GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrK in Phaeacidiphilus oryzae TH49

Align Fructokinase (EC 2.7.1.4) (characterized)
to candidate WP_037570570.1 BS73_RS07575 carbohydrate kinase

Query= reanno::Dino:3609413
         (308 letters)



>NCBI__GCF_000744815.1:WP_037570570.1
          Length = 308

 Score =  192 bits (487), Expect = 1e-53
 Identities = 135/318 (42%), Positives = 168/318 (52%), Gaps = 29/318 (9%)

Query: 1   MILCAGEALIDMLPRALPDGTAGFAPVAGGAVFNTAVALGRLGADVGLVTGLSRDLFGEV 60
           MI+ AGEALID++P    +G     P  GG  +NTAVAL RLG+     + +S D FGE 
Sbjct: 1   MIVVAGEALIDLVP----EGGQALYPRRGGGPYNTAVALARLGSATAFCSRVSTDAFGES 56

Query: 61  LMTALAAADVDSDMAVLSDRPTTLAFVTL-TDGHAQYAFYDENTAGRMLAPADMPDPGPE 119
           L+  L    VD+ +      PTTLA  +L  DG A Y FY E TA R+     +P+  PE
Sbjct: 57  LLAELRTNGVDTGLVQRGPEPTTLAVASLGADGSAGYTFYTEGTADRLFR---LPEALPE 113

Query: 120 VG-TLFFGGISLAVEPCAAAYEALCLK-AAAGRVVMLDPNIRPGFIKDETTFRARIDRML 177
               + FG  SL +EP A AYE +  + +A G    LDPNIR G I D   +RAR    L
Sbjct: 114 AARAVSFGTCSLVLEPGATAYERMLRRESARGLFTALDPNIRAGLIPDPDAYRARFRGWL 173

Query: 178 AVTDIVKVSDEDLAWLMG-PGDLAESAAALRARGPAVVCVTRGGAGVEAHTATG----IT 232
               ++K+S ED  WL G P D         A GP+ V VTRGG G+  H          
Sbjct: 174 PDVRLLKLSAEDAEWLGGTPRDWL-------ADGPSAVVVTRGGDGLSVHVQEAGEYREY 226

Query: 233 HVAAEAVEVVDTVGAGDTFNAGFLAGLAEAGALD----KDRLRALDAPVLTSALRLGAQA 288
           HV    V+VVDT+GAGDT NA  L  LAEAGA         L  +D P   + L   A+A
Sbjct: 227 HVPGHKVDVVDTIGAGDTVNAALLHRLAEAGAASGPGTGPGLGGVDWP---AVLDFAARA 283

Query: 289 AAITVSRAGANPPWRDEL 306
           AA+T SRAGANPP   E+
Sbjct: 284 AAVTCSRAGANPPTSAEV 301


Lambda     K      H
   0.320    0.136    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: 264
Number of extensions: 15
Number of successful extensions: 6
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: 308
Length of database: 308
Length adjustment: 27
Effective length of query: 281
Effective length of database: 281
Effective search space:    78961
Effective search space used:    78961
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 48 (23.1 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