GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11895 in Skermanella stibiiresistens SB22

Align Inositol transport system permease protein (characterized)
to candidate WP_051511581.1 N825_RS05320 ABC transporter permease

Query= reanno::WCS417:GFF2333
         (340 letters)



>NCBI__GCF_000576635.1:WP_051511581.1
          Length = 338

 Score =  213 bits (542), Expect = 6e-60
 Identities = 124/325 (38%), Positives = 194/325 (59%), Gaps = 27/325 (8%)

Query: 19  RLPTELSIFLVLIGIGLVFELFGWIVRDQSFLMNSQRLVLMILQVSIIGLLAIGVTQVII 78
           R   + S  L LI I +V  L         + ++++ +  ++   +++G++AIG+T VI+
Sbjct: 34  RFLVQYSNVLALIVILVVASLLS------PYFLSTRNIFNVLRGATMVGIVAIGMTYVIL 87

Query: 79  TTGIDLSSGSVLALSAMIAASLAQTSDFSRAVFPSLTDLPVWIPVAMGLGVGLLAGAING 138
             GIDLS GS++ LSA + AS A              D  + I  ++GL  GL+ G  NG
Sbjct: 88  NRGIDLSVGSLVGLSAALTASFA--------------DYGIGIAASIGLVSGLVLGLANG 133

Query: 139 SIIAVTGIPPFIATLGMMVSARGLARYYTEGQP--VSMLSDSYTAIGHG-----AMPVII 191
            +I    + PFIATLGMM+ ARGL   YT G    V   +D++T +G        +PV++
Sbjct: 134 LMITKLRLQPFIATLGMMIFARGLVFVYTNGSNIVVDKPTDAFTWLGSAYIGPVPVPVVV 193

Query: 192 FLVVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLIIVYSIAGLLAGLAGVVA 251
           F+++  +  + LRYT +G+  +A+G N +AAR SGINV R+ I VY I+G+LA  AGV+ 
Sbjct: 194 FVLIWALCALVLRYTVFGREIFAVGANEEAARLSGINVDRNKIRVYCISGVLAAFAGVIM 253

Query: 252 SARAATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVMASGFTFVGVD 311
           ++R   G+   G  +ELDAIAA +IGGT+  GGVG + GTV+G LIL  +++    + + 
Sbjct: 254 ASRLTVGEPNGGTLFELDAIAATLIGGTTFDGGVGSVHGTVLGVLILAFLSNVLNLLNIS 313

Query: 312 AYIQDIIKGLIIVVAVVIDQYRNKR 336
            Y Q ++KG+IIV+AVV+ ++R ++
Sbjct: 314 PYSQMLLKGVIIVLAVVVSEWRKRK 338


Lambda     K      H
   0.325    0.140    0.394 

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: 288
Number of extensions: 15
Number of successful extensions: 4
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: 340
Length of database: 338
Length adjustment: 28
Effective length of query: 312
Effective length of database: 310
Effective search space:    96720
Effective search space used:    96720
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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