GapMind for catabolism of small carbon sources

 

Alignments for a candidate for musK in Halomonas xinjiangensis TRM 0175

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_043527328.1 JH15_RS04270 ABC transporter ATP-binding protein

Query= BRENDA::Q8NMV1
         (376 letters)



>NCBI__GCF_000759345.1:WP_043527328.1
          Length = 373

 Score =  261 bits (667), Expect = 2e-74
 Identities = 160/372 (43%), Positives = 220/372 (59%), Gaps = 29/372 (7%)

Query: 18  EPTVKKFNLEIADGEFLVLVGPSGCGKSTTLRMLAGLENVTDGAIFIGDKDVTHVAPRDR 77
           E  +K  +L I  G+FL+LVGPSGCGKST +  +AGLE VT G+I I   DVT   P DR
Sbjct: 16  ERVLKDVSLSIDSGQFLILVGPSGCGKSTLMNAIAGLEPVTSGSISIAGDDVTWHTPADR 75

Query: 78  DIAMVFQNYALYPHMTVGENMGFALKIAGKSQDEINKRVDEAAATLGLTEFLERKPKALS 137
           DIAMVFQ+YALYP MTV +N+ F L++    + E    V+  A  L +++ LERKP  LS
Sbjct: 76  DIAMVFQSYALYPSMTVRQNISFGLEMRKVPKAEREAAVERVADLLQISQLLERKPSQLS 135

Query: 138 GGQRQRVAMGRAIVRNPQVFLMDEPLSNLDAKLRVQTRTQIAALQRKLGVTTVYVTHDQT 197
           GGQRQRVAMGRA+ R P+V+L DEPLSNLDAKLRV+ RT+I  L ++LG T VYVTHDQ 
Sbjct: 136 GGQRQRVAMGRALAREPKVYLFDEPLSNLDAKLRVEMRTEIKKLHQRLGTTIVYVTHDQI 195

Query: 198 EALTMGDRIAVLKDGYLQQVGAPRELYDRPANVFVAGFIGSPAMN-LGTFSVKDGD---- 252
           EA+T+ D IAV++DG + Q+G+P E+Y+ P ++FVAGF+GSP+MN +     K G+    
Sbjct: 196 EAMTLADCIAVMRDGKILQLGSPDEVYNNPVDMFVAGFMGSPSMNFINATLEKQGEQYHV 255

Query: 253 --ATSGHARIKLSPETLAAMTPEDN----GRITIGFRPE--ALEIIPEGESTDLSI-PIK 303
             AT G   + L P   +   PE +      + +G RPE  + E +  G++ + ++    
Sbjct: 256 RIATPGQDDLVL-PWPASREQPEMSEWVGKAVVLGLRPEHFSEEDVRLGDAAEGTLFNAS 314

Query: 304 LDFVEELGSDSFLYGKLVGEGDLGSSSEDVPESGQIVVRAAPNAAPAPGSVFHARIVEGG 363
           +  VE  G++  +   L   GD            ++  R  P    A G     R+  G 
Sbjct: 315 ITVVEPTGAEILIQLPL---GD-----------KEVTARVGPKCKVAAGETLALRVDMGM 360

Query: 364 QHNFSASTGKRL 375
              F   + +RL
Sbjct: 361 GVLFDPDSERRL 372


Lambda     K      H
   0.316    0.135    0.380 

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: 396
Number of extensions: 14
Number of successful extensions: 1
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: 376
Length of database: 373
Length adjustment: 30
Effective length of query: 346
Effective length of database: 343
Effective search space:   118678
Effective search space used:   118678
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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