GapMind for catabolism of small carbon sources

 

Aligments for a candidate for dctP in Pseudomonas stutzeri RCH2

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate GFF2613 Psest_2664 tripartite ATP-independent periplasmic transporter solute receptor, DctP family

Query= reanno::SB2B:6938088
         (339 letters)



>lcl|FitnessBrowser__psRCH2:GFF2613 Psest_2664 tripartite
           ATP-independent periplasmic transporter solute receptor,
           DctP family
          Length = 329

 Score =  337 bits (865), Expect = 2e-97
 Identities = 170/324 (52%), Positives = 224/324 (69%), Gaps = 2/324 (0%)

Query: 17  KASLLATVLGFSFGAV--AEPVEIKFSHVVAENTPKGQMALKFKELVESRLPGEYKVSVF 74
           K   LA  L FS   +  A+PV IKF+HVVA+NTPKGQ AL FK+L E RLPG+ KV V+
Sbjct: 5   KLKALACALSFSIAGLVHADPVTIKFAHVVADNTPKGQGALLFKKLAEERLPGKVKVEVY 64

Query: 75  PNSQLFGDNNELAALLLNDVQLVAPSLSKFERYTKKLQVFDLPFLFEDMDAVDRFQQSEA 134
           PNS LFGD  E+ ALLL DV ++APSL+KFE Y K +Q++DLPFLF+D+ A DRFQ    
Sbjct: 65  PNSSLFGDGKEMEALLLGDVHMLAPSLAKFEHYAKAIQIYDLPFLFDDLAAADRFQSGPQ 124

Query: 135 GQQLLNSMSRKGLVGLGYLHNGMKQFSANNALSLPGDAAGKKFRIMPSDVIAAQFEAVGA 194
           G+ LL +M  K + GL Y HNGMKQ SAN  L  P DA G KFR+  S V+  QF+AV A
Sbjct: 125 GKALLRAMEDKNITGLAYWHNGMKQLSANKPLREPKDARGLKFRVQASAVLDEQFKAVRA 184

Query: 195 IPVKKPFSEVFTLLQTRAIDGQENTWSNIYSKKFYEVQTHITESNHGVLDYMLVTSETFW 254
            P K  F+EV+  LQT  ++G ENTWSN  S+K +EVQ ++T S+HG++DYM++T+  FW
Sbjct: 185 NPRKMSFAEVYQGLQTGVVNGTENTWSNYESQKVHEVQPYMTASDHGLIDYMVITNTKFW 244

Query: 255 KSLPKDKREIIKQSMDEAVALGNKLALEKANEDRQLILDSKRVELVTLTPEQRQAWVNAM 314
             LP+D R  ++  M+E  A  N+ A +   + RQ I  S + E++ LTPEQR  W  AM
Sbjct: 245 NGLPEDLRGELETIMEEVTAEVNRQADDLNQQARQAIAASGKTEIIELTPEQRAQWREAM 304

Query: 315 RPVWSQFEDKIGKDLIEAAESANK 338
           +PVW +FE++IG +LIEAA++AN+
Sbjct: 305 KPVWKKFENEIGAELIEAAQAANR 328


Lambda     K      H
   0.316    0.132    0.368 

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: 300
Number of extensions: 8
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: 339
Length of database: 329
Length adjustment: 28
Effective length of query: 311
Effective length of database: 301
Effective search space:    93611
Effective search space used:    93611
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 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