GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Photobacterium gaetbulicola Gung47

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate WP_044623936.1 H744_RS23070 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::Smeli:SM_b21106
         (365 letters)



>NCBI__GCF_000940995.1:WP_044623936.1
          Length = 361

 Score =  316 bits (809), Expect = 7e-91
 Identities = 172/359 (47%), Positives = 229/359 (63%), Gaps = 25/359 (6%)

Query: 1   MAPVTLKKLVKRYGALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGAI 60
           MA V L  + K Y   + +H + L+++  EF+ LVGPSGCGKST LRMIAGLE+VS G +
Sbjct: 1   MAKVILNDVCKTYDKTQTIHDVKLDIESGEFLVLVGPSGCGKSTLLRMIAGLEDVSSGRV 60

Query: 61  EIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAAI 120
            I  R V D+    R ISMVFQSYALYPHMTV EN+ F LK    P  EI++R++EAA I
Sbjct: 61  HIDARDVTDVNASEREISMVFQSYALYPHMTVKENLAFGLKNIKMPTAEIESRISEAADI 120

Query: 121 LDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKLH 180
           L L+ LL RRP  LSGGQRQRVA+GR+IV+ P VFLFDEPLSNLDA LR Q+R E+ KLH
Sbjct: 121 LQLSELLNRRPQNLSGGQRQRVAIGRSIVQNPKVFLFDEPLSNLDAALRVQMRQELSKLH 180

Query: 181 ARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPMN 240
           +++++TMIYVTHDQVEAMTL+DRIVI+R G IEQ+GTP +V+ +PA  FVA F+G+P +N
Sbjct: 181 SKLKSTMIYVTHDQVEAMTLADRIVILRAGKIEQIGTPLEVYNQPANTFVAEFMGAPKIN 240

Query: 241 MEEAVLTDGKLAF-----------ASGATLPLPPRFRSLVREGQKVTFGLRPDDVYPSGH 289
           +  AV       F            +G+   LPP          KVT G+RP+      H
Sbjct: 241 LLTAVAEKSSEGFDLVFEGQSRLSIAGSLSHLPP--------DNKVTLGIRPE------H 286

Query: 290 GLHAGDADAVHEIELPVTITEPLGNETLVFTQFNGRDWVSRMLNPRPLRPGEAVPMSFD 348
                 ++    ++  VT +E LG+ T+V+  + G++   ++ +   L  G+   +  D
Sbjct: 287 ISIKAPSNEKTAMQATVTYSELLGDSTIVYLNYAGQEIRVKLASQEQLSVGDIFDLEID 345


Lambda     K      H
   0.320    0.137    0.397 

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: 323
Number of extensions: 13
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: 365
Length of database: 361
Length adjustment: 29
Effective length of query: 336
Effective length of database: 332
Effective search space:   111552
Effective search space used:   111552
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 24 2021. 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