GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruG in Shewanella sp. ANA-3

Align Fructose import permease protein FruG (characterized)
to candidate 7024901 Shewana3_2075 inner-membrane translocator (RefSeq)

Query= SwissProt::Q8G845
         (340 letters)



>FitnessBrowser__ANA3:7024901
          Length = 405

 Score =  132 bits (331), Expect = 2e-35
 Identities = 98/327 (29%), Positives = 164/327 (50%), Gaps = 22/327 (6%)

Query: 14  KGFKLDRQMIPTLAAVVIFILMIIMGQALFGTYIRLGFISSLFID----HAYLIILAVAM 69
           K   + R + P LA  ++ +  + +  + F    +   +    ID     A + +L++ M
Sbjct: 55  KSTSMGRYLWPLLALSILLLANLFIDSSFFNISYQDDRLYGSLIDILNRSAPVALLSIGM 114

Query: 70  TLPILTGGIDLSVGAIVAITAVVGLKLANAGVPAFLVMIIMLLIGAVFGLLAGT----LI 125
           +L I TGGIDLSVGA++AI   V    AN  +   + ++ ++  G + GLLAG     L+
Sbjct: 115 SLVIATGGIDLSVGAVMAIAGAV---CANLLLVPDISLVTVIAAGLIVGLLAGCINGGLV 171

Query: 126 EEFNMQPFIATLSTMFLARGLASIISTDSLTFPQGNDFSFISNVIKIIDNPKISNDLSFN 185
               +QP +ATL  M   RG+A +I+   +   Q   F+ I           +   L   
Sbjct: 172 SFLGIQPIVATLLLMVAGRGVAQLINQGQIITFQHPGFAAIG----------VGQFLGLP 221

Query: 186 VGVIIALVVVVFGYVFLHHTRTGRTIYAIGGSRSSAELMGLPVKRTQYIIYLTSATLAAL 245
           + V I + ++ F  + L  T  G  I A+G +  ++  +G+  K  +   Y  +   AAL
Sbjct: 222 MPVWIVIGMLTFSQLLLRKTALGLFIEAVGCNAKASRYLGINDKSIKLFAYGIAGLCAAL 281

Query: 246 ASIVYTANI-GSAKNTVGVGWELDAVASVVIGGTIITGGFGYVLGSVLGSLVRSILDPLT 304
           A ++ TA+I GS  N  G+  ELDAV +VVIGG  +TGG   ++ SV+G+L+   L    
Sbjct: 282 AGMISTADIQGSDANNAGLWLELDAVLAVVIGGAALTGGRFSLILSVVGALIIQTLATTI 341

Query: 305 SDFGVPAEWTTIVIGLMILVFVVLQRA 331
              G+PA++  ++  ++IL  ++LQ A
Sbjct: 342 IVSGLPAKFNLLIKAIVILTVLLLQSA 368


Lambda     K      H
   0.327    0.142    0.400 

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: 239
Number of extensions: 11
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: 340
Length of database: 405
Length adjustment: 30
Effective length of query: 310
Effective length of database: 375
Effective search space:   116250
Effective search space used:   116250
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: 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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