GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Rhodococcus qingshengii djl-6-2

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate WP_050657012.1 C1M55_RS18155 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::Dino:3607124
         (338 letters)



>NCBI__GCF_002893965.1:WP_050657012.1
          Length = 364

 Score =  317 bits (811), Expect = 4e-91
 Identities = 176/356 (49%), Positives = 229/356 (64%), Gaps = 25/356 (7%)

Query: 1   MAGIKIDKINKFY--GTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSG 58
           MA I   K +  Y    T A+  ++LDI DGEF+V VGPSG GKST LR LAGLE + SG
Sbjct: 1   MAEISYQKASCIYEGAGTLAVDSLDLDINDGEFIVLVGPSGSGKSTALRMLAGLEDIDSG 60

Query: 59  RIEIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAA 118
            I I G+D+T V   DRD+AMVFQ+YALYP+ TV ENM F +K+ G   + RK+++AEAA
Sbjct: 61  AITINGKDMTDVPSKDRDIAMVFQNYALYPNKTVGENMGFALKMRGVPVEERKKKVAEAA 120

Query: 119 RVLQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEG 178
           ++L L DYLDRKP +LSGGQRQRVA+GRAIV+ P VF  DEPLSNLDAKLRVQ R ++  
Sbjct: 121 KLLDLTDYLDRKPAKLSGGQRQRVAMGRAIVREPQVFCMDEPLSNLDAKLRVQTRTQIAA 180

Query: 179 LHKQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPA 238
           L ++LG T +YVTHDQVEAMTM D++ VL  G+++Q  SP +LY +P + FVA FIGSP 
Sbjct: 181 LQRRLGTTTVYVTHDQVEAMTMGDRVAVLKGGKLQQFASPTELYDRPANAFVAGFIGSPG 240

Query: 239 MNVFSSDV-------GLQDISLD-----------ASAAFVGCRPEHIEIVPDGDGHIAAT 280
           MN+ ++ V       G  ++ LD            ++  VG RPE  ++V  GDG IAA 
Sbjct: 241 MNLVTAPVSSGGVRFGDVEVPLDREQMAAIAAAGLASVTVGIRPEQFQVVAAGDG-IAAQ 299

Query: 281 VHVKERLGGESLLYLGLKGGG----QIVARVGGDDETKVGAAVSLRFSRHRLHQFD 332
           + + E LG ES +Y  + G       +VAR GG  + + G  +        +H FD
Sbjct: 300 IDLVEELGNESYIYAHVPGTEADPISLVARTGGRSKLQYGQTLGFERVDGLVHLFD 355


Lambda     K      H
   0.320    0.139    0.396 

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: 362
Number of extensions: 9
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: 338
Length of database: 364
Length adjustment: 29
Effective length of query: 309
Effective length of database: 335
Effective search space:   103515
Effective search space used:   103515
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: 49 (23.5 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