GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcB in Rhizobium leguminosarum 3841

Align Fructose import binding protein FrcB (characterized)
to candidate WP_003550404.1 RL_RS34880 D-ribose ABC transporter substrate-binding protein

Query= SwissProt::Q9F9B2
         (341 letters)



>NCBI__GCF_000009265.1:WP_003550404.1
          Length = 313

 Score =  111 bits (278), Expect = 2e-29
 Identities = 95/313 (30%), Positives = 146/313 (46%), Gaps = 24/313 (7%)

Query: 2   KKTVLSAAFGALAMGVAFASPSQAAEVSACLITKTDTNPFFVKMKEGAAAKAKELGVTLK 61
           ++  L+A  GALA+G A   P+ +A++ A +IT    NPFF     GA AKAKELG   +
Sbjct: 5   RRLTLAAFAGALALGTAL--PAFSADLIA-IITPAHDNPFFKAEAVGAEAKAKELGY--E 59

Query: 62  SYAGKIDGDSESQVAAIETCIADGAKGILIAASDTQGIVPQVQKARDAGLLVIALDTPLE 121
           +     D D+  Q   I+T I  GAK I++  +     V  V+KA+DAG+    +D  + 
Sbjct: 60  TLLMTHDDDANKQSEMIDTAIGRGAKAIILDNAGADASVAAVKKAKDAGIPSFLIDREIN 119

Query: 122 PLDAADATFATDNLLAGKLIGQWAAATLGDAAKEAKVAFLDLTPSQPSVDV-LRDQGFMI 180
               A A   ++N    +L  Q     +G+     K  +++L   +   +  +R QG+  
Sbjct: 120 ATGVAVAQIVSNNYQGAQLGAQEFVKLMGE-----KGNYVELVGKESDTNAGIRSQGY-- 172

Query: 181 GFGIDPKDPNKIGDEDDPRIVGHDITNGNEEGGRTAMENLLQKDPTINVVHTINEPAAAG 240
                    + I D  D + V     N ++    + ME +LQ +P I  V + N+  A G
Sbjct: 173 --------HDVIDDYPDLKSVAKQSANWSQTEAYSKMETILQANPDIKGVISGNDTMAMG 224

Query: 241 AYEALKSVGREKDVLIVSVDGGCPGVKNVAEGVIGATSQQYPLMMAALGIEAIKKFADTG 300
           A  AL++ GR KDV++V  DG      ++  G I AT  Q     A L +E    +    
Sbjct: 225 AIAALQAAGR-KDVIVVGFDGSNDVRDSIKSGGIKATVLQPAYAQAQLAVEQADAYIK-- 281

Query: 301 EKPTPTEGKDFVD 313
            K TP E K  +D
Sbjct: 282 NKTTPKEEKQLMD 294


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: 253
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: 341
Length of database: 313
Length adjustment: 28
Effective length of query: 313
Effective length of database: 285
Effective search space:    89205
Effective search space used:    89205
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: 48 (23.1 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