GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Herbaspirillum seropedicae SmR1

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate HSERO_RS22435 HSERO_RS22435 zinc-binding dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__HerbieS:HSERO_RS22435
          Length = 349

 Score =  315 bits (806), Expect = 2e-90
 Identities = 170/349 (48%), Positives = 225/349 (64%), Gaps = 9/349 (2%)

Query: 11  VKAFGWAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVP 70
           V A+G  A D    L     +RRATG  DV++ + +CG+CHSD H I + W  T YP VP
Sbjct: 3   VHAYGAHAADKP--LEHLHITRRATGAHDVQIDIAYCGICHSDLHQIRSEWAGTQYPCVP 60

Query: 71  GHEIVGVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHCENTIDTYGSIYFD 130
           GHEIVG V  VG+ V K KVGD VG+GC+V SC+SC  C +  E++C+N + TY     D
Sbjct: 61  GHEIVGRVAAVGAHVSKFKVGDVVGVGCIVDSCQSCPDCDEGLENYCDNMVGTYNGKTDD 120

Query: 131 GT-MTHGGYSDTMVADEHFIL--RWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKI 187
               T GGYS  +V  E ++L  R P+   L + APLLCAGITTYSPL+++G   PG K+
Sbjct: 121 APGWTMGGYSQQIVVHERYVLNIRHPE-ADLAAVAPLLCAGITTYSPLRHWGAG-PGKKV 178

Query: 188 GVVGLGGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSS 247
           GVVG+GGLGH+ +K+A A GA V     S+SKR +A + LGAD  +++ + E+M     S
Sbjct: 179 GVVGIGGLGHMGIKIAHAMGAHVVAFTTSDSKRADA-KALGADEVVVSRNAEEMAAHAKS 237

Query: 248 LDGIIDTVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFELP-VFSLLKGRKLLGGTINGGI 306
            D I++TV   H L     LLK  G + +VGAP  P   P VF+L+  R+ L G++ GGI
Sbjct: 238 FDFILNTVAAPHDLDAFLALLKREGTMTLVGAPATPHPSPNVFNLILKRRSLAGSLIGGI 297

Query: 307 KETQEMLDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDIAN 355
            ETQEMLDF A+H I AD+E+I  D +NTA ER++K DV+YRFVID A+
Sbjct: 298 PETQEMLDFCAEHGIVADIELIRADEINTAYERMLKGDVKYRFVIDNAS 346


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: 384
Number of extensions: 22
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: 349
Length adjustment: 29
Effective length of query: 336
Effective length of database: 320
Effective search space:   107520
Effective search space used:   107520
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