GapMind for catabolism of small carbon sources

 

Alignments for a candidate for srlE in Salinicoccus carnicancri Crm

Align PTS system glucitol/sorbitol-specific EIIB component; EII-Gut; Enzyme II-Gut; Glucitol/sorbitol-specific phosphotransferase enzyme IIB component; EC 2.7.1.198 (characterized)
to candidate WP_017549996.1 C792_RS0113515 PTS glucitol/sorbitol transporter subunit IIB

Query= SwissProt::O32333
         (336 letters)



>NCBI__GCF_000330705.1:WP_017549996.1
          Length = 338

 Score =  323 bits (829), Expect = 3e-93
 Identities = 167/338 (49%), Positives = 224/338 (66%), Gaps = 7/338 (2%)

Query: 4   YNAIKIVKGSGGFGGPLTVKPEEGKDTLLYITGGGAEPEIVEKIVNLTGCKAVNGFKTSV 63
           Y ++KI KGSGG+GGPL V P   K  ++ +TGGG +P + + I + TG +AV+GF T V
Sbjct: 2   YKSVKISKGSGGWGGPLMVTPSAEKPYVVSVTGGGIDP-LAQYIADQTGAEAVDGFNTKV 60

Query: 64  PEEQIFLVIIDCGGTLRCGIYPQKRIPTINVMPVGKSGPLAKFITEDIYVSAVGLNQISL 123
             +++  VIIDCGGT RCGIYP+  + T+N+   G SGPL +FI ED +VS V    I L
Sbjct: 61  DYDEMACVIIDCGGTARCGIYPKNDVLTVNLHGTGPSGPLMQFIKEDNFVSGVRERNIEL 120

Query: 124 ADSSA------EPIKSTKVPEEGKREFKYSADKKVSQSLAENSKSSIVQKIGMGAGKVVN 177
           ++          P+K      +  +E K  A +KV+ +  E  K   +++IG   G +V+
Sbjct: 121 SEDGGTSSDGTNPVKPAAAGRKTSKELKEEAKQKVADNKKEPEKKKFIERIGRAMGGIVS 180

Query: 178 TLYQAGRDAVQSMITTILPFMAFVAMLIGIIQGSGFGNWFAKILVPLAGNGIGLMILGFI 237
             YQAGR+ +  +I  ILPFMAFV+MLIGII  +G G+  A  + PLAGN +GL++L  I
Sbjct: 181 VFYQAGRETIDQVIKNILPFMAFVSMLIGIITFTGIGDLIANAVTPLAGNILGLLLLSVI 240

Query: 238 CSIPLLSALLGPGAVIAQIVGTLIGVEIGKGTIPPSLALPALFAINTQCACDFIPVGLGL 297
            S+P+LS +LGPGAVIAQ+VG LIGVEIG G IPP +ALPALFAIN Q   DF+PVGL L
Sbjct: 241 VSLPVLSPVLGPGAVIAQVVGVLIGVEIGNGNIPPEMALPALFAINPQAGADFVPVGLTL 300

Query: 298 AEAEPETVEVGVPSVLYSRFMIGVPRVAVAWVASIGLY 335
            EAEPET+EVGVP+VL+SR + G   V +A+  S  +Y
Sbjct: 301 GEAEPETIEVGVPAVLFSRAITGPLAVLIAFGFSFFIY 338


Lambda     K      H
   0.319    0.139    0.405 

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: 422
Number of extensions: 17
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: 336
Length of database: 338
Length adjustment: 28
Effective length of query: 308
Effective length of database: 310
Effective search space:    95480
Effective search space used:    95480
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 (21.7 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