GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Burkholderia phytofirmans PsJN

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate BPHYT_RS24470 BPHYT_RS24470 zinc-binding dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__BFirm:BPHYT_RS24470
          Length = 350

 Score =  343 bits (880), Expect = 4e-99
 Identities = 178/343 (51%), Positives = 234/343 (68%), Gaps = 5/343 (1%)

Query: 14  FGWAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVPGHE 73
           + +AA D T  L+PF+  RR     DV+++VLFCGVCHSD H   N W  T +P+VPGHE
Sbjct: 5   YAYAATDATAPLAPFEIQRRELRAHDVQMEVLFCGVCHSDLHQARNEWKNTVFPVVPGHE 64

Query: 74  IVGVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHCEN-TIDTYGSI-YFDG 131
           IVG VT VG  V K K GD VG+GCLV SCR+C SC ++ E +CEN  + TY  +   DG
Sbjct: 65  IVGRVTAVGLDVTKYKAGDLVGVGCLVDSCRTCASCKEDLEQYCENGFVGTYNGVDRVDG 124

Query: 132 TMTHGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIGVVG 191
             T+GGYS  +V DE F LR P+NL     APLLCAGITTYSPL+ +G   PG K+G+VG
Sbjct: 125 QTTYGGYSTQLVVDEAFTLRVPENLDPAGVAPLLCAGITTYSPLRTWGAG-PGKKVGIVG 183

Query: 192 LGGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSSLDGI 251
           LGGLGH+ VK+A+A GA V +   S SK ++A ++LGA   +++ +  +M+   +S D I
Sbjct: 184 LGGLGHMGVKLARAMGAHVVLFTTSPSKIEDA-KRLGAHEVVISKNAGEMEAHLNSFDLI 242

Query: 252 IDTVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFELP-VFSLLKGRKLLGGTINGGIKETQ 310
           ++TV   H L P  +LLK +G + +VGAPE     P VF+L+  R+ L G++ GGI ETQ
Sbjct: 243 VNTVAAQHDLNPFLNLLKRDGTMTLVGAPEHDHPSPQVFNLIFKRRRLAGSLIGGIAETQ 302

Query: 311 EMLDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDI 353
           EMLDF  +H IT+DVEVIPM  +N A ER++KSDV+YRFVID+
Sbjct: 303 EMLDFCGEHGITSDVEVIPMQGINEAFERMLKSDVKYRFVIDL 345


Lambda     K      H
   0.319    0.137    0.415 

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: 370
Number of extensions: 23
Number of successful extensions: 5
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: 365
Length of database: 350
Length adjustment: 29
Effective length of query: 336
Effective length of database: 321
Effective search space:   107856
Effective search space used:   107856
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.

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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