GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Synechococcus elongatus PCC 7942

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate Synpcc7942_0947 Synpcc7942_0947 ATPase

Query= TCDB::G3LHY9
         (356 letters)



>FitnessBrowser__SynE:Synpcc7942_0947
          Length = 355

 Score =  196 bits (497), Expect = 1e-54
 Identities = 110/346 (31%), Positives = 190/346 (54%), Gaps = 15/346 (4%)

Query: 4   ITLDHIRHAYGANPKSDKDYSLKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQPSH 63
           + L  +R AY  +     + SL     +   G    LLGPSGCGK+T L +I+GL QP+ 
Sbjct: 6   LELRQLRKAYSPSVVPVANLSL-----QLQPGEFLTLLGPSGCGKSTTLRLIAGLDQPTS 60

Query: 64  GRILFDGKDVTNLSTQSRNIAQVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRVRDI 123
           G I    +++T L    R++A VFQ   +Y  + V  NL   L+ R  + A++++R++ +
Sbjct: 61  GSIWLGDREITTLPPGDRDMAMVFQSYALYPHLNVRQNLTLGLQIRRTSAAEIEQRLQQV 120

Query: 124 LEMIDLASWARRKAQGLTADQKQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLRSQL 183
              ++L     R+   L+  Q+Q+++LGR LVR   +  L DEPL+ +D  ++  +R+Q+
Sbjct: 121 AHNLELDHLLDRRPAQLSGGQRQRVALGRALVRQP-SVFLLDEPLSNLDALLREQVRAQM 179

Query: 184 KRLHKQFGFTMVYVTHDQTEALTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYFIGS 243
           K L  Q    +VYVTHDQTEAL+ + ++ ++  G + Q+ +P  +++ P++ FV  FIGS
Sbjct: 180 KALFSQQASPVVYVTHDQTEALSLSHRIAILNGGHLQQLDSPDRIYQAPANAFVAGFIGS 239

Query: 244 PGMNFMPARIEGSTVKVGDETLTLEYAPKTSGTAKTELGIRPEFIRLG----REGMPITI 299
           P MN +P  I      +G   L +      +  ++   G+RPE ++L        +P+ +
Sbjct: 240 PRMNLLPLPIHSGQAWLGSRALPI--PSHLAARSQVLWGLRPEHLKLATPEVERAIPVQL 297

Query: 300 SKVEDIGRQKIVRARFADQP---IAIVVPEDADIPADARVTFDPSA 342
              E++G Q+++    A  P   + +++P D  IP D +VTF+P +
Sbjct: 298 HLTENLGMQRLLTVAIAANPEVRLRLLMPSDQPIPTDLQVTFEPES 343


Lambda     K      H
   0.321    0.137    0.405 

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: 269
Number of extensions: 13
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: 356
Length of database: 355
Length adjustment: 29
Effective length of query: 327
Effective length of database: 326
Effective search space:   106602
Effective search space used:   106602
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