GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Stutzerimonas stutzeri A1501

Align ABC transporter (characterized, see rationale)
to candidate WP_011913323.1 PST_RS11065 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:A0A166QFW2
         (381 letters)



>NCBI__GCF_000013785.1:WP_011913323.1
          Length = 371

 Score =  350 bits (898), Expect = e-101
 Identities = 189/366 (51%), Positives = 247/366 (67%), Gaps = 8/366 (2%)

Query: 1   MIKLKLDNVNKQLGGMRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICGGDL 60
           M  LK+ N+ K   G  I++ + L+I   EFVVFVGPSGCGKSTLLRLIAGL+ +  G +
Sbjct: 1   MADLKIHNLKKGFDGNEIIKGIDLDIRDREFVVFVGPSGCGKSTLLRLIAGLEEVSSGRI 60

Query: 61  LIDGRRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTDKTSLRERVLKTAQI 120
            +DGR + D+ P +R + MVFQ+YALYPHM+V  N+SF L LA  DK  +  ++   A+ 
Sbjct: 61  ELDGRDITDVSPAKRDLAMVFQTYALYPHMTVRKNMSFALDLAGADKQEVARKIEAAART 120

Query: 121 LQLDKLLQRKPKELSGGQRQRV----AMGRAMAREPDILLFDEPLSNLDASLRVQMRNEI 176
           L+L+ LL+RKP++LSGGQRQRV    A+GRA+ R P + LFDEPLSNLDA+LRVQMR E+
Sbjct: 121 LELEPLLERKPRQLSGGQRQRVAIGRAIGRAIVRNPKVFLFDEPLSNLDAALRVQMRLEL 180

Query: 177 ARLHDRLGSTMIYVTHDQVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGS 236
           +RLH  L +TMIYVTHDQVEAMTLADK+VVLNGGR+EQVGSP ELY  PA+ FVAGFLG+
Sbjct: 181 SRLHQELQATMIYVTHDQVEAMTLADKVVVLNGGRIEQVGSPMELYHHPANLFVAGFLGT 240

Query: 237 PRMNFLSARLQTPGETSLVDTLVWGI-TSLPFDSSNLAAGTPLSLGIRPEHVSLKAADGT 295
           P+M FL         +     L  G    LP   + L AG P++LGIRPEH++ + ++G 
Sbjct: 241 PKMGFLKGHASRVEASGCEVELDAGCRLFLPVSGATLKAGDPVTLGIRPEHLN-RGSEGN 299

Query: 296 AGVVVTA--VEYLGSETYVHLETGQDEPLICRCEVSAGWQAGDRVELLLDLDNLHLFDAD 353
             + V A   E LGS+TY H+ T   E L  R       + G+ + L L+  + HLFD+ 
Sbjct: 300 CQLTVKADVSERLGSDTYCHVVTRNGEQLTMRIRGDFTPRYGESLSLTLEAAHCHLFDSS 359

Query: 354 GVALSR 359
           G A+ +
Sbjct: 360 GQAVGQ 365


Lambda     K      H
   0.320    0.137    0.394 

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: 394
Number of extensions: 19
Number of successful extensions: 4
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: 381
Length of database: 371
Length adjustment: 30
Effective length of query: 351
Effective length of database: 341
Effective search space:   119691
Effective search space used:   119691
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 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