GapMind for catabolism of small carbon sources

 

Aligments for a candidate for AO353_03040 in Pseudomonas simiae WCS417

Align ABC transporter for L-Arginine and L-Citrulline, ATPase component (characterized)
to candidate GFF3439 PS417_17605 amino acid transporter

Query= reanno::pseudo3_N2E3:AO353_03040
         (254 letters)



>lcl|FitnessBrowser__WCS417:GFF3439 PS417_17605 amino acid
           transporter
          Length = 276

 Score =  318 bits (816), Expect = 6e-92
 Identities = 166/253 (65%), Positives = 202/253 (79%), Gaps = 3/253 (1%)

Query: 3   KLEVQDLHKRYGSHEVLKGVSLKAAAGDVISIIGSSGSGKSTFLRCINLLEQPHAGKILL 62
           KL+V+ +HKRYG HEVLKGVSL A  GDVIS+IG+SGSGKST LRCIN LEQP AG I L
Sbjct: 26  KLQVEGIHKRYGEHEVLKGVSLNARQGDVISLIGASGSGKSTMLRCINFLEQPDAGVITL 85

Query: 63  NNEELKLVANKDGALKAADPKQLQRMRSRLSMVFQHFNLWSHMTAMENIMEAPVHVLGMS 122
           +   +++   + G  +A    QLQ +R+RL+MVFQHFNLWSHMT +ENI  AP  VL +S
Sbjct: 86  DGISIEMRQGRAGT-RAPHQDQLQNLRTRLAMVFQHFNLWSHMTVLENITMAPRRVLDVS 144

Query: 123 KAEAREKAELYLAKVGVSHR-KDAYPGHMSGGEQQRVAIARALAMEPEVMLFDEPTSALD 181
            AEA ++A +YL KVG+  R  D YP  +SGG+QQRVAIARALAMEPE++LFDEPTSALD
Sbjct: 145 AAEAEKRARMYLDKVGLPSRVADQYPAFLSGGQQQRVAIARALAMEPEIILFDEPTSALD 204

Query: 182 PELVGDVLKVMQALAQEGRTMVVVTHEMGFAREVSNQLVFLHKGVVEESGNPREVLVNPQ 241
           PELVG+VLKV+Q LA+EGRTM++VTHEMGFAR+VS+Q++FLH+G VEE G+ R +L  P 
Sbjct: 205 PELVGEVLKVIQTLAEEGRTMLMVTHEMGFARQVSSQVLFLHQGRVEEHGDAR-ILDQPN 263

Query: 242 SERLQQFLSGSLK 254
           SERLQQFLS  LK
Sbjct: 264 SERLQQFLSNRLK 276


Lambda     K      H
   0.317    0.131    0.364 

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: 229
Number of extensions: 6
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: 254
Length of database: 276
Length adjustment: 25
Effective length of query: 229
Effective length of database: 251
Effective search space:    57479
Effective search space used:    57479
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 (21.7 bits)
S2: 47 (22.7 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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