GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Azospirillum brasilense Sp245

Align glycerol dehydrogenase (EC 1.1.1.6) (characterized)
to candidate AZOBR_RS07845 AZOBR_RS07845 glycerol dehydrogenase

Query= BRENDA::Q9WYQ4
         (364 letters)



>FitnessBrowser__azobra:AZOBR_RS07845
          Length = 364

 Score =  470 bits (1209), Expect = e-137
 Identities = 243/364 (66%), Positives = 279/364 (76%), Gaps = 1/364 (0%)

Query: 1   MITTTIFPGRYVQGAGAINILEEELSRFGERAFVVIDDFVDKNVLGENFFSSFTKVRVNK 60
           MITT IFP RYVQG GA++ L E+L+R G+    V D FV K + G    ++  +V +N 
Sbjct: 1   MITTAIFPARYVQGNGALDSLGEDLARLGKTVLAVTDSFVLKTLKGRLVEAAAGRVEMNI 60

Query: 61  QIFGGECSDEEIERLSGLVEEE-TDVVVGIGGGKTLDTAKAVAYKLKKPVVIVPTIASTD 119
           Q F GECSDEEIERL+GL      DVV GIGGGK LDTAKAVA+ L     IVPT+ASTD
Sbjct: 61  QEFRGECSDEEIERLTGLARAMGADVVAGIGGGKALDTAKAVAHALNARTAIVPTLASTD 120

Query: 120 APCSALSVIYTPNGEFKRYLFLPRNPDVVLVDTEIVAKAPARFLVAGMGDALATWFEAES 179
           APCSALSVIYTP G FKRYL LPRNPD+VLVDT +VA AP RFLV+GMGDAL+TWFEAE 
Sbjct: 121 APCSALSVIYTPEGAFKRYLVLPRNPDLVLVDTGVVASAPVRFLVSGMGDALSTWFEAED 180

Query: 180 CKQKYAPNMTGRLGSMTAYALARLCYETLLEYGVLAKRSVEEKSVTPALEKIVEANTLLS 239
           C+ K   NMTGR+G MTA+ALARLCY+TLLEYGVLAK + E+  VTPALE+IVEANTLLS
Sbjct: 181 CRIKRGGNMTGRVGPMTAFALARLCYDTLLEYGVLAKSACEQGVVTPALERIVEANTLLS 240

Query: 240 GLGFESGGLAAAHAIHNGLTVLENTHKYLHGEKVAIGVLASLFLTDKPRKMIEEVYSFCE 299
           GLGFESGGLAAAHA+HNGLT LE TH   HGEKVA G L  L LTD+P  +++EVY FC+
Sbjct: 241 GLGFESGGLAAAHAVHNGLTALEETHHCWHGEKVAFGTLTLLILTDRPPAVLDEVYGFCK 300

Query: 300 EVGLPTTLAEIGLDGVSDEDLMKVAEKACDKNETIHNEPQPVTSKDVFFALKAADRYGRM 359
            VGLPTTLAEIGL GVSDE L+  AE+AC + ETIHNEP  +T + V  A+KAAD  GR 
Sbjct: 301 AVGLPTTLAEIGLAGVSDERLLLAAERACAEGETIHNEPHEITPQRVLAAMKAADAEGRR 360

Query: 360 RKNL 363
           RK L
Sbjct: 361 RKGL 364


Lambda     K      H
   0.318    0.135    0.384 

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: 412
Number of extensions: 13
Number of successful extensions: 2
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: 364
Length of database: 364
Length adjustment: 29
Effective length of query: 335
Effective length of database: 335
Effective search space:   112225
Effective search space used:   112225
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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