GapMind for catabolism of small carbon sources

 

Aligments for a candidate for aglK in Phaeobacter inhibens BS107

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate GFF1302 PGA1_c13180 ABC transporter, ATP binding protein

Query= reanno::Smeli:SMc03065
         (362 letters)



>lcl|FitnessBrowser__Phaeo:GFF1302 PGA1_c13180 ABC transporter, ATP
           binding protein
          Length = 334

 Score =  343 bits (881), Expect = 3e-99
 Identities = 187/357 (52%), Positives = 243/357 (68%), Gaps = 27/357 (7%)

Query: 1   MTGLLLKDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDM 60
           M  + L+ + K++G V+VI  +DL I++GEF VFVGPSGCGKSTLLR+IAGLE+IT G +
Sbjct: 1   MGQIKLESVTKNFGPVEVIPPLDLTIEDGEFTVFVGPSGCGKSTLLRLIAGLEDITSGTI 60

Query: 61  FIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADM 120
            IDGE   ++PP+KRG+AMVFQSYALYPHM+V  N+AF M++A    +E  RR+  AA  
Sbjct: 61  RIDGEDATNIPPAKRGLAMVFQSYALYPHMSVRKNIAFPMKMAGIPADEQKRRIDNAAAA 120

Query: 121 LQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLS 180
           L LT YLDR P  LSGGQRQRVAIGRAI R P  FLFDEPLSNLDAALRV  R+EI++L 
Sbjct: 121 LNLTDYLDRRPGQLSGGQRQRVAIGRAIVREPAAFLFDEPLSNLDAALRVGMRLEISELH 180

Query: 181 ERMSDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAM 240
           +R++ TTMIYVTHDQVEAMT+AD+IVVL AG IEQVG+P+ELY  P N+FVA FIGSP M
Sbjct: 181 KRLA-TTMIYVTHDQVEAMTMADKIVVLQAGVIEQVGSPMELYRAPRNVFVAGFIGSPKM 239

Query: 241 NVIPATITATGQQTAVSLAGGKSVTLDVPTNASENGKTASFGVRPEDLRVTEADDFLFEG 300
           N++      TG Q A                       A+ G+RPE L ++E +  ++ G
Sbjct: 240 NLL------TGPQAA-------------------QHNAATIGIRPEHLSISETEG-MWAG 273

Query: 301 TVSIVEALGEVTLLYIEGLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFDTNG 357
           T+ + E LG  T  +++    ++P+  +  G   +G G++V  T D   LH F ++G
Sbjct: 274 TIGVSEHLGSDTFFHVQCDAFDDPLTVRASGELDLGYGERVFLTPDMTHLHRFGSDG 330


Lambda     K      H
   0.320    0.137    0.387 

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: 355
Number of extensions: 14
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: 362
Length of database: 334
Length adjustment: 29
Effective length of query: 333
Effective length of database: 305
Effective search space:   101565
Effective search space used:   101565
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: 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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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