GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdB in Pseudomonas stutzeri RCH2

Align 2-keto-isovalerate dehydrogenase component β subunit (EC 1.2.4.4) (characterized)
to candidate GFF2175 Psest_2218 Pyruvate/2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit

Query= metacyc::MONOMER-11684
         (327 letters)



>FitnessBrowser__psRCH2:GFF2175
          Length = 324

 Score =  259 bits (662), Expect = 6e-74
 Identities = 137/321 (42%), Positives = 209/321 (65%), Gaps = 3/321 (0%)

Query: 4   MSYIDAINLAMKEEMERDSRVFVLGEDVGRKGGVFKATAGLYEQFGEERVMDTPLAESAI 63
           +SY +A+  A++E ++RD R F++GEDVGR GG +  + GL E+FGE R+ DTPL+E A 
Sbjct: 5   ISYREALREALREALQRDERAFLMGEDVGRYGGTYAVSKGLLEEFGEARIRDTPLSELAF 64

Query: 64  AGVGIGAAMYGMRPIAEMQFADFIMPAVNQIISEAAKIRYRSNNDWSCPIVVRAPYGGGV 123
            G GIGAA+ GMRPI E+   +F + A++ +I+ AA +R+ S   +S P+V+R   G G 
Sbjct: 65  VGAGIGAALGGMRPIVEVMTVNFALLALDPLINTAATLRHMSGGQFSVPLVLRMATGAGR 124

Query: 124 HGALYHSQSVEAIFANQPGLKIVMPSTPYDAKGLLKAAVRDEDPVLFFEHKRAYRLIKGE 183
             A  HS S+E  FA+ PGLK++ P+T  DA+G+L  A++D DPVL FEH + Y L + E
Sbjct: 125 QLAAQHSHSLEGWFAHVPGLKVLAPATVEDARGMLWPALQDPDPVLIFEHAQLYNL-EDE 183

Query: 184 VPADDYVLPIGKADVKREGDDITVITYGLCVHFALQAAERLEKDGISAHVVDLRTVYPLD 243
           +P     + I  A V+R G D+++I YG  +H ALQAA++L ++GI+A V+DLR + PLD
Sbjct: 184 LP-PSMAVDIRSARVRRPGSDLSLIAYGGTLHKALQAADQLAEEGIAAEVIDLRVLRPLD 242

Query: 244 KEAIIEAASKTGKVLLVTEDTKEGSIMSEVAAIISEHCLFDLDAPIKRLAGPDIPAMPYA 303
           +  I+++  KT + L+V E  + GS+ +E+   I E   F+LDAP  R+   ++P +PYA
Sbjct: 243 EVTILDSVRKTRRALVVDEGWRSGSLSAEIITRIIEQGFFELDAPPARVCSAEVP-IPYA 301

Query: 304 PTMEKYFMVNPDKVEAAMREL 324
             +E+  +     + AA R+L
Sbjct: 302 RHLEEAALPQVPTIIAAARQL 322


Lambda     K      H
   0.319    0.136    0.392 

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: 261
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: 327
Length of database: 324
Length adjustment: 28
Effective length of query: 299
Effective length of database: 296
Effective search space:    88504
Effective search space used:    88504
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: 48 (23.1 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