GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glt in Rhizorhabdus wittichii RW1

Align Uncharacterized protein (characterized, see rationale)
to candidate WP_011952050.1 SWIT_RS06135 dicarboxylate/amino acid:cation symporter

Query= uniprot:A0A0C4Y5S4
         (436 letters)



>NCBI__GCF_000016765.1:WP_011952050.1
          Length = 421

 Score =  432 bits (1110), Expect = e-125
 Identities = 214/402 (53%), Positives = 293/402 (72%), Gaps = 1/402 (0%)

Query: 5   RLPTLIFIAMLLGVLAGTAAHHYAPDPAAAKSIADHLSILTDVFLRMIKMIIGPLVFATL 64
           RL   I  AM+ G++ G   +    DPA    +  H+SILT++FLR+IKMII PLVFATL
Sbjct: 4   RLTYYILGAMIAGIVVGITLNRTITDPATLTDVTGHISILTELFLRLIKMIIAPLVFATL 63

Query: 65  VSGIASMGDGKAVGRIGMKAMAWFIAASITSLLLGLLMANLLRPGDGMNLALPAADAASN 124
           V+GIA MGD  A+GR+G +++AWF+ AS+ SL LGL+M NLL+PG G +L LP   A++ 
Sbjct: 64  VTGIAHMGDTAALGRVGFRSIAWFLTASLMSLTLGLIMVNLLQPGVGADLVLPPEGASAG 123

Query: 125 LKTGALNLREFIAHMFPKSFVEAMATNEILQIVVFSLFFGFALGTLKDGIGKPVLAGIEG 184
           +     +L++F+ H+ PKSF EAMATNEILQIVVFS+F G A+  + +    P++ GIE 
Sbjct: 124 VSQADFSLKQFVTHLVPKSFFEAMATNEILQIVVFSVFTGVAITAVGERAA-PLVRGIEA 182

Query: 185 LSHVMLKITNYVMAFAPVGVFGAVAAVITAEGLGVLVVYAKLLGAVYLSLALLWVALIAG 244
           L  VML+IT+YVM FAP  VF AV   +  +G G+L+ + K +G+ YLS+ LLW  L+  
Sbjct: 183 LVQVMLQITDYVMRFAPFAVFAAVTTALAEQGPGILLSFGKFMGSFYLSMFLLWGLLLLL 242

Query: 245 GYFFLGRDVFRLLKMVRAPLMIGFATASSESAYPKVIEQLGRFGVKERITGFVLPLGYSF 304
            Y  +G     L++ +R P+++ F+TASSE+A+P+ +E L RFGV  RI  FVLPLGYSF
Sbjct: 243 CYLIVGGRSKLLIRYIREPILLAFSTASSEAAFPRTLEALDRFGVPPRIASFVLPLGYSF 302

Query: 305 NLDGSIMYTSFAALFVAQVYGIHLSLSQQVTMLLVLLVTSKGIAGVPRASLVVVAAVLPM 364
           NLDGS++Y +FA +F+AQ YGI L+ + QVTMLL+L+VTSKGIAGVPRASLV++++ L  
Sbjct: 303 NLDGSMIYCTFATMFIAQAYGIELTFAHQVTMLLILMVTSKGIAGVPRASLVIISSTLAF 362

Query: 365 FGLPEAGILLVLGIDHVLDMGRTVTNVLGNAIATTVVAKSEG 406
           F +PEAG+LL+L +DH LDMGR+ TNV+GNA+A+ +VAK EG
Sbjct: 363 FDIPEAGLLLILAVDHFLDMGRSATNVVGNAVASVIVAKWEG 404


Lambda     K      H
   0.325    0.141    0.401 

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: 403
Number of extensions: 18
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: 436
Length of database: 421
Length adjustment: 32
Effective length of query: 404
Effective length of database: 389
Effective search space:   157156
Effective search space used:   157156
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. 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