GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdA in Haloechinothrix alba DSM 45207

Align 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) (EC 1.2.4.4) (characterized)
to candidate WP_089303319.1 CHB84_RS20615 thiamine pyrophosphate-dependent dehydrogenase E1 component subunit alpha

Query= BRENDA::Q72GU1
         (367 letters)



>NCBI__GCF_900188115.1:WP_089303319.1
          Length = 341

 Score =  155 bits (391), Expect = 2e-42
 Identities = 99/316 (31%), Positives = 160/316 (50%), Gaps = 3/316 (0%)

Query: 38  LRRLYRDMLAARMLDERYTILIRTGKT-SFIAPAAGHEAAQVAIAHAIRPGFDWVFPYYR 96
           L ++YR M       E     ++ G+  S   P  G E A  A+  A+    D +   YR
Sbjct: 22  LTQMYRTMRLITSTGEHAVGEVKAGRLKSAFYPVRGLEGACAAMGVAMLTE-DQLVSNYR 80

Query: 97  DHGLALALGIPLKELFGQMLATKADPNKGRQMPEHPGSKALNFFTVASPIASHVPPAAGA 156
             G ALA G  L+ +  ++       +KG+    H   +++ F T    + S +P AAG 
Sbjct: 81  SLGDALAKGASLRSIVAEIYGRADGTSKGKGGAMHIHDQSVGFVTSTGVVGSGIPIAAGL 140

Query: 157 AISMKLLRTGQVAVCTFGDGATSEGDWYAGINFAAVQGAPAVFVCENNFYAISVDYRHQT 216
            ++ +L    +  V  FGDG TS G ++  +N A++   P VFVC+NN +A         
Sbjct: 141 GLAAQLDGAARAVVSVFGDGTTSIGAYHESMNLASLWNLPMVFVCQNNQWAEHTPIAEYA 200

Query: 217 HSPTIADKAHAFGIPGYLVDGMDVLASYYVVKEAVERARRGEGPSLVELRVYRYGPHSSA 276
            S  +A +A A+ +P   VDG D +A+   ++ A+ RAR G GP+ VE++ YR   HS +
Sbjct: 201 ASTDLAARAEAYAMPSLAVDGFDPIATAQQLRTALGRARNGGGPTFVEIKTYRLTGHSGS 260

Query: 277 DDDSRYRPKEEVAFWRKKDPIPRFRRFLEARGLWNEEWEEDVREEIRAELERGLKEAEEA 336
            D S Y P +E+A   ++DP P FRR+L   G+ +E+   +V +E+ AE+E     A+++
Sbjct: 261 SDYS-YMPTDELAAATERDPAPTFRRWLLDEGVLDEQALAEVDKEVIAEVEDAFAFAQDS 319

Query: 337 GPVPPEWMFADVFAEK 352
                   + DVFA++
Sbjct: 320 PQPAASERYTDVFADE 335


Lambda     K      H
   0.320    0.138    0.426 

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: 278
Number of extensions: 8
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: 367
Length of database: 341
Length adjustment: 29
Effective length of query: 338
Effective length of database: 312
Effective search space:   105456
Effective search space used:   105456
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 24 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