GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdA in Klebsiella michiganensis M5al

Align 2-keto-isovalerate dehydrogenase component α subunit (EC 1.2.4.4) (characterized)
to candidate BWI76_RS14160 BWI76_RS14160 ABC transporter substrate-binding protein

Query= metacyc::MONOMER-11683
         (330 letters)



>FitnessBrowser__Koxy:BWI76_RS14160
          Length = 320

 Score =  142 bits (358), Expect = 1e-38
 Identities = 110/321 (34%), Positives = 156/321 (48%), Gaps = 9/321 (2%)

Query: 11  LTDQEAVDMYRTMLLARKIDERMWLLNRSGKIP-FVISCQGQEAAQVGAAFALDREMDYV 69
           L  Q  +  YR M   R  +ER+   N SG IP F+    G+EA  VG    L    D++
Sbjct: 3   LNKQALLQAYRKMREIRTFEERLHQENTSGDIPGFIHLYTGEEAIAVGVCENLTNA-DFI 61

Query: 70  LPYYRDMGVVLAFGMTAKDLMMSGFAKAADPNSG-GRQMPGHFGQKKNRIVTGSSPVTTQ 128
              +R  G  +A G     +M   F K +    G G  M  H       ++  ++ V   
Sbjct: 62  GSTHRGHGHCIAKGCDIHGMMAEIFGKDSGLCRGKGGSM--HIADLSKGMLGANAIVGGA 119

Query: 129 VPHAVGIALAGRMEKKDIAAFVTFGEGSSNQGDFHEGANFAAVHKLPVIFMCENNKYAIS 188
            P A+G AL  +  K         G+G SNQG   E  N A V +LP IF+ ENN Y   
Sbjct: 120 PPLAIGAALTAKTLKTGNVGVSFTGDGGSNQGLVFEAINMAVVLQLPAIFIFENNGYGEG 179

Query: 189 VPYDKQVACENISDRAIGYGMPGVTVNGNDPLEVYQAVKEARERARRGEGPTLIETISYR 248
             +D  V   +I+ RA G+G+P VTV+G D   VY A  EA +RAR G GP++IE  ++R
Sbjct: 180 TGHDYAVGGRDIAGRAAGFGLPAVTVDGTDFFAVYDATAEAVKRAREGGGPSVIEAKAFR 239

Query: 249 LTPHSSDDDDSSYRGREEVEEAKKS-DPLLTYQAYLKETGLLSDEIEQTMLDEIMAIVNE 307
              H  + D + YR   EV+  ++  DPL  + A +K+   +S E    +  E+ A+V++
Sbjct: 240 WHGH-FEGDPALYRAEGEVQRLREQHDPLKIFTARVKQH--ISLEELAAIDAEVEALVDD 296

Query: 308 ATDEAENAPYAAPESALDYVY 328
           A  +A  A Y APE  L  VY
Sbjct: 297 AVFKARAAAYPAPEDLLTDVY 317


Lambda     K      H
   0.316    0.132    0.377 

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: 262
Number of extensions: 20
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: 330
Length of database: 320
Length adjustment: 28
Effective length of query: 302
Effective length of database: 292
Effective search space:    88184
Effective search space used:    88184
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: 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