GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK' in Klebsiella michiganensis M5al

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate BWI76_RS17830 BWI76_RS17830 ABC transporter ATP-binding protein

Query= uniprot:A8LLL2
         (373 letters)



>FitnessBrowser__Koxy:BWI76_RS17830
          Length = 364

 Score =  300 bits (769), Expect = 3e-86
 Identities = 177/361 (49%), Positives = 225/361 (62%), Gaps = 18/361 (4%)

Query: 1   MADLKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTL 60
           M  + L  V K+YGD  V+ +++L I  GE  V VGPSGCGKSTLLRMIAGLE+I+GG +
Sbjct: 1   MGSVVLNSVRKSYGDAHVIKDVSLTIPDGEFCVLVGPSGCGKSTLLRMIAGLEEISGGEV 60

Query: 61  EIDGTVVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALKIAKKSQAEIDAAVEAAAEK 120
            I+   V +V P  R IAMVFQSYALYP MTVRENM FALK+AK  +AEI+  V  AA  
Sbjct: 61  HINERNVTEVEPKLRDIAMVFQSYALYPQMTVRENMGFALKMAKLPKAEINQKVNEAAAL 120

Query: 121 LQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLK 180
           L L   L+RLPK LSGGQRQRVA+GR+IVR P+V+LFDEPLSNLDA LR   R EI +L 
Sbjct: 121 LGLEPLLERLPKDLSGGQRQRVAMGRAIVRKPQVFLFDEPLSNLDAKLRTQVRGEIRELH 180

Query: 181 EAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSPKM 240
             + ++T VYVTHDQ+EAMT+   IVVL  G I Q G+PLELY++P N FVA FIGSP++
Sbjct: 181 RRL-KTTSVYVTHDQIEAMTMGQMIVVLRDGRIEQAGTPLELYDRPANLFVAGFIGSPEI 239

Query: 241 NLLPGKIIGTGAQTTVEMTDG-------GRAVSDYPSDDSLMGAAVNVGVRPEDMVEAAP 293
           N LPG+++  G  T++ + DG       G  V+D        G  V   +RPE +     
Sbjct: 240 NQLPGEVVLNGNATSLRLKDGSLLALPAGLRVTD--------GQQVVYAIRPEQVNVVHE 291

Query: 294 GGDYVFEGKVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVTRLTAEPAKVHV 353
             D     KV   E  G    L+ +   G   ++ K +   K+  G    L  + + VH+
Sbjct: 292 ARDDALAAKVTAVENTGSDMQLFCDTGGGAFTSVFKQRLAVKE--GDKIWLQPKLSGVHL 349

Query: 354 F 354
           F
Sbjct: 350 F 350


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: 424
Number of extensions: 25
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: 364
Length adjustment: 30
Effective length of query: 343
Effective length of database: 334
Effective search space:   114562
Effective search space used:   114562
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 17 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