GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Sinorhizobium meliloti 1021

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate SMc00680 SMc00680 zinc-type alcohol dehydrogenase

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__Smeli:SMc00680
          Length = 347

 Score =  328 bits (841), Expect = 1e-94
 Identities = 166/341 (48%), Positives = 225/341 (65%), Gaps = 2/341 (0%)

Query: 13  AFGWAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVPGH 72
           A G+AA D +  L+PF F RR   + DV + + +CGVCHSD H   + WG +T+P+VPGH
Sbjct: 4   ARGYAATDASKPLAPFTFERREPRDDDVVIDIKYCGVCHSDIHQARDEWGNSTFPMVPGH 63

Query: 73  EIVGVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHCENTIDTYGSIYFDGT 132
           EIVG+V  VGS+V + K+GD VG+GC V SC +C     + E +    + TY  +  DGT
Sbjct: 64  EIVGIVRAVGSQVTRFKIGDRVGVGCFVDSCTTCAKRDLDLEQYLPGLVVTYNGVEADGT 123

Query: 133 MTHGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIGVVGL 192
            T GGYSD +V  E ++L  P+NLPLD+ APLLCAGIT YSPL+++    PG K+ +VGL
Sbjct: 124 PTQGGYSDHIVVKEGYVLSIPENLPLDAAAPLLCAGITLYSPLRHWKAG-PGKKVAIVGL 182

Query: 193 GGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSSLDGII 252
           GGLGH+ VK+A A GA+VTV+  + SK+++ L KLGAD +    D E       S D II
Sbjct: 183 GGLGHMGVKLAHAMGAEVTVLSQTLSKKEDGL-KLGADHYYATKDPETFTKLAGSFDLII 241

Query: 253 DTVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFELPVFSLLKGRKLLGGTINGGIKETQEM 312
            TV          +LLK +G+LV+VG PE P  +  FSL+  R+ + G++ G IKETQEM
Sbjct: 242 CTVAAEIDWNAYLNLLKVDGELVLVGIPENPVPVHAFSLVPARRSISGSMIGSIKETQEM 301

Query: 313 LDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDI 353
           LDF  +H I +++E I M+ +N A ER+V+SDVRYRFVID+
Sbjct: 302 LDFCGEHGIVSEIETIRMEQINEAYERVVRSDVRYRFVIDM 342


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: 325
Number of extensions: 10
Number of successful extensions: 3
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: 347
Length adjustment: 29
Effective length of query: 336
Effective length of database: 318
Effective search space:   106848
Effective search space used:   106848
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