GapMind for catabolism of small carbon sources

 

Aligments for a candidate for AO353_21725 in Phaeobacter inhibens BS107

Align ABC transporter for D-Glucosamine, putative ATPase component (characterized)
to candidate GFF3910 PGA1_65p00130 putative amino-acid ABC transporter, ATP-binding protein

Query= reanno::pseudo5_N2C3_1:AO356_00465
         (263 letters)



>lcl|FitnessBrowser__Phaeo:GFF3910 PGA1_65p00130 putative amino-acid
           ABC transporter, ATP-binding protein
          Length = 251

 Score =  225 bits (574), Expect = 6e-64
 Identities = 121/248 (48%), Positives = 161/248 (64%), Gaps = 7/248 (2%)

Query: 12  PLLDIRGLRKQYGPLEVLKGVDLSMQRGNVVTLIGSSGSGKTTLLRCVNMLEEFQGGQIV 71
           P + I GLRK +G   VL G+DL++Q G  + +IG SG+GK+TLLRC+N L+    G + 
Sbjct: 8   PAISITGLRKTFGDSVVLDGIDLTIQPGERIVIIGPSGTGKSTLLRCLNFLDAPDAGLV- 66

Query: 72  LDGESIGYDDIDGKRVRHPEKLIARHRAMTGMAFQQFNLFPHLTALQNVTLGLLKVKKLP 131
                IG  D+D  R    E L  R R  T   FQ + LF + TA +N+   L+ V+K P
Sbjct: 67  ----RIGDLDVDAARASKAEILALRRR--TAFVFQNYALFANKTAAENIMEALITVQKQP 120

Query: 132 KDEAVALAEKWLERVGLLERRDHFPGQLSGGQQQRVAIARAIAMNPSLMLFDEVTSALDP 191
           + EA A A + L   GL ++ D +P  LSGGQQQRV I RA+A+   LMLFDE TSALDP
Sbjct: 121 RAEAEARAREILAETGLADKADAYPASLSGGQQQRVGIGRAMALGAELMLFDEPTSALDP 180

Query: 192 ELVGEVLNVIKGLAEDGMTMLLVTHEMRFAFEVSDKIVFMNQGRIEEQGPPKELFERPQS 251
           E VGEVL ++  +AE+  TML+VTHEM+FA E++D++VFM  GRI EQGPP ++F+ PQ 
Sbjct: 181 EWVGEVLALMHKVAEERQTMLIVTHEMQFAREIADRVVFMEGGRIVEQGPPTQIFDAPQD 240

Query: 252 PRLAEFLK 259
           PR   FL+
Sbjct: 241 PRTRAFLR 248


Lambda     K      H
   0.320    0.138    0.392 

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: 158
Number of extensions: 3
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: 263
Length of database: 251
Length adjustment: 24
Effective length of query: 239
Effective length of database: 227
Effective search space:    54253
Effective search space used:    54253
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 47 (22.7 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint 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