GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Sinorhizobium meliloti 1021

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate SMc04393 SMc04393 ABC transporter ATP-binding protein

Query= reanno::WCS417:GFF4321
         (386 letters)



>FitnessBrowser__Smeli:SMc04393
          Length = 370

 Score =  362 bits (929), Expect = e-105
 Identities = 190/371 (51%), Positives = 252/371 (67%), Gaps = 8/371 (2%)

Query: 1   MATLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGG 60
           M+ L++ N+ K+YGA   + LK+I L I+EG FL+LVGPSGCGKSTL+N IAGLE IT G
Sbjct: 1   MSFLKITNLRKSYGA--LEILKDINLEIEEGGFLVLVGPSGCGKSTLLNTIAGLEPITSG 58

Query: 61  AIMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVA 120
            I I  + VSG+ P  RDIAMVFQSYALYP M+V  NI FG++IR +P+ + +  + +VA
Sbjct: 59  DIAINGRSVSGLHPSKRDIAMVFQSYALYPNMTVAGNIAFGMEIRGVPKEEREKAIKQVA 118

Query: 121 KLLQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
            +LQI HLL+RKP QLSGGQ+QRVAMGRAL R P+++LFDEPLSNLDAKLRV+MRTE+K 
Sbjct: 119 DMLQIGHLLDRKPSQLSGGQRQRVAMGRALVRNPQVFLFDEPLSNLDAKLRVDMRTEIKR 178

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIGSPP 240
           +H R+KTT VYVTHDQIEAMTL  K+AV+KDG++QQFGTP EIYNNPAN FVA F+GSP 
Sbjct: 179 LHHRMKTTIVYVTHDQIEAMTLATKIAVLKDGVLQQFGTPAEIYNNPANMFVADFMGSPA 238

Query: 241 MNFVPLRLQRKDGRLVALLDSGQA---RCELALNTTEAGLEDRDVILGLRPEQIMLAAGE 297
           MN +  +++    ++   L    A   R  +  N   +    ++V+ G+RPE +    G 
Sbjct: 239 MNLLKAQIETAGSQVSVTLARPNAEPLRLAVPHNGALSAYAGKEVVFGIRPEALTDPDGA 298

Query: 298 GDSASSI---RAEVQVTEPTGPDTLVFVQLNDTKVCCRLAPDVAPQVGETLTLQFDPSKV 354
             +A  +      ++V EP G DT    +L   ++  RL  D     G+T  L F+  K 
Sbjct: 299 DRNAQFVAEGECLIEVVEPAGSDTFAVTRLGGKEIVARLRADARIAPGQTSRLAFNLDKA 358

Query: 355 LLFDANTGERL 365
           + FD  + +R+
Sbjct: 359 VFFDPQSEKRI 369


Lambda     K      H
   0.318    0.135    0.382 

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: 400
Number of extensions: 15
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: 370
Length adjustment: 30
Effective length of query: 356
Effective length of database: 340
Effective search space:   121040
Effective search space used:   121040
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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