GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malF in Luteipulveratus mongoliensis MN07-A0370

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate WP_052597074.1 VV02_RS15280 sugar ABC transporter permease

Query= reanno::Koxy:BWI76_RS01825
         (514 letters)



>NCBI__GCF_001190945.1:WP_052597074.1
          Length = 302

 Score =  105 bits (261), Expect = 3e-27
 Identities = 76/257 (29%), Positives = 135/257 (52%), Gaps = 21/257 (8%)

Query: 250 KLSPGYTVTIGWDNFTRVFQDEGIQKPFFAIFVWTVVFSVLTVILTVAVGMVLACLVQWE 309
           +L+  YT  +G DN++R+ QD+   +      ++ V+F  L V++++A  ++L  + ++ 
Sbjct: 54  QLNGDYTF-VGADNYSRILQDDAFWQSLKVTGLYVVIFVPLIVVVSLAGAVLLHQMQRYT 112

Query: 310 ALKGKAIYRVLLILPYAVPSFISILIFKGLFNQSFGEINMMLSAL-FGIKPAWFSDPTTA 368
            L     +R LL +PY     ++ +++  +F    G +N  L  L FG  P         
Sbjct: 113 GL-----FRSLLFVPYLCSFVLAGIVWTWIFATD-GPLNAALGGLGFGSVPFISGSQLLV 166

Query: 369 RTMIIIVNTWLGYPYMMILCMGLLKAIPDDLYEASAMDGATPFQNFFKITLPLLIKPLTP 428
              + +V+ W G+ Y M++ +  LKA+P +++EA+ +DGA  ++ F+ ITLPLL +P+T 
Sbjct: 167 LGSLAMVSVWKGFGYSMLIFLAGLKALPAEVHEAARIDGAGAWRTFWHITLPLL-RPITL 225

Query: 429 -LMIASFAFNFNNFVLIQLLTNGGPDRLGTTTPAGYTDLLVSYTYRIAFEGGGGQDFGLA 487
            ++I      F  F  I ++T GGP+R              S  Y +  EG    DFG A
Sbjct: 226 FVLIIETIVGFQVFDTIYVMTGGGPNRASH-----------SLIYFLYDEGFKFFDFGYA 274

Query: 488 AAIATLIFLLVGLLAIV 504
           AA   ++F++V LL++V
Sbjct: 275 AAAGVVLFVIVLLLSLV 291



 Score = 26.2 bits (56), Expect = 0.002
 Identities = 13/51 (25%), Positives = 25/51 (49%), Gaps = 3/51 (5%)

Query: 67  YVYPGLAGMGLFVLFPLICTIAIAFTNYSSTNQLTF---ERAQQVLMDRSF 114
           +V P +   G+F   P++   A++ T+Y      TF   +   ++L D +F
Sbjct: 26  FVLPTVVIFGIFKFLPILGAGAMSLTDYQLNGDYTFVGADNYSRILQDDAF 76


Lambda     K      H
   0.325    0.140    0.426 

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: 337
Number of extensions: 15
Number of successful extensions: 3
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: 514
Length of database: 302
Length adjustment: 31
Effective length of query: 483
Effective length of database: 271
Effective search space:   130893
Effective search space used:   130893
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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