GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garK in Halomonas xinjiangensis TRM 0175

Align glycerate 2-kinase (EC 2.7.1.165) (characterized)
to candidate WP_043528409.1 JH15_RS07235 glycerate kinase

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



>NCBI__GCF_000759345.1:WP_043528409.1
          Length = 376

 Score =  405 bits (1040), Expect = e-117
 Identities = 208/372 (55%), Positives = 260/372 (69%)

Query: 1   MKIIIAPDSFKDSLSAEGVAQAIAAGLSEVWPQAQLIQCPMADGGEGTVDAVLAACKGEL 60
           M I+IAPDSFKD+L+A   A AIAAG+    PQA L  CPM DGGEGT+DA+L A   E 
Sbjct: 1   MHILIAPDSFKDALTASDAAAAIAAGIRRCLPQATLQCCPMGDGGEGTLDALLTATGAER 60

Query: 61  RRQQVRGPLGGTVEARWGWLADSHTAIIEMAEASGLQLVPPGQRDACTSTTYGTGELIRA 120
           R   V+  LG  ++A WGW A + TA +E+AEASGLQ +   +R A  STT+G GELI  
Sbjct: 61  REASVQDALGRALDAAWGWHAATRTAYVELAEASGLQQIAREERTALHSTTHGVGELIGE 120

Query: 121 ALDLGAERIILAIGGSATNDAGAGAMQALGAQLFDAEAQTLPPGGLALSRLAHISLENLD 180
           ALD GAER++L +GGSATNDAGAG + ALGA+L DAE  TLPPGG AL+ LA + L  LD
Sbjct: 121 ALDAGAERLVLTLGGSATNDAGAGMLVALGARLLDAEGDTLPPGGAALANLAELDLSGLD 180

Query: 181 PRLAQVRFEIAADVNNPLCGPHGASAIFGPQKGASPVHVQQLDAALGHFADHCARVLPKD 240
           PRLA ++ + A DV+NPL G  GASA+FGPQKGASP  V +LD AL  FAD  AR L ++
Sbjct: 181 PRLASLQVQTAVDVDNPLLGERGASAVFGPQKGASPAEVDRLDRALATFADVTARTLGEE 240

Query: 241 VRDEPGSGAAGGLGFAAKAFLGAQFRAGVEVVAELVGLEDAVRGADLVITGEGRFDAQTL 300
            R+ PG+GAAGG+GFA+ AFLGA  R G+E+V      E+ +  ADLVITGEG+ D Q+L
Sbjct: 241 YRERPGAGAAGGMGFASLAFLGASLRPGIELVMAQARFEERLAQADLVITGEGQLDGQSL 300

Query: 301 RGKTPFGVARIAGQHNVPVIVIAGTLGEGYEQMYAHGVAAAFALPAGPMSLEQACSEAPR 360
            GKTP G+AR A +H VP +V+AG LG  ++  +  GV AAFAL  GPMSL++A S    
Sbjct: 301 SGKTPIGIARAARRHGVPCVVLAGRLGAHWQAAHEEGVTAAFALADGPMSLDEALSRCSE 360

Query: 361 LLRERASDIARV 372
           LL +RA  + R+
Sbjct: 361 LLGDRAESVVRL 372


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: 403
Number of extensions: 15
Number of successful extensions: 1
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: 376
Length adjustment: 30
Effective length of query: 350
Effective length of database: 346
Effective search space:   121100
Effective search space used:   121100
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