GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Pseudomonas stutzeri RCH2

Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate GFF857 Psest_0871 ABC-type sugar transport systems, ATPase components

Query= reanno::acidovorax_3H11:Ac3H11_792
         (358 letters)



>FitnessBrowser__psRCH2:GFF857
          Length = 371

 Score =  196 bits (499), Expect = 6e-55
 Identities = 117/323 (36%), Positives = 190/323 (58%), Gaps = 19/323 (5%)

Query: 1   MARISL-DLAHSYKPNPQQDSDYALLPLKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLV 59
           MA ++L D+  SY   P          + ++ EDG     +GPSGCGK+T+L +++GL  
Sbjct: 1   MASVTLRDICKSYDGTP------ITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLED 54

Query: 60  PSHGKVLFDGRDVTRASPQERNIAQVFQFPVIYDTMTVAENLAFPLRNRKVPEGQIKQRV 119
            + G +L D + V    P++R++  VFQ   +Y  MTVAEN+AF L+   V + +IK+RV
Sbjct: 55  ITSGDLLIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRV 114

Query: 120 GVIAEMLEMSGQLNQRAAGLAADAKQKISLGRGLVRADVAAVLFDEPLTVIDPHLKWQLR 179
             +AE+L++   L ++   L+   +Q++++GR +VR +    LFDEPL+ +D  L+ Q+R
Sbjct: 115 EAVAEILQLDKLLERKPKDLSGGQRQRVAIGRTMVR-EPKVFLFDEPLSNLDAFLRVQMR 173

Query: 180 RKLKQIHHELKLTLIYVTHDQVEALTFADQVVVMTRGKAVQVGSADALFERPAHTFVGHF 239
            ++ ++H  ++ T+IYVTHDQVEA+T AD++VV+  G+  QVG    L+  P + FV  F
Sbjct: 174 IEIARLHQRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGF 233

Query: 240 IGSPGMNFLPAH---RDGENLSV---AGHRLASPV-GRAL-PAGALQVGIRPEYLALAQP 291
           +GSP MNF+         E +++   +G+ L  PV G A+ P   L +GIRPE+  +  P
Sbjct: 234 LGSPQMNFVEVRAISASPETVTIELPSGYPLTLPVDGSAVSPGDPLTLGIRPEHFVM--P 291

Query: 292 QQAG-ALPGTVVQVQDIGTYQML 313
            +A     G +   + +G Y +L
Sbjct: 292 DEADFTFHGQITVAERLGQYNLL 314


Lambda     K      H
   0.320    0.136    0.395 

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: 297
Number of extensions: 15
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: 358
Length of database: 371
Length adjustment: 29
Effective length of query: 329
Effective length of database: 342
Effective search space:   112518
Effective search space used:   112518
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 (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