GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PfGW456L13_1895 in Marinomonas arctica 328

Align ABC transporter for D-Galactose and D-Glucose, permease component 1 (characterized)
to candidate WP_111608577.1 DK187_RS17245 sugar ABC transporter permease

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1895
         (302 letters)



>NCBI__GCF_003259225.1:WP_111608577.1
          Length = 301

 Score =  249 bits (636), Expect = 6e-71
 Identities = 126/301 (41%), Positives = 194/301 (64%), Gaps = 3/301 (0%)

Query: 4   VAVFSKAS-PFDALQRWLPKLVLAPSMLIVLVGFYGYII-WTFILSFTNSSFMPSYKWVG 61
           +A  +K S P  A +  +  L+ +  M IV +G +   + ++ +LSFT S   P++ WVG
Sbjct: 1   MATSTKVSIPRRAKRVQISSLLASTPMAIVAIGVFVVCVGYSVMLSFTKSRLFPNFNWVG 60

Query: 62  LQQYMRLMDNDRWWVASKNLALFGGMFISISLVLGVFLAVLLDQRIRKEGFIRTVYLYPM 121
           L QY RL    RW V+ +NL ++G +FI + L+ G F+AV LDQ++R E   RT++LYP 
Sbjct: 61  LDQYERLWGTSRWVVSVENLLIYGILFIVLCLIAGFFMAVFLDQKVRFESGFRTLFLYPY 120

Query: 122 ALSMIVTGTAWKWLLNPGLGLDKMLRDWGWEGFRLDWLVDQDRVVYCLVIAAVWQASGFV 181
           A+S++VTG  W+W++ P LG+  +++  GW  F    LVD    +Y ++IAAVWQ+SG V
Sbjct: 121 AMSLVVTGLVWQWMMEPSLGIQNVVQRMGWSSFEFAPLVDPQYAIYGVLIAAVWQSSGLV 180

Query: 182 MAMFLAGLRGVDQSIIRAAQVDGASLPTIYLKIVLPSLRPVFFSAFMILAHIAIKSFDLV 241
           MA+ LAGLRG+D  I +AA+VDG      YL IVLP +RPV  ++ ++LA   ++ +DL+
Sbjct: 181 MALMLAGLRGIDGEIWKAARVDGIPTWQTYLFIVLPMMRPVMITSVVLLAVGVVRVYDLI 240

Query: 242 AAMTAGGPGYSSDLPAMFMYSFTFSRGQMGIGSASAMLMLGAVLTILVPYLYSE-LRGKR 300
            A T GGPG S+++PA F+     +RG +G+G A+A +ML  VL ++ P++Y E +R  +
Sbjct: 241 VAQTGGGPGMSTEMPAKFVIDHITARGNVGLGMAAATMMLLPVLLVIGPWIYREYVRPAK 300

Query: 301 H 301
           H
Sbjct: 301 H 301


Lambda     K      H
   0.329    0.141    0.448 

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: 326
Number of extensions: 17
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: 302
Length of database: 301
Length adjustment: 27
Effective length of query: 275
Effective length of database: 274
Effective search space:    75350
Effective search space used:    75350
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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