GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garK in Amycolatopsis halophila YIM 93223

Align glycerate 2-kinase (EC 2.7.1.165) (characterized)
to candidate WP_051400108.1 AMYHA_RS19785 glycerate kinase

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



>NCBI__GCF_000504245.1:WP_051400108.1
          Length = 384

 Score =  287 bits (734), Expect = 4e-82
 Identities = 169/371 (45%), Positives = 221/371 (59%), Gaps = 9/371 (2%)

Query: 2   KIIIAPDSFKDSLSAEGVAQAIAAGLSEVWPQAQLIQCPMADGGEGTVDAVLAACKGELR 61
           +++IAPD FK SLSA  VA  +AAGL    P   + + P+ADGG+GT+DA LAA      
Sbjct: 3   QVVIAPDKFKGSLSAPEVAAHVAAGLRRARPGLDVREVPVADGGDGTLDAALAA---GFT 59

Query: 62  RQQVR--GPLGGTVEARWGWLADSHTAIIEMAEASGLQLVPPGQRDACTSTTYGTGELIR 119
           R  VR  GP G  V+  +       TA++E+A+ SGL  +P  +     +T++GTGE+IR
Sbjct: 60  RVPVRASGPTGEAVDTAYA--RRGGTAVVELADVSGLSRLPGRRLAPLAATSFGTGEVIR 117

Query: 120 AALDLGAERIILAIGGSATNDAGAGAMQALGAQLFDAEAQTLPPGGLALSRLAHISLENL 179
           AALD G   I+L +GGSA  D GAG  +ALG +L D +   L PGG AL+RLA   +  L
Sbjct: 118 AALDDGCRTIVLGLGGSACTDGGAGMARALGVRLLDPDGADLSPGGAALTRLATADVSGL 177

Query: 180 DPRLAQVRFEIAADVNNPLCGPHGASAIFGPQKGASPVHVQQLDAALGHFADHCARVLPK 239
            P +A+    +A+DV+NPL G HGA+A++GPQKGA    V  LDAAL  +A+   R    
Sbjct: 178 HPAVAEADIVVASDVDNPLLGEHGAAAVYGPQKGADTEQVALLDAALARWAEVLQRDTNV 237

Query: 240 D--VRDEPGSGAAGGLGFAAKAFLGAQFRAGVEVVAELVGLEDAVRGADLVITGEGRFDA 297
           D      PG+GAAGG+GFAA A LGA  R G+E + +LVG    + GA LV+TGEG  D 
Sbjct: 238 DPATATRPGAGAAGGVGFAALALLGAVLRPGIEYLLDLVGFHRQLAGASLVVTGEGSLDE 297

Query: 298 QTLRGKTPFGVARIAGQHNVPVIVIAGTLGEGYEQMYAHGVAAAFALPAGPMSLEQACSE 357
           QTLRGK P GVA  A    VPV+ +AG      E + A G AAA+AL        +  +E
Sbjct: 298 QTLRGKAPAGVAAAAHAAGVPVVAVAGRCLLASETLTASGFAAAYALTDIESDPRRCVAE 357

Query: 358 APRLLRERASD 368
           A  LL   A+D
Sbjct: 358 AGPLLERLATD 368


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: 449
Number of extensions: 23
Number of successful extensions: 3
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: 384
Length adjustment: 30
Effective length of query: 350
Effective length of database: 354
Effective search space:   123900
Effective search space used:   123900
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