GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03635 in Klebsiella michiganensis M5al

Align ABC-type sugar transport system, periplasmic component protein (characterized, see rationale)
to candidate BWI76_RS14855 BWI76_RS14855 periplasmic binding protein/LacI transcriptional regulator

Query= uniprot:D8IZC6
         (316 letters)



>FitnessBrowser__Koxy:BWI76_RS14855
          Length = 317

 Score =  226 bits (575), Expect = 7e-64
 Identities = 118/315 (37%), Positives = 191/315 (60%), Gaps = 8/315 (2%)

Query: 3   KNTIAIACSTLL-----LAAAAQPAMAADKPLKSVGVTVGDLANPFFVAIAKGAESGAHK 57
           K  +AIA + ++     LA AA  A    K +  +G+ V D++NPFF A+ + A+  A K
Sbjct: 6   KAWLAIAVAAVITTMTGLAPAASAAPQESKKIARIGLMVQDMSNPFFSAMERNAKQAAAK 65

Query: 58  INPDAKVTVVSSKYDLNTQVGQIENFIANKVDLIVLNAADSKGVGPAVKKAQKAGIVVVA 117
           I   A + V  ++ DL  Q  QI+ FI  KVDLI+++A D  G+ PA+++A+ AGI+V+A
Sbjct: 66  IG--ATLNVQDAQVDLANQNTQIDAFIQQKVDLIIISAVDESGIEPAIQRAKAAGIIVIA 123

Query: 118 VDVAAAGADVTVMSDNTMAGAESCKFLAEKLQGKGNVVIVNGPPVSAVMDRVTGCKAEFK 177
           VD  A GAD  +M++   AG  SC++L  ++ GKG V++V+G P+  ++DR+ GCK   +
Sbjct: 124 VDTPAKGADAAIMTNAIQAGETSCEYLFSQMGGKGKVLLVDGTPIQTIIDRIKGCKNVAQ 183

Query: 178 KSPGIKILSDNQNAGGSRDGGMTTMSNLLAAQPKIDAVFAINDPTAIGAELAIRQAKRSD 237
           K P IKI+   Q +   R  G+   +++L A P +  +F +NDP+A+GA LA+ QA ++ 
Sbjct: 184 KYPDIKIVG-QQASRNDRASGLMVTTDMLTANPDVSGIFGMNDPSALGAVLAVEQAGKAG 242

Query: 238 IKWISGVDGAPDAERALKDSKSLFAASPAQDPYGMAAESVAIGYAVMNGRAPQQKVKLLP 297
              ++GVDG+P+A   LK   S F  +  Q+P  M  +++++   +++G+    +  L+P
Sbjct: 243 AINVTGVDGSPEAVEELKRGGSPFIGTATQNPGEMVRQAISLAQDMVDGKPIASRTVLIP 302

Query: 298 VKLITRDNVADYQGW 312
             L+TRDNV  Y GW
Sbjct: 303 SVLVTRDNVGSYPGW 317


Lambda     K      H
   0.314    0.129    0.360 

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: 255
Number of extensions: 9
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: 316
Length of database: 317
Length adjustment: 27
Effective length of query: 289
Effective length of database: 290
Effective search space:    83810
Effective search space used:    83810
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 48 (23.1 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