GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Halomonas desiderata SP1

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate WP_086510784.1 BZY95_RS15425 ABC transporter ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_791
         (363 letters)



>NCBI__GCF_002151265.1:WP_086510784.1
          Length = 373

 Score =  186 bits (472), Expect = 9e-52
 Identities = 127/361 (35%), Positives = 197/361 (54%), Gaps = 20/361 (5%)

Query: 3   LALDSISKKVGAQTWLYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVTVD 62
           L ++++ K  G++  L D+SLA+ SG   +L+G +  GK++LM  +AGL+  T+G + + 
Sbjct: 4   LEINNVCKDFGSEQVLKDVSLAIDSGEFLILVGPSGCGKSTLMNAIAGLEPVTSGEIRIA 63

Query: 63  GKDVTGMPVRDRNVAMVYQQFINYPSMKVAANIASPLKLRG--EKNIDARVREIASRLHI 120
           G+ VT     +R++AMV+Q +  YPSM V  NI+  L++R   +   +A V  +A  L I
Sbjct: 64  GESVTWQTPAERDIAMVFQSYALYPSMTVRQNISFGLEMRKVPKAEREAAVERVADLLQI 123

Query: 121 DMFLDRYPAELSGGQQQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFAAG 180
              L+R P++LSGGQ+QRVA+ RALA+   + L DEPL NLD KLR ++R E+ +L    
Sbjct: 124 GHLLERKPSQLSGGQRQRVAMGRALAREPKVYLFDEPLSNLDAKLRVDMRTEIKKLHQRL 183

Query: 181 QSTVVYATTEPGEALLLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNLMA 240
            +T+VY T +  EA+ L    AV+ +G++LQ G   EV++ P  L VA     P MN ++
Sbjct: 184 GTTIVYVTHDQIEAMTLADCIAVMRDGRILQLGSPDEVYNDPVDLFVAGFMGSPSMNFIS 243

Query: 241 AS------ATAQGVRLQGGAELTLPLPQGAAT-AAGLTVGVRA-SALRVH------ARPG 286
           A+      A    V   G   L LP PQ   T A G  VG R    LR        AR G
Sbjct: 244 ATLVGGSGAYRLRVETPGEETLELPWPQERETPALGEKVGERVILGLRPEHFTEDDARLG 303

Query: 287 D----VSVAGVVELAEISGSDTFVHASTPWGDLVAQLTGVHYFELGTAITLHLDPAQAYV 342
           +    V++   + + E +G+D  +      G+  A++      + G  +TL +D  +A +
Sbjct: 304 EYAEGVALTPRITVVEPTGADILLQLKLGDGEATARVGPKCRVKAGERLTLRIDMGRAVM 363

Query: 343 F 343
           F
Sbjct: 364 F 364


Lambda     K      H
   0.318    0.133    0.375 

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: 262
Number of extensions: 9
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: 363
Length of database: 373
Length adjustment: 30
Effective length of query: 333
Effective length of database: 343
Effective search space:   114219
Effective search space used:   114219
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 (21.7 bits)
S2: 49 (23.5 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