GapMind for catabolism of small carbon sources

 

Alignments 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:

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