GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ltaE in Acidovorax sp. GW101-3H11

Align L-allo-threonine aldolase (EC 4.1.2.49) (characterized)
to candidate Ac3H11_4475 Low-specificity L-threonine aldolase (EC 4.1.2.48)

Query= BRENDA::O07051
         (338 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4475
          Length = 355

 Score =  330 bits (846), Expect = 3e-95
 Identities = 177/352 (50%), Positives = 233/352 (66%), Gaps = 19/352 (5%)

Query: 5   DLRSDTVTQPTDAMRQCMLHAEVGDDVYGEDPGVNALEAYGADLLGKEAALFVPSGTMSN 64
           D RSDTVTQPT AMR+ M  A +GDDV+ +DP VNAL+ + A+LLG EAALF PSGT +N
Sbjct: 3   DFRSDTVTQPTPAMREAMFKAPLGDDVFADDPSVNALQDHAAELLGFEAALFAPSGTQTN 62

Query: 65  LLAVMSHCQRGEGAVLGSAAHIYRYEAQGSAVLGSVALQPVPMQADGSLALADVRAAIAP 124
           L+A+  HCQRG+ A++G + H YR+EA G AVLGS+  QPV  Q DG+L +AD+ AAI P
Sbjct: 63  LIALWGHCQRGDEAIVGQSWHTYRWEAGGMAVLGSIQPQPVETQPDGTLRVADIAAAIKP 122

Query: 125 DDVHFTPTRLVCLENTHNGKVLPLPYLREMRELVDEHGLQLHLDGARLFNAVVASG---- 180
           DD HF  TRLV LENT  G+VLP  Y+ ++ +L    GL +HLDGAR+FNA  A+     
Sbjct: 123 DDPHFARTRLVVLENTTGGQVLPPAYIADVAQLARSRGLAMHLDGARMFNAATANAARNG 182

Query: 181 ----HTVRELVAPFDSVSICLSKGLGAPVGSLLVGSHAFIARARRLRKMVGGGMRQAGIL 236
                  R L + FDS S+CLSKGLGAPVGSL++GS  FI +ARR RK++GGGMRQAG+L
Sbjct: 183 TDVYAEARALCSHFDSASLCLSKGLGAPVGSLVLGSRDFIRQARRTRKILGGGMRQAGVL 242

Query: 237 AQAGLFALQQHVVRLADDHRRARQLAEGLA----ALPGI--RLDLAQVQTNMVFLQLTSG 290
           A AG +ALQ HV RLADDH    +LA+GLA    + P +  ++ +   QTN++F  L + 
Sbjct: 243 AAAGSYALQHHVRRLADDHANLDRLAQGLAEANRSHPVLKDKITVLPWQTNILFTDLHAE 302

Query: 291 ESAPLLAFMKARGI-----LFSGYGELRLVTHLQIHDDDIEEVIDAFTEYLG 337
            +    A++   G+     L+ G   LR VTHL + + D+   +D    + G
Sbjct: 303 VAPAFTAWLAQHGVRVTSSLYGGATRLRWVTHLDVSEADVTAALDCVARFTG 354


Lambda     K      H
   0.322    0.137    0.396 

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: 398
Number of extensions: 16
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: 338
Length of database: 355
Length adjustment: 29
Effective length of query: 309
Effective length of database: 326
Effective search space:   100734
Effective search space used:   100734
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