GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garK in Echinicola vietnamensis KMM 6221, DSM 17526

Align glycerate 2-kinase (EC 2.7.1.165) (characterized)
to candidate Echvi_4031 Echvi_4031 glycerate kinase

Query= metacyc::MONOMER-20837
         (380 letters)



>FitnessBrowser__Cola:Echvi_4031
          Length = 370

 Score =  170 bits (431), Expect = 5e-47
 Identities = 115/327 (35%), Positives = 170/327 (51%), Gaps = 12/327 (3%)

Query: 1   MKIIIAPDSFKDSLSAEGVAQAIAAGLSEVWPQAQLIQCPMADGGEGTVDAVLAACKGEL 60
           M I+IAP++FK ++ A+  A  I   L +    A+  +CP+ADGG+GT    L   + +L
Sbjct: 1   MNILIAPNAFKGTIPADRAAALIEEVLRQYLSHAEYQRCPIADGGDGT--CFLLGNQLKL 58

Query: 61  RRQQVRGPLG-GTVEARWGWLADSHT-AIIEMAEASGLQLVPPGQRDACTSTTYGTGELI 118
            + +  G    G  E    +L +S   A I+++  SGL  +PP   +A  ++T+GTG+LI
Sbjct: 59  NKIEAVGLNAIGLTEQGLIFLNESRKEAWIDVSTLSGLAGLPPFGVNAQLTSTFGTGQLI 118

Query: 119 RAALDLGAERIILAIGGSATNDAGAGAMQALGAQLFDAEAQTLP---PGGLALSRLAHIS 175
             A+  GAE IIL +GGSAT D G G ++ALG    D   + +P   PG   L R+AHI 
Sbjct: 119 MEAIRRGAEHIILGLGGSATVDMGTGILRALGYLFLDKNGREIPMFSPG--FLERIAHI- 175

Query: 176 LENLDPRLAQVRFEIAADVNNPLCGPHGASAIFGPQKGASPVHVQQLDAALGHFADHCAR 235
                  + +VRF    DV N   G  GA  +FGPQKG S       ++A     +    
Sbjct: 176 --QRPVAMNKVRFTCLCDVKNTFFGSQGAIPVFGPQKGLSEADQHVFESAAKGVFELLKA 233

Query: 236 VLPKDVRDEPGSGAAGGLGFAAKAFLGAQFRAGVEVVAELVGLEDAVRGADLVITGEGRF 295
                + D+PG GAAGG+     AF   +   G     E V +++ V  AD VITGEG+F
Sbjct: 234 KGDGQLTDQPGFGAAGGIALGLSAFFSVKIEEGAHYFFEQVNMQEKVSWADWVITGEGKF 293

Query: 296 DAQTLRGKTPFGVARIAGQHNVPVIVI 322
           D+Q+  GK  + +  +A +H    ++I
Sbjct: 294 DSQSAAGKGSYKLLGLANKHQKKTLLI 320


Lambda     K      H
   0.318    0.135    0.398 

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: 291
Number of extensions: 17
Number of successful extensions: 4
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: 380
Length of database: 370
Length adjustment: 30
Effective length of query: 350
Effective length of database: 340
Effective search space:   119000
Effective search space used:   119000
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.

Links

Downloads

Related tools

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