GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Stenotrophomonas chelatiphaga DSM 21508

Align LacK, component of Lactose porter (characterized)
to candidate WP_057508148.1 ABB28_RS08100 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= TCDB::Q01937
         (363 letters)



>NCBI__GCF_001431535.1:WP_057508148.1
          Length = 362

 Score =  326 bits (836), Expect = 5e-94
 Identities = 179/365 (49%), Positives = 241/365 (66%), Gaps = 8/365 (2%)

Query: 1   MAEVRLTDIRKSYGSLEV-IKGVNLEVSSGEFVVFVGPSGCGKSTLLRMIAGLEDISSGE 59
           MA+V+L  +RK Y + +V +K    EV+ GE +V VGPSGCGKSTLLRMIAGLE+IS G 
Sbjct: 1   MAKVQLQGVRKVYDNGQVAVKDATFEVADGELMVLVGPSGCGKSTLLRMIAGLEEISGGT 60

Query: 60  LTIGGTVMNDVDPSKRGIAMVFQTYALYPHMTVRENMGFALRFAGMAKDEIERRVNAAAK 119
           LTIG  V+NDV P  R IAMVFQ+YALYPHMTV EN+ F L+  G  K  I++R++ AA+
Sbjct: 61  LTIGERVVNDVAPKDRDIAMVFQSYALYPHMTVAENLAFGLKLRGHDKATIDKRISEAAQ 120

Query: 120 ILELDALMDRKPKALSGGQRQRVAIGRAIVRQPDVFLFDEPLSNLDAELRVHMRVEIARL 179
            L L  +MD+ PKA+SGGQRQRVA+GRA+VR+P VFL DEPLSNLDA+LR  +R EIA+L
Sbjct: 121 TLGLTDMMDKLPKAMSGGQRQRVALGRALVREPAVFLLDEPLSNLDAKLRHSVRTEIAQL 180

Query: 180 HKELNATIVYVTHDQVEAMTLADKIVVMRGGIVEQVGAPLALYDDPDNMFVAGFIGSPRM 239
           H++L  T++YVTHDQVEAMTL  +IVV++ G+++Q+  P+ LYD P N+FVAGF+GSP M
Sbjct: 181 HRKLGTTMIYVTHDQVEAMTLGQRIVVLKDGVIQQIDTPMELYDRPANLFVAGFLGSPAM 240

Query: 240 NFLPAVVIGQAEGGQVTVALKARPDTQLTVACATPPQGGDAVTVGVRPEHFLPAGSG-DT 298
           N L   +   A G  V+      P   L  A   P      + VGVRPEH  PA +G + 
Sbjct: 241 NVLRGTLQASASGVVVSDGDWKAP---LGHATIDPRWLDKPIAVGVRPEHLQPADAGAEW 297

Query: 299 QLTAHVDVVEHLGNTSYVYAHTVPGEQIIIEQEERRHGGRYGDEIAVGISAKTSFLFDA- 357
              A ++ +E +GN   ++ + V G+  +  +   R     G+ + + +       FDA 
Sbjct: 298 TFEARIEGIEPVGNE--IFVNLVSGQHALTMRVAPRALPAVGETLKLAVQPNALHFFDAE 355

Query: 358 SGRRI 362
           +G R+
Sbjct: 356 TGERL 360


Lambda     K      H
   0.320    0.137    0.390 

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: 351
Number of extensions: 7
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: 363
Length of database: 362
Length adjustment: 29
Effective length of query: 334
Effective length of database: 333
Effective search space:   111222
Effective search space used:   111222
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 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