GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglB in Cronobacter universalis NCTC 9529

Align D-galactose-binding periplasmic protein DGAL aka MglB aka B2150, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate WP_007699692.1 AFK65_RS13215 galactose/glucose ABC transporter substrate-binding protein MglB

Query= TCDB::P0AEE5
         (332 letters)



>NCBI__GCF_001277175.1:WP_007699692.1
          Length = 332

 Score =  611 bits (1575), Expect = e-180
 Identities = 308/332 (92%), Positives = 321/332 (96%), Gaps = 1/332 (0%)

Query: 1   MNKKVLTLSAVMASMLFGAAAHAADTRIGVTIYKYDDNFMSVVRKAIEQDAKAAPDVQLL 60
           MNKKVLTLSAVM+ MLFG AA AAD RIGVTIYKYDDNFMSVVRKAIE++A A+ DVQLL
Sbjct: 1   MNKKVLTLSAVMSCMLFGTAAQAAD-RIGVTIYKYDDNFMSVVRKAIEKEASASSDVQLL 59

Query: 61  MNDSQNDQSKQNDQIDVLLAKGVKALAINLVDPAAAGTVIEKARGQNVPVVFFNKEPSRK 120
           MNDSQNDQSKQNDQIDVLLAKGVK+LAINLVDPAAAGTVIEKARGQN+P+VFFNKEPSRK
Sbjct: 60  MNDSQNDQSKQNDQIDVLLAKGVKSLAINLVDPAAAGTVIEKARGQNIPIVFFNKEPSRK 119

Query: 121 ALDSYDKAYYVGTDSKESGIIQGDLIAKHWAANQGWDLNKDGQIQFVLLKGEPGHPDAEA 180
           ALDSYDKAYYVGTDSKESGIIQGDLIAKHW AN GWDLNKDGQIQ+VLLKGEPGHPDAEA
Sbjct: 120 ALDSYDKAYYVGTDSKESGIIQGDLIAKHWKANAGWDLNKDGQIQYVLLKGEPGHPDAEA 179

Query: 181 RTTYVIKELNDKGIKTEQLQLDTAMWDTAQAKDKMDAWLSGPNANKIEVVIANNDAMAMG 240
           RTTYVIKELNDKGIKT+QLQLDTAMWDTAQAKDKMDAWLSGPNANKIEVVIANNDAMAMG
Sbjct: 180 RTTYVIKELNDKGIKTQQLQLDTAMWDTAQAKDKMDAWLSGPNANKIEVVIANNDAMAMG 239

Query: 241 AVEALKAHNKSSIPVFGVDALPEALALVKSGALAGTVLNDANNQAKATFDLAKNLADGKG 300
           AVEALKAHNKSS+PVFGVDALPEALALVKSGALAGTVLNDANNQAKATFDLAKNLA GKG
Sbjct: 240 AVEALKAHNKSSVPVFGVDALPEALALVKSGALAGTVLNDANNQAKATFDLAKNLAAGKG 299

Query: 301 AADGTNWKIDNKVVRVPYVGVDKDNLAEFSKK 332
           AADGTNWKI+NKVVR+PYVGVDKDNLAE + K
Sbjct: 300 AADGTNWKIENKVVRIPYVGVDKDNLAEITSK 331


Lambda     K      H
   0.313    0.129    0.363 

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: 534
Number of extensions: 9
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: 332
Length of database: 332
Length adjustment: 28
Effective length of query: 304
Effective length of database: 304
Effective search space:    92416
Effective search space used:    92416
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