GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araWsh in Saccharomonospora cyanea NA-134

Align Inner-membrane translocator (characterized, see rationale)
to candidate WP_005457271.1 SACCYDRAFT_RS14745 ABC transporter permease

Query= uniprot:A0KWY6
         (405 letters)



>NCBI__GCF_000244975.1:WP_005457271.1
          Length = 369

 Score =  307 bits (786), Expect = 4e-88
 Identities = 172/344 (50%), Positives = 231/344 (67%), Gaps = 10/344 (2%)

Query: 63  LWPLLALSILLLANLFIDSSFFNISYQDDRLYGSLIDILNRSAPVALLSIGMSLVIATGG 122
           +WP+LAL+ LL+ N+ +  SFF+I  QD  LYGSLIDIL   AP  L+++GM+LVIAT G
Sbjct: 18  VWPVLALAALLVVNVVVTPSFFDIRLQDGHLYGSLIDILKNGAPTLLIALGMTLVIATRG 77

Query: 123 IDLSVGAVMAIAGAV-CANLLLVPD----ISLVTVIAAGLIVGLLAGCINGGLVSFLGIQ 177
           IDLSVGAV+AIAGAV C ++    D     +    +   L + LL G  NG LVS LGIQ
Sbjct: 78  IDLSVGAVVAIAGAVACTSIAGANDPGGASAAFLAMTLALALCLLLGAWNGFLVSVLGIQ 137

Query: 178 PIVATLLLMVAGRGVAQLINQGQIITFQHPGFAAIGVGQFLGLPMPVWIVIGMLTFSQLL 237
           PI+ATL+LM AGRG+A LI  GQI+T  +  +AA+G G FL LP+ + I +G+     +L
Sbjct: 138 PIIATLVLMTAGRGIAMLITDGQIVTVNNGTYAAVGAG-FLVLPVAILISLGVFVLVAVL 196

Query: 238 LRKTALGLFIEAVGCNAKASRYLGINDKSIKLFAYGIAGLCAALAGMISTADIQGSDANN 297
            RKTALG+ IEAVG N  ASR  G+  ++I    Y  A LCA +AG++ +A++  +DANN
Sbjct: 197 TRKTALGMLIEAVGVNPTASRLAGVRSRTIVWTVYVFAALCAGVAGLMISANVSAADANN 256

Query: 298 AGLWLELDAVLAVVIGGAALTGGRFSLILSVVGALIIQTLATTIIVSGLPAKFNLLIKAI 357
           AGLW+ELDA+LAVVIGG AL+GGR+SL  ++VGAL+IQTL TT+   G+P++  L+ KA+
Sbjct: 257 AGLWIELDAILAVVIGGTALSGGRYSLTGTLVGALLIQTLTTTVYTIGIPSEVTLVFKAL 316

Query: 358 VILTVLLLQSAKFRRQLSALFKSKRHADAKPAEKATSAKASAAT 401
           V++ V LLQS K R    AL +  R      A+   + +   AT
Sbjct: 317 VVIAVCLLQSPKAR----ALLRRNRTPAVAQADIGDAPEPRGAT 356


Lambda     K      H
   0.323    0.136    0.379 

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: 365
Number of extensions: 21
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: 405
Length of database: 369
Length adjustment: 30
Effective length of query: 375
Effective length of database: 339
Effective search space:   127125
Effective search space used:   127125
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 (22.0 bits)
S2: 50 (23.9 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