GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Synechococcus elongatus PCC 7942

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate Synpcc7942_0947 Synpcc7942_0947 ATPase

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__SynE:Synpcc7942_0947
          Length = 355

 Score =  251 bits (640), Expect = 3e-71
 Identities = 147/367 (40%), Positives = 212/367 (57%), Gaps = 24/367 (6%)

Query: 4   IHCQALAKHYAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGTLRI 63
           +  + L K Y+     +  L L +  GEF+ LLGPSGCGKST LR+IAGL+  + G++ +
Sbjct: 6   LELRQLRKAYSPSVVPVANLSLQLQPGEFLTLLGPSGCGKSTTLRLIAGLDQPTSGSIWL 65

Query: 64  GGTVVNDLPARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAALLN 123
           G   +  LP  +R++AMVFQ+YALYPH++V  N+  GL+  +  AAEI++R+++VA  L 
Sbjct: 66  GDREITTLPPGDRDMAMVFQSYALYPHLNVRQNLTLGLQIRRTSAAEIEQRLQQVAHNLE 125

Query: 124 LEALLERKPRAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRLHQR 183
           L+ LL+R+P  +SGGQ+QR A+ RA+++ PSVFL DEPLSNLDA LR Q+R  +K L  +
Sbjct: 126 LDHLLDRRPAQLSGGQRQRVALGRALVRQPSVFLLDEPLSNLDALLREQVRAQMKALFSQ 185

Query: 184 LRTTTVYVTHDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAMNFL 243
             +  VYVTHDQ EA++L+ R+ ++  G + Q  SP  +Y+ P N F AGFIG+P MN L
Sbjct: 186 QASPVVYVTHDQTEALSLSHRIAILNGGHLQQLDSPDRIYQAPANAFVAGFIGSPRMNLL 245

Query: 244 SGTVQRQDGQLFIETAHQRWALTGERF----SRLRHAMAVKLAVRPDHVRIAGEREPAAS 299
              +            H   A  G R     S L     V   +RP+H+++A    P   
Sbjct: 246 PLPI------------HSGQAWLGSRALPIPSHLAARSQVLWGLRPEHLKLA---TPEVE 290

Query: 300 LTCPVSVELVEILGADALLTTRCG---DQTLTALVPADRLPQPGATLTLALDQHELHVFD 356
              PV + L E LG   LLT       +  L  L+P+D+ P P   L +  +    H F 
Sbjct: 291 RAIPVQLHLTENLGMQRLLTVAIAANPEVRLRLLMPSDQ-PIP-TDLQVTFEPESQHWFC 348

Query: 357 VESGENL 363
             +G+ L
Sbjct: 349 PSTGDRL 355


Lambda     K      H
   0.321    0.137    0.403 

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: 347
Number of extensions: 16
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: 406
Length of database: 355
Length adjustment: 30
Effective length of query: 376
Effective length of database: 325
Effective search space:   122200
Effective search space used:   122200
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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