GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruG in Paraburkholderia bryophila 376MFSha3.1

Align Fructose import permease protein FruG (characterized)
to candidate H281DRAFT_05272 H281DRAFT_05272 monosaccharide ABC transporter membrane protein, CUT2 family

Query= SwissProt::Q8G845
         (340 letters)



>FitnessBrowser__Burk376:H281DRAFT_05272
          Length = 365

 Score =  202 bits (515), Expect = 8e-57
 Identities = 116/317 (36%), Positives = 185/317 (58%), Gaps = 9/317 (2%)

Query: 18  LDRQMIPTLAAVVIFILMIIMGQALFGTYIRLGFISSLFIDHAYLIILAVAMTLPILTGG 77
           +D + +P    +++F  +   G  ++  +     +  L +D+A+L+I+A+ MT  I++GG
Sbjct: 12  VDPRTLPIAVTILLFCALFGFGSVMYTGFFSWQVLLDLLVDNAFLLIVAIGMTFVIVSGG 71

Query: 78  IDLSVGAIVAITAVVGLKLANA-GVPAFLVMIIMLLIGAVFGLLAGTLIEEFNMQPFIAT 136
           IDLSVG++VA+T +V   L+    +  ++++ I+L++G VFG + G LI  F +Q FI T
Sbjct: 72  IDLSVGSVVALTTIVEAVLSERYHLSVWVIVPIVLVMGTVFGAVQGALIHFFRLQAFIVT 131

Query: 137 LSTMFLARGLASIISTDSLTFPQGNDFSFISNVIKIIDNPKISNDLSFNVGVIIALVVVV 196
           L+ MF ARGL  +I+T S+T       +  +  + I      +N       V+IA V ++
Sbjct: 132 LAGMFFARGLCFLITTQSITITDPTFHAISAFRLDIGIGSVTAN-------VLIAFVALL 184

Query: 197 FGYVFLHHTRTGRTIYAIGGSRSSAELMGLPVKRTQYIIYLTSATLAALASIVYTANIGS 256
                 H TR GR +YA+GG+  SA LMGLPV  T+  +Y  S   +AL   V+T  + S
Sbjct: 185 GAIYVAHFTRFGRNVYAVGGNARSALLMGLPVAHTRIGVYALSGFCSALGGAVFTFYVLS 244

Query: 257 AKNTVGVGWELDAVASVVIGGTIITGGFGYVLGSVLG-SLVRSILDPLTSDFGVPAEWTT 315
                G G ELDA+A+ VIGGT++TGG GYV+GS+ G  ++ +I   +T D  + + WT 
Sbjct: 245 GYGLQGQGMELDAIAATVIGGTLLTGGVGYVVGSLFGVGILGTIQTLITFDGTLSSWWTR 304

Query: 316 IVIGLMILVFVVLQRAV 332
           IVIG ++  F +LQR +
Sbjct: 305 IVIGALLCAFCLLQRLI 321


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: 331
Number of extensions: 17
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: 340
Length of database: 365
Length adjustment: 29
Effective length of query: 311
Effective length of database: 336
Effective search space:   104496
Effective search space used:   104496
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.

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