GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ltaE in Desulfacinum infernum DSM 9756

Align L-allo-threonine aldolase (EC 4.1.2.49) (characterized)
to candidate WP_073041906.1 BUB04_RS17520 low specificity L-threonine aldolase

Query= BRENDA::O07051
         (338 letters)



>NCBI__GCF_900129305.1:WP_073041906.1
          Length = 347

 Score =  266 bits (679), Expect = 7e-76
 Identities = 164/341 (48%), Positives = 204/341 (59%), Gaps = 11/341 (3%)

Query: 4   IDLRSDTVTQPTDAMRQCMLHAEVGDDVYGEDPGVNALEAYGADLLGKEAALFVPSGTMS 63
           I L SDT T+PTDAMR+ M  AEVGD+  GEDP VN L     DLLGKEAALF+P GTM 
Sbjct: 2   IPLASDTETKPTDAMRRAMAVAEVGDEQKGEDPTVNRLLERVCDLLGKEAALFLPGGTMC 61

Query: 64  NLLAVMSHCQRGEGAVLGSAAHIYRYEAQGSAVLGSVALQPVPMQ----ADGSLALADVR 119
           NL+++ +H Q G+  +    AHI R E+ GS     V ++PV  +      G+L  A  +
Sbjct: 62  NLISIKTHTQPGDAVLADHMAHIIRAESGGSPFASGVLIEPVFSERGIFTPGALEEAYAK 121

Query: 120 AAIAPDDVHFTPTRLVCLENTHN---GKVLPLPYLREMRELVDEHGLQLHLDGARLFNAV 176
              AP     TP RLVC+E THN   G V  L  LR + +   E GL LH+DGARL NAV
Sbjct: 122 VRTAPWPYAPTP-RLVCVEQTHNFGGGTVWKLDELRAVHDKARELGLALHMDGARLLNAV 180

Query: 177 VASGHTVRELVAPFDSVSICLSKGLGAPVGSLLVGSHAFIARARRLRKMVGGGMRQAGIL 236
           VA G   RE  A  DSV I  +KGLGAPVG++L GS  FIARAR  + M GG MRQAGI+
Sbjct: 181 VAGGVPAREFAACVDSVWIDFTKGLGAPVGAVLAGSADFIARARLYKHMFGGAMRQAGIV 240

Query: 237 AQAGLFALQQHVVRLADDHRRARQLAEGLAALPGIRLDLAQVQTNMVFLQLTS-GESAP- 294
           A   L AL  HV RLA+DH  AR+L  GL+ +PGIR+   + +TNMVF ++   G   P 
Sbjct: 241 AAGCLHALDHHVERLAEDHENARRLDRGLSDIPGIRVLTPEPETNMVFFEIPGLGMGVPA 300

Query: 295 LLAFMKARGILFSGYG-ELRLVTHLQIHDDDIEEVIDAFTE 334
             A  K RG+   G G  +R VTHL +  +DI+  +    E
Sbjct: 301 FTAEAKRRGVSLVGIGCGIRAVTHLDVSREDIDRAVAILAE 341


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: 357
Number of extensions: 19
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: 338
Length of database: 347
Length adjustment: 29
Effective length of query: 309
Effective length of database: 318
Effective search space:    98262
Effective search space used:    98262
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 24 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