GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Sinorhizobium meliloti 1021

Align D-xylulose reductase (EC 1.1.1.9) (characterized)
to candidate SMc01992 SMc01992 alcohol dehydrogenase

Query= reanno::Dino:3607129
         (347 letters)



>FitnessBrowser__Smeli:SMc01992
          Length = 346

 Score =  495 bits (1275), Expect = e-145
 Identities = 245/346 (70%), Positives = 287/346 (82%)

Query: 1   MARALVLEAARKLALRDIDLPDELGPEDVRIAIDTVGVCGSDVHYYTHGKIGPFVVKQPM 60
           MA+ALVLE   +L+LRDI +  +L P DV I I TVGVCGSDVHYYTHGKIGPFVV +PM
Sbjct: 1   MAKALVLEKKGQLSLRDIPVRRDLSPTDVLIGIRTVGVCGSDVHYYTHGKIGPFVVNEPM 60

Query: 61  VLGHEAAGIVTEIGAAVTHLALGDRVCMEPGIPNGSSKASKLGVYNVDPAVQFWATPPVH 120
           +LGHEAAG+V E+G+ V HL  GDRVCMEPGIP+ SS++SKLG+YNVDP+V+FWATPPVH
Sbjct: 61  ILGHEAAGVVLEVGSQVRHLKKGDRVCMEPGIPDLSSRSSKLGIYNVDPSVRFWATPPVH 120

Query: 121 GCLTPSVVHPAAFTFKLPDHVSFAEGAMVEPFAIGMQAAAKARIKPGDVALVTGAGPIGV 180
           GCLTP VVHPAAFT++LPDHVSFAEGAMVEPFAIG+QAA +A I+PGDV  V GAGPIG+
Sbjct: 121 GCLTPEVVHPAAFTYRLPDHVSFAEGAMVEPFAIGVQAALRAGIRPGDVGAVMGAGPIGM 180

Query: 181 MVALAALAGGCAKVFVSDLVEDKLAIAAGYDNIHPILIPRDNPAEVLQEATEGWGADVVF 240
           M ALAALAGGC+KV+V+DL + KL +   Y+ I  I + +   +E L  AT GWGADVVF
Sbjct: 181 MTALAALAGGCSKVYVADLAQPKLDVIGAYEGIETINVRQQAVSEALAGATGGWGADVVF 240

Query: 241 ECAGAAASIQAALEAAAPAGCVVWVGMPVDPVPVDIVLAQSRELRMETVFRYANMYDRAI 300
           EC+GAA +I A    A P G VV VGMPV+PVP DIV  Q++ELR+ETVFRYAN+YDRAI
Sbjct: 241 ECSGAAPAILALPSLARPGGTVVLVGMPVEPVPFDIVGMQAKELRIETVFRYANVYDRAI 300

Query: 301 ALLASGKVDLKPLISATFPFEDSIAAFDRAVEARPTDVKIQIKMGA 346
            L+ASGKVDLKPLISAT PF++SIAAFDRAVEARPTDVKIQI+M A
Sbjct: 301 ELIASGKVDLKPLISATIPFDESIAAFDRAVEARPTDVKIQIEMPA 346


Lambda     K      H
   0.321    0.137    0.408 

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: 447
Number of extensions: 17
Number of successful extensions: 1
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: 347
Length of database: 346
Length adjustment: 29
Effective length of query: 318
Effective length of database: 317
Effective search space:   100806
Effective search space used:   100806
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 (21.8 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