GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garK in Kocuria turfanensis HO-9042

Align glycerate 2-kinase (EC 2.7.1.165) (characterized)
to candidate WP_062736047.1 AYX06_RS12490 glycerate kinase

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



>NCBI__GCF_001580365.1:WP_062736047.1
          Length = 416

 Score =  274 bits (701), Expect = 3e-78
 Identities = 161/378 (42%), Positives = 215/378 (56%), Gaps = 8/378 (2%)

Query: 2   KIIIAPDSFKDSLSAEGVAQAIAAGLSEVWPQAQLIQCPMADGGEGTVDAVLAACKGELR 61
           ++++APD FK +L+A   A+A+AAG+   WP A++   P+ADGGEGTVDA +AA   +LR
Sbjct: 16  RVVVAPDKFKGTLTAPEAAEALAAGVRRHWPGARVSTVPLADGGEGTVDAAVAA-GAQLR 74

Query: 62  RQQVRGPLGGTVEARWGWLA---DSHTAIIEMAEASGLQLVPPGQRDACTSTTYGTGELI 118
           R  VRG LG  V ARW  L     S TA++E A+A+GL  V P    A  + +YG G+LI
Sbjct: 75  RTAVRGALGARVRARWALLTAENGSTTAVVESAQAAGLDQVRPSPATARAAHSYGCGQLI 134

Query: 119 RAALDLGAERIILAIGGSATNDAGAGAMQALGAQLFDAEAQTLPPGGLALSRLAHISLEN 178
           RAALD GA  +++ +GGSA  D G+GA++ALG ++ D     +P GG  L R A +    
Sbjct: 135 RAALDAGAADVVVGLGGSAMTDGGSGALRALGLEVLDDGGAPVPLGGAGLLRAARLDASG 194

Query: 179 LDPRLAQVRFEIAADVNNPLCGPHGASAIFGPQKGASPVHVQQLDAALGHFADHCARVLP 238
           LDPRL  VR  +A DV NPL GP GA+ +F  QKGA      +LDAAL  +A   A    
Sbjct: 195 LDPRLRSVRLRLAVDVQNPLYGPAGAAHVFAGQKGADAGARAELDAALRRWAALLAGTPG 254

Query: 239 KDVRDEPGSGAAGGLGFAAKAFLGAQFRAGVEVVAELVGLEDAVRGADLVITGEGRFDAQ 298
                 PG+GAAGG      A   A    G E+VA LVGLE  ++ ADL++ GEG  D Q
Sbjct: 255 SRPFRRPGAGAAGGFPSGFLALTPAVLEGGFELVAALVGLEQHLQRADLLLVGEGSLDEQ 314

Query: 299 TLRGKTPFGVARIAGQHNVPVIVIAGTLGEGYEQMYAHGVAAAFAL----PAGPMSLEQA 354
           +L+GK P   A +A    +PV  +AG L     Q+   GV AA +L    P+   +  +A
Sbjct: 315 SLQGKAPLAAAAVAAARGIPVAAVAGRLSLSARQLREAGVGAAASLVDVAPSEAEARARA 374

Query: 355 CSEAPRLLRERASDIARV 372
              AP    E    + RV
Sbjct: 375 GHYAPLAAAEALRQLDRV 392


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: 459
Number of extensions: 30
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: 416
Length adjustment: 31
Effective length of query: 349
Effective length of database: 385
Effective search space:   134365
Effective search space used:   134365
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 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