GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacI in Sinorhizobium meliloti 1021

Align Xylose/arabinose import permease protein XacI (characterized, see rationale)
to candidate SMc04394 SMc04394 ABC transporter permease

Query= uniprot:D4GP37
         (309 letters)



>FitnessBrowser__Smeli:SMc04394
          Length = 293

 Score =  143 bits (361), Expect = 4e-39
 Identities = 95/309 (30%), Positives = 158/309 (51%), Gaps = 39/309 (12%)

Query: 14  SLVEDVNLRRVAQYALVVFFLGFFLVPLETGIMTAIKTNESVAR----SLP---FAPPVG 66
           +++    L R   Y+ ++ F  + L+PL   ++ ++K  + + +    +LP      P  
Sbjct: 8   NVISHNRLTRALIYSALILFALYSLLPLYVMLVNSLKPLDEIRQGGMLNLPQTWTVEPWL 67

Query: 67  EGFTLGNIQFALEQLSGSFFNSLIMSIPATIGSVLFGSMAAYGLTMVNWRAQ-----MGM 121
             ++   I      L   F NS++M +PA   S + G++  Y LT   WR        GM
Sbjct: 68  SAWSTAQIGVQPTGLRPFFINSILMVVPAVAISTIIGALNGYVLT--KWRFPGANIFFGM 125

Query: 122 LMLFVVGVFVPYQAVLVPLARFWNNIFPLARMIEPMVASIPFFQGYHAELVPLVITHIAY 181
           L+L     F+P+Q VL+P+AR    +                  G    +  L++ H+ Y
Sbjct: 126 LLL---SCFIPFQIVLIPMARILGIL------------------GIAGSIWGLILVHVVY 164

Query: 182 GIPICTILFRSYYQSLPNSLVEAGKIDGASITKIYRRIILPISKPMFGVVFIYQFTQIYN 241
           GI   T+ FR+YY++ P  LV A +IDGAS  +I+RRI+LP S P+  V  I+QFT I+N
Sbjct: 165 GIGFTTLYFRNYYEAFPTELVRAAQIDGASFFQIFRRILLPSSGPIIVVSVIWQFTNIWN 224

Query: 242 EFLFAFTLVTGSDAPAAPVTLVLPAIGASTSGI-NFGIRMSAAFLAAVPTLILYVAFAEQ 300
           +FLF  +    S   + P+T+ L  + +S++G+  + +  + A LAA+PTLI+Y+     
Sbjct: 225 DFLFGASF---SGPYSTPMTVALNNLVSSSTGVKEYNVHFAGAILAALPTLIVYIVSGRY 281

Query: 301 FAKGLRTEA 309
           F +GL + A
Sbjct: 282 FVRGLMSGA 290


Lambda     K      H
   0.328    0.141    0.413 

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: 253
Number of extensions: 9
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: 309
Length of database: 293
Length adjustment: 27
Effective length of query: 282
Effective length of database: 266
Effective search space:    75012
Effective search space used:    75012
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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