GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuE in Halomonas desiderata SP1

Align ABC transporter substrate-binding protein (characterized, see rationale)
to candidate WP_086510099.1 BZY95_RS11690 ABC transporter substrate-binding protein

Query= uniprot:A0A166QFS3
         (424 letters)



>NCBI__GCF_002151265.1:WP_086510099.1
          Length = 429

 Score =  471 bits (1212), Expect = e-137
 Identities = 231/417 (55%), Positives = 300/417 (71%), Gaps = 5/417 (1%)

Query: 8   LPAALLTLCAGLPSLSSAADLTISCGAVGAELQLCKEAVQAWSKQTGNNVEVVSTPNSAT 67
           L A+ LTL   + + + AA +TI+CG  G     C E  + W+++TG+ V VV+TP S T
Sbjct: 18  LVASGLTL---VTTQAQAATITIACGD-GGSADFCPELARQWAQETGHEVAVVTTPQSGT 73

Query: 68  ERLSFYQQILSAQSSDIDIIQIDMVWPGMLAKHLLDLREVLPANATQGYFQAQVDNATVN 127
           E LS YQQ+L ++SSDID++ +D VWPG+LA HL+DL + LP +A++G+F A +DN TV+
Sbjct: 74  ETLSLYQQLLGSKSSDIDVLMVDTVWPGLLAAHLIDLADYLPEDASEGFFPAMIDNNTVD 133

Query: 128 GRLVTMPWFTDSGLLYYRKDLLEKYNQQVPRTWEEMTATARNIQQAERTAGNPNAWGYIF 187
            RL+ +PW++D+GLLYYR+DLLEKY+  VP TWE++T  AR IQ AER AGN    G++F
Sbjct: 134 DRLLALPWYSDAGLLYYRRDLLEKYDHDVPETWEQLTEIAREIQNAEREAGNERMHGFVF 193

Query: 188 QGRAYEGLTCNALEWISSQPEGGLVNSRGDIVVNSQASRTALTLAKSWVGDISPRGVLNY 247
           QGRAYEGLT NALEWI+S   G +V+  G+I VN+  +  ALTLA SWVGDI+PRGV NY
Sbjct: 194 QGRAYEGLTTNALEWIASYGGGTIVDDDGNITVNNPQAAEALTLAASWVGDIAPRGVRNY 253

Query: 248 TEEEGRGVFQSGNALFMRNWPYVWALVQGQDSAVKDKVGVAPLPRGGETGTHASTLGGWG 307
            EEE RG+FQSGNA+FMRNWPY WAL Q   +A++ K GVAPLP  G  G   +TLGGW 
Sbjct: 254 MEEEARGLFQSGNAVFMRNWPYAWALGQADGTAIQGKFGVAPLPH-GSAGESVATLGGWS 312

Query: 308 LAVSRYSAHPKLAAELVSYLTSAQEQKHRALIGAYNPVIESLYQDPELLAAMPYYAQLHS 367
            AVSRYS +P LAAELV+YLT+  +QK  A+    NP   +LYQD E+L   P+  +L+ 
Sbjct: 313 WAVSRYSKNPDLAAELVAYLTAEAQQKAHAIRFGMNPTRVTLYQDKEVLEVQPFIGELYD 372

Query: 368 ILNDGVMRPASITADRYPRVSNAFFDRVHGVLAGELPVDQALAELESELTRIKRRNW 424
            L  GV RPA++T + Y RVSNAFF+RVH VL+G+L  +QAL +LE EL RI RR W
Sbjct: 373 TLVSGVPRPANVTGEHYTRVSNAFFNRVHDVLSGDLTAEQALGQLERELNRISRRGW 429


Lambda     K      H
   0.316    0.131    0.392 

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: 507
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: 424
Length of database: 429
Length adjustment: 32
Effective length of query: 392
Effective length of database: 397
Effective search space:   155624
Effective search space used:   155624
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 51 (24.3 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