GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TT_C0328 in Marinomonas arctica 328

Align Glucose-binding protein aka TT_C0328, component of The glucose/mannose porter TTC0326-8 plus MalK1 (ABC protein, shared with 3.A.1.1.25) (characterized)
to candidate WP_111608605.1 DK187_RS17240 carbohydrate ABC transporter substrate-binding protein

Query= TCDB::Q72KX2
         (414 letters)



>NCBI__GCF_003259225.1:WP_111608605.1
          Length = 397

 Score =  150 bits (378), Expect = 8e-41
 Identities = 103/336 (30%), Positives = 155/336 (46%), Gaps = 13/336 (3%)

Query: 14  LSALAQGGKLEIFSWW-AGDEGPALEALIRLYKQKYPGVEVINATVTGGAGVNARAVLKT 72
           +SA  Q   LE+  WW +G E  A+  L   +  K    + ++  V    G NARA+   
Sbjct: 1   MSASVQAADLEVIHWWTSGGEQKAVTVLAEEFN-KLGNDKWVDTAVA--LGENARALTMQ 57

Query: 73  RMLGGDPPDTFQVHAGMELIGTWVVANRMEDLSALFRQEGWLQAF-PKGLIDLISYKGGI 131
           R+LGGD P   Q +   +     +    + DL+ +  +EGW     P  +++     GGI
Sbjct: 58  RILGGDAPGAAQFNTSRQF-EELIEEGLLLDLTPVAEKEGWTDFIRPSSILNPCMKDGGI 116

Query: 132 WSVPVNIHRSNVMWYLPAKLKEWGVNPPRTWDEFLATCQTLKQKGLEAPLAL-GENWTQQ 190
           + VPVNIH +  +W       E GV  P TW+EFL+    +++ G   PLA  G+ W ++
Sbjct: 117 YCVPVNIHSAQWLWTNKKVFAEVGVKEPNTWEEFLSVAPKIREAGY-IPLAFGGQGWQER 175

Query: 191 HLWESVALAVLGPDDWNNLWNGKLKFTDPKAV--RAWEVFGRVLDCANKDAAGLSWQQAV 248
           H+++ V + V     WN LW  K       A   + +E FG +    +  A G +W  A 
Sbjct: 176 HVFDVVLIGVTDEAFWNRLWKDKSVDAAGSAQMRKVFETFGALRQFTDAGAPGRNWNDAT 235

Query: 249 DRVVQGKAAFNVMGDWAAGYMTTTLKLKPGTDFAWAPSPGTQGVFMMLSDSFGLPKGAKN 308
           + V+ GKAA  VMGDWA G      K+    D+   P P  +    +  D+F  PK +  
Sbjct: 236 NMVITGKAAAQVMGDWARGEFAAADKVAE-VDYGCIPGPSKRPYLTLGGDAFIFPKSSDQ 294

Query: 309 RQNA--INWLRLVGSKEGQDTFNPLKGSIAARLDSD 342
              A  +    ++ S   Q  FN  KGS+  R D D
Sbjct: 295 NLEAAQMKLASMMLSPYIQAKFNNTKGSLPVRADVD 330


Lambda     K      H
   0.319    0.134    0.429 

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: 510
Number of extensions: 29
Number of successful extensions: 5
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: 414
Length of database: 397
Length adjustment: 31
Effective length of query: 383
Effective length of database: 366
Effective search space:   140178
Effective search space used:   140178
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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