GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glk in Rhizobium freirei PRF 81

Align glucokinase (EC 2.7.1.2) (characterized)
to candidate WP_004117842.1 RHSP_RS13800 ROK family protein

Query= reanno::SB2B:6938110
         (299 letters)



>NCBI__GCF_000359745.1:WP_004117842.1
          Length = 308

 Score =  145 bits (366), Expect = 1e-39
 Identities = 105/302 (34%), Positives = 142/302 (47%), Gaps = 14/302 (4%)

Query: 2   MRMGVDLGGTKIELVALGEDGSELFRKRIATPR----EYQGTLNAVVTLVNEAEATLGTQ 57
           M +  D+GG+ I+          L   R  TPR    E+   L  V+     AEA  G  
Sbjct: 1   MIVSFDIGGSAIKGGIARSMTDILPLARRPTPRHDFAEFVAVLREVI-----AEAG-GKP 54

Query: 58  GSLGIGIPGVISPYTGLVKNANSTWINGHPLDRDLGALLNREVRVANDANCFAVSEAVDG 117
             L   I GV+ P T  +  AN   I+G  L  DL A L   V +ANDA+CFA++EA+ G
Sbjct: 55  TCLSFSIAGVVDPDTQALTCANIRCIDGRHLAADLEAELGYPVLIANDADCFAMAEAMSG 114

Query: 118 AAAGKRVVFGAILGTGCGAGLAFDGRVHEGGNGIGGEWGHNPL----PWMRPDEFNTTEC 173
           A  G R+VFGAILGTG G GL  DGR+     G  GEWGH P+        P       C
Sbjct: 115 AGRGHRIVFGAILGTGVGGGLVADGRLVNAAGGFAGEWGHGPIIASFAGDPPAAIPAYPC 174

Query: 174 FCGNKDCIETFVSGTGFVRDFRNSGGTAQNGAEIMSLVDAGDELANLVFDRYLDRLARSL 233
            CG K C++T     G  R  +   G   +  EI+      D  A    D  +D +A  L
Sbjct: 175 GCGQKGCVDTVGGARGIERLHKTLYGAELSSEEIIDRWLKDDTQAQRTIDVMIDLVASPL 234

Query: 234 AHVINMLDPDAIVLGGGMSNVQAIYARLPAILPKYVVGRECRTPVVQNLYGCSSGVRGAA 293
           A  +N+     + +GGG+SNV+ + ARL   +   ++ +  R  VV +      G+ GAA
Sbjct: 235 ALTVNITGATIVPVGGGLSNVEPLLARLDQAVRARILRKFGRPLVVPSQCKLEPGLIGAA 294

Query: 294 WL 295
            L
Sbjct: 295 LL 296


Lambda     K      H
   0.320    0.139    0.429 

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: 295
Number of extensions: 14
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: 299
Length of database: 308
Length adjustment: 27
Effective length of query: 272
Effective length of database: 281
Effective search space:    76432
Effective search space used:    76432
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 Sep 24 2021. 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