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_RS03140 BWI76_RS03140 alcohol dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__Koxy:BWI76_RS03140
          Length = 339

 Score =  227 bits (578), Expect = 4e-64
 Identities = 117/339 (34%), Positives = 193/339 (56%), Gaps = 13/339 (3%)

Query: 16  WAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVPGHEIV 75
           +AA++    LS +++       +DV ++V +CG+CHSD  MI N WG ++YP+V GHE++
Sbjct: 7   YAAKEAGADLSLWEYDAGDLKPEDVEVQVEYCGICHSDLSMIDNEWGMSSYPLVAGHEVI 66

Query: 76  GVVTEVGSKVEK--VKVGDNVGIGCLVGSCRSCESCCDNRESHC-ENTIDTYGSIYFDGT 132
           G V  +GS  +   +KVG  VGIG    SC  C++C      +C E ++ T         
Sbjct: 67  GRVAALGSAAQDKGLKVGQKVGIGWTARSCGHCDACISGNHVNCLEGSVPTI-------- 118

Query: 133 MTHGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIGVVGL 192
           +  GG++D + AD  +++  P+N+ L+S  P+LC GIT + PL  + +    +++GV+G+
Sbjct: 119 INRGGFADKLRADWQWVIPLPENVDLESAGPMLCGGITVFKPLLMHHVTA-NSRVGVIGI 177

Query: 193 GGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSSLDGII 252
           GGLGH+A+K+  A GA+VT    + +K +E L  +GAD  + + D E +K      D II
Sbjct: 178 GGLGHIAIKLLHAMGAEVTAFSSNPAKEQEVLA-MGADRVVNSRDPEALKALAGQFDLII 236

Query: 253 DTVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFELPVFSLLKGRKLLGGTINGGIKETQEM 312
           +TV V+    P F+ L   G    VGA  KPF +P F+L+ G + + G+  G   E +++
Sbjct: 237 NTVAVDLDWQPYFEALAYGGNFHTVGAVMKPFPVPAFTLIGGDRSISGSATGNPAELRKL 296

Query: 313 LDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVI 351
           + FA +  +    E+ PM  +N A++ + +   RYR V+
Sbjct: 297 MKFAGRSKVAPTTELFPMSQINEALKHVREGKARYRVVL 335


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: 283
Number of extensions: 18
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: 339
Length adjustment: 29
Effective length of query: 336
Effective length of database: 310
Effective search space:   104160
Effective search space used:   104160
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