GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK' in Brucella inopinata BO1

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate WP_008510722.1 BIBO1_RS17945 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:A8LLL2
         (373 letters)



>NCBI__GCF_000182725.1:WP_008510722.1
          Length = 350

 Score =  297 bits (761), Expect = 3e-85
 Identities = 171/360 (47%), Positives = 222/360 (61%), Gaps = 24/360 (6%)

Query: 1   MADLKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTL 60
           M ++ L G+ K +G + VL  I+L+I  GE +V VGPSGCGKSTLLRM+AGLE I+GG L
Sbjct: 1   MKEVSLRGITKTFGQLTVLDRIDLEIHSGEFLVLVGPSGCGKSTLLRMVAGLEPISGGDL 60

Query: 61  EIDGTVVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALKIAKKSQAEIDAAVEAAAEK 120
            I G   N++ P +R IAMVFQSYAL+PHMT REN+ F  +I  +  AE  A V+ AA  
Sbjct: 61  VIGGERANELAPQKRNIAMVFQSYALFPHMTARENIGFGPRIRGEKAAETAAKVDHAASI 120

Query: 121 LQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLK 180
           L L  YLDR P+ LSGGQRQRVA+GR+IVR+P V+LFDEPLSNLDA LRV  R EI  L 
Sbjct: 121 LNLHSYLDRYPRQLSGGQRQRVAMGRAIVREPSVFLFDEPLSNLDAQLRVQMRTEIKALH 180

Query: 181 EAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSPKM 240
           + + +ST++YVTHDQ+EAMT+A RIVV+  G I Q+G+PL+LY++P N+FVA FIGSP M
Sbjct: 181 QRL-KSTVIYVTHDQIEAMTMADRIVVMNQGKIQQIGAPLDLYDRPANKFVAGFIGSPSM 239

Query: 241 NLLPGKI------IGTGAQTTVEMTDGGRAVSDYPSDDSLMGAAVNVGVRPEDMVEAAPG 294
           + +PG +       G G +  V     G               A   G+RPE+ V A  G
Sbjct: 240 SFIPGTVADGFFCTGEGEKIAVSAAAKG-------------ARAAEAGIRPENFVIAREG 286

Query: 295 GDYVFEGKVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVTRLTAEPAKVHVF 354
                   V + E  G  T +Y    +GE       + IH    G+   +TA    +H+F
Sbjct: 287 AGLTL--VVEVIEPTGPETHIYGRI-AGEPVRAVFRERIHL-APGEQVPVTAGSEHIHLF 342


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: 393
Number of extensions: 23
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: 373
Length of database: 350
Length adjustment: 29
Effective length of query: 344
Effective length of database: 321
Effective search space:   110424
Effective search space used:   110424
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: 49 (23.5 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