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_1680 Synpcc7942_1680 Sulphate transport system permease protein 1

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__SynE:Synpcc7942_1680
          Length = 338

 Score =  202 bits (513), Expect = 2e-56
 Identities = 121/314 (38%), Positives = 172/314 (54%), Gaps = 25/314 (7%)

Query: 23  LDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGTLRIGGTVVNDLPARERNVAMVF 82
           +DL +  G  V LLGPSG GKST+LR+IAGLE    G + + G    +   R+R +  VF
Sbjct: 21  VDLTVETGSLVALLGPSGSGKSTLLRLIAGLEQPDSGRIFLTGRDATNESVRDRQIGFVF 80

Query: 83  QNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAALLNLEALLERKPRAMSGGQQQR 142
           Q+YAL+ H++V  NIAFGL   K    ++  RV E+  L+ L  L +R P  +SGGQ+QR
Sbjct: 81  QHYALFKHLTVRKNIAFGLELRKHTKEKVRARVEELLELVQLTGLGDRYPSQLSGGQRQR 140

Query: 143 AAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRLHQRLRTTTVYVTHDQLEAMTLA 202
            A+ARA+   P V L DEP   LDAK+R  LR  +++LH  +  TTV+VTHDQ EAM +A
Sbjct: 141 VALARALAVQPQVLLLDEPFGALDAKVRKDLRSWLRKLHDEVHVTTVFVTHDQEEAMEVA 200

Query: 203 DRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAMNFLSGTVQRQDGQLFIETAHQR 262
           D++++M  G++ Q GSPAE+Y  P   F   FIG   +   S  + +  G   ++T H  
Sbjct: 201 DQIVVMNHGKVEQIGSPAEIYDNPATPFVMSFIGPVNVLPNSSHIFQAGG---LDTPHP- 256

Query: 263 WALTGERFSRLRHAMAVKLAVRPDHVRIAGEREPAASLTCPVSVELVEILGADALLTTRC 322
                            ++ +RP  + IA +  P    T P  ++ +  LG +     R 
Sbjct: 257 -----------------EVFLRPHDIEIAIDPIPE---TVPARIDRIVHLGWEVQAEVRL 296

Query: 323 GD-QTLTALVPADR 335
            D Q L A +P DR
Sbjct: 297 EDGQVLVAHLPRDR 310


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: 338
Number of extensions: 7
Number of successful extensions: 1
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: 338
Length adjustment: 30
Effective length of query: 376
Effective length of database: 308
Effective search space:   115808
Effective search space used:   115808
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 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