GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08260 in Sinorhizobium meliloti 1021

Align Branched-chain amino acid ABC transporter,substrate-binding periplasmic component (characterized, see rationale)
to candidate SMc00078 SMc00078 Leu/Ile/Val-binding protein

Query= uniprot:G8ALJ3
         (366 letters)



>FitnessBrowser__Smeli:SMc00078
          Length = 368

 Score =  343 bits (879), Expect = 6e-99
 Identities = 174/360 (48%), Positives = 236/360 (65%), Gaps = 2/360 (0%)

Query: 9   VAVAATAMTASVAKADIAVATAGPITGQYATFGEQMKKGIEQAVADINAAGGVLGQKLKL 68
           +A+AA+   A +A ADI +    P+TG  A FGEQ+K G E AV  IN+AGGV G+KL +
Sbjct: 9   MALAASVAFAPLAHADITIGVITPLTGPVAAFGEQVKNGAEAAVEAINSAGGVNGEKLVV 68

Query: 69  EVGDDACDPKQAVAVANQLAKAGVKFVAGHFCSGSSIPASQVYAEEGVLQISPASTNPKL 128
           ++ DDA +PKQAV+VANQLA  G+++V G   SG+S+PAS V AE G+L ++P +T P L
Sbjct: 69  KIVDDAGEPKQAVSVANQLAGEGIQYVVGPVLSGTSMPASDVLAENGILMVTPTATTPDL 128

Query: 129 TEQNLKNVFRVCGRDDQQGQIAGKYLLENYKGKNVAILHDKSAYGKGLADETQKALNAGG 188
           T + L NV R CGRDDQQ  +A  Y+++N+K K VA+LHDK AYGKGLAD  + A+NAGG
Sbjct: 129 TTRGLWNVLRTCGRDDQQAVVAADYVVKNFKDKRVAVLHDKGAYGKGLADGFKAAINAGG 188

Query: 189 QKEKIYEAYTAGEKDYSALVSKLKQEAVDVVYVGGYHTEAGLLARQMKDQGLNAPIVSGD 248
             E +YE  T GEKD+ A+V++LK E VDVVY GGYH E GLLARQM DQG+ A ++ GD
Sbjct: 189 ITEVVYEGLTPGEKDFGAIVTRLKAENVDVVYFGGYHAEGGLLARQMHDQGVKAQLLGGD 248

Query: 249 ALVTNEYWAITGPAGENTMMTFGPDPREMPEAKEAVEKFRKAGYEPEGYTLYTYAALQIW 308
            L   E+WAI G A   T+ T   D    P A   +E  +      E +TL  YAA+Q+ 
Sbjct: 249 GLSNTEFWAIGGEAASGTVYTNASDATRNPAAAPVIEALKAKNIPAEAFTLNAYAAVQVL 308

Query: 309 AEAAKQANST-DSAKIADVLRK-NSYNTVIGKIGFDAKGDVTSPAYVWYRWNNGQYAQVK 366
               ++A ST D+  +A  ++   + +TVIGK+ +   GD+TSP++  Y+W  GQ   V+
Sbjct: 309 KAGIEKAGSTEDATAVATAIKSGEAIDTVIGKLTYGESGDLTSPSFSLYKWEGGQSVAVE 368


Lambda     K      H
   0.312    0.129    0.366 

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: 437
Number of extensions: 15
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: 366
Length of database: 368
Length adjustment: 30
Effective length of query: 336
Effective length of database: 338
Effective search space:   113568
Effective search space used:   113568
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