GapMind for catabolism of small carbon sources

 

Aligments for a candidate for livJ in Sinorhizobium meliloti 1021

Align Solute-binding (Aliphatic amino acid) component of ABC transporter (characterized, see rationale)
to candidate SMa0576 SMa0576 Leu or Leu/Val/Ile transport binding protein

Query= uniprot:Q1MDE9
         (367 letters)



>FitnessBrowser__Smeli:SMa0576
          Length = 363

 Score =  262 bits (669), Expect = 1e-74
 Identities = 136/365 (37%), Positives = 213/365 (58%), Gaps = 2/365 (0%)

Query: 3   LKTLTATLVASLAFAPLAHADITIGLIAPLTGPVAAYGDQVKNGAQTAVDEINKKGGILG 62
           ++ L      + A A  + A++ IG+  P++G +A  G Q++ GA+ AV  IN  GG+LG
Sbjct: 1   MRHLFTAAALAFALASQSEAEVLIGVAGPMSGKLAWTGTQLRRGAEMAVANINAAGGVLG 60

Query: 63  EKVVLELADDAGEPKQGVSAANKVVGDGIRFVVGPVTSGVAIPVSDVLAENGVLMVTPTA 122
           ++V L +ADD  +P+Q ++AA K+V DG  FV+G   SG +IP S + A  GVL ++P++
Sbjct: 61  QQVRLIVADDFCDPRQALAAAEKLVADGAVFVIGHYCSGASIPASKIYAAAGVLQISPSS 120

Query: 123 TAPDLTKRGLTNVLRTCGRDDQQAEVAAKYVLKNFKDKRVAIVNDKGAYGKGLADAFKAT 182
           T P LT++G  NV R C RDD Q   A  Y+  ++ D ++AI++D   YGKGLAD  K  
Sbjct: 121 TNPMLTEQGHANVFRVCSRDDAQGHKAGNYLADHWGDSKIAILHDNTTYGKGLADETKKQ 180

Query: 183 LNAGGITEVVNDAITPGDKDFSALTTRIKSEKVDVVYFGGYHPEGGLLARQLHDLAANAT 242
           LN  G+TE V  + TPG  D+S     +++  + V+Y GGYH E  L+ R   D A    
Sbjct: 181 LNMRGVTEAVYQSYTPGKDDYSVEVAALQTAHIAVLYLGGYHTEAALMVRAARDRAYPVQ 240

Query: 243 IIGGDGLSNTEFWAIGTDAAGGTIFTNASDATKSPDSKAAADALAAKNIPAEAFTLNAYA 302
           +I GD  +   F  I   AA GT+FT  +D  ++ ++    +   A+N   +++TL++Y 
Sbjct: 241 LISGDDTATEAFGLIAGPAAEGTLFTFVADPRRNAEAAEVVERFRAENFEPDSWTLHSYG 300

Query: 303 AVEVLKAGIEKAGSAEDAEAVATALKDGKEIPTAIGKVTYGETGDLTSQSFSLYKWEAGK 362
           A E+    + KA S  D +AV  AL++  +  T +G++ + + GDLT QS+  Y W++G+
Sbjct: 301 AAEIWAQAVTKANSL-DLQAVIAALRE-DQFDTVLGRIDFDKKGDLTVQSWVWYVWKSGE 358

Query: 363 IVAAE 367
            V  E
Sbjct: 359 YVPVE 363


Lambda     K      H
   0.312    0.131    0.362 

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: 342
Number of extensions: 17
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: 367
Length of database: 363
Length adjustment: 30
Effective length of query: 337
Effective length of database: 333
Effective search space:   112221
Effective search space used:   112221
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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