GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrK in Bradyrhizobium sp. BTAi1

Align Fructokinase (EC 2.7.1.4) (characterized)
to candidate WP_012041226.1 BBTA_RS04345 carbohydrate kinase

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



>NCBI__GCF_000015165.1:WP_012041226.1
          Length = 315

 Score =  220 bits (560), Expect = 4e-62
 Identities = 132/306 (43%), Positives = 160/306 (52%), Gaps = 2/306 (0%)

Query: 1   MILCAGEALIDMLPRALPDGTAGFAPVAGGAVFNTAVALGRLGADVGLVTGLSRDLFGEV 60
           MIL  G+ALID +P  L DG  G  PV GG+  N  V L RLGA  G V G+S DLFG +
Sbjct: 1   MILSCGDALIDFVPARLADGRDGLRPVVGGSCLNVPVGLARLGAPAGFVGGISTDLFGSM 60

Query: 61  LMTALAAADVDSDMAVLSDRPTTLAFVTLTDGHAQYAFYDENTAGRMLAPADMPDPGPEV 120
           +     A+ VD   A  S   TTLAFV    G AQYAFYD  TA R         P   +
Sbjct: 61  IAAHAQASGVDLSHATRSADQTTLAFVRHVGGEAQYAFYDAETAARKWTYRHGSIPFTSI 120

Query: 121 GTLFFGGISLAVEPCAAAYEALCLKAAAGRVVMLDPNIRPGFIKDETTFRARIDRMLAVT 180
             +  G  +L  +  AA   AL      G  +  DPN RP  ++D+  +R ++D   A  
Sbjct: 121 DAIHVGSTTLIHDLGAAETRALIAATQGGVTISFDPNCRPNLVQDKAAYRVQMDGFAASA 180

Query: 181 DIVKVSDEDLAWLMGPGDLAESAAALRARGPAVVCVTRGGAGVEA-HTATGITHVAAEAV 239
           D++K+SD D  +L G  D A  A AL ARG  +V VTRG  G    H   G   VAA AV
Sbjct: 181 DLIKMSDVDFDYLHGHDDYAARAEALLARGAKLVVVTRGPKGALGWHAGAGAAEVAAPAV 240

Query: 240 EVVDTVGAGDTFNAGFLAGLAEAGALDKDRLRALDAPVLTSALRLGAQAAAITVSRAGAN 299
           EVVDT+GAGD+F AG L  L   G L K  L  L A  L   L   A  AA+T +R GA+
Sbjct: 241 EVVDTIGAGDSFQAGLLFALHRLGRLGKAALAELTATELRKVLAFAAACAAVTCTREGAD 300

Query: 300 PP-WRD 304
           PP W D
Sbjct: 301 PPRWAD 306


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: 216
Number of extensions: 11
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: 308
Length of database: 315
Length adjustment: 27
Effective length of query: 281
Effective length of database: 288
Effective search space:    80928
Effective search space used:    80928
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.

Links

Downloads

Related tools

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