GapMind for catabolism of small carbon sources

 

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

Align Putative beta-xyloside ABC transporter, permease component, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR (characterized)
to candidate H281DRAFT_02703 H281DRAFT_02703 monosaccharide ABC transporter membrane protein, CUT2 family

Query= TCDB::G4FGN4
         (313 letters)



>FitnessBrowser__Burk376:H281DRAFT_02703
          Length = 333

 Score =  239 bits (609), Expect = 9e-68
 Identities = 129/307 (42%), Positives = 184/307 (59%), Gaps = 8/307 (2%)

Query: 13  IFLILIAIVVFLGVTTREFLTVENIFTVILNVSFIAIMSFGMTMVIITSGIDLSVGSILG 72
           +F  L+ I + L + + EFLT   +  +++ VS + I + G T VIITSGIDLSVGS++ 
Sbjct: 29  LFAALVIICIALSIASPEFLTTSTLTNIMVQVSVVGIAAVGGTFVIITSGIDLSVGSLVA 88

Query: 73  AASVVMGLLMDEKGLSP------FLSVVIGLAVGVGFGLANGLLITKARLAPFISTLGML 126
              +V   +M   G SP         +   LAVG   G  NGL +   RL PFI TL M+
Sbjct: 89  LTGMVAATVM--AGSSPGAIGLGIAGLCAALAVGAAAGALNGLAVAWLRLVPFIVTLAMM 146

Query: 127 SVGRGLAYVMSGGWPISPFPESFTVHGQGMVGPVPVPVIYMAVIGVIAHIFLKYTVTGRR 186
           ++ RGL   +S G     FP +FT  G   V  +P+P+I M VI VI H+ L+ T  G +
Sbjct: 147 AMARGLTLAISDGRTKFDFPNAFTAFGAKTVAGLPMPMIVMLVIFVIGHVLLRKTTFGHQ 206

Query: 187 IYAIGGNMEASKLVGIKTDRILILVYTINGFLAAFAGFLLTAWLGVAQPNAGQGYELDVI 246
           ++A+GGN EA++L GI   R++ L Y + G  AA AG +L   L  A P+A  G EL VI
Sbjct: 207 VFAVGGNQEAARLAGIPVHRVVFLTYMLAGVTAAIAGIVLAGRLNSALPSAANGLELQVI 266

Query: 247 AATVIGGTSLSGGEGTILGAFLGAVIMGVLRNGMILLGVSSFWQQVVIGIVIIIAIAIDQ 306
           AA VIGGTSL+GG G+I+G F+G V++GV+  G+ LLGV+ FW Q + G VI  A+ +D 
Sbjct: 267 AAVVIGGTSLAGGRGSIVGTFIGVVLIGVINVGLSLLGVNPFWTQFIQGGVIFAAVLLDA 326

Query: 307 IRRAKER 313
           + + +++
Sbjct: 327 LSQRRKQ 333


Lambda     K      H
   0.328    0.145    0.421 

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: 302
Number of extensions: 18
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: 313
Length of database: 333
Length adjustment: 28
Effective length of query: 285
Effective length of database: 305
Effective search space:    86925
Effective search space used:    86925
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: 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