GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsB in Paraburkholderia bryophila 376MFSha3.1

Align ABC-type sugar transport system, periplasmic component protein (characterized, see rationale)
to candidate H281DRAFT_03822 H281DRAFT_03822 monosaccharide ABC transporter substrate-binding protein, CUT2 family

Query= uniprot:D8IUD0
         (314 letters)



>FitnessBrowser__Burk376:H281DRAFT_03822
          Length = 320

 Score =  300 bits (768), Expect = 3e-86
 Identities = 163/316 (51%), Positives = 214/316 (67%), Gaps = 3/316 (0%)

Query: 1   MNKFTRRHFAIA-ALACAVLPGAAMAQTP--AKPKVALVMKSLANEFFLNMENGAREYQK 57
           M +  RR   IA ALA A L  AA A T     PK+ALV+KS+ + F + M N A+ YQ+
Sbjct: 1   MTQEMRRRVLIAGALAAAGLTRAAGAATVEGGMPKIALVLKSINDPFTVAMANAAKNYQQ 60

Query: 58  ANASKFDLIANGIKDEQDTANQIKIVEQMIVSKVNALVIAPADSKALVPVVKKAIDAGII 117
             AS+F L   G   E DTA QI+IV+ +I +K+NA+VIAP+ SK L  VV +AI AGII
Sbjct: 61  HYASQFALTVRGTATEADTAGQIRIVDDLIKAKMNAIVIAPSGSKPLTAVVARAIKAGII 120

Query: 118 VVNIDNKLDDAALKEKGITVPFVGPDNRKGAKLAGDYLGKQLQKGDKVAIIEGVSTTFNA 177
           VV+IDN LDDA+     I+VPFVGPDNRKGA L  +YL  +LQ GD+V IIEG++   NA
Sbjct: 121 VVSIDNPLDDASQDAAKISVPFVGPDNRKGATLVANYLAGRLQAGDQVGIIEGIAADRNA 180

Query: 178 QQRTLGFQDAMKDVGANVVTVQSGQWEIDQGNKVAASILNAHPDIKAILAGNDNMALGAV 237
           Q+RT G++D M   G  VV  Q+  WE  +G  VA+ +L  HP I+ +L  NDNMA+GA 
Sbjct: 181 QERTAGYRDVMSTAGMQVVATQAADWEYGKGRDVASKMLGQHPQIRGLLCANDNMAMGAA 240

Query: 238 AAIRAAGKTGKVQLVGYDNINAIKPMLKDGRVLATVDQFAQQQAVFGIETALKALSEKKP 297
            A+R AG+TG V + GY+ I AIKP++ DG VLATV+QFA +QAVFG++ ALKA++E++ 
Sbjct: 241 DAVRDAGRTGGVYITGYNAIEAIKPLIADGHVLATVNQFADRQAVFGMDVALKAVTEQRK 300

Query: 298 QSALGGVVETKVSLVT 313
           Q  L   +ET + LVT
Sbjct: 301 QRELSRTIETPLQLVT 316


Lambda     K      H
   0.315    0.131    0.355 

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: 237
Number of extensions: 5
Number of successful extensions: 1
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: 314
Length of database: 320
Length adjustment: 27
Effective length of query: 287
Effective length of database: 293
Effective search space:    84091
Effective search space used:    84091
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 48 (23.1 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