GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Acidovorax sp. GW101-3H11

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate Ac3H11_2066 SN-glycerol-3-phosphate transport ATP-binding protein UgpC (TC 3.A.1.1.3)

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



>FitnessBrowser__acidovorax_3H11:Ac3H11_2066
          Length = 355

 Score =  276 bits (706), Expect = 6e-79
 Identities = 160/361 (44%), Positives = 220/361 (60%), Gaps = 17/361 (4%)

Query: 2   TGLLLKDIRKSYG----AVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITG 57
           + L +  I K +G    +V+V+  +D+ +  GEF++ VGPSGCGKSTLL +IAGL+E T 
Sbjct: 3   SSLDIAGINKRFGKGDKSVEVLRKVDIHVAPGEFLILVGPSGCGKSTLLNIIAGLDEPTE 62

Query: 58  GDMFIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGA 117
           G++ I G+ V  +PP  R IAMVFQSYALYP ++V DN+ F + + +  K E  +R+   
Sbjct: 63  GEIRIGGKNVVGMPPRDRDIAMVFQSYALYPTLSVADNIGFALEMRKMPKPERQKRIDEV 122

Query: 118 ADMLQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIA 177
           A MLQ++  LDR P  LSGGQRQRVA+GRA+ R P++FLFDEPLSNLDA LRV  R EI 
Sbjct: 123 AAMLQISHLLDRRPSQLSGGQRQRVAMGRALARQPQLFLFDEPLSNLDAKLRVEMRAEIK 182

Query: 178 KLSERMSDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGS 237
           +L  + S  T +YVTHDQVEAMTL  RI V+  G ++Q+G P E+Y RPAN +VA FIGS
Sbjct: 183 RL-HQASGITSVYVTHDQVEAMTLGSRIAVMKGGVVQQLGTPDEIYNRPANTYVATFIGS 241

Query: 238 PAMNVIPATITATGQQTAVSLAGGKSVTLDVPTNASENGKTASFGVRPEDLRVTEADDFL 297
           P MN++   +  TG Q  +    G ++ L  P +++        GVRPE L + E     
Sbjct: 242 PTMNLLRGAV--TGGQFGIQ---GAALNLAPPPSSANE---VLLGVRPEHLVMQETAP-- 291

Query: 298 FEGTVSIVEALGEVTLLYIEGLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFDTNG 357
           + G VS+VE  G  T + ++    +  +  +     RV  G+ V      A  H FD   
Sbjct: 292 WRGRVSVVEPTGPDTYVMVDTAAGS--VTLRTDAQTRVQPGEHVGLALAPAHAHWFDAQS 349

Query: 358 Q 358
           +
Sbjct: 350 E 350


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: 339
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: 362
Length of database: 355
Length adjustment: 29
Effective length of query: 333
Effective length of database: 326
Effective search space:   108558
Effective search space used:   108558
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.

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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