GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Cupriavidus basilensis 4G11

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate RR42_RS00870 RR42_RS00870 isovaleryl-CoA dehydrogenase

Query= CharProtDB::CH_091785
         (379 letters)



>FitnessBrowser__Cup4G11:RR42_RS00870
          Length = 396

 Score =  297 bits (761), Expect = 3e-85
 Identities = 157/383 (40%), Positives = 244/383 (63%), Gaps = 5/383 (1%)

Query: 1   MDFNLTREQELVRQMVREFAENEVKPIAAEIDETERFPMENVKKMGQYGMMGIPFSKEYG 60
           + F+L  + E++R+ V  +A+ E+ P AAEID T++FPM+  KKMG  G++GI  ++EYG
Sbjct: 10  LKFDLGEDIEMLRETVCNWAQAELAPRAAEIDRTDQFPMDAWKKMGDLGVLGITVAEEYG 69

Query: 61  GAGGDVLSYIIAVEELSKVCGTTGVILSAHTSLCASLINEHGTEEQKQKYLVPLAKGEKI 120
           GA    L+++IA+EE+S+   + G+   AH++LC + I+ +GT  QK +YL  L  G+ I
Sbjct: 70  GANMGYLAHMIAMEEISRASASVGLSYGAHSNLCVNQIHRNGTAAQKARYLPKLVSGDWI 129

Query: 121 GAYGLTEPNAGTDSGAQQTVAVLEGDHYVINGSKIFITNGGVADTFVIFAMTDRTKGTKG 180
           GA  ++EPNAG+D  + +  A  +GDHYV+NG+K++ITNG   D  V++A T+   G +G
Sbjct: 130 GALAMSEPNAGSDVVSMKLRADFKGDHYVLNGTKMWITNGPDCDVLVVYAKTEPDLGARG 189

Query: 181 ISAFIIEKGFKGFSIGKVEQKLGIRASSTTELVFEDMIVPVENMIGKEGKGFPIAMKTLD 240
           ++AFI+EKG KGFS+ +   KLG+R S T ELVF+D+ VPVEN++G E  G  + M  LD
Sbjct: 190 MTAFIVEKGMKGFSVAQKLDKLGMRGSHTGELVFQDVEVPVENILGGENLGAKVLMSGLD 249

Query: 241 GGRIGIAAQALGIAEGAFNEARAYMKERKQFGRSLDKFQGLAWMMADMDVAIESAR-YLV 299
             R  ++   +GI +   +    Y+ +RKQFG+S+ +FQ +   +ADM   +++AR YL 
Sbjct: 250 YERAVLSGGPVGIMQACMDVITPYIHDRKQFGQSIGEFQLIQGKVADMYTTLQAARSYLY 309

Query: 300 YKAAYLKQAGLPYT----VDAARAKLHAANVAMDVTTKAVQLFGGYGYTKDYPVERMMRD 355
                L   G  +      D A   L+ A  A  +  ++VQ+ GG GY  +YPV R+ RD
Sbjct: 310 TVGKNLDSLGKDHVRQVRKDCAAVILYTAEKATWMAGESVQILGGNGYINEYPVGRLWRD 369

Query: 356 AKITEIYEGTSEVQKLVISGKIF 378
           AK+ EI  GTSE+++++I  ++F
Sbjct: 370 AKLYEIGAGTSEIRRMLIGRELF 392


Lambda     K      H
   0.317    0.135    0.377 

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: 406
Number of extensions: 15
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: 379
Length of database: 396
Length adjustment: 30
Effective length of query: 349
Effective length of database: 366
Effective search space:   127734
Effective search space used:   127734
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: 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