GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Klebsiella michiganensis M5al

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate BWI76_RS11535 BWI76_RS11535 putative oxidoreductase, Zn-dependent and NAD(P)-binding protein

Query= curated2:Q72L62
         (343 letters)



>FitnessBrowser__Koxy:BWI76_RS11535
          Length = 358

 Score =  160 bits (404), Expect = 6e-44
 Identities = 114/361 (31%), Positives = 185/361 (51%), Gaps = 31/361 (8%)

Query: 1   MRALAKLAPE-EGLTLVDRPVPEPGPGEILVRVEAASICGTDLHIWKWDAWARGRIRPPL 59
           M+ALA+      G  ++D P P  GP ++++ ++AA+ICG D+  +  D+   G  +   
Sbjct: 1   MKALARFGKAFGGYKMIDVPEPVCGPDDVVIEIKAAAICGADMKHYNVDS---GSDQFNS 57

Query: 60  VTGHEFSGVVEAVGPGVKRPQVGDHV-SLESHVVCHACPACRTGNYHVCLNTKILGVDRD 118
           + GHEF+G +  VG  VK  +VG  V S  S  VC  CPAC  G++  C     LG+D +
Sbjct: 58  IRGHEFAGAIVRVGDKVKDWKVGQRVVSDNSGHVCGVCPACEQGDFLCCAEKVNLGLDNN 117

Query: 119 ---GGFAEYVVVPAE-------NAWVNPKDLPFEVAAILEPFGNAVHTVYAGSG-VSGKS 167
              GGF++Y +VP E         W  P  + +E AA+L+P  NA  ++   S  + G+ 
Sbjct: 118 TWGGGFSKYCLVPGEILKIHRHALWEIPPGVDYEDAAVLDPICNAYKSLAQQSKFLPGQD 177

Query: 168 VLITGAGPIGLMAAMVARASGAGPILV---SDPNPYRLAFARPY-ADRLVNPLEEDLLEV 223
           V++ G GP+GL +  +AR  GA  I++    +    R   A+   A  +VN   ED++  
Sbjct: 178 VVVFGTGPLGLFSVQMARIMGAVNIVMVGLEEDVAVRFPIAKALGATAVVNASTEDVVAR 237

Query: 224 VRRVTGS-GVEVLLEFSGNEAAIHQGLMALIPGGEARILGIPSDPIRFDLAGELVMRGIT 282
            + + G   + +++E SG   A+ Q +  L P GE   +G+   P+ F +        IT
Sbjct: 238 CQAICGKDNLGLVIECSGANIALKQSIEMLRPNGEVVRVGMGFQPLDFSI------NDIT 291

Query: 283 AFG--IAGRRLWQT--WMQGTALVYSGRVDLSPLITHRLPLSRYREAFGLLASGQAVKVI 338
            +   I G   + +  W     L+ SG + + P+ITHR+ LS++RE F  +    A+KVI
Sbjct: 292 TWNKSIIGHMAYDSTSWRNAIRLLASGAIKVKPMITHRIGLSQWREGFDAMVDKTAIKVI 351

Query: 339 L 339
           +
Sbjct: 352 M 352


Lambda     K      H
   0.321    0.140    0.432 

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: 362
Number of extensions: 21
Number of successful extensions: 7
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: 343
Length of database: 358
Length adjustment: 29
Effective length of query: 314
Effective length of database: 329
Effective search space:   103306
Effective search space used:   103306
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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