GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Maridesulfovibrio zosterae DSM 11974

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_051249582.1 H589_RS0101625 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_000425265.1:WP_051249582.1
          Length = 390

 Score =  259 bits (661), Expect = 1e-73
 Identities = 148/345 (42%), Positives = 207/345 (60%), Gaps = 34/345 (9%)

Query: 3   NTKTNWIIGAVALLVLPLILQS-FGNAWVRIADLALLYVLLALGLNIVVGYAGLLDLGYV 61
           +T    ++ A  LL   +     FG     +A   ++Y+ L LGLNIVVG AG+LDLGY+
Sbjct: 68  STTVPMVVWAFLLLAFAIAYPHLFGRYAQDVAINCMVYICLGLGLNIVVGLAGMLDLGYI 127

Query: 62  AFYAVGAYLFALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTL 121
           AFY +GAY +AL++  +                  S W+ +P++A +A     ++G  ++
Sbjct: 128 AFYGLGAYTYALLSVTY----------------KISFWLCLPLSAAVAGLGACIIGYCSM 171

Query: 122 KLRGDYLAIVTLGFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGF 181
           ++RGDYLAIVTLGF EI+R+  NN    ++LTNGP G+  I +  ++  D    +     
Sbjct: 172 RMRGDYLAIVTLGFAEIVRMVFNNW---MSLTNGPNGITGIKAPGIYWPDFTNGMTFEHL 228

Query: 182 DINSVTLYYYLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAF 241
            +  ++L YY+ L LVV ++I  YRL  SRIGRAW AIREDE AA+ MGI T  MKLLA+
Sbjct: 229 WLKKLSLIYYVILALVVFTIIAVYRLNHSRIGRAWEAIREDETAAEVMGIPTFYMKLLAY 288

Query: 242 GMGASFGGVSGAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALP 301
             GA FGG++GA + A   FVSPESF+ +ES M+++MVVLGG+G IPGVILGA+ L ALP
Sbjct: 289 CTGACFGGMAGAFYAARMRFVSPESFTFLESAMVLSMVVLGGMGSIPGVILGALALIALP 348

Query: 302 EVLRYVAGPLQAMTDGRLDSAILRQLLIALAMIIIMLLRPRGLWP 346
           E+ R              D  + R L+    M ++ML RP+GL P
Sbjct: 349 EIFR--------------DFELYRMLVFGGVMTLMMLFRPQGLLP 379


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: 383
Number of extensions: 20
Number of successful extensions: 4
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: 390
Length adjustment: 30
Effective length of query: 328
Effective length of database: 360
Effective search space:   118080
Effective search space used:   118080
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.

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