Alignments for a candidate for TM1750 in Synechococcus elongatus PCC 7942

GapMind for catabolism of small carbon sources

Alignments for a candidate for TM1750 in Synechococcus elongatus PCC 7942

Align TM1750, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate Synpcc7942_2236 Synpcc7942_2236 ATPase

Query= TCDB::Q9X272
         (328 letters)



>FitnessBrowser__SynE:Synpcc7942_2236
          Length = 554

 Score =  194 bits (493), Expect = 4e-54
 Identities = 104/257 (40%), Positives = 166/257 (64%), Gaps = 11/257 (4%)

Query: 11  KPLLQTVDLKKYFPQGKRILKAVDGISIEIKEGETLGLVGESGCGKSTLGRTILKLLRPD 70
           +PLLQ   L   +       +AV  +S  +  G TLGLVGESGCGKS+L R ++ L+   
Sbjct: 298 QPLLQVEQLGITYRGRSTAFQAVQNLSFTLPAGLTLGLVGESGCGKSSLARCLVGLVPAS 357

Query: 71  GGKIFFEGKDITNLNDKEMKPYRKKMQIIFQDPLGSLNPQMTVGRIIEDPLIIHKIGTKK 130
            G+I+ + + +   + ++ +  R+ +Q++FQDP  +L+P+ TVG  I +PL I     K+
Sbjct: 358 EGQIWLDQQPLDLRSSRDRQRLRQTVQMVFQDPAAALDPRWTVGSAILEPLRI-----KQ 412

Query: 131 ERRKR------VEELLDMVGIGREFINSFPHEFSGGQQQRIGIARALALNPKFIVCDEPV 184
            RR R      +++ L  V +  +  + +PHEFSGGQ+QRI IARAL   P+ ++CDE V
Sbjct: 413 PRRDRTADQRLLKQWLQRVDLPTDIGDRYPHEFSGGQRQRICIARALIGQPRLLICDESV 472

Query: 185 SALDVSIQAQIIDLLEEIQQKMGISYLFIAHNLAVVEHISHKVAVMYLGKIVEYGDVDKI 244
           SALDVS+QAQI++LL+++Q ++G++YLFI+H+LAVV ++S ++ VM  G++ E    +++
Sbjct: 473 SALDVSVQAQILNLLKQLQAELGLTYLFISHDLAVVRYMSDRILVMNQGQLEEDSPTEQL 532

Query: 245 FLNPIHPYTRALLKSVP 261
           F  P   YTR L+ ++P
Sbjct: 533 FQRPQSDYTRRLIAAIP 549



 Score =  159 bits (402), Expect = 2e-43
 Identities = 96/268 (35%), Positives = 158/268 (58%), Gaps = 20/268 (7%)

Query: 12  PLLQTVDLKKYFPQGKRILKAVDGISIEIKEGETLGLVGESGCGKSTLGRTILKLLRPDG 71
           PLL+   L+  F  G+ I  A+ G+ + ++ GE++G+VGESG GKS     I  LL    
Sbjct: 4   PLLEIRQLQICF--GEAI--ALQGLDLVVQPGESVGIVGESGSGKSVACLAIPGLLPKTA 59

Query: 72  ---GKIFFEG------KDITNLNDKEMKPYR-KKMQIIFQDPLGSLNPQMTVGRIIEDPL 121
              G+I F        +D+  L ++E++  R  ++  IFQ+PL SLNP  + G  + + +
Sbjct: 60  RCSGQIAFRSVAGQSSRDLLTLPERELRQLRGDRLGFIFQEPLSSLNPVFSAGFQLLEAI 119

Query: 122 IIHKIGTKKERRKRVEELLDMVGIGRE------FINSFPHEFSGGQQQRIGIARALALNP 175
             H   ++ E ++RV  LL  V + RE       +  +PH+ SGGQ+QR+ IA ALA NP
Sbjct: 120 QQHLPLSQAEAQQRVIALLQEVQLIREPSQAAQILRRYPHQLSGGQRQRLMIAIALAANP 179

Query: 176 KFIVCDEPVSALDVSIQAQIIDLLEEIQQKMGISYLFIAHNLAVVEHISHKVAVMYLGKI 235
             ++ DEP +ALD ++QA ++ LL  +QQ+  ++ +F++H+L V+  ++ +V V+Y G++
Sbjct: 180 DLLLADEPTTALDATVQASVLQLLRRLQQQRQMAMIFVSHDLGVIAEVADRVVVLYRGQV 239

Query: 236 VEYGDVDKIFLNPIHPYTRALLKSVPKI 263
           VE G V  +  +P HPYT+ L+   P+I
Sbjct: 240 VEQGRVADVLNSPQHPYTQGLVACRPQI 267


Lambda     K      H
   0.321    0.142    0.417 

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: 497
Number of extensions: 19
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 328
Length of database: 554
Length adjustment: 32
Effective length of query: 296
Effective length of database: 522
Effective search space:   154512
Effective search space used:   154512
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: 51 (24.3 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources