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_0947 Synpcc7942_0947 ATPase

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



>FitnessBrowser__SynE:Synpcc7942_0947
          Length = 355

 Score =  276 bits (705), Expect = 8e-79
 Identities = 158/366 (43%), Positives = 225/366 (61%), Gaps = 20/366 (5%)

Query: 4   LELRNVNKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGGAIL 63
           LELR + K Y P +   + N+ L++  GEFL L+GPSGCGKST +  IAGL+  + G+I 
Sbjct: 6   LELRQLRKAYSPSVVP-VANLSLQLQPGEFLTLLGPSGCGKSTTLRLIAGLDQPTSGSIW 64

Query: 64  VDDADISGMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDEEVARVSKLL 123
           + D +I+ + P DRD+AMVFQSYALYP ++VR N+  GL+IR+   AEI++ + +V+  L
Sbjct: 65  LGDREITTLPPGDRDMAMVFQSYALYPHLNVRQNLTLGLQIRRTSAAEIEQRLQQVAHNL 124

Query: 124 QIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKLMHQ 183
           +++HLL R+P QLSGGQ+QRVA+GRAL R+P ++L DEPLSNLDA LR ++R +MK +  
Sbjct: 125 ELDHLLDRRPAQLSGGQRQRVALGRALVRQPSVFLLDEPLSNLDALLREQVRAQMKALFS 184

Query: 184 RLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFIGSPPMNF 243
           +  +  VYVTHDQ EA++L  ++A++  G +QQ  +P  IY  PAN FVA FIGSP MN 
Sbjct: 185 QQASPVVYVTHDQTEALSLSHRIAILNGGHLQQLDSPDRIYQAPANAFVAGFIGSPRMNL 244

Query: 244 IPLRLQRKDGRLLALLDSGQA---RCELPLGMQDAGLEDREVILGIRPEQIILANGEANG 300
           +PL +            SGQA      LP+    A     +V+ G+RPE + LA  E   
Sbjct: 245 LPLPIH-----------SGQAWLGSRALPIPSHLAARS--QVLWGLRPEHLKLATPEVE- 290

Query: 301 LPTIRAEVQVTEPTGPDTLVFVNL-NDTKVCCRLAPDVAPAVGETLTLQFDPAKVLLFDA 359
              I  ++ +TE  G   L+ V +  + +V  RL       +   L + F+P     F  
Sbjct: 291 -RAIPVQLHLTENLGMQRLLTVAIAANPEVRLRLLMPSDQPIPTDLQVTFEPESQHWFCP 349

Query: 360 KTGERL 365
            TG+RL
Sbjct: 350 STGDRL 355


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: 360
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: 386
Length of database: 355
Length adjustment: 30
Effective length of query: 356
Effective length of database: 325
Effective search space:   115700
Effective search space used:   115700
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: 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