GapMind for catabolism of small carbon sources

 

Aligments for a candidate for SM_b21216 in Pseudomonas fluorescens FW300-N1B4

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate Pf1N1B4_5115 Maltose/maltodextrin transport ATP-binding protein MalK (EC 3.6.3.19)

Query= reanno::Smeli:SM_b21216
         (360 letters)



>lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_5115 Maltose/maltodextrin
           transport ATP-binding protein MalK (EC 3.6.3.19)
          Length = 381

 Score =  285 bits (728), Expect = 2e-81
 Identities = 159/353 (45%), Positives = 218/353 (61%), Gaps = 7/353 (1%)

Query: 4   LEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDILIG 63
           L++ N+ K+ G +  L+ + + + +GEF+V +G SGCGKSTLL +IAGL    GGD+LI 
Sbjct: 4   LKLDNVNKQLGGMRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICGGDLLID 63

Query: 64  ERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARLLQI 123
            R V  + P++R + MVFQSYALYP++SV  NI FGL++ +  +    + V  TA++LQ+
Sbjct: 64  GRRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTDKTSLRERVLKTAQILQL 123

Query: 124 ENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLHQML 183
           + LL RKP +LSGGQRQRVA+GRA+ R P + LFDEPLSNLDA LR++MR E+ RLH  L
Sbjct: 124 DKLLQRKPKELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLHDRL 183

Query: 184 RTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMNILD 243
            +T++YVTHDQ+EAMTLA +I V+  GR+EQ+ +P E+Y+RPA+ +VAGF+GSP MN L 
Sbjct: 184 GSTMIYVTHDQVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMNFLS 243

Query: 244 AEMTANG---LKIEGCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRLAAGSEAQRLTASV 300
           A +   G   L       +  LP   +  A AG  + +GIRPE + L A      +   V
Sbjct: 244 ARLQTPGETSLVDTLVWGITSLPFDSSNLA-AGTPLSLGIRPEHVSLKAADGTAGVV--V 300

Query: 301 EVVELTGPELVTTATVGSQRITACLPPRTAVGM-GSAHAFTFDGTALHLFDPE 352
             VE  G E       G      C    +A    G       D   LHLFD +
Sbjct: 301 TAVEYLGSETYVHLETGQDEPLICRCEVSAGWQAGDRVELLLDLDNLHLFDAD 353


Lambda     K      H
   0.320    0.136    0.385 

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: 369
Number of extensions: 13
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: 360
Length of database: 381
Length adjustment: 30
Effective length of query: 330
Effective length of database: 351
Effective search space:   115830
Effective search space used:   115830
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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