GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PfGW456L13_1897 in Synechococcus elongatus PCC 7942

Align ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized)
to candidate Synpcc7942_1406 Synpcc7942_1406 ATPase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1897
         (386 letters)



>FitnessBrowser__SynE:Synpcc7942_1406
          Length = 368

 Score =  190 bits (483), Expect = 5e-53
 Identities = 125/358 (34%), Positives = 196/358 (54%), Gaps = 24/358 (6%)

Query: 6   LRNVNKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGGAILVD 65
           L  V K +       +  +  +++ GE L LVGPSGCGK+TL+  IAG E++  G+I + 
Sbjct: 9   LDRVCKQFSGSSLAAVDQVSFELEAGEILGLVGPSGCGKTTLLRMIAGFESLQSGSIQLA 68

Query: 66  DADIS----GMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDEEVARVSK 121
              ++     + P+ R + MVFQ YAL+P ++V DN+ FGL+ RK   A   + +A    
Sbjct: 69  GETVATAQRSLPPETRSVGMVFQDYALFPHLTVLDNVCFGLRDRKGSAAVARQALA---- 124

Query: 122 LLQIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKLM 181
           L+ +E L  R P +LSGGQQQRVA+ RALA +P + L DEPLSNLD ++R+ +R E++ +
Sbjct: 125 LVGLEGLERRYPHELSGGQQQRVALARALAPQPPLILLDEPLSNLDVQVRLRLRQELRDI 184

Query: 182 HQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFIGSPPM 241
            ++ + T + VTHDQ EA+++ D+VAVM+ G  +Q G P++++ +PA+ FVA F+     
Sbjct: 185 LRQAQATAILVTHDQEEALSICDRVAVMRLGRFEQIGQPEELFQHPASRFVAEFLSQ--A 242

Query: 242 NFIPLRLQRKDGRLLALLDSGQARCELPLGMQDAGLEDREVILGIRPEQIIL-ANGEANG 300
           NF+    Q    R +          E P G++ +       ++ +R E ++L  + E  G
Sbjct: 243 NFLATEYQGDAWRTVL------GDFEAPGGLEGSRTGGEPPVVMVRQEDVLLHPHPEGTG 296

Query: 301 LPTIRAEVQVTEPTGPDTLVFVNLNDTKVCCRLAP-DVAPAVGETLTLQFDPAKVLLF 357
           L      V+  +  G D   FV L        L P   A AVG  + +Q    +  L+
Sbjct: 297 L------VRDRQFLGRDYRYFVQLPAGLEIQVLGPVSEAIAVGTAVQVQLRTGQARLY 348


Lambda     K      H
   0.319    0.138    0.393 

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: 320
Number of extensions: 11
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: 386
Length of database: 368
Length adjustment: 30
Effective length of query: 356
Effective length of database: 338
Effective search space:   120328
Effective search space used:   120328
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 (21.7 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