GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Billgrantia desiderata SP1

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate WP_086511129.1 BZY95_RS17245 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::psRCH2:GFF857
         (371 letters)



>NCBI__GCF_002151265.1:WP_086511129.1
          Length = 380

 Score =  412 bits (1060), Expect = e-120
 Identities = 212/367 (57%), Positives = 265/367 (72%), Gaps = 5/367 (1%)

Query: 1   MASVTLRDICKSYDGTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGDL 60
           MA++ L DI K +D T + + +DL++ D EFVVFVGPSGCGKSTLLR+IAGLE  TSGD+
Sbjct: 1   MATLQLHDIVKRFDDTEVIKGVDLEVNDREFVVFVGPSGCGKSTLLRMIAGLESATSGDI 60

Query: 61  LIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAEI 120
           LID  R+N++ P +R + MVFQSYALYPHMTV +NM F LKLA V K E +R+V   A I
Sbjct: 61  LIDGVRMNEVGPAERGLAMVFQSYALYPHMTVEDNMGFSLKLAGVPKEERRRKVREAASI 120

Query: 121 LQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARLH 180
           LQL+ LLERKPK LSGGQRQRVAIGR +VR P +FLFDEPLSNLDA LRVQMRIE+ARLH
Sbjct: 121 LQLEPLLERKPKALSGGQRQRVAIGRAIVRNPSIFLFDEPLSNLDAALRVQMRIELARLH 180

Query: 181 QRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLGSPQMN 240
           + + +TMIYVTHDQ+EAMT+ADKIVVL  G + QVG P+ LYH+P+NRFVAGF+GSP+MN
Sbjct: 181 EELDATMIYVTHDQIEAMTMADKIVVLQGGVVEQVGSPMELYHHPRNRFVAGFIGSPKMN 240

Query: 241 FVEVRAISASPETVTIELPSGYPLTLPVDGSAVSPGDPLTLGIRPEHFVMPDEADFTFHG 300
           F+EV  +SA+   V + LP G   T+PVDGS +   D LTLGIRPEH  +  +   +  G
Sbjct: 241 FLEVERVSAAATGVEVRLPDGDTCTVPVDGSGLD-DDALTLGIRPEHLQLDPQGPLS--G 297

Query: 301 QITVAERLGQYNLLYLTLERLQDVITLCVDGNLRVTEGETFAAGLKADKCHLFRENGEAC 360
           +I V ERLG    LY+ ++    ++T+  DGN+    G++   G + D  HLF   G A 
Sbjct: 298 RIEVIERLGGVTSLYVRMQ--NTLVTVSADGNVDSRVGDSLRFGFERDCAHLFDGEGLAL 355

Query: 361 TRHYREP 367
               R P
Sbjct: 356 PSLARHP 362


Lambda     K      H
   0.322    0.139    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: 451
Number of extensions: 14
Number of successful extensions: 4
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: 371
Length of database: 380
Length adjustment: 30
Effective length of query: 341
Effective length of database: 350
Effective search space:   119350
Effective search space used:   119350
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 (21.9 bits)
S2: 50 (23.9 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