GapMind for catabolism of small carbon sources

 

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

Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate Ac3H11_2066 SN-glycerol-3-phosphate transport ATP-binding protein UgpC (TC 3.A.1.1.3)

Query= reanno::acidovorax_3H11:Ac3H11_792
         (358 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2066
          Length = 355

 Score =  202 bits (515), Expect = 8e-57
 Identities = 127/360 (35%), Positives = 206/360 (57%), Gaps = 17/360 (4%)

Query: 5   SLDLAHSYKPNPQQDSDYALL-PLKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLVPSHG 63
           SLD+A   K   + D    +L  + +    G    L+GPSGCGK+T+LNI++GL  P+ G
Sbjct: 4   SLDIAGINKRFGKGDKSVEVLRKVDIHVAPGEFLILVGPSGCGKSTLLNIIAGLDEPTEG 63

Query: 64  KVLFDGRDVTRASPQERNIAQVFQFPVIYDTMTVAENLAFPLRNRKVPEGQIKQRVGVIA 123
           ++   G++V    P++R+IA VFQ   +Y T++VA+N+ F L  RK+P+ + ++R+  +A
Sbjct: 64  EIRIGGKNVVGMPPRDRDIAMVFQSYALYPTLSVADNIGFALEMRKMPKPERQKRIDEVA 123

Query: 124 EMLEMSGQLNQRAAGLAADAKQKISLGRGLVRADVAAVLFDEPLTVIDPHLKWQLRRKLK 183
            ML++S  L++R + L+   +Q++++GR L R      LFDEPL+ +D  L+ ++R ++K
Sbjct: 124 AMLQISHLLDRRPSQLSGGQRQRVAMGRALAR-QPQLFLFDEPLSNLDAKLRVEMRAEIK 182

Query: 184 QIHHELKLTLIYVTHDQVEALTFADQVVVMTRGKAVQVGSADALFERPAHTFVGHFIGSP 243
           ++H    +T +YVTHDQVEA+T   ++ VM  G   Q+G+ D ++ RPA+T+V  FIGSP
Sbjct: 183 RLHQASGITSVYVTHDQVEAMTLGSRIAVMKGGVVQQLGTPDEIYNRPANTYVATFIGSP 242

Query: 244 GMNFLPAHRDGENLSVAGH--RLASPVGRALPAGALQVGIRPEYLALAQPQQAGALPGTV 301
            MN L     G    + G    LA P      A  + +G+RPE+L +   Q+     G V
Sbjct: 243 TMNLLRGAVTGGQFGIQGAALNLAPPPS---SANEVLLGVRPEHLVM---QETAPWRGRV 296

Query: 302 VQVQDIG--TYQMLTAKVGEHTVKARFTPETRLPSSGDTAWLQVLGEHTCYY--KNEELL 357
             V+  G  TY M+    G  +V  R   +TR+   G+   L +   H  ++  ++EE L
Sbjct: 297 SVVEPTGPDTYVMVDTAAG--SVTLRTDAQTRV-QPGEHVGLALAPAHAHWFDAQSEERL 353


Lambda     K      H
   0.320    0.136    0.395 

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: 295
Number of extensions: 13
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: 358
Length of database: 355
Length adjustment: 29
Effective length of query: 329
Effective length of database: 326
Effective search space:   107254
Effective search space used:   107254
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 (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