GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Hyphomicrobium sulfonivorans WDL6

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_083509693.1 APY04_RS10565 high-affinity branched-chain amino acid ABC transporter permease LivM

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_001541235.1:WP_083509693.1
          Length = 474

 Score =  261 bits (668), Expect = 2e-74
 Identities = 163/351 (46%), Positives = 213/351 (60%), Gaps = 28/351 (7%)

Query: 10  IGAVALLVLP---LILQSFGNA--WV-RIADLALLYVLLALGLNIVVGYAGLLDLGYVAF 63
           IG  ALL+ P   L+L   G A  W+       L+YV+LA GLNIVVG AGLLDLGYVAF
Sbjct: 109 IGLAALLIFPFFALLLTGQGGAVKWIDNFGVQILIYVMLAWGLNIVVGLAGLLDLGYVAF 168

Query: 64  YAVGAYLFALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKL 123
           YAVGAY +AL+A+           A  P     + WI +P+A +LAAF+G +LG P L+L
Sbjct: 169 YAVGAYAYALIAT-------YVIPATVPGLGPWAFWICLPIAGILAAFWGILLGFPVLRL 221

Query: 124 RGDYLAIVTLGFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRL------E 177
           RGDYLAIVTL FGEIIR+ L N    V +TNG  G+ +   +  FGL    R       +
Sbjct: 222 RGDYLAIVTLAFGEIIRLVLINW---VEVTNGNAGI-RTPYITFFGLPFSSRTGETTFGD 277

Query: 178 VFGFD----INSVTLYYYLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINT 233
           VF       ++     YY  L L ++  +   RL+   IGRAW A+REDEIA +++GINT
Sbjct: 278 VFSLPGSPAVHRSMFLYYTILALALLVAVATQRLRRLPIGRAWEAMREDEIACRSLGINT 337

Query: 234 RNMKLLAFGMGASFGGVSGAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILG 293
            N KL AF +GA FGG++GA FGA QGFV+P SF  MES  I+A+VVLGG+G + GV + 
Sbjct: 338 VNTKLTAFAIGAMFGGLAGAFFGARQGFVNPRSFEFMESATILAIVVLGGMGSLVGVAIA 397

Query: 294 AVLLSALPEVLRYVAGPLQAMTDGRLDSAILRQLLIALAMIIIMLLRPRGL 344
           AV +    E+LR +   L+ +     D    R L+  LAM+++M+ RPRGL
Sbjct: 398 AVAVIGGIELLRELTF-LKQIFGPEFDPGQYRMLIFGLAMVLMMIWRPRGL 447


Lambda     K      H
   0.328    0.144    0.430 

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: 468
Number of extensions: 19
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: 358
Length of database: 474
Length adjustment: 31
Effective length of query: 327
Effective length of database: 443
Effective search space:   144861
Effective search space used:   144861
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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