GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Burkholderia phytofirmans PsJN

Align butyryl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate BPHYT_RS28040 BPHYT_RS28040 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-13470
         (379 letters)



>FitnessBrowser__BFirm:BPHYT_RS28040
          Length = 377

 Score =  348 bits (894), Expect = e-100
 Identities = 174/377 (46%), Positives = 253/377 (67%)

Query: 1   MDFTLTNEQKFVEQMVSEFTENEVKPIAAEIDETERFPLETVEKFAKYGMMGMPFPVEYG 60
           MD   T+EQ+ +     +F   ++ P A + D   + P E V +  + G +GM  P E+G
Sbjct: 1   MDSFYTDEQRMIRDAARDFATEQLAPHAGQWDREAQLPAEVVRQMGELGFLGMIVPAEWG 60

Query: 61  GSGTDYLSYIIAVEGLAKSCTSSSTILSAHTSLCAAPIYDWGTEEQKQKYLVPLAKGEKL 120
           GS TDY++Y +A+E +A  C + +T++S H S+   PI ++GTE QK +YL  LA G ++
Sbjct: 61  GSYTDYVAYALALEEIAAGCAACATLMSVHNSVGCGPILNFGTEAQKDRYLQDLATGRRI 120

Query: 121 GAFGLTEPNAGTDAAGQQTTAVLEGDHYVLNGQKIFITNGAYADTFVIFAMTDRSKGTRG 180
           GAF LTEP AG++A   +T AVL    ++LNG K F+TNG+ AD  ++FA+TD  +G RG
Sbjct: 121 GAFCLTEPQAGSEANNLRTRAVLRDGKWILNGSKQFVTNGSRADLAIVFAVTDPDRGKRG 180

Query: 181 ITAFIVEKDFPGFSIGKSEDKLGIRASSTTELIFENCIVPKENMLGKEGKGFTVAMHTLD 240
           +TAFIV  D PGF++GK E KLGIRAS T  +  ++C VP+ N+LG+ G+G  +A+  L+
Sbjct: 181 LTAFIVPTDTPGFNVGKPEHKLGIRASDTCPISLDDCAVPEANLLGEPGEGLRIALSNLE 240

Query: 241 GGRIGIAAQALGLAEGALAEALNYMKERKQFGKALYKFQGLAWMVAELDTKIEAVKQLVY 300
           GGRIGIAAQA+G+A  A   A  Y  ER QFGKAL + Q +A M+A++ T++ A + LV+
Sbjct: 241 GGRIGIAAQAVGIARAAFDAARLYANERIQFGKALKEHQTIANMLADMATRLNAARLLVH 300

Query: 301 KAAVNKQMGLPYSVEAARAKLAAATVAMETTTKVVQIFGGYGFTKDYPVERMMRDAKITE 360
            AA  +  G P   EA++AKL A+ +A E  +  +QI GGYG+ +DY VER  RDA+IT+
Sbjct: 301 HAARLRTAGKPCLSEASQAKLFASELAEEICSNAIQIHGGYGYLEDYAVERHYRDARITQ 360

Query: 361 IYEGTSQVQKMVISANL 377
           IYEGTS+VQ+M+I+ ++
Sbjct: 361 IYEGTSEVQRMLIARHV 377


Lambda     K      H
   0.316    0.132    0.372 

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: 288
Number of extensions: 3
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: 379
Length of database: 377
Length adjustment: 30
Effective length of query: 349
Effective length of database: 347
Effective search space:   121103
Effective search space used:   121103
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 (21.6 bits)
S2: 50 (23.9 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