GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Herbaspirillum seropedicae SmR1

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate HSERO_RS22750 HSERO_RS22750 sugar ABC transporter ATP-binding protein

Query= BRENDA::Q97UY8
         (353 letters)



>FitnessBrowser__HerbieS:HSERO_RS22750
          Length = 377

 Score =  193 bits (490), Expect = 7e-54
 Identities = 111/296 (37%), Positives = 176/296 (59%), Gaps = 20/296 (6%)

Query: 1   MVRIIVKNVSKVFKKGKVVALDNVNINIENGERFGILGPSGAGKTTFMRIIAGLDVPSTG 60
           M  + +K + K +  G+   L  +N++I +GE   ++GPSG GK+T +R++ GL+  S G
Sbjct: 1   MAHVNIKQLRKTYD-GRADVLAGLNLDIRDGEFCVLVGPSGCGKSTLLRMLCGLEEISGG 59

Query: 61  ELYFDDRLVASNGKLIVPPEDRKIGMVFQTWALYPNLTAFENIAFPLTNMKMSKEEIRKR 120
           EL    ++V       +PP +R I MVFQ++ALYP++  ++N+AF L     SK +I  R
Sbjct: 60  ELAIGGQVVNH-----LPPAERGIAMVFQSYALYPHMNVYKNMAFGLKVAGNSKSDIDAR 114

Query: 121 VEEVAKILDIHHVLNHFPRELSGGQQQRVALARALVKDPSLLLLDEPFSNLDARMRDSAR 180
           +   A IL I H+L   PRELSGGQ+QRVA+ RA+V+ P L L DEP SNLDA +R   R
Sbjct: 115 IRHAAAILKIDHLLQRLPRELSGGQRQRVAIGRAIVRQPRLFLFDEPLSNLDAALRVQTR 174

Query: 181 ALVKEVQSRLGVTLLVVSHDPADIFAIADRVGVLVKGKLVQVGKPEDLYDNPVSIQVASL 240
             + ++  +L  T++ V+HD  +   + D++ V+ +G++ Q G P +LY  P ++ VA  
Sbjct: 175 LEIAKLHRQLAATIVYVTHDQVEAMTLGDKIVVMHEGRIQQAGTPLELYQQPQNLFVAGF 234

Query: 241 IG--EINELEGKVT---NEGV---VIGSLRF-----PVSVSSDRAI-IGIRPEDVK 282
           IG  ++N  +G VT   + GV   + G LR      P+ V+   A+ +G+R E ++
Sbjct: 235 IGSPKMNFFQGVVTRCDDSGVQVEIAGGLRLLADVDPLGVTPGAAVTLGLRAEQIR 290


Lambda     K      H
   0.319    0.139    0.390 

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: 266
Number of extensions: 14
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: 353
Length of database: 377
Length adjustment: 30
Effective length of query: 323
Effective length of database: 347
Effective search space:   112081
Effective search space used:   112081
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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