GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garK in Paraburkholderia phymatum STM815

Align glycerate 2-kinase (EC 2.7.1.165) (characterized)
to candidate WP_012404191.1 BPHY_RS24710 glycerate kinase

Query= BRENDA::P23524
         (381 letters)



>NCBI__GCF_000020045.1:WP_012404191.1
          Length = 395

 Score =  393 bits (1010), Expect = e-114
 Identities = 202/381 (53%), Positives = 264/381 (69%), Gaps = 1/381 (0%)

Query: 1   MKIVIAPDSYKESLSASEVAQAIEKGFREIFPDAQYVSVPVADGGEGTVEAMIAATQGAE 60
           MKIVIAPDS+KESLSA+EVA  IE GFREIFPD QY  +P+ADGGEGTV+A+  A  G  
Sbjct: 1   MKIVIAPDSFKESLSAAEVATQIEAGFREIFPDFQYQRLPIADGGEGTVDALFEAISGQR 60

Query: 61  RHAWVTGPLGEKVNASWGISGDGKTAFIEMAAASGLELVPAEKRDPLVTTSRGTGELILQ 120
           R   V+ PLG  V A + I  +G T  IEMAAASGL LV   +RDP +T+SRGTGELI+ 
Sbjct: 61  RQVTVSDPLGRPVQAEYAILSNG-TGVIEMAAASGLHLVAPHERDPRITSSRGTGELIVD 119

Query: 121 ALESGATNIIIGIGGSATNDGGAGMVQALGAKLCDANGNEIGFGGGSLNTLNDIDISGLD 180
           AL  G  + I+GIGGSATNDGGAG++QALG +L D+ G ++  GG  L+ L  ID +  D
Sbjct: 120 ALSVGVRHFIVGIGGSATNDGGAGLLQALGVRLVDSKGADLASGGAVLSQLAHIDQTRAD 179

Query: 181 PRLKDCVIRVACDVTNPLVGDNGASRIFGPQKGASEAMIVELDNNLSHYAEVIKKALHVD 240
           PRLK+C   VACDV NPL+G NGA+ +FGPQKGA+  MI ELD  L ++A VIK+ L  D
Sbjct: 180 PRLKECYFEVACDVDNPLIGGNGATAVFGPQKGATPQMIAELDEALGNFAAVIKRDLDAD 239

Query: 241 VKDVPGAGAAGGMGAALMAFLGAELKSGIEIVTTALNLEEHIHDCTLVITGEGRIDSQSI 300
           V+ +PG+GAAGG+GAAL+  L A L+ GIEIV  A+ + + + +  LV+TGEG ID Q+ 
Sbjct: 240 VRSLPGSGAAGGLGAALIGVLHARLRPGIEIVCEAMRVADAVQEADLVVTGEGCIDGQTA 299

Query: 301 HGKVPIGVANVAKKYHKPVIGIAGSLTDDVGVVHQHGIDAVFSVLTSIGTLDEAFRGAYD 360
            GK P+G+A +A ++  PVI I G++      V+ +GIDAVF  +    ++++AF+ A  
Sbjct: 300 RGKAPVGIAKIASQFGVPVIAIGGAVAGSADKVYANGIDAVFPSVQRACSIEQAFQDAAV 359

Query: 361 NICRASRNIAATLAIGMRNAG 381
           N+   +RN AA L+IG    G
Sbjct: 360 NVRTTARNTAAVLSIGAHTFG 380


Lambda     K      H
   0.315    0.135    0.385 

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: 471
Number of extensions: 23
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: 381
Length of database: 395
Length adjustment: 30
Effective length of query: 351
Effective length of database: 365
Effective search space:   128115
Effective search space used:   128115
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: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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