GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Klebsiella michiganensis M5al

Align glycerol dehydrogenase (EC 1.1.1.6) (characterized)
to candidate BWI76_RS00815 BWI76_RS00815 glycerol dehydrogenase

Query= BRENDA::B2ZPN8
         (367 letters)



>FitnessBrowser__Koxy:BWI76_RS00815
          Length = 367

 Score =  684 bits (1765), Expect = 0.0
 Identities = 341/367 (92%), Positives = 352/367 (95%)

Query: 1   MDRIIQSPGKYIQGAGAIKRLGDYLKPLAERWLVVGDKFVLGFAEEMLRKSLADAGLAAE 60
           MDRIIQSPGKYIQGA A+ RLG YLKPLAERWL+VGDKFVLGFAEE LRKSLADAGL  E
Sbjct: 1   MDRIIQSPGKYIQGADAMTRLGGYLKPLAERWLIVGDKFVLGFAEEKLRKSLADAGLVGE 60

Query: 61  IAPFGGECSHNEINRLRDIAGNAKCTAVLGIGGGKTLDTAKALAHFMNVPVAIAPTIAST 120
           IAPFGGECSHNEINRLR IA +A+CTAVLGIGGGKTLDTAKALAHFMN+PV IAPTIAST
Sbjct: 61  IAPFGGECSHNEINRLRGIADSAQCTAVLGIGGGKTLDTAKALAHFMNLPVVIAPTIAST 120

Query: 121 DAPCSALSVIYTDEGEFDSYLMLPRNPNMVIVDTQIVAGAPARLLAAGIGDALATWFEAR 180
           DAPCSALSVIY+D+GEFDSYLMLPRNPNMVIVDTQIVAGAPARLLAAGIGDALATWFEAR
Sbjct: 121 DAPCSALSVIYSDDGEFDSYLMLPRNPNMVIVDTQIVAGAPARLLAAGIGDALATWFEAR 180

Query: 181 ACSRSGATTMAGGKCTQAALALAELCYNTLLEEGEKAMLAAEQHVVTPALERVVEANTYL 240
           ACSRSGATTMAGGKCTQAALALAELCYNTL+EEGEKAMLAAEQHVVTPALERV+EANTYL
Sbjct: 181 ACSRSGATTMAGGKCTQAALALAELCYNTLIEEGEKAMLAAEQHVVTPALERVIEANTYL 240

Query: 241 SGVGFESGGLAAAHAIHNGMTAIPDAHHYYHGEKVAFGTLTQLVLENAPVDEIETVAALC 300
           SGVGFESGGLAAAHAIHNG+TAIPDAHHYYHGEKVAFGTLTQLVLENAPV+EIETVAALC
Sbjct: 241 SGVGFESGGLAAAHAIHNGLTAIPDAHHYYHGEKVAFGTLTQLVLENAPVEEIETVAALC 300

Query: 301 HSVGLPITLAQLDIKGDIPTKMRLVAEAACAEGETIHNMPGGVDSDQVYAALLVADQYGQ 360
           HSVGLPITLAQLDIK DIP KMR VAEAACAEGETIHNMPGG   DQVYAALLVADQYGQ
Sbjct: 301 HSVGLPITLAQLDIKADIPGKMRTVAEAACAEGETIHNMPGGATPDQVYAALLVADQYGQ 360

Query: 361 RFLQEWE 367
           RFLQEWE
Sbjct: 361 RFLQEWE 367


Lambda     K      H
   0.319    0.134    0.395 

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: 655
Number of extensions: 19
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: 367
Length of database: 367
Length adjustment: 30
Effective length of query: 337
Effective length of database: 337
Effective search space:   113569
Effective search space used:   113569
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