GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galactonolactonase in Flavobacterium beibuense F44-8

Align D-galactono-lactonase (EC 3.1.1.-) (characterized)
to candidate WP_052123248.1 Q763_RS05865 lactonase family protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3314
         (389 letters)



>NCBI__GCF_000769915.1:WP_052123248.1
          Length = 370

 Score =  214 bits (544), Expect = 4e-60
 Identities = 129/371 (34%), Positives = 203/371 (54%), Gaps = 20/371 (5%)

Query: 18  VQVASAEDYQLLVGSYT-AGQSQGIYRLAFDSRTGQ--IDASPLQVIKSANPSWLTLSKD 74
           + + + ++Y L++G+YT A +S+GIY   F+++TG+  + +S   VI   NPS++T+S D
Sbjct: 13  ISLHAQDNYNLIIGTYTNACESEGIYVYDFNTKTGEATLKSSSQGVI---NPSYVTVSAD 69

Query: 75  QRHLFVVNENGPGQTDPVGRVSSFAIDPKTHALSLISQVQSLGNEPTHSSLSIDGSHLFV 134
            + L+ VNENG   T     VS+F     +  +  I++  S G +P +  +  D  H+ V
Sbjct: 70  NKFLYSVNENGEEST-----VSAFNYMASSGKIEFINKKDSKGADPCY--IINDDKHVIV 122

Query: 135 SNYSVAEDPGGTLAVLPVAADGKLKAVVQMSSHPASRVNPERQASAHVHSTIPSPDGRYV 194
           +NY+     GGT+AV      G L    Q+  H  S +N +RQ   HVH    SPD  Y+
Sbjct: 123 ANYT-----GGTIAVFAKDKHGGLTKAKQVVKHSGSSINKDRQEGPHVHMVYFSPDKNYI 177

Query: 195 FANDLGADKVFAYRFDPKANPELPLTPATPAFVQLPPGSGPRHLLFSADGKHAWLTMEMS 254
           FANDLG DK+  Y+++  A     +       V++  GSGPRHL+FS +    ++  E+ 
Sbjct: 178 FANDLGTDKISVYKYNKNATDGSKVLTLADT-VEVKKGSGPRHLVFSPNNVFFYVLQELD 236

Query: 255 AQVAVFDYHDGQLEQTQMVDLAAGQPVSDKAAAALHASADGKFLYVSNRGTANQLLVFAI 314
             +  F Y  G++E+ Q   +          AA +H S DGKFLY +NRG AN + VF +
Sbjct: 237 GTLTAFSYVKGKIEKIQESTIVTPYFTGQTGAADIHISHDGKFLYATNRGDANTISVFRV 296

Query: 315 DPATGHLSELQRRAVEGDHPREFSLDPSGKFLLIANQKSNQIVVVERDARTGLLGKTVQK 374
             A G ++ +Q+   EG  PR F+  P   +LL+ANQ SN +++ +RD  TG+L  T + 
Sbjct: 297 H-ANGKVNLVQQATTEGIGPRNFTFGPKEDYLLVANQISNDVIIFKRDRTTGMLTDTEKC 355

Query: 375 LPMDAPSDLRF 385
           + + +P  L F
Sbjct: 356 IELCSPVCLVF 366


Lambda     K      H
   0.316    0.132    0.382 

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: 372
Number of extensions: 22
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: 389
Length of database: 370
Length adjustment: 30
Effective length of query: 359
Effective length of database: 340
Effective search space:   122060
Effective search space used:   122060
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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