GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malF in Herbaspirillum seropedicae SmR1

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate HSERO_RS16725 HSERO_RS16725 ABC transporter permease

Query= reanno::psRCH2:GFF850
         (521 letters)



>FitnessBrowser__HerbieS:HSERO_RS16725
          Length = 299

 Score = 95.9 bits (237), Expect = 2e-24
 Identities = 75/245 (30%), Positives = 115/245 (46%), Gaps = 15/245 (6%)

Query: 267 FTGFANFSRVLTEPSIREPFMQIFAWTFAFAGLTVVFTLAVGLVLASLLQWELVRGKAFY 326
           F G  NF+  L   S+ +  + +F   F     +++    +GL LA LL  + V  K F+
Sbjct: 51  FIGLDNFT-YLAGDSLAQ--LSLFNTVFYTVSASIL-KFMLGLWLAILLN-KNVPLKTFF 105

Query: 327 RLMLILPYAVPGFISILVFRGLFNQNFGEINLLLE--GLFGIRPDWFSDPSLARTMILIV 384
           R +++LP+ VP  +S L F  L++  F  I+  L   GL     D+  DP  AR   +  
Sbjct: 106 RAIVLLPWIVPTALSALAFWWLYDAQFSVISWALHKMGLIDRYIDFLGDPWNARWSTVFA 165

Query: 385 NTWLGYPYMLLLCMGLLQAIPRDQYEASAIDGASPLDNLLRITLPQLIKPLMPLLIACFA 444
           N W G P++ +  +  LQ I    YEA+AIDGA+P      +TLP L   +  ++     
Sbjct: 166 NVWRGIPFVAISLLAGLQTISPSLYEAAAIDGATPWQQFRHVTLPLLTPIIAVVMTFSVL 225

Query: 445 FNFNNFVLITLLTRGGPDIIGATTPAGTTDLLVSYTYRIAFQDSGQDFALAAAIATMIFI 504
           F F +F LI +LTRGG        P   T L+ + +++ A          A A   + F+
Sbjct: 226 FTFTDFQLIYVLTRGG--------PLNATHLMATLSFQRAIPGGALGEGAALATYMIPFL 277

Query: 505 LVGAM 509
           L   M
Sbjct: 278 LAAIM 282



 Score = 28.1 bits (61), Expect = 5e-04
 Identities = 17/60 (28%), Positives = 32/60 (53%), Gaps = 4/60 (6%)

Query: 72  NRRMYAQRYIFPSVAGMLVFVIFPLLYTVGIGFTNYSGTNLLSQAQVERYHLSQTYLAGE 131
           NR +    ++ P+V  ++VF+ +PL   + +GFT+       S   ++ +    TYLAG+
Sbjct: 8   NRNVLGMLFMAPAVILLVVFLTYPLGLGIWLGFTDTKIGGEGSFIGLDNF----TYLAGD 63


Lambda     K      H
   0.327    0.142    0.429 

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: 414
Number of extensions: 19
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: 521
Length of database: 299
Length adjustment: 31
Effective length of query: 490
Effective length of database: 268
Effective search space:   131320
Effective search space used:   131320
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (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