GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Pseudomonas stutzeri RCH2

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate GFF1243 Psest_1276 Zn-dependent alcohol dehydrogenases

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__psRCH2:GFF1243
          Length = 351

 Score =  332 bits (851), Expect = 9e-96
 Identities = 174/345 (50%), Positives = 233/345 (67%), Gaps = 5/345 (1%)

Query: 13  AFGWAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVPGH 72
           + G+AA D +  L+P+ FSRR  G  DVR+++LFCGVCHSD H   N W  T YP VPGH
Sbjct: 4   SIGYAALDPSTPLAPYSFSRREVGPNDVRIEILFCGVCHSDLHTARNEWNNTLYPSVPGH 63

Query: 73  EIVGVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHCEN-TIDTY-GSIYFD 130
           EIVG V+ VG+ V K K GD  G+GCLV SCR+C SC +  E +CEN  + TY G  +  
Sbjct: 64  EIVGRVSAVGANVSKFKAGDIAGVGCLVDSCRTCSSCGEGLEQYCENGFVGTYNGPAFGG 123

Query: 131 GTMTHGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIGVV 190
           G  T GGYSD +V DE ++LR      L + APLLCAGITTYSPL+ + +  PG K+GVV
Sbjct: 124 GENTLGGYSDNIVVDEKYVLRINHTDNLAAVAPLLCAGITTYSPLRQWKVG-PGQKVGVV 182

Query: 191 GLGGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSSLDG 250
           GLGGLGH+AVK+A A GA+V +   S  KR++AL +LGA   +++ ++++M    +S D 
Sbjct: 183 GLGGLGHMAVKIANAMGAKVVLFTTSPDKREDAL-RLGAAEVVVSKNKDEMAAHANSFDF 241

Query: 251 IIDTVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFELP-VFSLLKGRKLLGGTINGGIKET 309
           I++TV   H L    +LLK +  + +VGAP  P   P VF L+  R+ + G++ GGI ET
Sbjct: 242 ILNTVAAPHNLDAFVNLLKRDATMTLVGAPASPHPSPSVFGLIFKRRRIAGSLIGGIAET 301

Query: 310 QEMLDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDIA 354
           QEMLDF A+H I +D+E+I M  +N A ER++KSDV+YRFVID+A
Sbjct: 302 QEMLDFCAEHGIVSDIEMIRMQDINDAYERMLKSDVKYRFVIDMA 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: 350
Number of extensions: 16
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: 351
Length adjustment: 29
Effective length of query: 336
Effective length of database: 322
Effective search space:   108192
Effective search space used:   108192
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