GapMind for catabolism of small carbon sources

 

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

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate WP_035129644.1 Q763_RS00100 ATP-binding cassette domain-containing protein

Query= uniprot:A8LLL2
         (373 letters)



>NCBI__GCF_000769915.1:WP_035129644.1
          Length = 267

 Score =  114 bits (285), Expect = 3e-30
 Identities = 73/243 (30%), Positives = 125/243 (51%), Gaps = 8/243 (3%)

Query: 4   LKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTLEID 63
           +++  +EK++GD KVL  I+   + G+  + +G SG GK+ +L+ + G+     G++  D
Sbjct: 2   IEIKDIEKSFGDTKVLKGISTTFETGKTNLIIGRSGSGKTVMLKTLLGIHTPEKGSISFD 61

Query: 64  GTVVNDVPPAQR-----GIAMVFQSYALYPHMTVRENMSFALKI-AKKSQAEIDAAVEAA 117
           G + +++   ++      I MVFQ  AL+  M V +N++F LK+   K   EI   V   
Sbjct: 62  GRIYSELTRDEKRSLRTEIGMVFQGSALFDSMNVEDNVAFPLKMFTNKRGREIKDRVNEV 121

Query: 118 AEKLQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIA 177
            E++ L     + P  +SGG ++RVAI R+IV +PK    DEP S LD    +    E+ 
Sbjct: 122 LERVNLVDANYKFPNEISGGMQKRVAIARAIVNNPKYLFCDEPNSGLDPETSILID-ELI 180

Query: 178 QLKEAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGS 237
           Q      + T V  THD    + +  +IV L  G     G+  ++ E   N+ + +F+ S
Sbjct: 181 QEITREYDMTTVINTHDMNSVLQIGEKIVFLKNGIKEWEGTNEQILE-TRNKSIVEFVYS 239

Query: 238 PKM 240
            ++
Sbjct: 240 SEL 242



 Score = 24.6 bits (52), Expect = 0.003
 Identities = 15/54 (27%), Positives = 27/54 (50%), Gaps = 1/54 (1%)

Query: 289 VEAAPGGDYVFEGKVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVT 342
           +E + G   V +G ++ T   G+  L+   + SG+   +  L GIH   KG ++
Sbjct: 7   IEKSFGDTKVLKG-ISTTFETGKTNLIIGRSGSGKTVMLKTLLGIHTPEKGSIS 59


Lambda     K      H
   0.316    0.135    0.379 

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: 206
Number of extensions: 10
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 373
Length of database: 267
Length adjustment: 27
Effective length of query: 346
Effective length of database: 240
Effective search space:    83040
Effective search space used:    83040
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: 48 (23.1 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