GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Klebsiella michiganensis M5al

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate BWI76_RS03320 BWI76_RS03320 alcohol dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__Koxy:BWI76_RS03320
          Length = 352

 Score =  297 bits (761), Expect = 3e-85
 Identities = 158/349 (45%), Positives = 215/349 (61%), Gaps = 7/349 (2%)

Query: 11  VKAFGWAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGF---TTYP 67
           +K FG+AA++    L+P  F RRA  + D+ +++ +CGVCHSD H I ++W     T YP
Sbjct: 1   MKTFGYAAQNAQSGLAPMSFERRALRDDDLAIEINYCGVCHSDLHQIRDDWRSWNPTVYP 60

Query: 68  IVPGHEIVGVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHCEN--TIDTYG 125
            +PGHEI+G V EVG  V   K+GD V +G +V SCR C+ C    E  C    T+    
Sbjct: 61  SIPGHEIIGTVIEVGPNVTHYKIGDAVAVGTIVDSCRVCDQCRRGEEQMCREFPTMTYNS 120

Query: 126 SIYFDGTMTHGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGT 185
           S   DG  T GGYS  ++  E F+LR P+ L     APLLCAGIT YSPL+ + +  PG+
Sbjct: 121 SDRHDGKTTLGGYSKHIIVREEFVLRMPEGLDAARAAPLLCAGITVYSPLRTWNVG-PGS 179

Query: 186 KIGVVGLGGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGAR 245
           ++GV+G+GGLGH+AVK A   GA VTVI  +E+K  EA   LGAD+ L+++  + MK A 
Sbjct: 180 RVGVIGIGGLGHLAVKFAAGLGAHVTVITRTEAKTAEA-RALGADTTLISNSDDAMKAAT 238

Query: 246 SSLDGIIDTVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFELPVFSLLKGRKLLGGTINGG 305
           SS D IIDT+PV H ++    LL   G LV+VGA           L+ GR+ + G+ +GG
Sbjct: 239 SSFDVIIDTIPVEHDVSAYVQLLDVEGALVIVGALGNMAGFNSLPLIMGRRCITGSPSGG 298

Query: 306 IKETQEMLDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDIA 354
           I ETQEMLDF  K  I  + E+I +  +N A ER+ + +V YRFVID+A
Sbjct: 299 IAETQEMLDFCGKTGILPECEMIAIAEINEAFERMERGEVHYRFVIDMA 347


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: 324
Number of extensions: 18
Number of successful extensions: 6
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: 352
Length adjustment: 29
Effective length of query: 336
Effective length of database: 323
Effective search space:   108528
Effective search space used:   108528
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