GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c07300 in Sinorhizobium meliloti 1021

Align Inositol transport system sugar-binding protein (characterized)
to candidate SMa0218 SMa0218 ABC transporter substrate-binding protein

Query= reanno::Phaeo:GFF715
         (316 letters)



>FitnessBrowser__Smeli:SMa0218
          Length = 316

 Score =  117 bits (292), Expect = 5e-31
 Identities = 98/317 (30%), Positives = 149/317 (47%), Gaps = 20/317 (6%)

Query: 11  ATTVAAAPMMLATTASAEGEKYILVSHAPDSDSWWNTIKNGIALAGEQMNVE--VEYRNP 68
           A   A    +L +TA A   K  ++ +   S  ++N +  G   A  Q  V+  V+Y N 
Sbjct: 9   AALAAGLATLLTSTALAADVKATMIIYLDPSVQFFNPVVKGAQDAAAQFGVDLDVQYAN- 67

Query: 69  PTGDLADMARIIEQAAASGPNGIITTLSDYDVLSGPIKAAVDSGVDVIIMNSGTPDQARE 128
              D      +IE A ASG +GI   +S  D     I AAV +G+ VI  N+   D A+ 
Sbjct: 68  --NDPVRQNDLIESATASGVDGIAVAISSSDAFDESICAAVKAGIIVIGFNNDDLDGAKG 125

Query: 129 VGALMYVGQPEYDAGHAAGMRA-KADGVGSFLCVNHYISSPSSTERCQGFADGLGVD--- 184
                YVG  E  +G+  G R  K  G+ S   V +    P   E     A G G++   
Sbjct: 126 NCRQAYVGMDELASGYELGNRMIKEFGLKSGDVVFNPREIP---EASFAVARGGGIEKAM 182

Query: 185 ----LGDQMIDSGQDPAEIKNRVLAYLNTNPETDAILTLGPTSADPTLLALDENGMAGDI 240
               +  + + +G DPAE +N +  +L  NP   A+   G  ++     A+ + G+  DI
Sbjct: 183 TENGIKVETVRAGLDPAEAQNIIAQFLIANPNVKALFGTGSVTSTVGAGAIKDAGV--DI 240

Query: 241 YFGTFDLGEEIVKGLKSGVINWGIDQQPFLQAYLPVVVLTNYHRYGVLPGNNINSGPG-F 299
            FG FDL  EIV  ++SG +   +DQQP+LQ Y P+  +    +YG+ P  +I++G G F
Sbjct: 241 PFGGFDLAVEIVNAVESGAMYATMDQQPYLQGYYPIAQIALAKKYGLTP-TDIDTGQGAF 299

Query: 300 VTKDGLEKVEEFAGEYR 316
           + K  +  V+   G YR
Sbjct: 300 LDKTRIGSVKPLIGSYR 316


Lambda     K      H
   0.315    0.134    0.393 

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: 264
Number of extensions: 14
Number of successful extensions: 3
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: 316
Length of database: 316
Length adjustment: 27
Effective length of query: 289
Effective length of database: 289
Effective search space:    83521
Effective search space used:    83521
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: 48 (23.1 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