GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Sinorhizobium meliloti 1021

Align Leu/Ile/Val-binding protein LivJ aka B3460 aka LIV-BP, component of Leucine; leucine/isoleucine/valine porter (characterized)
to candidate SMc00078 SMc00078 Leu/Ile/Val-binding protein

Query= TCDB::P0AD96
         (367 letters)



>FitnessBrowser__Smeli:SMc00078
          Length = 368

 Score =  293 bits (750), Expect = 5e-84
 Identities = 153/359 (42%), Positives = 228/359 (63%), Gaps = 9/359 (2%)

Query: 3   IKGKALLAGCIALAFSNMALAEDIKVAVVGAMSGPVAQYGDQEFTGAEQAVADINAKGGI 62
           + G AL A   ++AF+ +A A DI + V+  ++GPVA +G+Q   GAE AV  IN+ GG+
Sbjct: 6   LTGMALAA---SVAFAPLAHA-DITIGVITPLTGPVAAFGEQVKNGAEAAVEAINSAGGV 61

Query: 63  KGNKLQIVKYDDACDPKQAVAVANKVVNDGIKYVIGHLCSSSTQPASDIYEDEGILMITP 122
            G KL +   DDA +PKQAV+VAN++  +GI+YV+G + S ++ PASD+  + GILM+TP
Sbjct: 62  NGEKLVVKIVDDAGEPKQAVSVANQLAGEGIQYVVGPVLSGTSMPASDVLAENGILMVTP 121

Query: 123 AATAPELTARGYQLILRTTGLDSDQGPTAAKYILEKVKPQRIAIVHDKQQYGEGLARAVQ 182
            AT P+LT RG   +LRT G D  Q   AA Y+++  K +R+A++HDK  YG+GLA   +
Sbjct: 122 TATTPDLTTRGLWNVLRTCGRDDQQAVVAADYVVKNFKDKRVAVLHDKGAYGKGLADGFK 181

Query: 183 DGLKKGNANVVFFDGITAGEKDFSTLVARLKKENIDFVYYGGYHPEMGQILRQARAAGLK 242
             +  G    V ++G+T GEKDF  +V RLK EN+D VY+GGYH E G + RQ    G+K
Sbjct: 182 AAINAGGITEVVYEGLTPGEKDFGAIVTRLKAENVDVVYFGGYHAEGGLLARQMHDQGVK 241

Query: 243 TQFMGPEGVANVSLSNIAGESAEGLLVTKPKNYDQVPANKPIVDAIKAKKQDPSGAFVWT 302
            Q +G +G++N     I GE+A G + T   +  + PA  P+++A+KA K  P+ AF   
Sbjct: 242 AQLLGGDGLSNTEFWAIGGEAASGTVYTNASDATRNPAAAPVIEALKA-KNIPAEAFTLN 300

Query: 303 TYAALQSLQAGLNQ---SDDPAEIAKYLKA-NSVDTVMGPLTWDEKGDLKGFEFGVFDW 357
            YAA+Q L+AG+ +   ++D   +A  +K+  ++DTV+G LT+ E GDL    F ++ W
Sbjct: 301 AYAAVQVLKAGIEKAGSTEDATAVATAIKSGEAIDTVIGKLTYGESGDLTSPSFSLYKW 359


Lambda     K      H
   0.314    0.133    0.380 

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: 412
Number of extensions: 20
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: 367
Length of database: 368
Length adjustment: 30
Effective length of query: 337
Effective length of database: 338
Effective search space:   113906
Effective search space used:   113906
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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