GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK' in Methylocystis bryophila S285

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate WP_245300279.1 B1812_RS18275 sulfate/molybdate ABC transporter ATP-binding protein

Query= uniprot:A8LLL2
         (373 letters)



>NCBI__GCF_002117405.1:WP_245300279.1
          Length = 353

 Score =  181 bits (459), Expect = 3e-50
 Identities = 113/300 (37%), Positives = 165/300 (55%), Gaps = 11/300 (3%)

Query: 6   LTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTLEIDGT 65
           + GVE  +G    L +++LDI  GEL+  +GPSG GK+TLLR+IAGL     G +  D  
Sbjct: 1   MEGVELDFGSYPALRDVSLDIAGGELVALLGPSGSGKTTLLRVIAGLNSPHRGAVFFDAL 60

Query: 66  VVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALK----IAKKSQAEIDAAVEAAAEKL 121
               +   +R +  VFQ+YAL+ HM+V +N++F LK     ++  + EI A V    E +
Sbjct: 61  NATSLSVQERRVGFVFQNYALFKHMSVADNVAFGLKARPRASRPPKREIAARVAELLELV 120

Query: 122 QLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLKE 181
           QL     R P  LSGGQRQRVA+ R++  +P+V L DEP   LDA +R   R  + ++ +
Sbjct: 121 QLEGLGQRYPAQLSGGQRQRVALARALAIEPRVLLLDEPFGALDARVRKDLRRWLREIHK 180

Query: 182 AMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSP--- 238
               +T V+VTHDQ EAM LA R+VVL  G I Q GSP  LY++P + FV  F+G     
Sbjct: 181 RTGLTT-VFVTHDQDEAMELADRVVVLNQGRIEQAGSPAALYDRPASAFVLSFVGEAVAL 239

Query: 239 KMNLLPGKIIGTGAQTTVE---MTDGGRAVSDYPSDDSLMGAAVNVGVRPEDMVEAAPGG 295
            + +  G +   G +  V+   + DG   V   P+D ++ GA  +      + +   P G
Sbjct: 240 PVTVKQGHVSLGGRELHVDAHNLRDGQARVFFRPADIAIAGAGPSALEGRVEALRRTPSG 299


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: 334
Number of extensions: 17
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: 373
Length of database: 353
Length adjustment: 29
Effective length of query: 344
Effective length of database: 324
Effective search space:   111456
Effective search space used:   111456
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 Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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