR KGF E I   P  K
Sbjct: 130 LIGSDFIEEGRKAGRWLLQDSTGKPGPIRVVELQGTVGSAPAIDRMKGFHEVIDTDPRFK 189

Query: 183 IIRSQSGDFTRSKGKEVMESFIKAENNGKNICMVYAHNDDMVIGAIQAIKEAGLKPGKDI 242
           ++RSQSGDFTR+KGKEVME+F+KAE  G +I +++AHNDDM IGAIQAI+EAGL PGKDI
Sbjct: 190 LVRSQSGDFTRAKGKEVMEAFLKAE--GGHIDVLFAHNDDMAIGAIQAIEEAGLTPGKDI 247

Query: 243 LTGSIDGVPDIYKAMMDGEANASVELTPNMAGPAFDALEKYKKDGTMPEKLTLTKSTLYL 302
              SIDGV   ++AM  G+ NA++E  P         +        +P+++ + +  ++ 
Sbjct: 248 RIVSIDGVRGAFEAMKAGKLNATIECNPLFGAQLAQLIRDVHAGKPVPKRIVVEEG-VFT 306

Query: 303 PDTAKEELEKKK 314
            D A   L  +K
Sbjct: 307 QDQAAAALPGRK 318


Lambda     K      H
   0.313    0.130    0.363 

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: 265
Number of extensions: 10
Number of successful extensions: 3
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: 318
Length of database: 319
Length adjustment: 27
Effective length of query: 291
Effective length of database: 292
Effective search space:    84972
Effective search space used:    84972
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 48 (23.1 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