GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdB in Sphingomonas wittichii RW1

Align branched-chain-2-oxoacid decarboxylase (subunit 2/2) (EC 4.1.1.72) (characterized)
to candidate WP_011951687.1 SWIT_RS04275 alpha-ketoacid dehydrogenase subunit beta

Query= BRENDA::Q9HIA4
         (319 letters)



>NCBI__GCF_000016765.1:WP_011951687.1
          Length = 327

 Score =  265 bits (677), Expect = 1e-75
 Identities = 148/324 (45%), Positives = 208/324 (64%), Gaps = 10/324 (3%)

Query: 1   MNMVQALNSAMDLKMSEDDSVIILGEDVG--RDGGVFRVTDGLQAKYGPQRVIDTPLSEL 58
           M M+ A+N A+   M E+  +++LGEDV    DGGVF  T GL  ++G  RV  TP+SE 
Sbjct: 7   MTMIDAINRALHDAMEENGKILLLGEDVADPEDGGVFGATRGLSTRFGEDRVKSTPISEQ 66

Query: 59  GIVGMAIGMAVNGLKPIPEIQFQDFIYTSMDQIINQMAKIRYRSGGDYTVPLVLRTPVGG 118
            IVG AIG ++ G +P+ E+   +F+  +MD ++N  AK+R+ SGG  +VP+ +RT  G 
Sbjct: 67  AIVGAAIGASLVGYRPVAEVMLMNFMTVAMDMLVNHAAKLRFMSGGQTSVPITVRTMTGS 126

Query: 119 GIKGGLYHSQSGEAYFAHTAGLTVVSPSNPYDAKGLLISAIESPDPVIFLEPKRLYRAQK 178
           G+  G  HS   EA+FAHTAG+ VV PS+  DA GLL SAI+  DPVIF+E   +Y AQ 
Sbjct: 127 GLSLGGQHSDFVEAWFAHTAGMKVVIPSSANDAYGLLRSAIDDADPVIFVETLPIYWAQG 186

Query: 179 VEVPDEKYTIPLRKANVLKQGNDVTIVTYGSMVPTVMSVA---SKSKYDVEVIDLRTIAP 235
            EV  E+  IP+ KA V ++G+D+TI+ YG MV   ++VA   +K    VEVIDLRT++P
Sbjct: 187 -EVSFER--IPIGKARVCREGSDLTIIAYGQMVSHSLTVATELAKQGKSVEVIDLRTVSP 243

Query: 236 MDRDTIISSVKKTGRVVIVHEAPRTLGVGAEISAMISERAIEYLYAPIVRVTGPDTPFPY 295
            DR+T+++SV KTGR +IVHEA +  GVGAEI+++I E     L AP+ R+     P P+
Sbjct: 244 WDRETVLASVAKTGRALIVHEAVKEYGVGAEIASVIGEALFGRLVAPVQRLGAAYCPVPF 303

Query: 296 R--LEEYYLPNEGRINAALDRVMS 317
              LE+ + PN   I AA   ++S
Sbjct: 304 SKPLEQAFAPNAESIGAAAAALLS 327


Lambda     K      H
   0.318    0.137    0.388 

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: 282
Number of extensions: 14
Number of successful extensions: 5
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: 319
Length of database: 327
Length adjustment: 28
Effective length of query: 291
Effective length of database: 299
Effective search space:    87009
Effective search space used:    87009
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: 48 (23.1 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