GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Escherichia coli BW25113

Align L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized)
to candidate 15894 b1776 predicted oxidoreductase, Zn-dependent and NAD(P)-binding (NCBI)

Query= BRENDA::P07913
         (341 letters)



>FitnessBrowser__Keio:15894
          Length = 358

 Score =  164 bits (414), Expect = 4e-45
 Identities = 113/364 (31%), Positives = 190/364 (52%), Gaps = 32/364 (8%)

Query: 1   MKALSKL-KAEEGIWMTDVPVPELGHNDLLIKIRKTAICGTDVHIYNWDEWSQKTIPVPM 59
           MKAL++  KA  G  M DVP P  G  D++I+I+  AICG D+  YN D  S +      
Sbjct: 1   MKALARFGKAFGGYKMIDVPQPMCGPEDVVIEIKAAAICGADMKHYNVDSGSDE---FNS 57

Query: 60  VVGHEYVGEVVGIGQEVKGFKIGDRV--SGEGHITCGHCRNCRGGRTHLCRNTIGVGVNR 117
           + GHE+ G +  +G++VK +K+G RV     GH+ CG C  C  G    C   + +G++ 
Sbjct: 58  IRGHEFAGCIAQVGEKVKDWKVGQRVVSDNSGHV-CGVCPACEQGDFLCCTEKVNLGLDN 116

Query: 118 ---PGCFAEYLVIPA-------FNAFKIPDNISDDLAAIFDPFGNAVHTAL--SFDLVGE 165
               G F++Y ++P           ++IPD +  + AA+ DP  NA  +    S  L G+
Sbjct: 117 NTWGGGFSKYCLVPGEILKIHRHALWEIPDGVDYEDAAVLDPICNAYKSIAQQSKFLPGQ 176

Query: 166 DVLVSGAGPIGIMAAAVAKHVGARNVVITDVNE---YRLELARKMGITRAVNVAKENLND 222
           DV+V G GP+G+ +  +A+ +GA N+V+  + E    R  +A+++G T  VN + E++  
Sbjct: 177 DVVVIGTGPLGLFSVQMARIMGAVNIVVVGLQEDVAVRFPVAKELGATAVVNGSTEDVVA 236

Query: 223 VMAELGMTEGFDVGLEMSGAPPAFRTMLDTMNHGGRIAM--LGIPPSDMSIDWTKVIFKG 280
              ++   +   + +E SGA  A +  ++ +   G +    +G  P D SI+        
Sbjct: 237 RCQQICGKDNLGLVIECSGANIALKQAIEMLRPNGEVVRVGMGFKPLDFSINDITA---- 292

Query: 281 LFIKGIYGREMFE--TWYKMAALIQSG-LDLSPIITHRFSIDDFQKGFDAMRSGQSGKVI 337
            + K I G   ++  +W     L+ SG + + P+ITHR  +  +++GFDAM    + KVI
Sbjct: 293 -WNKSIIGHMAYDSTSWRNAIRLLASGAIKVKPMITHRIGLSQWREGFDAMVDKTAIKVI 351

Query: 338 LSWD 341
           +++D
Sbjct: 352 MTYD 355


Lambda     K      H
   0.322    0.140    0.433 

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: 345
Number of extensions: 22
Number of successful extensions: 4
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: 341
Length of database: 358
Length adjustment: 29
Effective length of query: 312
Effective length of database: 329
Effective search space:   102648
Effective search space used:   102648
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 (21.9 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