GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcB in Ruegeria conchae TW15

Align Fructose import binding protein FrcB (characterized)
to candidate WP_029622083.1 G7G_RS0115750 sugar ABC transporter substrate-binding protein

Query= SwissProt::Q9F9B2
         (341 letters)



>NCBI__GCF_000192475.1:WP_029622083.1
          Length = 339

 Score =  480 bits (1236), Expect = e-140
 Identities = 240/339 (70%), Positives = 282/339 (83%), Gaps = 1/339 (0%)

Query: 3   KTVLSAAFGALAMGVAFASPSQAAEVSACLITKTDTNPFFVKMKEGAAAKAKELGVTLKS 62
           + +L  A  A A+  A AS +QAA  + CLITKTDTNPFFVKMKEGA AKA+ELG+TLK+
Sbjct: 2   RNLLKLAASATALTFAAAS-AQAAGETVCLITKTDTNPFFVKMKEGATAKAEELGMTLKA 60

Query: 63  YAGKIDGDSESQVAAIETCIADGAKGILIAASDTQGIVPQVQKARDAGLLVIALDTPLEP 122
           +AGK+DGD E+QV AIETCI DGAKGIL+ ASDT  IVP V++ARDAG+LVIALDTPL P
Sbjct: 61  FAGKVDGDHETQVQAIETCILDGAKGILLTASDTSSIVPAVKQARDAGVLVIALDTPLSP 120

Query: 123 LDAADATFATDNLLAGKLIGQWAAATLGDAAKEAKVAFLDLTPSQPSVDVLRDQGFMIGF 182
           +D+ADATFATDN  AG LIGQWA A +GDAA +AK+A LDL  SQP+VDVLR+QGF+ GF
Sbjct: 121 IDSADATFATDNYKAGLLIGQWAKAKMGDAAADAKIATLDLNVSQPTVDVLRNQGFLDGF 180

Query: 183 GIDPKDPNKIGDEDDPRIVGHDITNGNEEGGRTAMENLLQKDPTINVVHTINEPAAAGAY 242
           G+D  DPN IGDE D R+VG D+T+GNEEGGR AMENLL KD +INVVHTINEPAAAGAY
Sbjct: 181 GVDLADPNVIGDETDARLVGSDVTDGNEEGGRRAMENLLAKDSSINVVHTINEPAAAGAY 240

Query: 243 EALKSVGREKDVLIVSVDGGCPGVKNVAEGVIGATSQQYPLMMAALGIEAIKKFADTGEK 302
           EALKS+GRE DVLIVSVDGGCPGV+NV  GVIGATSQQYPL+MA+LG+EA+KK+A+ G K
Sbjct: 241 EALKSIGRENDVLIVSVDGGCPGVQNVEAGVIGATSQQYPLLMASLGVEAVKKWAEEGVK 300

Query: 303 PTPTEGKDFVDTGVSLVADKPVSGVESIDTKTGMEKCWG 341
           P  T GKDF DTGV+L+ D+PV GVES+    G++ CWG
Sbjct: 301 PENTPGKDFYDTGVALITDQPVDGVESLSVAEGLDLCWG 339


Lambda     K      H
   0.313    0.132    0.372 

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: 470
Number of extensions: 19
Number of successful extensions: 1
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: 341
Length of database: 339
Length adjustment: 28
Effective length of query: 313
Effective length of database: 311
Effective search space:    97343
Effective search space used:    97343
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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