GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Cereibacter sphaeroides ATCC 17029

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate WP_011840164.1 RSPH17029_RS00495 ABC transporter ATP-binding protein

Query= uniprot:A8LLL2
         (373 letters)



>NCBI__GCF_000015985.1:WP_011840164.1
          Length = 367

 Score =  322 bits (825), Expect = 1e-92
 Identities = 184/363 (50%), Positives = 243/363 (66%), Gaps = 12/363 (3%)

Query: 1   MADLKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTL 60
           MA L++  + K++    VL +I+L I++GE +VFVGPSGCGKSTLLRMI GLE  T GT+
Sbjct: 1   MAFLEIRSLCKSFESYPVLKDIDLSIEKGEFVVFVGPSGCGKSTLLRMITGLETPTSGTI 60

Query: 61  EIDGTVVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALKIAKKSQAEIDAAVEAAAEK 120
            I+  V+NDV PA+RG AMVFQSYALYPHMTV +N+SF L++++K +A I   VE AA  
Sbjct: 61  AIEDEVINDVDPARRGTAMVFQSYALYPHMTVFQNISFGLRMSRKPKALIRERVEKAAAI 120

Query: 121 LQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLK 180
           L+L + LDR P  LSGGQ+QRVAIGR+IVR+P+V+LFDEPLSNLDA LRV  R E+ +L 
Sbjct: 121 LRLDKLLDRKPAQLSGGQKQRVAIGRAIVREPRVFLFDEPLSNLDAELRVQMRAELLELH 180

Query: 181 EAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSPKM 240
           E +  +TM+YVTHDQVEAMTLA ++VV++GG I Q G PL+LY+ P+N FVA F+GSPKM
Sbjct: 181 ERL-GTTMIYVTHDQVEAMTLADKMVVMSGGRIQQYGRPLDLYDDPDNRFVAGFVGSPKM 239

Query: 241 NLLPGKIIGTGAQ-TTVEMTDGGRAVSDYPSDDSLM-GAAVNVGVRPEDM----VEAAPG 294
           N L   +   GA     ++  GG A    P  +SL  GA +++G+RPE +       AP 
Sbjct: 240 NFLSATVTSAGADGLRADLAAGGAAA--LPLIESLAPGARIDIGIRPEQLSVVPAGQAPS 297

Query: 295 GDYV-FEGKVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVTRLTAEPAKVHV 353
            D V   G+VA+ E LG  + L+      +D  IG     H    G+  R+ A  + V V
Sbjct: 298 ADAVSVAGRVALIEDLGAESYLHLHL--ADDSRIGVRTARHAAHLGEEVRVAAPASGVLV 355

Query: 354 FKD 356
           F +
Sbjct: 356 FDE 358


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: 419
Number of extensions: 22
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: 367
Length adjustment: 30
Effective length of query: 343
Effective length of database: 337
Effective search space:   115591
Effective search space used:   115591
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 10 2024. 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