GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Marinobacter adhaerens HP15

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate GFF960 HP15_939 spermidine/putrescine ABC transporter ATPase subunit

Query= reanno::Dino:3607124
         (338 letters)



>FitnessBrowser__Marino:GFF960
          Length = 372

 Score =  235 bits (600), Expect = 1e-66
 Identities = 139/328 (42%), Positives = 194/328 (59%), Gaps = 28/328 (8%)

Query: 4   IKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRIEIG 63
           + I  I+K +  T A+ ++NLDI  GE    +G SG GKSTLLR LAG E  ++G I + 
Sbjct: 15  LSIRGISKSFDGTLAVDNVNLDIHKGEIFALLGGSGSGKSTLLRMLAGFETPNAGSIMLD 74

Query: 64  GRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARVLQL 123
           G+DVT + P  R   M+FQSYAL+PHMTV +N+  G+K +       ++R+A   +++++
Sbjct: 75  GQDVTALPPFLRPTNMMFQSYALFPHMTVEQNIAMGLKQDKLPKSEIRDRVAAMLKLVKM 134

Query: 124 EDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLHKQL 183
           E Y  RKP QLSGGQ+QRVA+ R++ K P + L DEP+  LD KLR +M++EL  + + +
Sbjct: 135 EPYARRKPQQLSGGQQQRVALARSLAKRPKLLLLDEPMGALDKKLRTEMQLELVEILENV 194

Query: 184 GATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMNVF- 242
           GAT + VTHDQ EAMTMA +I ++ +GRI Q+GSP+D+Y  PNSR  AEFIGS  +N+F 
Sbjct: 195 GATCLMVTHDQEEAMTMASRIAIMAQGRIAQIGSPIDIYESPNSRMTAEFIGS--VNIFE 252

Query: 243 -------SSDVGLQDISLDA--------------SAAFVGCRPEHIEIVPD-GDGH---I 277
                  +  V L    LDA              +A  V  RPE I + PD  DG     
Sbjct: 253 AHIREDEADSVTLTSDLLDAPVFIDRGVTTPAESTATLVALRPEKIYLTPDKPDGENNWS 312

Query: 278 AATVHVKERLGGESLLYLGLKGGGQIVA 305
             TV     LG  +  Y+ L  G ++ A
Sbjct: 313 CGTVDNIAYLGDITSYYVKLASGKRVQA 340


Lambda     K      H
   0.320    0.139    0.396 

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: 300
Number of extensions: 11
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: 338
Length of database: 372
Length adjustment: 29
Effective length of query: 309
Effective length of database: 343
Effective search space:   105987
Effective search space used:   105987
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