GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11885 in Acidovorax sp. GW101-3H11

Align Rhizopine-binding protein (characterized, see rationale)
to candidate Ac3H11_611 Putative sugar ABC transport system, periplasmic binding protein YtfQ precursor

Query= uniprot:A0A0N9WNI6
         (308 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_611
          Length = 322

 Score =  127 bits (318), Expect = 5e-34
 Identities = 94/303 (31%), Positives = 158/303 (52%), Gaps = 15/303 (4%)

Query: 8   ASLALSLMLASGA-ALADLRIGVSMSQFDDTWLTYLRESMDKQAKSMPDGVKLQFEDARS 66
           AS+ ++ +L S A A   L +G S    +  W T   ES+   AK    G++L+F DA+ 
Sbjct: 14  ASVPVAALLPSTAWAQKPLVLGFSQVGAESEWRTANTESIKSAAKEA--GIELKFSDAQQ 71

Query: 67  DVVKQLSQVESFISQKVDAIVVNPVDTAATRKITEAAVKAGIPLVYVNRRPDDLKLPKGV 126
               Q+  + SFI+QKVD I  +PV  +    +   A  A IP+V  +R  +       V
Sbjct: 72  KQENQIKAIRSFIAQKVDVIAFSPVVESGWEPVLREAKAAKIPVVLTDRAVNTKDTSLYV 131

Query: 127 ITVASNDLEAGQMQMQYLAEKM---KGKGDIVILLGDLANNSTTNRTKGVKEVLAKYPGI 183
             + S+ +E G+   ++L EKM   KG+ +IV L G + +    +R KG +E++   P  
Sbjct: 132 TFMGSDFVEEGRKAGRWLVEKMKDQKGEVNIVELQGTVGSAPAIDRKKGFEEIIKADPKF 191

Query: 184 KIDQEQTGTWSRDKGMTLVNDWL-TQGRKFDAIVSNNDEMAIGAAMALKQAGVEKG-SVL 241
           KI + QTG ++R KG  ++  +L  +G+K + + ++ND+MAIGA  A+++AG++    ++
Sbjct: 192 KIIRSQTGDFTRAKGKEVMEAFLKAEGKKINVLYAHNDDMAIGAIQAIEEAGMKPAKDIV 251

Query: 242 IAGVDGTPDGLRAVKKGDLAVSVFQDANGQAVDSIDAAVKMAKNEPVEQAVWVPYRLITP 301
           I  +D       A+  G L VSV  + +      + AAVK      ++    VP R++T 
Sbjct: 252 IISIDAVKGAFEAMIAGKLNVSV--ECSPLLGPQLMAAVK-----DIKAGKAVPKRIVTE 304

Query: 302 ENV 304
           E +
Sbjct: 305 EGI 307


Lambda     K      H
   0.315    0.130    0.360 

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: 223
Number of extensions: 12
Number of successful extensions: 2
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: 308
Length of database: 322
Length adjustment: 27
Effective length of query: 281
Effective length of database: 295
Effective search space:    82895
Effective search space used:    82895
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.5 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