GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bmpA in Nitriliruptor alkaliphilus DSM 45188

Align Basic membrane lipoprotein, component of General nucleoside uptake porter, NupABC/BmpA (transports all common nucleosides as well as 5-fluorocytidine, inosine, deoxyuridine and xanthosine) (Martinussen et al., 2010) (Most similar to 3.A.1.2.12). NupA is 506aas with two ABC (C) domains. NupB has 8 predicted TMSs, NupC has 9 or 10 predicted TMSs in a 4 + 1 (or 2) + 4 arrangement (characterized)
to candidate WP_169786887.1 NITAL_RS18225 BTAD domain-containing putative transcriptional regulator

Query= TCDB::D2BKA1
         (350 letters)



>NCBI__GCF_000969705.1:WP_169786887.1
          Length = 989

 Score =  129 bits (325), Expect = 3e-34
 Identities = 88/250 (35%), Positives = 131/250 (52%), Gaps = 22/250 (8%)

Query: 117 AKNNPKSNFVIVDSVIKDQKNVASATFADNESAYLAGVAAAKATKTNKIGFIGG-MQSDV 175
           A+ +P+++FV++DSV     NV  A FA++E ++L G AAA  + T +IGFIG  +   +
Sbjct: 735 AREHPETHFVVLDSVYDPHPNVTYARFAEHEGSFLVGAAAALTSATGRIGFIGAIVDLPI 794

Query: 176 ITRFEKGYEAGAKSVNPDIKVDVQYAGSFSDAA--KGKTIAA----AMYGAGDDVVYQCA 229
           + RF+ G+EAGA+ V PDI++D  Y     D++  +  T+AA    A+Y  G DVVY  A
Sbjct: 795 LWRFQAGFEAGARHVAPDIEIDSVYLTGHPDSSGFESPTLAAHAATALYRGGADVVYHAA 854

Query: 230 GGVGTGVFSEAKALNSTKNEADKVWVIGVDQDQ---------EYLGKYKSKDGKDSNFVL 280
           G  G G+F  A A   +  +A  +W IGVD D+           L  Y   D K    +L
Sbjct: 855 GHAGLGLFETAVA--ESGRQARHLWAIGVDADEYRNEHVYGGTKLWDYGPDDWKP--HLL 910

Query: 281 VSTIKEVGNVVKDIADKTKDGKFPGGTIVTYDLKNGGVNLGLDSA-NSEIKDAVAKAKAD 339
            S +K     V D     + G+   G + T+DL NGGV+          +   +   KAD
Sbjct: 911 TSMLKRFDRAVHDSIVDFRAGRLEAG-LRTFDLANGGVDYATSGGFIDHLVPQLENLKAD 969

Query: 340 IIDGKITVPS 349
           I+ G+I VP+
Sbjct: 970 IVAGRIEVPT 979


Lambda     K      H
   0.310    0.128    0.353 

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: 627
Number of extensions: 32
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: 350
Length of database: 989
Length adjustment: 36
Effective length of query: 314
Effective length of database: 953
Effective search space:   299242
Effective search space used:   299242
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 (21.8 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Apr 09 2024. 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